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micronodular pattern of random distribution&#44; &#8220;tree-in-bud&#8221; images&#44; along with apical subpleural blebs&#44; linear fibrotic lines and distortion of the normal bronchovascular architecture &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Flexible bronchoscopy presented inflammatory changes of the mucosa and mucopurulent sputum&#46; BAL&#44; in the context of infection&#44; showed a concordant neutrophilic cellular profile &#40;860&#44;000<span class="elsevierStyleHsp" style=""></span>total cells&#47;mL&#44; with 84&#37; neutrophils&#41;&#46; The cytopathological study was negative and microbiological workup allowed for the identification of C<span class="elsevierStyleItalic">orynebacterium species</span> and <span class="elsevierStyleItalic">Acinetobacter baumannii</span>&#46; Serum immunoglobulins were normal&#44; as were complement levels and serum angiotensin-converting enzyme titers&#46; There were positive anti-nuclear antibodies with positive anti-cytoskeleton fibers and anti-vimentin antibodies&#44; and negative anti-neutrophil cytoplasmic antibodies &#40;ANCAs&#41;&#46; His serological panel was negative for syphilis&#44; B and C hepatitis and Human Immunodeficiency virus &#40;HIV&#41;-1&#47;2 infection&#44; but presented high IgM and IgG titers for cytomegalovirus&#44; Epstein&#8211;Barr and herpes simplex virus-1&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">He underwent a multiple-lobe surgical lung biopsy&#44; which was suggestive of alveolar proteinosis with some fibrotic trace&#46; It revealed aspects of diffuse alveolar occupation by eosinophilic&#44; Periodic-Acid-Schiff positive proteinaceous material&#44; with a light macrophagic reaction&#44; together with abnormal lobular architecture&#44; diffuse septal fibrosis with focal collagen deposition and some multinucleate foreign body giant cells with cholesterol crystal clefts &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; There were no granulomas&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">By this time absent serum monocytes and low B and NK cell counts had been acknowledged&#46; Indeed&#44; severe monocytopenia had been ignored for years&#44; as had low B and NK cell blood counts on previous blood workup&#46; At this moment&#44; suspicion about a possible immunodeficiency syndrome associated with diffuse parenchymal lung disease was assessed&#46; A peripheral blood sample was studied by a detailed flow cytometry at a Histocompatibility Center Laboratory &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; It revealed an almost complete absence of monocytes &#40;CD14&#43;&#44; CD300E&#43;&#41;&#44; B cells &#40;CD19&#43;CD20&#43;&#41; and NK cells &#40;CD56&#43;&#44; CD3&#8722;&#41;&#46; Additionally&#44; there was no detectable myeloid or plasmacytoid population of dendritic cells &#8211; DCs &#8211; &#40;CD16&#43;&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">Bone marrow biopsy disclosed hypocellularity with megakaryocytic dysplasia and maturative abnormalities&#46; Marrow immunophenotyping revealed very scarce monocytes &#40;0&#46;4&#37;&#41;&#44; mainly consisting of immature forms &#40;promonocytes&#41;&#44; absence of CD34&#43; B cell precursors&#44; and scarce myeloid DCs and absent plasmacytoid DCs or CD34&#43; cells compromised with this lineage&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The patient fulfilled the diagnostic criteria for <span class="elsevierStyleItalic">Dendritic cell</span>&#44; <span class="elsevierStyleItalic">Monocyte</span>&#44; <span class="elsevierStyleItalic">B and NK Lymphoid Human Deficiency &#40;DCML&#41; Syndrome</span>&#44; as suggested by Bigley and Collin&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> He presented cutaneous epidermodysplasia with several in situ carcinomas&#59; mycobacterial infection &#8211; two episodes of PT&#59; severe blood monocytopenia&#44; B cell and NK cell deficiencies&#59; absolute blood DCs deficiency&#59; hypocelullar bone marrow with megakaryocytic dysplasia&#59; and normal immunoglobulins&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">DCML&#44; also known as &#8220;autosomic dominant and sporadic monocytopenia&#8221;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> or &#8220;MonoMAC&#8221;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a>&#44; is a novel immunodeficiency syndrome&#44; primarily described in 2010 by Vinh and colleagues&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> It results from one of several known GATA-2 mutations<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> determining a progressive and selective loss of bone-marrow multi-lymphoid progenitors &#8211; pluripotent cells that originate DC&#44; monocytes and lymphoid cells &#8211; and partial depletion of granulocyte-macrophage progenitors &#40;although sufficient to sustain granulopoiesis&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The associated deficit of DCs and the understanding of the immunoregulatory mechanisms were highlighted in 2011 by Bigley&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> DC depletion is associated with a marked increase in fms-like tyrosine-kinase ligand &#40;FLT3L&#41; and concomitant loss of regulatory T cells&#44; which can contribute to auto-immune phenomena&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6&#44;7</span></a> Remarkably&#44; despite the near absence of monocytes&#44; tecidual macrophages &#8211; like