A Case of Multicystic Dysplastic Kidney Presenting as a Single Midline Pelvic Cyst.

IF 0.7 Q4 UROLOGY & NEPHROLOGY
Case Reports in Nephrology and Dialysis Pub Date : 2023-07-04 eCollection Date: 2023-01-01 DOI:10.1159/000530925
Kristin M Ebert, Christina B Ching
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引用次数: 0

Abstract

We present an unusual case of a female neonate presenting with a single midline pelvic cyst. Prenatal imaging was suggestive of multicystic dysplastic kidney (MCDK), but postnatal imaging was atypical for this diagnosis given the location and singular cyst noted. The patient ultimately underwent surgical exploration and was diagnosed with an ectopic MCDK. Ectopic MCDK should be considered in the differential diagnosis of unilocular cystic pelvic lesions identified in the perinatal period.

Abstract Image

Abstract Image

一例表现为单一中线盆腔囊肿的多囊性肾脏发育不良病例
我们接诊了一例不寻常的新生女婴,她患有单发中线盆腔囊肿。产前影像学检查提示多囊发育不良肾(MCDK),但考虑到囊肿的位置和单发性,产后影像学检查并不典型。患者最终接受了手术探查,并被诊断为异位多囊肾。在围产期发现的单眼盆腔囊性病变的鉴别诊断中,应考虑异位MCDK。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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