Geller Stephen A, Dubinsky Marla C, Poordad F Fred, Vasiliauskas Eric A, Cohen Arthur H, Abreu Maria T, Tran Tram, Martin Paul, Vierling John M, Targan Stephan R
Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Am J Surg Pathol. 2004 Sep;28(9):1204-11. doi: 10.1097/01.pas.0000128665.12063.97.
6-Thioguanine (6-TG) has been used as an alternative thiopurine for inflammatory bowel disease (IBD) patients not responsive to or intolerant of azathioprine (AZA) and 6-mercaptopurine (6-MP). 6-TG-related hepatotoxicity, including liver biochemistry value elevations, sinusoidal collagen deposition on electron microscopy, and veno-occlusive disease, have been described related to its use as therapy for neoplastic disease.
We studied 38 liver biopsies from patients treated with 6-TG, almost all of whom (n = 125) received 6-TG for 1 to 3 years at the Inflammatory Bowel Disease Center at Cedars-Sinai Medical Center. All biopsies were fixed in 4% buffered formalin and prepared in the usual manner. Hematoxylin and eosin, Masson's trichrome (trichrome), and reticulin silver impregnation (reticulin) stained slides were studied. In 23 cases, tissue was also prospectively fixed in glutaraldehyde and processed for electron microscopy.
In 20 of the 37 patients studied (53%), nodular regeneration of varying degree was seen with reticulin. In only 4 of these 20 instances (11% of the total) were the changes seen with hematoxylin and eosin and in 3 of the 4, only in retrospect after studying the reticulin preparation. Minimal fibrosis was seen with trichrome in only 13 biopsies (34%), but sinusoidal collagen deposition was observed in 14 of the 23 cases studied with electron microscopy (60%). The biopsy from the 1 patient with nodular hyperplasia obvious with hematoxylin and eosin also demonstrated changes of venous outflow obstruction.
6-TG-treated IBD patients are at significant risk for nodular hyperplasia, early fibrosis and, less often, venous outflow disease (Budd-Chiari). The natural history of these changes is unknown and follow-up biopsies are needed to determine histologic and clinical sequela. Patients not demonstrating nodular hyperplasia or fibrosis who continue with 6-TG because there are no better therapeutic choices should be periodically rebiopsied.
6-硫鸟嘌呤(6-TG)已被用作对硫唑嘌呤(AZA)和6-巯基嘌呤(6-MP)无反应或不耐受的炎症性肠病(IBD)患者的替代硫嘌呤类药物。与6-TG相关的肝毒性,包括肝生化值升高、电子显微镜下的窦性胶原沉积和肝静脉闭塞病,已被描述与其用于肿瘤疾病治疗有关。
我们研究了38例接受6-TG治疗患者的肝活检标本,几乎所有患者(n = 125)在雪松西奈医疗中心炎症性肠病中心接受了1至3年的6-TG治疗。所有活检标本均用4%缓冲福尔马林固定,并按常规方法制备。研究了苏木精和伊红染色、马松三色染色(三色染色)和网状纤维银浸染(网状纤维)染色的玻片。在23例病例中,组织也前瞻性地用戊二醛固定并进行电子显微镜检查。
在37例研究患者中的20例(53%),网状纤维染色可见不同程度的结节状再生。在这20例中,只有4例(占总数的11%)在苏木精和伊红染色中可见变化,其中3例仅在研究网状纤维标本后回顾性发现。三色染色仅在13例活检标本(34%)中可见轻度纤维化,但在23例接受电子显微镜检查的病例中有14例(60%)观察到窦性胶原沉积。1例苏木精和伊红染色显示明显结节性增生的患者的活检标本也显示出静脉流出道梗阻的变化。
接受6-TG治疗的IBD患者有发生结节性增生、早期纤维化的显著风险,较少发生静脉流出道疾病(布加综合征)。这些变化的自然病程尚不清楚,需要进行随访活检以确定组织学和临床后遗症。对于因没有更好的治疗选择而继续使用6-TG且未表现出结节性增生或纤维化的患者,应定期重新进行活检。