Fiel M I, Shukla D, Saraf N, Xu R, Schiano T D
The Lillian and Henry M. Stratton-Hans Popper Department of Pathology, The Mount Sinai Medical Center, New York, New York 10029, USA.
Transpl Infect Dis. 2008 Jun;10(3):184-9. doi: 10.1111/j.1399-3062.2007.00258.x. Epub 2007 Oct 1.
Infrequently, hepatitis C (HCV) appears to be the cause of hepatic granulomas. Interferon therapy for HCV has been increasingly associated with the development of sarcoidosis.
We sought to determine the incidence of hepatic granulomas in patients with recurrent HCV post liver transplantation (LT).
Between 1994 and 2005, 820 patients were transplanted for HCV at our institution. The pathology database was searched for patients having recurrent HCV and granulomas. At Mount Sinai Medical Center, protocol biopsies have been performed for the last 2 years in patients receiving pegylated interferon-alpha2b and ribavirin (PEG) for recurrent HCV. Review of slides from explanted livers, pre- and post-perfusion biopsies, and all allograft biopsies were evaluated. Lipogranulomas were excluded because of their frequent association with steatosis.
A total of 10,225 liver biopsies were performed on HCV patients, and 25 (0.24%) showed non-caseating epithelioid granulomas. Hepatic granulomas were detected in 14 post-LT HCV patients; 9 patients received PEG. Typically, only 1 lobular granuloma was found. None of these patients had granulomas in the native liver or in any biopsy before interferon therapy; 6/9 patients had undetectable HCV-RNA levels, and 4 had sustained viral response. No other cause for granuloma formation was identified in the 6 patients.
Hepatic granulomas are infrequently found in HCV liver biopsies and rarely found in post-LT biopsies with recurrent HCV. When present, they occur more commonly in patients receiving and virologically responding to PEG therapy. The presence of granulomas in patients with HCV being treated with PEG may not warrant an extensive etiologic work-up for granulomatous hepatitis unless otherwise clinically indicated.
丙型肝炎病毒(HCV)很少会引发肝肉芽肿。针对HCV的干扰素疗法与结节病的发生越来越相关。
我们试图确定肝移植(LT)后复发性HCV患者肝肉芽肿的发生率。
1994年至2005年间,我们机构有820例患者因HCV接受移植。在病理数据库中搜索复发性HCV和肉芽肿患者。在西奈山医学中心,过去两年对接受聚乙二醇化干扰素-α2b和利巴韦林(PEG)治疗复发性HCV的患者进行了方案活检。对移植肝、灌注前和灌注后活检以及所有同种异体移植活检的切片进行评估。脂肪肉芽肿因其常与脂肪变性相关而被排除。
对HCV患者共进行了10225次肝活检,其中25例(0.24%)显示非干酪样上皮样肉芽肿。在14例LT后HCV患者中检测到肝肉芽肿;9例患者接受了PEG治疗。通常,仅发现1个小叶肉芽肿。这些患者在干扰素治疗前的原肝或任何活检中均未发现肉芽肿;9例患者中有6例HCV-RNA水平检测不到,4例有持续病毒应答。6例患者未发现其他肉芽肿形成原因。
肝肉芽肿在HCV肝活检中很少见,在LT后复发性HCV活检中也很少见。如果存在,它们更常见于接受PEG治疗且病毒学应答的患者中。接受PEG治疗的HCV患者出现肉芽肿,除非有其他临床指征,否则可能无需对肉芽肿性肝炎进行广泛的病因检查。