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一名感染人类免疫缺陷病毒且患有卡波西肉瘤的患者的卡斯特曼病。

Castleman disease in an HIV-infected patient with Kaposi sarcoma.

作者信息

Saif M W

机构信息

Division of Hematology/Oncology, University of Alabama at Birmingham, Wallace Tumor Institute, USA.

出版信息

AIDS Read. 2001 Nov;11(11):572-6.

Abstract

Multicentric Castleman disease (MCD) is a heterogeneous lymphoproliferative disorder, characterized by systemic symptoms, generalized lymphadenopathy, hepatosplenomegaly, proteinuria, and rash. The clinical course is variable and may range from indolent to aggressive, fulminating in a rapidly fatal illness. Mortality is usually from infective complications and less commonly from malignancies, such as lymphoma or Kaposi sarcoma. The association of concurrent or preceding Castleman disease with Kaposi sarcoma is well documented. Castleman disease developed in a 51-year-old patient with AIDS about 10 months after diagnosis of Kaposi sarcoma. MCD was found to be associated with human herpesvirus 8/Kaposi sarcoma-associated herpesvirus.

摘要

多中心Castleman病(MCD)是一种异质性淋巴增殖性疾病,其特征为全身症状、全身性淋巴结肿大、肝脾肿大、蛋白尿和皮疹。临床病程多变,可从惰性发展为侵袭性,迅速恶化为快速致命性疾病。死亡率通常源于感染性并发症,较少源于恶性肿瘤,如淋巴瘤或卡波西肉瘤。Castleman病与卡波西肉瘤同时发生或先于卡波西肉瘤出现的关联已有充分记录。一名51岁的艾滋病患者在诊断为卡波西肉瘤约10个月后患上了Castleman病。发现MCD与人类疱疹病毒8/卡波西肉瘤相关疱疹病毒有关。

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