alveolar macrophages &#8211; are preserved but are probably functionally defective&#44; explaining the possible feature of PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> It has been suggested that tecidual macrophages may originate from local proliferation&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">This progressive form of bone marrow lymphoid failure&#44; at a given point in time&#44; assumes features of a distinct form of myelodysplasia<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> with composed deficiency of monocytes&#44; B&#44; NK and DCs subsets&#44; along with proneness to mycobacterial&#44; fungal and viral infections&#44; epidermodysplasia verruciformis and in situ carcinomas related to chronic HPV infection&#44; and the possible development of PAP in a significant number of patients&#46; Cases may be sporadic or of autosomal dominant heredity&#44; and tend to present in the third or fourth decades of life &#8211; although previous unnoticed monocytopenia might have been present several decades earlier along with an ill-defined history of unusual infections starting at an early age&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">Unlike monocytopenia&#44; NK and B cell deficiencies are generally not easily detected in regular blood counts due to the preservation of peripheral T cells&#46; Patients tend to present normocellular or hypocellular &#40;89&#37;&#41; marrows&#44; always with megakaryocyte dysplasia&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Severe perineal HPV infection from adolescence is a common feature&#44; progressing with variously diffuse epidermodysplasia verruciformis&#44; apparently as a result of the combined monocyte and NK cell deficiencies&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Weight loss and constitutional symptoms are frequently reported&#44;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> but the natural history is marked by prominent recurrent infections by mycobacteria&#44; aerobic bacteria and fungus&#46; Although not an universal finding&#44; mycobacterial infection is seen in the majority of patients<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> and possibly derives from defective phagocytosis resulting from GATA2 mutation&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> as well as from impairment of the IL-12&#47;INF-&#947; axis induced by the cellular deficiencies&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">In advanced disease&#44; progression to acute myeloblastic leukemia is frequent and autoimmune phenomena &#8211; lupus-like syndrome&#44; multiple sclerosis &#8211; may also occur in a fraction of patients&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Regarding the emergence of parenchymal lung disease in DCML&#44; PAP occurs in 33&#37; of patients &#40;36&#37; in sporadic and 29&#37; in autosomal-dominant patients&#41;&#44; with a median onset age of 42 years&#44; and without detectable anti granulocyte-macrophage colony-stimulating factor &#40;GM-CSF&#41; antibodies&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> The impossibility to perform anti-GM-CSF antibody testing at our Center is a limitation in this case report&#46; However&#44; as the patient fulfilled all the diagnostic criteria proposed by Bigley and Collin&#44; we can speculate that anti-GM-CSF antibodies would probably not be present in this case either&#44; according to what is reported on patients with DCML&#46;</p><p id="par0085" class="elsevierStylePara elsevierViewall">It apparently results from monocyte&#47;macrophage dysfunction<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> with metabolism and phagocytic impairment &#40;induced by GATA-2 mutations&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> although some believe that mycobacterial infection may play a pathogenetic role&#46; Therapeutic administration of GM-CSF does not seem to have a significant effect&#44; but whole-lung lavage may present moderate success&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">A remarkable aspect of this case is that the patient&#39;s diffuse parenchymal lung disease was histologically consistent with chronic PAP that evolved to fibrosis&#46; As already suggested by some authors&#44; established fibrotic burden probably results from the tecidual reaction to long-lasting subclinical proteinosis&#44; although it is possible that the history of recurrent bacterial and mycobacterial infections may have also contributed&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Generally&#44; PAP CT pattern is not strictly alveolar as many patients present a &#8220;mosaic attenuation pattern&#8221; with ground glass opacification&#44; or airspace consolidation&#44; over a background of thickened interlobular septae&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">11&#44;12</span></a> Moreover&#44; there are various reports of pulmonary fibrosis of various degrees associated with PAP&#44; sometimes diagnosed several years after disease onset&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10&#8211;17</span></a> In some cases the onset of PAP was clearly established prior to fibrosis&#44; using serial lung biopsies&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15&#44;17</span></a> A review by Holbert regarding CT findings in a small group of patients with PAP found substantial fibrosis in 2 cases&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Interestingly&#44; a recent paper from Ishii also found that a