梅干腹综合征：一例罕见病例报告。
Prune belly syndrome: A rare case report.
作者信息
Gyawali Siddinath, Gyawali Balkrishna, Ghimire Bhumika, Shrestha Bibek, Khanal Pratima, Dahal Geha Raj, Koirala Dinesh Prasad
机构信息
Institute of Medicine, Tribhuvan University Teaching Hospital Kathmandu Nepal.
Manmohan Memorial Institute of Health Sciences Kathmandu Nepal.
出版信息
Clin Case Rep. 2024 Jun 17;12(6):e8922. doi: 10.1002/ccr3.8922. eCollection 2024 Jun.
KEY CLINICAL MESSAGE
In babies presenting with an omphalocele, other components of the prune belly syndrome should be scrutinized for early diagnosis and timely intervention.
ABSTRACT
A male baby on his 13th day of life presented with an omphalocele. On evaluation, he had congenital absence of left kidney and bilateral cryptorchidism. Therefore, he was diagnosed with prune belly syndrome. He responded well to abdminoplasty, and wait and watch policy was applied for his cryptorchidism.
关键临床信息
对于患有脐膨出的婴儿，应仔细检查梅干腹综合征的其他组成部分，以便早期诊断和及时干预。
摘要
一名出生13天的男婴患有脐膨出。经评估，他先天性左肾缺如且双侧隐睾。因此，他被诊断为梅干腹综合征。他对腹壁成形术反应良好，对于隐睾采取了观察等待策略。
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