Department of Pathology, Massachusetts General Hospital, 55 Fruit St, Boston, MA 02114, USA.
Arch Pathol Lab Med. 2012 Jun;136(6):618-22. doi: 10.5858/arpa.2011-0214-OA.
Hepatotoxicity is an important side effect of thiopurine analog treatment for inflammatory bowel disease. A variety of histopathologic findings have been observed in patients with inflammatory bowel disease with thiopurine-induced hepatotoxicity, including nodular regenerative hyperplasia, vascular injury, and cholestasis.
To describe the histologic features shared by 3 cases of thiopurine-induced hepatotoxicity in patients with inflammatory bowel disease.
We identified 3 patients with inflammatory bowel disease who developed hepatotoxicity due to 6-mercaptopurine from the educational files of the Department of Pathology at Massachusetts General Hospital (Boston). Histology slides (stained with hematoxylin-eosin, trichrome, periodic-acid Schiff with diastase digestion, and iron stains) and patients' medical records were reviewed retrospectively.
All 3 patients were receiving 6-mercaptopurine monotherapy at therapeutic doses, had normal thiopurine metabolite levels, and presented with elevated aminotransferase levels. Biopsies from all 3 cases exhibited a pattern of centrilobular hepatocyte injury characterized by ceroid-laden macrophages, hepatocyte anisonucleosis, and increased lipofuscin pigment, as well as centrilobular steatosis. Aminotransferase levels trended downward and either normalized or remained at borderline elevated levels after 6-mercaptopurine dose was reduced (in 1 patient) or discontinued (in 2 patients).
Recognition of a pattern of centrilobular injury enables pathologists to suggest thiopurine-induced liver injury as the cause of elevated aminotransferases in patients with inflammatory bowel disease.
硫嘌呤类似物治疗炎症性肠病会引起肝毒性,这是一个重要的副作用。在硫嘌呤诱导的炎症性肠病肝毒性患者中观察到多种组织病理学发现,包括结节性再生性增生、血管损伤和胆汁淤积。
描述 3 例炎症性肠病患者因硫嘌呤引起的肝毒性的组织学特征。
我们从马萨诸塞州总医院(波士顿)病理学系的教学档案中确定了 3 例因 6-巯基嘌呤而发生炎症性肠病肝毒性的患者。回顾性分析组织学切片(苏木精-伊红、三色、过碘酸希夫染色伴消化酶和铁染色)和患者病历。
所有 3 例患者均接受 6-巯基嘌呤单药治疗,剂量为治疗剂量,硫嘌呤代谢物水平正常,且出现氨基转移酶水平升高。3 例活检均表现为中央小叶肝细胞损伤模式,特征为含类脂褐素的巨噬细胞、肝细胞异型核和脂褐素色素增加,以及中央小叶脂肪变性。氨基转移酶水平下降,在降低 6-巯基嘌呤剂量(1 例)或停药(2 例)后,要么正常化,要么保持在边缘升高水平。
认识到中央小叶损伤的模式可以使病理学家提示炎症性肠病患者的氨基转移酶升高是由硫嘌呤引起的肝损伤所致。