marked cystic and interstitial appearance might be particularly related to hereditary or secondary forms of PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> Thus&#44; a lung fibrotic pattern may be encountered in the context of chronic secondary PAP &#40;sometimes subclinical&#41;&#44; namely in the context of DMCL syndrome&#46;</p><p id="par0095" class="elsevierStylePara elsevierViewall">Regarding treatment options&#44; hematopoietic stem cell transplantation is seen as potentially curative for DMCL patients&#44; even for subjects with established respiratory failure&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;3</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">This entity should be considered as a possible etiology of unexplained persistent monocytopenia&#44; high susceptibility to opportunistic infections and simultaneous epidermodysplasia verruciformis&#44; with possible development of secondary PAP potentially progressing to fibrotic change&#46; Further characterization of DMCL syndrome&#44; studies addressing the pathogenetic mechanisms of interstitial fibrosis in patients with PAP and the different reactions of lung parenchyma in this disease will be important in the near future&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">At the time of this publication&#44; arrangements are being made to investigate the specific GATA-2 mutation involved in this patient&#46; Ideally&#44; genetic testing should always be accomplished in order to expand the knowledge of orphan diseases such as DCML&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Ethical disclosures</span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Protection of human and animal subjects</span><p id="par0110" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this study&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Confidentiality of data</span><p id="par0115" class="elsevierStylePara elsevierViewall">The authors declare that they have followed the protocols of their work center on the publication of patient data and that all the patients included in the study received sufficient information and gave their written informed consent to participate in the study&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Right to privacy and informed consent</span><p id="par0120" class="elsevierStylePara elsevierViewall">The authors have obtained the written informed consent of the patients or subjects mentioned in the article&#46; The corresponding author is in possession of this document&#46;</p></span></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Conflicts of interest</span><p id="par0125" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Case report of a male patient with a five-decade follow-up history in a tertiary care hospital distinguished for malabsorption syndrome&#44; failure-to-thrive&#44; meningitis and recurrent bacterial&#44; fungal and mycobacterial pulmonary infections&#46; Additionally&#44; he developed epidermodysplasia verruciformis&#44; several in situ spinocellular carcinomas and an uncharacteristic parenchymal lung disease&#46; Surgical lung biopsy suggested pulmonary alveolar proteinosis with fibrotic change&#46; Retrospectively&#44; severe monocytopenia had been overlooked in the past&#44; as well as low B and NK cell blood counts&#46; Flow cytometry confirmed the absence of the previous cell subsets along with an undetectable population of dendritic blood cells&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Dendritic cell&#44; monocyte&#44; B and NK lymphoid Human Deficiency Syndrome &#40;DCMLS&#41; is a novel rare immunodeficiency described in 2010&#44; linked to GATA-2 mutation&#46; This syndrome should be highlighted as a rare cause of acquired PAP&#44; with a radiological pattern encompassing potential fibrotic change&#46; Failure to recognize monocytopenia may impede the chance to diagnose&#46;</p></span>"
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        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Relato de um caso cl&#237;nico de um doente do sexo masculino com um historial de acompanhamento de cinco d&#233;cadas&#44; num hospital de cuidados terci&#225;rios&#44; caracterizado por um s&#237;ndrome de malabsor&#231;&#227;o&#44; insufici&#234;ncia de crescimento&#44; meningite e infec&#231;&#245;es pulmonares bacterianas&#44; f&#250;ngicas e micobacterianas recorrentes&#46; Al&#233;m disso&#44; desenvolveu epidermodisplasia verruciforme&#44; diversos carcinomas espinocelulares in situ e uma doen&#231;a pulmonar parenquimatosa n&#227;o definida&#46; Uma bi&#243;psia pulmonar cir&#250;rgica sugeriu uma Proteinose Alveolar Pulmonar com altera&#231;&#245;es fibr&#243;ticas&#46; Em retrospectiva&#44; uma monocitopenia grave negligenciada no passado&#44; bem como uma baixa contagem de c&#233;lulas B &#40;linf&#243;citos B&#41; e NK &#40;c&#233;lulas &#8216;natural killer&#8217;&#41;&#46; Uma citometria de fluxo confirmou a aus&#234;ncia dos subconjuntos de c&#233;lulas anteriores&#44; juntamente com uma popula&#231;&#227;o indetect&#225;vel de c&#233;lulas dendr&#237;ticas sangu&#237;neas&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">A S&#237;ndrome de Defici&#234;ncia Humana de c&#233;lulas dendr&#237;ticas&#44; mon&#243;citos&#44; linf&#243;ides B e NK &#233; uma rara imunodefici&#234;ncia descrita recentemente em 2010 e relacionada com a muta&#231;&#227;o do gene GATA-2&#46; Esta s&#237;ndrome dever&#225; ser referida como uma causa rara de PAP &#40;proteinose alveolar pulmonar&#41; adquirida&#44; com um padr&#227;o radiol&#243;gico que poder&#225; apresentar uma potencial altera&#231;&#227;o fibri&#243;tica&#46; A aus&#234;ncia de reconhecimento da monocitopenia pode impedir a oportunidade de chegar a este diagn&#243;stico&#46;</p></span>"
