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与特纳综合征相关的子宫非典型息肉样腺肌瘤。三例报告,包括对“雌激素相关”子宫内膜肿瘤及与特纳综合征相关肿瘤的综述。

Atypical polypoid adenomyoma of the uterus associated with Turner's syndrome. A report of three cases, including a review of "estrogen-associated" endometrial neoplasms and neoplasms associated with Turner's syndrome.

作者信息

Clement P B, Young R H

机构信息

Department of Pathology, Vancouver General Hospital, British Columbia, Canada.

出版信息

Int J Gynecol Pathol. 1987;6(2):104-13. doi: 10.1097/00004347-198706000-00002.

Abstract

The clinical and pathological features of three atypical polypoid adenomyomas of the uterus that were associated with Turner's syndrome are described. The patients, at least two of whom had been on long-term exogenous estrogens, were in their third decade and presented with abnormal vaginal bleeding. In two cases an exophytic mass protruded through the external os and clinically suggested a malignant tumor. The histological (and in one case, the ultrastructural) findings were similar to those of previously described cases of atypical polypoid adenomyoma. The clinical findings in these cases suggest that some atypical polypoid adenomyomas may be a complication of prolonged estrogenic stimulation. The association between Turner's syndrome and other gynecological neoplasms is reviewed.

摘要

本文描述了三例与特纳综合征相关的非典型息肉样腺肌瘤的临床和病理特征。患者年龄均在三十多岁,至少两人长期使用外源性雌激素,均出现异常阴道出血症状。其中两例患者有外生性肿物自宫颈外口突出,临床提示为恶性肿瘤。组织学(其中一例为超微结构)检查结果与先前报道的非典型息肉样腺肌瘤病例相似。这些病例的临床发现提示,一些非典型息肉样腺肌瘤可能是长期雌激素刺激的并发症。本文还综述了特纳综合征与其他妇科肿瘤之间的关联。

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