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

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 func...

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Main Authors: Ya-Nan Qin, Chang-Ming Tao, Tian-Tian Guo, Jing-Jing Liu, Wei-Chang Luan, Chun-Hua Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Medicine
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Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2025.1654316/full
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author Ya-Nan Qin
Chang-Ming Tao
Tian-Tian Guo
Jing-Jing Liu
Wei-Chang Luan
Chun-Hua Liu
author_facet Ya-Nan Qin
Chang-Ming Tao
Tian-Tian Guo
Jing-Jing Liu
Wei-Chang Luan
Chun-Hua Liu
author_sort Ya-Nan Qin
collection DOAJ
description 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 β-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.
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publishDate 2025-08-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Medicine
spelling doaj-art-5a85ba02fb784e24b9ec8de2c02008d12025-08-20T04:14:18ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2025-08-011210.3389/fmed.2025.16543161654316Case Report: Hepatocellular adenoma due to long-term oral stanozolol administrationYa-Nan Qin0Chang-Ming Tao1Tian-Tian Guo2Jing-Jing Liu3Wei-Chang Luan4Chun-Hua Liu5Department of Infectious Diseases, Liaocheng People's Hospital, Liaocheng, ChinaDepartment of Infectious Diseases, Liaocheng People's Hospital, Liaocheng, ChinaImaging Department, Liaocheng People's Hospital, Liaocheng, ChinaDepartment of Infectious Diseases, Liaocheng People's Hospital, Liaocheng, ChinaEmergency Department, Liaocheng People's Hospital, Liaocheng, ChinaDepartment of Infectious Diseases, Liaocheng People's Hospital, Liaocheng, ChinaThis 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 β-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.https://www.frontiersin.org/articles/10.3389/fmed.2025.1654316/fullaplastic anemiastanozololandrogenscase reporthepatocellular adenoma
spellingShingle Ya-Nan Qin
Chang-Ming Tao
Tian-Tian Guo
Jing-Jing Liu
Wei-Chang Luan
Chun-Hua Liu
Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration
Frontiers in Medicine
aplastic anemia
stanozolol
androgens
case report
hepatocellular adenoma
title Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration
title_full Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration
title_fullStr Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration
title_full_unstemmed Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration
title_short Case Report: Hepatocellular adenoma due to long-term oral stanozolol administration
title_sort case report hepatocellular adenoma due to long term oral stanozolol administration
topic aplastic anemia
stanozolol
androgens
case report
hepatocellular adenoma
url https://www.frontiersin.org/articles/10.3389/fmed.2025.1654316/full
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