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          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Epidermodysplasia verruciformis on patient&#39;s hands&#44; trunk and head&#46;</p>"
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                      "titulo" => "Dendritic cell&#44; monocyte&#44; B and NK lymphoid deficiency defines the lost lineages of a new GATA-2 dependent myelodysplastic syndrome"
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                        0 => array:2 [
                          "etal" => false
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                      "doi" => "10.3324/haematol.2011.048355"
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                        "fecha" => "2011"
                        "volumen" => "96"
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                    0 => array:2 [
                      "titulo" => "The human syndrome of dendritic cell&#44; monocyte&#44; B and NK lymphoid deficiency"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "V&#46; Bigley"
                            1 => "M&#46; Haniffa"
                            2 => "S&#46; Doulatov"
                            3 => "X&#46;N&#46; Wang"
                            4 => "R&#46; Dickinson"
                            5 => "N&#46; McGovern"
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                    0 => array:2 [
                      "doi" => "10.1084/jem.20101459"
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                        "tituloSerie" => "J Exp Med"
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                        "volumen" => "208"
                        "paginaInicial" => "227"
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                    0 => array:2 [
                      "titulo" => "Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria&#44; fungi&#44; papillomaviruses&#44; and myelodysplasia"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "D&#46;C&#46; Vinh"
                            1 => "S&#46;Y&#46; Patel"
                            2 => "G&#46; Uzel"
                            3 => "V&#46;L&#46; Anderson"
                            4 => "A&#46;F&#46; Freeman"
                            5 => "K&#46;N&#46; Olivier"
                          ]
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                      ]
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Case report
A novel immunodeficiency syndrome as a rare cause of secondary pulmonary alveolar proteinosis: A diagnosis after 5 decades
Uma nova síndrome da imunodeficiência como causa rara de proteinose alveolar pulmonar: um diagnóstico após 5 décadas
Pedro G. Ferreiraa,
Corresponding author
p_goncalof@hotmail.com

Corresponding author.
, Lina Carvalhob, Fernanda Gamboaa
a Pulmonology Department, Coimbra Hospital and University Centre, Coimbra, Portugal
b Anatomopathology Department, Coimbra Hospital and University Centre, Coimbra, Portugal
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supervised by the Tuberculosis District Center&#46; In his forties he started presenting recurrent processes of bronchitis with isolation of <span class="elsevierStyleItalic">Haemophilus influenzae</span> and <span class="elsevierStyleItalic">Streptococcus pneumoniae</span>&#46; He also started dermatological consultations for epidermodysplasia verruciformis that gradually developed on his hands&#44; upper limbs&#44; torso&#44; and neck&#44; and severe perineal condylomas that were repeatedly treated with electrodessication and curettage &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Since then&#44; he has been diagnosed six times with in situ cutaneous spinocellular carcinoma&#46; His skin biopsies typically revealed dyskeratotic spinocellular carcinomas and &#8220;bowenoid papulosis&#8221; of a verruciform nature&#44; with abnormalities in the granulosa cell layer suggesting infection by human papillomavirus &#40;HPV&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">At the age of 47&#44; one of his admissions to the Pulmonology Department was for <span class="elsevierStyleItalic">Aspergillus fumigatus</span> lung infection &#40;the patient did not fulfill the criteria for allergic bronchopulmonary mycosis&#41;&#46; A complete investigation for cystic fibrosis was performed and&#44; after a borderline sweat test&#44; he showed normal spermogram and negative Cystic Fibrosis Transmembrane Conductance Regulator &#40;CFTR&#41; genotype mutation study&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Gradually&#44; he started developing parenchymal lung disease&#44; initially with reticulomicronodular pattern with upper lobe predominance on chest radiograph&#46; In his fifties&#44; computed tomography &#40;CT&#41; scan showed a septal thickening pattern with reticulation&#44; traction bronchiectasis and micronodulation&#46; Pulmonary function tests presented moderately severe restriction by spirometry &#40;<span class="elsevierStyleItalic">Tiffeneau</span> index of 0&#46;74&#44; Forced Vital Capacity 57&#46;2&#37;&#44; forced expiratory volume in one second 52&#46;8&#37;&#41;&#44; corrected to normal by plethysmographic lung volumes &#40;total