Niaz Sana, Naz Sahira, Raziq Rumaissa Abdul
Sana Niaz, MBBS, FCPS, Department of Neonatology, Indus Hospital & Health Network, Karachi, Pakistan.
Sahira Naz, MBBS, FCPS, Department of Pediatrics, Indus Hospital & Health Network, Karachi, Pakistan.
Pak J Med Sci. 2022 Jan;38(2):426-429. doi: 10.12669/pjms.38.ICON-2022.5771.
Congenital Pouch Colon (CPC) is a rare anorectal malformation (ARM) in which a part of or the entire colon is replaced by pouch-like dilatation. Males are more likely to be diagnosed with the condition compared to females. The highest incidence of the disease is in South Asia, with a significant number of cases reported from India. Early diagnosis can be made when there are hypoechogenic lesions on antenatal ultrasound scans. We report a case of a neonate with routine antenatal scans who presented with a distended abdomen and inability to pass feces. The diagnosis was made in the early neonatal period, followed by surgical management.
先天性袋状结肠（CPC）是一种罕见的肛肠畸形（ARM），其中部分或整个结肠被袋状扩张所取代。与女性相比，男性更易被诊断出患有此病。该疾病在南亚发病率最高，印度报告了大量病例。当产前超声扫描出现低回声病变时可作出早期诊断。我们报告一例新生儿病例，该患儿在常规产前扫描时被发现，出生后出现腹部膨隆且无法排便。在新生儿早期作出诊断，随后进行了手术治疗。
