| Literature DB >> 29589251 |
Keizo Kato1,2, Hiroshi Abe3, Noriko Hanawa3, Junya Fukuzawa4, Ryota Matsuo4, Takeshi Yonezawa3, Sadahiro Itoh3, Yoshiyuki Sato3, Makiko Ika3, Shohei Shimizu3, Shinji Endo3, Hiroshi Hano5, Asami Izu6, Masahiko Sugitani6, Akihito Tsubota7.
Abstract
A 32-year-old Japanese woman was admitted to our hospital for the diagnosis and treatment of multiple liver tumors. She had been receiving 125 mg testosterone enanthate every 2 weeks following female-to-male gender identity disorder (GID) diagnosis at 20 years of age. Ultrasonography, computed tomography, and magnetic resonance imaging showed 11 hepatic nodular tumors with a maximum diameter of 28 mm. Liver tumors with hepatocellular adenoma (HCA) were diagnosed with needle biopsy. Segmentectomy of the left lateral lobe including two lesions, subsegmentectomy of S6 including two lesions, enucleation of each tumor in S5 and S7, and open surgical radiofrequency ablation for each tumor in S4 and S7 were performed. Immunohistochemical specimens showed that the tumor cells were diffusely and strongly positive for glutamine synthetase and that the nuclei were ectopically positive for β-catenin. Thus, the tumors were diagnosed as β-catenin-activated HCA (b-HCA). Transcatheter arterial chemoembolization plus subsequent radiofrequency ablation was performed for the 3 residual lesions in S4 and S8. Although testosterone enanthate was being continued for GID, no recurrence was observed until at least 22 months after the intensive treatments. HCA development in such patients receiving testosterone should be closely monitored using image inspection.Entities:
Keywords: Gender identity disorder; Testosterone; β-Catenin-activated hepatocellular adenoma
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Year: 2018 PMID: 29589251 DOI: 10.1007/s12328-018-0854-4
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265