lung capacity 80&#46;8&#37;&#44; residual volume 109&#46;2&#37;&#41;&#44; with a moderately affected diffusion capacity &#40;DLCO 54&#37;&#41;&#44; while maintaining satisfactory blood gas analysis at room air &#40;pO<span class="elsevierStyleInf">2</span> 80<span class="elsevierStyleHsp" style=""></span>mmHg&#44; pCO<span class="elsevierStyleInf">2</span> 41<span class="elsevierStyleHsp" style=""></span>mmHg&#44; SaO<span class="elsevierStyleInf">2</span> 96&#37;&#41;&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">At his last admission&#44; at the age of 61 years&#44; he presented a more pronounced diffuse interstitial reticulomicronodular pattern and progressive emaciation&#46; He complained of productive cough with high volume purulent sputum and worsened dyspnea &#40;grade III mMRC&#41;&#46; High-resolution chest CT showed a more profuse septal thickening&#44; micronodular pattern of random distribution&#44; &#8220;tree-in-bud&#8221; images&#44; along with apical subpleural blebs&#44; linear fibrotic lines and distortion of the normal bronchovascular architecture &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Flexible bronchoscopy presented inflammatory changes of the mucosa and mucopurulent sputum&#46; BAL&#44; in the context of infection&#44; showed a concordant neutrophilic cellular profile &#40;860&#44;000<span class="elsevierStyleHsp" style=""></span>total cells&#47;mL&#44; with 84&#37; neutrophils&#41;&#46; The cytopathological study was negative and microbiological workup allowed for the identification of C<span class="elsevierStyleItalic">orynebacterium species</span> and <span class="elsevierStyleItalic">Acinetobacter baumannii</span>&#46; Serum immunoglobulins were normal&#44; as were complement levels and serum angiotensin-converting enzyme titers&#46; There were positive anti-nuclear antibodies with positive anti-cytoskeleton fibers and anti-vimentin antibodies&#44; and negative anti-neutrophil cytoplasmic antibodies &#40;ANCAs&#41;&#46; His serological panel was negative for syphilis&#44; B and C hepatitis and Human Immunodeficiency virus &#40;HIV&#41;-1&#47;2 infection&#44; but presented high IgM and IgG titers for cytomegalovirus&#44; Epstein&#8211;Barr and herpes simplex virus-1&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">He underwent a multiple-lobe surgical lung biopsy&#44; which was suggestive of alveolar proteinosis with some fibrotic trace&#46; It revealed aspects of diffuse alveolar occupation by eosinophilic&#44; Periodic-Acid-Schiff positive proteinaceous material&#44; with a light macrophagic reaction&#44; together with abnormal lobular architecture&#44; diffuse septal fibrosis with focal collagen deposition and some multinucleate foreign body giant cells with cholesterol crystal clefts &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; There were no granulomas&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">By this time absent serum monocytes and low B and NK cell counts had been acknowledged&#46; Indeed&#44; severe monocytopenia had been ignored for years&#44; as had low B and NK cell blood counts on previous blood workup&#46; At this moment&#44; suspicion about a possible immunodeficiency syndrome associated with diffuse parenchymal lung disease was assessed&#46; A peripheral blood sample was studied by a detailed flow cytometry at a Histocompatibility Center Laboratory &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; It revealed an almost complete absence of monocytes &#40;CD14&#43;&#44; CD300E&#43;&#41;&#44; B cells &#40;CD19&#43;CD20&#43;&#41; and NK cells &#40;CD56&#43;&#44; CD3&#8722;&#41;&#46; Additionally&#44; there was no detectable myeloid or plasmacytoid population of dendritic cells &#8211; DCs &#8211; &#40;CD16&#43;&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">Bone marrow biopsy disclosed hypocellularity with megakaryocytic dysplasia and maturative abnormalities&#46; Marrow immunophenotyping revealed very scarce monocytes &#40;0&#46;4&#37;&#41;&#44; mainly consisting of immature forms &#40;promonocytes&#41;&#44; absence of CD34&#43; B cell precursors&#44; and scarce myeloid DCs and absent plasmacytoid DCs or CD34&#43; cells compromised with this lineage&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The patient fulfilled the diagnostic criteria for <span class="elsevierStyleItalic">Dendritic cell</span>&#44; <span class="elsevierStyleItalic">Monocyte</span>&#44; <span class="elsevierStyleItalic">B and NK Lymphoid Human Deficiency &#40;DCML&#41; Syndrome</span>&#44; as suggested by Bigley and Collin&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> He presented cutaneous epidermodysplasia with several in situ carcinomas&#59; mycobacterial infection &#8211; two episodes of PT&#59; severe blood monocytopenia&#44; B cell and NK cell deficiencies&#59; absolute blood DCs deficiency&#59; hypocelullar bone marrow with megakaryocytic dysplasia&#59; and normal immunoglobulins&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">DCML&#44; also known as &#8220;autosomic dominant and sporadic monocytopenia&#8221;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> or &#8220;MonoMAC&#8221;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a>&#44; is a novel immunodeficiency syndrome&#44; primarily described in 2010 by Vinh and colleagues&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> It results from one of several known GATA-2 mutations<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> determining a progressive and selective