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病例报告:长期口服司坦唑醇导致肝细胞腺瘤。

Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration.

作者信息

Qin Ya-Nan, Tao Chang-Ming, Guo Tian-Tian, Liu Jing-Jing, Luan Wei-Chang, Liu Chun-Hua

机构信息

Department of Infectious Diseases, Liaocheng People's Hospital, Liaocheng, China.

Imaging Department, Liaocheng People's Hospital, Liaocheng, China.

出版信息

Front Med (Lausanne). 2025 Aug 20;12:1654316. doi: 10.3389/fmed.2025.1654316. eCollection 2025.

DOI:10.3389/fmed.2025.1654316
PMID:40909442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12404949/
Abstract

This article presents a case of a 15-year-old male with a 6-year history of aplastic anemia treated with long-term oral stanozolol to promote hematopoiesis. Throughout this period, he underwent regular outpatient follow-up assessments of blood and liver function parameters. While abnormal liver function was recorded on several occasions and treated with oral hepatoprotective drugs, no abdominal imaging test was conducted. On this occasion, the patient was admitted to hospital with abdominal pain. Abdominal imaging revealed a liver tumor of undetermined nature. A diagnosis of -catenin-activated hepatocellular adenoma was subsequently confirmed via hepatic perforation biopsy. Considering the high bleeding risk, transcatheter hepatic artery embolization was performed as a preventative measure. Stanozolol was discontinued immediately after diagnosis and replaced with platelet-boosting therapy using romiplostim. A repeat abdominal CT scan performed 4 months after discontinuation of the drug showed a significant reduction in lesion size, which continued to be closely monitored. Hepatocellular adenoma is a rare clinical scenario. This case, supported by complete data and gold-standard pathologic diagnosis, provided valuable insights, suggesting that patients on long-term androgen therapy with aplastic anemia constituted a high-risk group for hepatocellular adenoma, and highlighted the need to optimize management strategies.

摘要

本文介绍了一例15岁男性再生障碍性贫血患者的病例,该患者长期口服司坦唑醇以促进造血,病程长达6年。在此期间,他定期在门诊进行血液和肝功能参数的随访评估。虽然多次记录到肝功能异常并使用口服保肝药物进行治疗,但未进行腹部影像学检查。此次,患者因腹痛入院。腹部影像学检查发现一个性质不明的肝脏肿瘤。随后通过肝穿刺活检确诊为β-连环蛋白激活型肝细胞腺瘤。考虑到出血风险高,作为预防措施进行了经导管肝动脉栓塞术。诊断后立即停用司坦唑醇,改用罗米司亭进行升血小板治疗。停药4个月后进行的重复腹部CT扫描显示病灶大小显著缩小,此后继续密切监测。肝细胞腺瘤是一种罕见的临床情况。该病例有完整的数据和金标准病理诊断支持,提供了有价值的见解,表明再生障碍性贫血长期接受雄激素治疗的患者是肝细胞腺瘤的高危人群,并强调了优化管理策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b84/12404949/e63147c70ad2/fmed-12-1654316-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b84/12404949/b2a7df625edc/fmed-12-1654316-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b84/12404949/e63147c70ad2/fmed-12-1654316-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b84/12404949/b2a7df625edc/fmed-12-1654316-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b84/12404949/e63147c70ad2/fmed-12-1654316-g002.jpg

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