Brucellosis as a rare cause of granulomatous hepatitis with hepatic and bone marrow granulomas: A case report.

IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Hepatology Forum Pub Date : 2021-09-15 eCollection Date: 2021-09-01 DOI:10.14744/hf.2021.2021.0038
Kendal Yalcin, Elif Tugba Tuncel, Feyzullah Ucmak, Remzi Bestas
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引用次数: 1

Abstract

Brucellosis is a zoonotic infection that may involve the liver in a variety of ways, however, data on the histopathology of liver effects in brucellosis are limited. Brucellosis is generally characterized by a high fever, joint or back pain, and hepatosplenomegaly. This report illustrates a case of granulomatous hepatitis with granulomas in the liver and bone marrow in a patient who presented with non-specific symptoms, hepatomegaly, splenomegaly, digital clubbing, and laboratory signs of intrahepatic cholestasis. Granulomas were detected in the bone marrow and hepatic specimens. The diagnosis of brucellosis was based on the isolation of Brucella mellitensis in a blood culture and serum agglutination titers of 1:640. Treatment for brucellosis led to improved laboratory and clinical findings. Brucellosis should be considered in regions where it is endemic in cases of an elevated transaminase level and related clinical findings. Brucellosis should also be considered in the differential diagnosis of intrahepatic cholestasis and/or granulomas in hepatic and bone marrow biopsies. This case report provides valuable histopathological features and detailed information of liver involvement in a case of brucellosis.

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布鲁氏菌病是肉芽肿性肝炎合并肝和骨髓肉芽肿的罕见病因:1例报告。
布鲁氏菌病是一种人畜共患感染,可能以多种方式累及肝脏,然而,关于布鲁氏菌病对肝脏影响的组织病理学数据有限。布鲁氏菌病的一般特征是高烧、关节或背部疼痛以及肝脾肿大。本报告报告一例肉芽肿性肝炎,伴有肝脏和骨髓肉芽肿,患者表现为非特异性症状,肝肿大,脾肿大,手指棒状和肝内胆汁淤积的实验室体征。骨髓及肝脏标本均可见肉芽肿。布鲁氏菌病的诊断是基于在血液培养中分离到梅利特布鲁氏菌和血清凝集滴度为1:640。对布鲁氏菌病的治疗改善了实验室和临床结果。在出现转氨酶水平升高和相关临床表现的布鲁氏菌病流行地区,应考虑考虑布鲁氏菌病。在肝内胆汁淤积和/或肉芽肿的肝和骨髓活检鉴别诊断中也应考虑布鲁氏菌病。本病例报告提供了有价值的组织病理学特征和肝脏受累的详细信息的情况下,布鲁氏菌病。
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CiteScore
1.90
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12.50%
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