Sharma Rakesh M, Sinha Sanjay, Kishan Hari B, De Padua Michelle
Department of Urological Oncology, Basavatarakam Indo-American Cancer Institute and Research Centre, Hyderabad, Telangana, India.
Department of Urology, Apollo Hospitals, Hyderabad, Telangana, India.
BMJ Case Rep. 2018 Jan 23;2018:bcr-2017-223117. doi: 10.1136/bcr-2017-223117.
A 40-year-old normotensive woman presented with abnormal facial hair for 4 years and amenorrhoea for 13 years. Hormonal, biochemical and haematological evaluation showed isolated elevation of serum testosterone and free testosterone. Her follicle-stimulating hormone and luteinising hormone were in the premenopausal range. Until recently she had reconciled to early 'menopause' and visited beauty clinics but never sought medical evaluation. Imaging revealed an enhancing left adrenal mass with fat densities and venous thrombus extending through the inferior vena cava to a 7 cm mass in the right atrium. She underwent left kidney-preserving surgery utilising hypothermic cardiopulmonary bypass with early clamping of the pulmonary artery without circulatory arrest. Histology showed adrenocortical carcinoma with composite incidental myelolipoma and neoplastic thrombus. At 2 months, testosterone has normalised and she is doing well. Isolated testosterone-secreting adrenocortical carcinoma with massive venous thrombus is rare as is coincidental composite macroscopic myelolipoma.
一名40岁血压正常的女性,面部毛发异常4年,闭经13年。激素、生化和血液学检查显示血清睾酮和游离睾酮单独升高。她的促卵泡生成素和促黄体生成素处于绝经前范围。直到最近,她一直以为自己是过早“绝经”,并去过美容诊所,但从未寻求过医学评估。影像学检查发现左侧肾上腺有一强化肿块,伴有脂肪密度,静脉血栓延伸至下腔静脉并形成右心房内一个7厘米的肿块。她接受了保留左肾的手术,采用低温体外循环,早期夹闭肺动脉,未进行循环阻断。组织学检查显示为肾上腺皮质癌,合并偶然发现的髓样脂肪瘤和肿瘤性血栓。术后2个月,睾酮已恢复正常,她情况良好。孤立性分泌睾酮的肾上腺皮质癌伴大量静脉血栓罕见,巧合的复合性大体髓样脂肪瘤也很罕见。