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一名患有常染色体显性多囊肾病患者的子宫平滑肌瘤发生巨大囊性变。

Massive cystic degeneration of a uterine leiomyoma in a patient with autosomal dominant polycystic kidney disease.

作者信息

Tomimatsu Takuji, Sugihara Mika, Nakamura Takafumi, Kashihara Naoki, Shimoya Koichiro

机构信息

Department of Obstetrics and Gynecology, Kawasaki Medical School, Kurashiki, Japan.

出版信息

Gynecol Obstet Invest. 2015;79(3):168-71. doi: 10.1159/000369996. Epub 2015 Feb 3.

Abstract

BACKGROUND

A uterine cyst occurring as an extrarenal manifestation of autosomal dominant polycystic kidney disease (ADPKD) is extremely rare.

CASE

A 46-year-old Japanese woman was referred with a large abdominal mass causing severe abdominal distension. A large uterine cyst as an extrarenal manifestation of ADPKD was strongly suspected. First, we managed this patient by aspirating the cyst fluid through a small laparotomy. A year later, the cyst recurred and the patient underwent hysterectomy. Massive cystic degeneration of a uterine leiomyoma was diagnosed histologically.

CONCLUSION

We described the rare case of massive cystic degeneration of a uterine leiomyoma in a patient with ADPKD, in which a causal relationship was suspected.

摘要

背景

作为常染色体显性多囊肾病(ADPKD)肾外表现的子宫囊肿极为罕见。

病例

一名46岁的日本女性因巨大腹部肿块导致严重腹胀前来就诊。强烈怀疑是作为ADPKD肾外表现的巨大子宫囊肿。首先,我们通过小切口剖腹术抽吸囊液对该患者进行治疗。一年后,囊肿复发,患者接受了子宫切除术。组织学诊断为子宫平滑肌瘤的大量囊性变。

结论

我们描述了一例ADPKD患者子宫平滑肌瘤大量囊性变的罕见病例,怀疑二者存在因果关系。

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