Granulomatous liver disease in Thailand: a 20-year retrospective clinicoradiopathological analysis.

IF 3.3 Q2 GASTROENTEROLOGY & HEPATOLOGY
Siwanon Nawalerspanya, Apichat Kaewdech, Naichaya Chamroonkul, Pimsiri Sripongpun
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Abstract

Objective: Granulomatous liver disease (GLD) is a rare condition with various aetiologies and is characterised by the formation of hepatic granulomas. A comprehensive evaluation of GLD from a broad perspective is lacking. We aimed to investigate the aetiology and the clinicoradiopathological characteristics of patients with GLD in recent decades in Thailand.

Methods: This retrospective study was conducted at a tertiary care centre in Thailand. All patients who underwent liver biopsy between 2003 and 2023 were reviewed. Patients with a histopathological report of granulomas in liver specimens were included. Clinical presentations, radiological data, and laboratory data closest to the procedure date were also collected.

Results: Of the 4384 liver biopsy specimens collected during the study period, 89 (2%) had GLD. Of these, 58.4% were men, with the following aetiologies: 61 (68.5%) infectious, 16 (18%) non-infectious, and 12 (13.5%) undetermined. Common presentations included abnormal liver test results (81.4%) and fever (56.1%). Among infectious granulomas, mycobacterial infections (tuberculosis: 28; non-tuberculous mycobacteria (NTM): 11) were predominant. Compared with other causes, NTM was associated with a significantly lower body mass index, more extragastrointestinal involvement, and lower serum albumin levels. Caseating-type granulomas were also observed in 16% of non-mycobacterial cases. Nearly 40% of patients with GLD demonstrated no focal lesions on liver imaging, whereas multifocal lesions were found in a third of patients.

Conclusions: Infectious causes, especially mycobacterial infections, remain the primary aetiology of GLD in Thailand. Granuloma types are not pathognomonic of specific diseases, emphasising the need for extensive evaluation beyond liver biopsy to determine the underlying aetiology.

泰国肉芽肿性肝病:20年回顾性临床放射病理学分析
目的:肉芽肿性肝病(GLD)是一种病因多样的罕见疾病,以肝脏肉芽肿的形成为特征。缺乏从宏观角度对GLD的综合评价。我们的目的是调查近几十年来泰国GLD患者的病因和临床放射病理学特征。方法:本回顾性研究在泰国三级保健中心进行。回顾了2003年至2023年间所有接受肝活检的患者。包括肝标本肉芽肿组织病理学报告的患者。临床表现、放射学数据和最接近手术日期的实验室数据也被收集。结果:在研究期间收集的4384例肝活检标本中,89例(2%)发生GLD。其中,58.4%为男性,其病因如下:感染性61例(68.5%),非感染性16例(18%),未确定的12例(13.5%)。常见表现为肝脏检查结果异常(81.4%)和发热(56.1%)。在感染性肉芽肿中,分枝杆菌感染(结核:28;非结核分枝杆菌(NTM): 11个。与其他原因相比,NTM与明显较低的体重指数、更多的胃肠外受累和较低的血清白蛋白水平相关。在16%的非分枝杆菌病例中也观察到干酪样型肉芽肿。近40%的GLD患者在肝脏影像学上未发现局灶性病变,而三分之一的患者发现多灶性病变。结论:感染原因,尤其是分枝杆菌感染,仍然是泰国GLD的主要病因。肉芽肿类型不是特定疾病的病理特征,强调需要在肝活检之外进行广泛的评估以确定潜在的病因。
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来源期刊
BMJ Open Gastroenterology
BMJ Open Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.90
自引率
3.20%
发文量
68
审稿时长
2 weeks
期刊介绍: BMJ Open Gastroenterology is an online-only, peer-reviewed, open access gastroenterology journal, dedicated to publishing high-quality medical research from all disciplines and therapeutic areas of gastroenterology. It is the open access companion journal of Gut and is co-owned by the British Society of Gastroenterology. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around continuous publication, publishing research online as soon as the article is ready.
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