Suppr超能文献

[以肝脏疾病表现的霍奇金病。两例报告(作者译)]

[Hodgkin's disease presenting as an hepatic disease. Report of two cases (author's transl)].

作者信息

Urbano-Márquez A, Grau Junyent J M, Sala M, Estruch R, Bruguera M, Rozman C

出版信息

Med Clin (Barc). 1981 Mar 25;76(6):255-8.

PMID:7253732
Abstract

During the course of Hodgkin's disease there is a low incidence of clinical manifestations of liver involvement: less than 15% of the patients present jaundice at some time during the evolution of their disease. The initial manifestation of Hodgkin's disease as an hepatic illness is a rare event. Two such cases are herein reported. The first patient was a 68 year-old male with a febrile illness of one month duration who 15 days before admission presented painless jaundice, dark urine, and discolored stools. The clinical work-up pointed to the possible existence of an extrahepatic cholestasis. At laparotomy a normal biliary tree was found, and surgical liver biopsy disclosed severe tissue cholestasis and a granulomatous portal reaction constituted by white blood cells, eosinophiles and histiocytes, most of them atypical and some showing features of Reed-Sternberg cells. The second patient was a 21 year-old male with a febrile illness of four months duration who developed jaundice and progressive mental obtundation one week before admission. The biochemical studies demonstrated severe pancytopenia and signs of advanced liver failure. Percutaneous liver biopsy disclosed a normal hepatic architecture and the presence of numerous atypical histiocytes in the portal areas. Lymphography showed sizeable pelvic and paraaortic lymph nodes. Subsequent laparotomy for lymph node biopsy confirmed the diagnosis of Hodgkin's disease, nodular sclerosis type. The authors suggest that hepatic Hodgkin's disease must be considered in the differential diagnosis of any febrile illness with jaundice.

摘要

在霍奇金病病程中,肝脏受累的临床表现发生率较低:在疾病进展过程中,不到15%的患者会出现黄疸。霍奇金病最初表现为肝脏疾病是罕见事件。本文报告两例这样的病例。首例患者为68岁男性,发热病程1个月,入院前15天出现无痛性黄疸、深色尿和大便变色。临床检查提示可能存在肝外胆汁淤积。剖腹手术时发现胆道树正常,手术肝活检显示严重的组织胆汁淤积以及由白细胞、嗜酸性粒细胞和组织细胞构成的肉芽肿性门脉反应,其中大多数细胞不典型,部分呈现里德-斯腾伯格细胞特征。第二例患者为21岁男性,发热病程4个月,入院前1周出现黄疸并进行性精神迟钝。生化检查显示严重全血细胞减少和晚期肝功能衰竭迹象。经皮肝活检显示肝结构正常,门脉区存在大量非典型组织细胞。淋巴管造影显示盆腔和腹主动脉旁有肿大淋巴结。随后的剖腹手术进行淋巴结活检确诊为结节硬化型霍奇金病。作者建议,在对任何伴有黄疸的发热性疾病进行鉴别诊断时,必须考虑肝脏霍奇金病。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验