He Ying, Gao Yu-Tao, Sun Li
Department of Gynecological Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen 518116, Guangdong Province, China.
Department of Gynecological Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
World J Clin Cases. 2023 Feb 26;11(6):1341-1348. doi: 10.12998/wjcc.v11.i6.1341.
Functioning gonadotroph adenomas are extremely rare pituitary tumors that secrete gonadotropins and exhibit distinct clinical manifestations. Here, we report a case of functioning gonadotroph adenoma in a reproductive-aged woman and discuss its diagnosis and management.
A 21-year-old female patient with abdominal pain, irregular menstruation, hyperestrogenemia, and an ovarian mass was included. Brain magnetic resonance imaging (MRI) revealed a pituitary macroadenoma, and transsphenoidal surgery relieved her clinical symptoms. Before transsphenoidal surgery, plasma CA125, estradiol levels were elevated, while prolactin, luteinizing hormone, follicle-stimulating hormone, PROG, cortisol, FT4, thyroid-stimulating hormone, parathyroid hormone, and GH levels were maintained at normal levels. After transsphenoidal surgery, the patient was diagnosed with a functioning gonadotroph adenoma. During follow-up, pelvic ultrasound confirmed normal-sized ovaries in the patient, the menstrual cycle returned to regular, and her hormones were maintained within a normal range. There was no evidence of tumor recurrence after two years of follow-up.
Early diagnosis of functioning gonadotroph adenomas should be considered in patients with hyperestrogenism, irregular menstruation, large or recurrent ovarian cysts, and visual field defects. Pituitary MRI should be performed, and transsphenoidal surgery is recommended for the management of this disease.
促性腺激素分泌型垂体腺瘤是极为罕见的垂体肿瘤,可分泌促性腺激素并表现出独特的临床表现。在此,我们报告一例育龄期女性促性腺激素分泌型垂体腺瘤病例,并讨论其诊断与治疗。
纳入一名21岁女性患者,其有腹痛、月经不规律、高雌激素血症及卵巢肿物。脑部磁共振成像(MRI)显示垂体大腺瘤,经蝶窦手术缓解了她的临床症状。经蝶窦手术前,血浆CA125、雌二醇水平升高,而催乳素、黄体生成素、卵泡刺激素、孕酮、皮质醇、游离甲状腺素、促甲状腺激素、甲状旁腺激素及生长激素水平维持在正常范围。经蝶窦手术后,该患者被诊断为促性腺激素分泌型垂体腺瘤。随访期间,盆腔超声证实患者卵巢大小正常,月经周期恢复规律,激素水平维持在正常范围内。随访两年无肿瘤复发迹象。
对于有高雌激素血症、月经不规律、卵巢囊肿较大或复发以及视野缺损的患者,应考虑早期诊断促性腺激素分泌型垂体腺瘤。应进行垂体MRI检查,推荐经蝶窦手术治疗该病。