摘要
Multicystic dysplastic kidney (MCDK) is a congenital maldevelopment in which the renal cortex is characteristically replaced by numerous cysts of multiple sizes. MCDK presenting as a single predominant large cyst in morphology is less common. We report on the prenatal imaging findings and perinatal management of a fetus with MCDK unusually presenting as a single predominant large cyst, erroneously interpreted as a severe fetal hydronephrosis. Details of the perinatal history, radiological evaluation, morphological characteristic, and clinical aspect of this case are presented. We also discuss a few studies addressing the sensitivity of magnetic resonance urography for the prenatal diagnosis of MCDK.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 227-231 |
| 頁數 | 5 |
| 期刊 | Pediatrics and Neonatology |
| 卷 | 52 |
| 發行號 | 4 |
| DOIs | |
| 出版狀態 | 已發佈 - 8月 2011 |
| 對外發佈 | 是 |
UN SDG
此研究成果有助於以下永續發展目標
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SDG 3 良好的健康和福祉
ASJC Scopus subject areas
- 兒科、圍產兒和兒童健康
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