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Leydig cell tumor of ovary with primary hyperparathyroidism: A rare association

机译:伴有原发性甲状旁腺功能亢进的卵巢Leydig细胞瘤:一种罕见的关联

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Leydig cell tumors of ovary are extremely rare sex cord stromal tumors that account for <0.2% of ovarian cancers. Most of these tumors can cause hyperandrogenism. A 54 year old multiparous postmenopausal woman, known diabetic and hypertensive, presented with progressive virilization, bone pains and depressed mood for 2 years. Diagnostic evaluation revealed markedly elevated testosterone with normal dehydroepiandrosterone sulphate. Computerized tomography of abdomen showed right ovarian mass with multiple cysts in both kidneys. Biochemical investigations revealed hyperglycemia, hypercalcemia, hypophosphatemia and elevated parathormone (PTH) levels. Sestamibi scan for parathyroids was suggestive of right inferior parathyroid adenoma. Histopathology of the resected right ovarian tumor was consistent with leydig cell tumor of ovary. Postoperatively serum testosterone and blood glucose levels were normalized, but PTH levels remained high. PTH levels were normalized after resection of parathyroid adenoma.
机译:卵巢的Leydig细胞肿瘤是极为罕见的性索间质肿瘤,占卵巢癌的<0.2%。这些肿瘤大多数会引起雄激素过多。一名54岁的绝经后多产妇女,已知患有糖尿病和高血压,持续2年出现逐步性勃起,骨痛和情绪低落。诊断评估显示,正常脱氢表雄酮硫酸盐可使睾丸激素显着升高。腹部计算机断层扫描显示两个肾脏的右卵巢有多个囊肿。生化研究表明,高血糖,高血钙,低磷血症和副激素(PTH)水平升高。 Sestamibi甲状旁腺扫描提示右下甲状旁腺腺瘤。切除的右卵巢肿瘤的组织病理学与卵巢莱迪希氏细胞瘤一致。术后血清睾丸激素和血糖水平恢复正常,但PTH水平仍然很高。甲状旁腺腺瘤切除后PTH水平恢复正常。

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