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表现为红细胞增多症的卵巢泡膜细胞增生症

Ovarian Hyperthecosis Presenting as Polycythemia.

作者信息

Jaiswal Gayatri, Varsha Fnu, Bononi Patricia, Dimech Christina, Dharia Ashni

机构信息

Division of Endocrinology, Allegheny Health Network, Pittsburgh, Pennsylvania.

出版信息

AACE Clin Case Rep. 2024 Dec 2;11(2):89-92. doi: 10.1016/j.aace.2024.11.008. eCollection 2025 Mar-Apr.

Abstract

BACKGROUND/OBJECTIVE: A 58-year-old postmenopausal woman presented with polycythemia on routine laboratory examinations along with long-standing hirsutism. The objective of this report is to highlight polycythemia as a rare presenting feature of ovarian hyperthecosis (OH).

CASE REPORT

A 58-year-old woman presented with elevated hemoglobin and hematocrit levels in the primary care setting on routine laboratory examinations. On further workup, she was found to have elevated testosterone levels. Further history was relevant for excessive facial hair, frontal hair loss, and deepened voice. Examination findings were consistent with significant hirsutism. Adrenal and ovarian imaging was negative for tumor. The patient elected to have laparoscopic bilateral oophorectomy, which revealed OH on surgical pathology. After 2 months of surgery, the total testosterone levels became normal, and polycythemia resolved.

DISCUSSION

In a postmenopausal woman, hirsutism with virilization should generally prompt urgent investigation because these signs are associated with malignant androgen-secreting tumors of the adrenal gland and ovaries. However, these symptoms can also be the result of benign causes such as OH.

CONCLUSION

This case is a rare illustration of OH in a postmenopausal woman presenting with polycythemia secondary to severe hyperandrogenism. Suspicion for this condition is crucial in evaluation for rare causes of polycythemia because if left untreated, it can lead to increased morbidity and mortality.

摘要

背景/目的:一名58岁的绝经后女性在常规实验室检查中出现红细胞增多症,同时伴有长期多毛症。本报告的目的是强调红细胞增多症作为卵巢泡膜细胞增生症(OH)一种罕见的表现特征。

病例报告

一名58岁女性在基层医疗单位进行常规实验室检查时,血红蛋白和血细胞比容水平升高。进一步检查发现,她的睾酮水平升高。进一步询问病史发现有面部毛发过多、额部脱发和声音变深。体格检查结果与明显的多毛症相符。肾上腺和卵巢影像学检查未发现肿瘤。患者选择接受腹腔镜双侧卵巢切除术,手术病理显示为OH。术后2个月,总睾酮水平恢复正常,红细胞增多症也得到缓解。

讨论

在绝经后女性中,多毛症伴男性化通常应促使进行紧急检查,因为这些体征与肾上腺和卵巢分泌雄激素的恶性肿瘤有关。然而,这些症状也可能是由OH等良性原因引起的。

结论

该病例罕见地说明了一名绝经后女性因严重高雄激素血症继发红细胞增多症而患OH。在评估红细胞增多症的罕见病因时,怀疑这种疾病至关重要,因为如果不治疗,可能会导致发病率和死亡率增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af28/11973594/38fb1a0de001/gr1.jpg

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本文引用的文献

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A Case of Ovarian Hyperthecosis in a Postmenopausal Woman.
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