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一名出现肝功能障碍和肝紫癜的患者的恶性组织细胞增多症。

Malignant histiocytosis in a patient presenting with hepatic dysfunction and peliosis hepatis.

作者信息

Fine K D, Solano M, Polter D E, Tillery G W

机构信息

Department of Internal Medicine, Baylor University Medical Center, Dallas, Texas.

出版信息

Am J Gastroenterol. 1995 Mar;90(3):485-8.

PMID:7872292
Abstract

In this article, we report the case of a 36-yr-old patient presenting with manifestations of portal hypertension, hepatic dysfunction, and fever who proved to have peliosis hepatis on liver biopsy. A thorough work-up revealed no obvious etiology. At autopsy, malignant histiocytosis of the liver and bone marrow was diagnosed. This case represents the first report of the association of peliosis hepatis with this rare histiocytic neoplasm and exemplifies the need for persistence in the search for malignancy, particularly hematological malignancy, in the patient with unexplained peliosis. The clinical similarity of peliosis hepatis associated with hematological malignancy and bacillary peliosis is also discussed.

摘要

在本文中,我们报告了一例36岁患者,其表现为门静脉高压、肝功能不全和发热,肝脏活检证实为肝紫癜病。全面检查未发现明显病因。尸检时,诊断为肝脏和骨髓恶性组织细胞增多症。该病例是肝紫癜病与这种罕见组织细胞肿瘤关联的首例报告,例证了对于不明原因肝紫癜病患者持续排查恶性肿瘤,尤其是血液系统恶性肿瘤的必要性。文中还讨论了与血液系统恶性肿瘤相关的肝紫癜病和杆菌性紫癜在临床上的相似性。

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