Sicilia Vitaliano, Earle Jonathan, Mezitis Spyros G E
Department of Internal Medicine, Lenox Hill Hospital, New York, New York, USA.
Endocr Pract. 2006 Jul-Aug;12(4):417-21. doi: 10.4158/EP.12.4.417.
To report a case of a follicle-stimulating hormone (FSH)-secreting pituitary adenoma, which manifested with oligomenorrhea, dysmenorrhea, and multiple bilateral ovarian cysts.
We present a case report of a 29-year-old woman, including detailed laboratory, radiologic, and pathologic findings, who was diagnosed as having an FSH-secreting pituitary tumor. The pertinent literature is also reviewed.
A 29-year-old woman, after experiencing oligomenorrhea and increasing abdominal girth for >1 year, presented with an acute abdomen. Ultrasonography revealed multicystic ovaries >15 cm in maximal diameter, causing bilateral adnexal torsion. After bilateral ovarian cystectomies, ultrasound study showed recurrence of the cysts. Relevant laboratory data were as follows: serum FSH 6.8 mIU/mL, luteinizing hormone 0.1 mIU/mL, prolactin 67 ng/mL, human chorionic gonadotropin <2 mIU/mL, progesterone 3.5 ng/dL, estradiol 237 pg/mL, thyrotropin 1.8 microIU/mL, testosterone <4 ng/dL, insulin 8.0 microIU/mL, and fasting plasma glucose 87 mg/dL. Magnetic resonance imaging (MRI) of the brain revealed a 2.5-cm pituitary mass, although the patient had no symptoms of pituitary dysfunction. Transsphenoidal removal of the mass was performed, and pathology studies were positive for FSH-secreting adenoma. Repeated MRI at 3 months showed an 0.8-cm residual tumor. The patient refused adjuvant radiotherapy. Regular menses resumed within 2 months postoperatively, and she later successfully became pregnant. Almost 3 years after treatment, the patient remained asymptomatic, results of pituitary function tests were normal, and follow-up MRI showed no signs of tumor regrowth.
Although very uncommon, gonadotropin-secreting pituitary adenomas should be considered in the differential diagnosis of new-onset oligomenorrhea and dysmenorrhea, especially if associated with multicystic ovaries on ultrasound study, even in the absence of elevated levels of serum gonadotropins. Furthermore, we propose that it may be acceptable to withhold adjuvant radiotherapy in patients who are asymptomatic after transsphenoidal surgical excision of these tumors.
报告一例分泌促卵泡生成素(FSH)的垂体腺瘤病例,该病例表现为月经过少、痛经和双侧多发性卵巢囊肿。
我们报告一例29岁女性的病例,包括详细的实验室、影像学和病理学检查结果,该患者被诊断为分泌FSH的垂体肿瘤。同时对相关文献进行综述。
一名29岁女性,在经历了1年多的月经过少和腹围增加后,出现急腹症。超声检查显示双侧卵巢多囊,最大直径>15 cm,导致双侧附件扭转。双侧卵巢囊肿切除术后,超声检查显示囊肿复发。相关实验室数据如下:血清FSH 6.8 mIU/mL,促黄体生成素0.1 mIU/mL,催乳素67 ng/mL,人绒毛膜促性腺激素<2 mIU/mL,孕酮3.5 ng/dL,雌二醇237 pg/mL,促甲状腺激素1.8 μIU/mL,睾酮<4 ng/dL,胰岛素8.0 μIU/mL及空腹血糖87 mg/dL。脑部磁共振成像(MRI)显示垂体有一个2.5 cm的肿块,尽管患者无垂体功能障碍症状。行经蝶窦肿块切除术,病理研究证实为分泌FSH的腺瘤。术后三个月复查MRI显示有一个0.8 cm的残留肿瘤。患者拒绝辅助放疗。术后2个月内月经恢复正常,随后成功怀孕。治疗后近3年,患者无症状,垂体功能测试结果正常,随访MRI未显示肿瘤复发迹象。
虽然分泌促性腺激素的垂体腺瘤非常罕见,但在新发月经过少和痛经的鉴别诊断中应考虑到,尤其是超声检查发现有多囊卵巢时,即使血清促性腺激素水平未升高。此外,我们建议对于经蝶窦手术切除这些肿瘤后无症状的患者,可不进行辅助放疗。