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伴有男性化的卵巢类固醇细胞瘤中的原发性骨髓化生:一例报告

Agnogenic myeloid metaplasia in an ovarian steroid cell tumor with virilization: a case report.

作者信息

Huang Ching-Wen, Hsueh Swei, Chang Ming-Yang

机构信息

Department of Pathology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan, Taiwan.

出版信息

J Reprod Med. 2004 Sep;49(9):765-8.

Abstract

BACKGROUND

Extramedullary hematopoiesis in patients without hematologic disorders is very rare and has apparently never been described previously in association with an ovarian steroid cell tumor.

CASE

An 18-year-old woman was admitted to our clinic due to primary amenorrhea. the On examination she had significant facial hirsutism, clitoromegaly and and Adam's apple. The serum level of testosterone was elevated. A 7-cm, right ovarian mass was enucleated during laparotomy. Histology revealed a steroid cell tumor with foci of myeloid metaplasia; bony trabecula formation was present. There was no evidence of hematologic or systemic disease. The hormone values became normal 1 month postoperatively.

CONCLUSION

This report describes a patient with agnogenic myeloid metaplasia in an ovarian steroid cell tumor with virilization; this association was not previously reported.

摘要

背景

在无血液系统疾病的患者中,髓外造血非常罕见,此前显然从未有过与卵巢类固醇细胞瘤相关的描述。

病例

一名18岁女性因原发性闭经入住我院。检查发现她有明显的面部多毛、阴蒂肥大和喉结。血清睾酮水平升高。剖腹手术中摘除了一个7厘米的右侧卵巢肿块。组织学检查显示为伴有髓样化生灶的类固醇细胞瘤;存在骨小梁形成。没有血液系统或全身性疾病的证据。术后1个月激素值恢复正常。

结论

本报告描述了一名患有卵巢类固醇细胞瘤并伴有男性化表现的特发性髓样化生患者;这种关联此前未见报道。

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