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特发性胆汁淤积作为霍奇金淋巴瘤的一种副肿瘤现象

Idiopathic cholestasis as a paraneoplastic phenomenon in Hodgkin's lymphoma.

作者信息

Barta Stefan K, Yahalom Joachim, Shia Jinru, Hamlin Paul A

机构信息

Department of Medicine, St. Luke's Roosevelt Hospital Center, New York, NY, USA.

出版信息

Clin Lymphoma Myeloma. 2006 Jul;7(1):77-82. doi: 10.3816/CLM.2006.n.044.

Abstract

Paraneoplastic cholestasis is an uncommon presenting symptom in Hodgkin's lymphoma (HL). Two distinct entities causing this clinical picture have been described: idiopathic cholestasis and vanishing bile duct syndrome (VBDS). We report a patient with idiopathic cholestasis and early-stage HL with favorable risk factors whose liver biopsy results were consistent with intrahepatic cholestasis and no ductopenia. Other causes for cholestatic jaundice were ruled out. He was treated with subtotal lymphoid irradiation and subsequently experienced a steady improvement in his liver function tests to near normal over 21 months. This case illustrates a rare paraneoplastic phenomenon, and a review of the available literature is included. We also discuss the differences between HL-related idiopathic cholestasis and VBDS. The distinction between these 2 diseases has prognostic implications: idiopathic cholestasis is usually reversible in early-stage HL after treatment, whereas patients who develop VBDS commonly die from their disease. There is no established approach to the management of paraneoplastic cholestasis. We postulate that single-modality radiation therapy alone should be considered a valid treatment alternative in early-stage HL with idiopathic cholestasis.

摘要

副肿瘤性胆汁淤积是霍奇金淋巴瘤(HL)中一种不常见的临床表现。已经描述了导致这种临床表现的两种不同情况:特发性胆汁淤积和消失性胆管综合征(VBDS)。我们报告了一名患有特发性胆汁淤积和早期HL且具有有利风险因素的患者,其肝活检结果与肝内胆汁淤积一致且无胆管减少。排除了胆汁淤积性黄疸的其他病因。他接受了次全淋巴照射治疗,随后在21个月内肝功能检查稳步改善至接近正常。本病例说明了一种罕见的副肿瘤现象,并对现有文献进行了综述。我们还讨论了HL相关的特发性胆汁淤积和VBDS之间的差异。这两种疾病的区分具有预后意义:特发性胆汁淤积在早期HL治疗后通常是可逆的,而发生VBDS的患者通常死于该疾病。目前尚无处理副肿瘤性胆汁淤积的既定方法。我们推测,对于患有特发性胆汁淤积的早期HL,单纯采用单模态放射治疗应被视为一种有效的治疗选择。

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