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J Pediatr Hematol Oncol ; 46(2): e191-e194, 2024 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-38277621

RESUMO

X-linked inhibitor of apoptosis protein (XIAP) deficiency is an inborn error of immunity (IEI). Allogeneic hematopoietic cell transplantation (HCT) is currently the only curative therapy available for XIAP deficiency. Granulomatous and lymphocytic interstitial lung disease (GLILD) is a common immune-related lung complication of IEIs. We present a 6-year-old boy with XIAP deficiency and GLILD. Computed tomography showed lung nodes but no symptoms. Before HCT, GLILD was not managed with immunosuppressive therapy, because he was asymptomatic. The HCT procedure was subsequently performed. The post-HCT course was uneventful; follow-up computed tomography on day 46 showed nodules had disappeared. HCT could potentially ameliorate GLILD like other inflammatory processes associated with the underlying IEIs.


Assuntos
Imunodeficiência de Variável Comum , Doenças Genéticas Ligadas ao Cromossomo X , Transplante de Células-Tronco Hematopoéticas , Doenças Pulmonares Intersticiais , Transtornos Linfoproliferativos , Masculino , Humanos , Criança , Proteínas Inibidoras de Apoptose Ligadas ao Cromossomo X/genética , Doenças Pulmonares Intersticiais/etiologia , Doenças Pulmonares Intersticiais/terapia , Transtornos Linfoproliferativos/terapia , Transtornos Linfoproliferativos/complicações , Transplante de Células-Tronco Hematopoéticas/métodos , Imunodeficiência de Variável Comum/complicações
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