loss of bone-marrow multi-lymphoid progenitors &#8211; pluripotent cells that originate DC&#44; monocytes and lymphoid cells &#8211; and partial depletion of granulocyte-macrophage progenitors &#40;although sufficient to sustain granulopoiesis&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The associated deficit of DCs and the understanding of the immunoregulatory mechanisms were highlighted in 2011 by Bigley&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> DC depletion is associated with a marked increase in fms-like tyrosine-kinase ligand &#40;FLT3L&#41; and concomitant loss of regulatory T cells&#44; which can contribute to auto-immune phenomena&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6&#44;7</span></a> Remarkably&#44; despite the near absence of monocytes&#44; tecidual macrophages &#8211; like alveolar macrophages &#8211; are preserved but are probably functionally defective&#44; explaining the possible feature of PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> It has been suggested that tecidual macrophages may originate from local proliferation&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">This progressive form of bone marrow lymphoid failure&#44; at a given point in time&#44; assumes features of a distinct form of myelodysplasia<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> with composed deficiency of monocytes&#44; B&#44; NK and DCs subsets&#44; along with proneness to mycobacterial&#44; fungal and viral infections&#44; epidermodysplasia verruciformis and in situ carcinomas related to chronic HPV infection&#44; and the possible development of PAP in a significant number of patients&#46; Cases may be sporadic or of autosomal dominant heredity&#44; and tend to present in the third or fourth decades of life &#8211; although previous unnoticed monocytopenia might have been present several decades earlier along with an ill-defined history of unusual infections starting at an early age&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">Unlike monocytopenia&#44; NK and B cell deficiencies are generally not easily detected in regular blood counts due to the preservation of peripheral T cells&#46; Patients tend to present normocellular or hypocellular &#40;89&#37;&#41; marrows&#44; always with megakaryocyte dysplasia&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Severe perineal HPV infection from adolescence is a common feature&#44; progressing with variously diffuse epidermodysplasia verruciformis&#44; apparently as a result of the combined monocyte and NK cell deficiencies&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Weight loss and constitutional symptoms are frequently reported&#44;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> but the natural history is marked by prominent recurrent infections by mycobacteria&#44; aerobic bacteria and fungus&#46; Although not an universal finding&#44; mycobacterial infection is seen in the majority of patients<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> and possibly derives from defective phagocytosis resulting from GATA2 mutation&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> as well as from impairment of the IL-12&#47;INF-&#947; axis induced by the cellular deficiencies&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">In advanced disease&#44; progression to acute myeloblastic leukemia is frequent and autoimmune phenomena &#8211; lupus-like syndrome&#44; multiple sclerosis &#8211; may also occur in a fraction of patients&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Regarding the emergence of parenchymal lung disease in DCML&#44; PAP occurs in 33&#37; of patients &#40;36&#37; in sporadic and 29&#37; in autosomal-dominant patients&#41;&#44; with a median onset age of 42 years&#44; and without detectable anti granulocyte-macrophage colony-stimulating factor &#40;GM-CSF&#41; antibodies&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> The impossibility to perform anti-GM-CSF antibody testing at our Center is a limitation in this case report&#46; However&#44; as the patient fulfilled all the diagnostic criteria proposed by Bigley and Collin&#44; we can speculate that anti-GM-CSF antibodies would probably not be present in this case either&#44; according to what is reported on patients with DCML&#46;</p><p id="par0085" class="elsevierStylePara elsevierViewall">It apparently results from monocyte&#47;macrophage dysfunction<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> with metabolism and phagocytic impairment &#40;induced by GATA-2 mutations&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> although some believe that mycobacterial infection may play a pathogenetic role&#46; Therapeutic administration of GM-CSF does not seem to have a significant effect&#44; but whole-lung lavage may present moderate success&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">A remarkable aspect of this case is that the patient&#39;s diffuse parenchymal lung disease was histologically consistent with chronic PAP that evolved to fibrosis&#46; As already suggested by some authors&#44; established fibrotic burden probably results from the tecidual reaction to long-lasting subclinical proteinosis&#44; although it is possible that the history of recurrent bacterial and mycobacterial infections may have also contributed&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Generally&#44; PAP CT pattern is not strictly alveolar as many patients present a &#8220;mosaic attenuation pattern&#8221; with