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作 者:Lily S Cheng Richard J Wood
机构地区:[1]Department of Surgery,Division of Pediatric Surgery,University of Virginia,Charlottesville,Virginia,USA [2]Department of Pediatric Colorectal and Pelvic Reconstructive Surgery,Nationwide Children's Hospital,Columbus,Ohio,USA
出 处:《World Journal of Pediatric Surgery》2024年第3期233-236,共4页世界小儿外科杂志(英文)
基 金:the National Institute of Diabetes and Digestive and Kidney Diseases(Grant number:K08DK133673).
摘 要:OVERVIEW OF SHORT-SEGMENT HIRSCHSPRUNG DISEASE The most common variant of Hirschsprung disease(HSCR)is short-segment or recto-sigmoid disease.The majority(70%-85%)of HSCR is limited to the rectum or sigmoid colon.1 These patients usually present in the neonatal period with'typical'signs and symp-toms:failure to pass meconium within the first 24-48 hours,abdominal distention,vomiting,explosive passage of stool/gas,and failure to thrive.12 Patients may also present with signs and symptoms of Hirschsprung-associated enterocolitis(HAEC),which include abdom-inal tenderness,fever,explosive diarrhea,and bloody stools.3 Rectal irrigation is usually an effective first-line management strategy in patients with short-segment HSCR and is the mainstay of treatment for HAEC.
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