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长期使用雄激素类固醇治疗再生障碍性贫血并伴有家族性腺瘤性息肉病导致的多发性肝腺瘤。

Multiple hepatic adenomas caused by long-term administration of androgenic steroids for aplastic anemia in association with familial adenomatous polyposis.

作者信息

Nakao A, Sakagami K, Nakata Y, Komazawa K, Amimoto T, Nakashima K, Isozaki H, Takakura N, Tanaka N

机构信息

Department of Surgery, Shobara Red Cross Hospital, Japan.

出版信息

J Gastroenterol. 2000;35(7):557-62. doi: 10.1007/s005350070081.

Abstract

We report a rare case of hepatic adenomas (HA), in a 20-year-old Japanese girl treated for 6 years with anabolic androgens for aplastic anemia. In a review of the world literature using computer MEDLINE search, we found only 17 cases of androgen-induced HA published between 1975 and 1998 in the English-language literature. The patient was referred to us because of liver lesions detected during a follow-up examination for familial adenomatous polyposis. After being diagnosed with aplastic anemia at 14 years of age, she had been treated with oxymetholone (30 mg/day) for 6 years. Laboratory evaluation revealed normal liver function. Ultrasonography (US) and computed tomography (CT) demonstrated multiple liver lesions. Histopathological examinations of biopsied specimens from the liver tumor showed HA. After the patient was diagnosed with HA, oxymetholone was tapered off. Patients taking androgenic-anabolic steroids should be carefully monitored with US and CT and tumor markers should be measured. This report may be helpful in identifying the population who is at risk of developing hepatic sex hormone-related tumors.

摘要

我们报告了一例罕见的肝腺瘤(HA)病例,患者为一名20岁的日本女孩,因再生障碍性贫血接受合成代谢雄激素治疗6年。通过计算机检索MEDLINE数据库查阅世界文献,我们发现1975年至1998年期间英文文献中仅报道了17例雄激素诱导的HA。该患者因在家族性腺瘤性息肉病的随访检查中发现肝脏病变而转诊至我们科室。她14岁时被诊断为再生障碍性贫血,接受羟甲烯龙(30毫克/天)治疗6年。实验室检查显示肝功能正常。超声检查(US)和计算机断层扫描(CT)显示肝脏有多个病变。对肝肿瘤活检标本进行的组织病理学检查显示为HA。患者被诊断为HA后,逐渐减少羟甲烯龙的用量。服用雄激素合成代谢类固醇的患者应通过US和CT进行仔细监测,并检测肿瘤标志物。本报告可能有助于识别有发生肝脏性激素相关肿瘤风险的人群。

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