ground glass opacification&#44; or airspace consolidation&#44; over a background of thickened interlobular septae&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">11&#44;12</span></a> Moreover&#44; there are various reports of pulmonary fibrosis of various degrees associated with PAP&#44; sometimes diagnosed several years after disease onset&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10&#8211;17</span></a> In some cases the onset of PAP was clearly established prior to fibrosis&#44; using serial lung biopsies&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15&#44;17</span></a> A review by Holbert regarding CT findings in a small group of patients with PAP found substantial fibrosis in 2 cases&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Interestingly&#44; a recent paper from Ishii also found that a marked cystic and interstitial appearance might be particularly related to hereditary or secondary forms of PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> Thus&#44; a lung fibrotic pattern may be encountered in the context of chronic secondary PAP &#40;sometimes subclinical&#41;&#44; namely in the context of DMCL syndrome&#46;</p><p id="par0095" class="elsevierStylePara elsevierViewall">Regarding treatment options&#44; hematopoietic stem cell transplantation is seen as potentially curative for DMCL patients&#44; even for subjects with established respiratory failure&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;3</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">This entity should be considered as a possible etiology of unexplained persistent monocytopenia&#44; high susceptibility to opportunistic infections and simultaneous epidermodysplasia verruciformis&#44; with possible development of secondary PAP potentially progressing to fibrotic change&#46; Further characterization of DMCL syndrome&#44; studies addressing the pathogenetic mechanisms of interstitial fibrosis in patients with PAP and the different reactions of lung parenchyma in this disease will be important in the near future&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">At the time of this publication&#44; arrangements are being made to investigate the specific GATA-2 mutation involved in this patient&#46; Ideally&#44; genetic testing should always be accomplished in order to expand the knowledge of orphan diseases such as DCML&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Ethical disclosures</span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Protection of human and animal subjects</span><p id="par0110" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this study&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Confidentiality of data</span><p id="par0115" class="elsevierStylePara elsevierViewall">The authors declare that they have followed the protocols of their work center on the publication of patient data and that all the patients included in the study received sufficient information and gave their written informed consent to participate in the study&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Right to privacy and informed consent</span><p id="par0120" class="elsevierStylePara elsevierViewall">The authors have obtained the written informed consent of the patients or subjects mentioned in the article&#46; The corresponding author is in possession of this document&#46;</p></span></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Conflicts of interest</span><p id="par0125" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Case report of a male patient with a five-decade follow-up history in a tertiary care hospital distinguished for malabsorption syndrome&#44; failure-to-thrive&#44; meningitis and recurrent bacterial&#44; fungal and mycobacterial pulmonary infections&#46; Additionally&#44; he developed epidermodysplasia verruciformis&#44; several in situ spinocellular carcinomas and an uncharacteristic parenchymal lung disease&#46; Surgical lung biopsy suggested pulmonary alveolar proteinosis with fibrotic change&#46; Retrospectively&#44; severe monocytopenia had been overlooked in the past&#44; as well as low B and NK cell blood counts&#46; Flow cytometry confirmed the absence of the previous cell subsets along with an undetectable population of dendritic blood cells&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Dendritic cell&#44; monocyte&#44; B and NK lymphoid Human Deficiency Syndrome &#40;DCMLS&#41; is a novel rare immunodeficiency described in 2010&#44; linked to GATA-2 mutation&#46; This syndrome should be highlighted as a rare cause of acquired PAP&#44; with a radiological pattern encompassing potential fibrotic change&#46; Failure to recognize monocytopenia may impede the chance to diagnose&#46;</p></span>"
