关键词: EBV-associated polymorphic B-cell lymphoproliferative disorder HIV-associated CD8+ T-cell skin infiltrative disease antiretroviral therapy erythroderma

Mesh : Humans Male Adult CD8-Positive T-Lymphocytes / immunology Epstein-Barr Virus Infections / complications immunology drug therapy Lymphoproliferative Disorders / drug therapy immunology diagnosis Acquired Immunodeficiency Syndrome / drug therapy complications immunology Herpesvirus 4, Human / immunology HIV Infections / drug therapy complications immunology Treatment Outcome Antiretroviral Therapy, Highly Active B-Lymphocytes / immunology

来  源:   DOI:10.2169/internalmedicine.2687-23   PDF(Pubmed)

Abstract:
Human immunodeficiency virus (HIV)-associated CD8+ T-cell skin infiltrative disease with severe erythroderma has rarely been reported. While HIV-positive patients are prone to develop lymphoma, which is often associated with Epstein-Barr virus, polymorphic lymphoproliferative disorder is rare, accounting for <5% of cases. We herein report a 41-year-old HIV-positive man who presented with a fever, erythroderma, and lymphadenopathy and was diagnosed with the coexistence of both diseases. His condition improved significantly with continued antiretroviral therapy. This case suggests that HIV-induced immunodeficiency is central to the pathogenesis of both entities and that improvement of the immunodeficient state is an effective treatment.
摘要:
人类免疫缺陷病毒(HIV)相关的CD8T细胞皮肤浸润性疾病伴严重红皮病的报道很少。虽然HIV阳性患者容易患上淋巴瘤,通常与爱泼斯坦-巴尔病毒有关,多形性淋巴增生性疾病是罕见的,占病例的5%。我们在此报告一名41岁的HIV阳性男子,他出现了发烧,红皮病,和淋巴结病,并被诊断为两种疾病并存。通过持续的抗逆转录病毒治疗,他的病情明显改善。这种情况表明,HIV诱导的免疫缺陷对两种实体的发病机理至关重要,并且改善免疫缺陷状态是有效的治疗方法。
公众号