一名被诊断为晚发型联合免疫缺陷症患者的严重胃肠道巨细胞病毒感染

Georgina Sauqué Pintos, Arnau Antolí Gil, Gemma Rocamora Blanch, Renzo Avila Espinoza, Rosario Taco Sánchez, Núria Sabé Fernández, X. Solanich Moreno
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引用次数: 0

摘要

晚发型联合免疫缺陷症(LOCID)是普通可变免疫缺陷症(CVID)的一种罕见变异型,通常影响那些出现机会性感染(OI)和/或 CD4+ T 淋巴细胞低下的成年患者。由于这种病症的罕见性,诊断延误很常见,从而增加了发病率和死亡率。我们报告了一名 66 岁男性患者的病例,他出现了严重的胃肠道巨细胞病毒(CMV)感染,抗病毒治疗和抗巨细胞病毒特异性人免疫球蛋白治疗均无效,最终因未确诊的 LOCID 而死亡。
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Severe gastrointestinal cytomegalovirus infection in a patient diagnosed with late onset combined immunodeficiency
Late onset combined immunodeficiency (LOCID) is a rare variant of common variable immunodeficiency (CVID), typically affecting adult patients who present with opportunistic infections (OI) and/or low CD4+ T lymphocytes. Diagnostic delay is common due to the rareness of this entity, increasing morbidity and mortality. We report on a 66-year-old male who developed a severe gastrointestinal cytomegalovirus (CMV) infection, refractory to antiviral treatment and anti-cytomegalovirus specific human immunoglobulin administration, with a fatal outcome due to an undiagnosed LOCID.
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