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        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Relato de um caso cl&#237;nico de um doente do sexo masculino com um historial de acompanhamento de cinco d&#233;cadas&#44; num hospital de cuidados terci&#225;rios&#44; caracterizado por um s&#237;ndrome de malabsor&#231;&#227;o&#44; insufici&#234;ncia de crescimento&#44; meningite e infec&#231;&#245;es pulmonares bacterianas&#44; f&#250;ngicas e micobacterianas recorrentes&#46; Al&#233;m disso&#44; desenvolveu epidermodisplasia verruciforme&#44; diversos carcinomas espinocelulares in situ e uma doen&#231;a pulmonar parenquimatosa n&#227;o definida&#46; Uma bi&#243;psia pulmonar cir&#250;rgica sugeriu uma Proteinose Alveolar Pulmonar com altera&#231;&#245;es fibr&#243;ticas&#46; Em retrospectiva&#44; uma monocitopenia grave negligenciada no passado&#44; bem como uma baixa contagem de c&#233;lulas B &#40;linf&#243;citos B&#41; e NK &#40;c&#233;lulas &#8216;natural killer&#8217;&#41;&#46; Uma citometria de fluxo confirmou a aus&#234;ncia dos subconjuntos de c&#233;lulas anteriores&#44; juntamente com uma popula&#231;&#227;o indetect&#225;vel de c&#233;lulas dendr&#237;ticas sangu&#237;neas&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">A S&#237;ndrome de Defici&#234;ncia Humana de c&#233;lulas dendr&#237;ticas&#44; mon&#243;citos&#44; linf&#243;ides B e NK &#233; uma rara imunodefici&#234;ncia descrita recentemente em 2010 e relacionada com a muta&#231;&#227;o do gene GATA-2&#46; Esta s&#237;ndrome dever&#225; ser referida como uma causa rara de PAP &#40;proteinose alveolar pulmonar&#41; adquirida&#44; com um padr&#227;o radiol&#243;gico que poder&#225; apresentar uma potencial altera&#231;&#227;o fibri&#243;tica&#46; A aus&#234;ncia de reconhecimento da monocitopenia pode impedir a oportunidade de chegar a este diagn&#243;stico&#46;</p></span>"
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          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Epidermodysplasia verruciformis on patient&#39;s hands&#44; trunk and head&#46;</p>"
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                      "titulo" => "Dendritic cell&#44; monocyte&#44; B and NK lymphoid deficiency defines the lost lineages of a new GATA-2 dependent myelodysplastic syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:2 [
                            0 => "V&#46; Bigley"
                            1 => "M&#46; Collin"
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                      "doi" => "10.3324/haematol.2011.048355"
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                        "tituloSerie" => "Haematologica"
                        "fecha" => "2011"
                        "volumen" => "96"
                        "paginaInicial" => "1081"
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                0 => array:2 [
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                    0 => array:2 [
                      "titulo" => "The human syndrome of dendritic cell&#44; monocyte&#44; B and NK lymphoid deficiency"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "V&#46; Bigley"
                            1 => "M&#46; Haniffa"
                            2 => "S&#46; Doulatov"
                            3 => "X&#46;N&#46; Wang"
                            4 => "R&#46; Dickinson"
                            5 => "N&#46; McGovern"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1084/jem.20101459"
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                        "tituloSerie" => "J Exp Med"
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                        "volumen" => "208"
                        "paginaInicial" => "227"
                        "paginaFinal" => "234"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/21242295"
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                ]
              ]
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              "identificador" => "bib0015"
              "etiqueta" => "3"
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                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria&#44; fungi&#44; papillomaviruses&#44; and myelodysplasia"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "D&#46;C&#46; Vinh"
                            1 => "S&#46;Y&#46; Patel"
                            2 => "G&#46; Uzel"
                            3 => "V&#46;L&#46; Anderson"
                            4 => "A&#46;F&#46; Freeman"
                            5 => "K&#46;N&#46; Olivier"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1182/blood-2009-03-208629"
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "2010"
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                        "link" => array:1 [
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/20040766"
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                ]
              ]
            ]
            3 => array:3 [
              "identificador" => "bib0020"
              "etiqueta" => "4"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome&#58; diagnostic features and clinical implications"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "Calvo K&#46;R&#46;"
                            1 => "D&#46;C&#46; Vinh"
                            2 => "I&#46; Maric"
                            3 => "W&#46; Wang"
                            4 => "P&#46; Noel"
                            5 => "M&#46; Stetler-Stevenson"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.3324/haematol.2011.041152"
                      "Revista" => array:6 [
                        "tituloSerie" => "Haematologica"
                        "fecha" => "2011"
                        "volumen" => "96"
                        "paginaInicial" => "1221"
                        "paginaFinal" => "1225"
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/21508125"
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              "etiqueta" => "5"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection &#40;MonoMAC&#41; syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
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Pulmonology

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