Garcia Daniel Jose, Hamade Mohamad, Lin Li, Matias Matias, Sobhan Armaan, Zaritsky Mario, Thorson Chad
Department of Surgery, University of Miami, PO Box 016960 (C203), Miami, FL 33101, United States.
Department of Radiology, University of Miami, 1150 NW 14th St #511, Miami, FL 33136, United States.
J Surg Case Rep. 2024 Dec 5;2024(12):rjae766. doi: 10.1093/jscr/rjae766. eCollection 2024 Dec.
Congenital colonic stenosis (CCS) is a rare cause of intestinal obstruction, most commonly presenting in the neonatal period. We present a case of delayed CCS and describe the diagnostic challenges experienced. A 16-week-old female patient presented with persistent failure to thrive associated with signs of intestinal obstruction. Prior encounters included investigation for pyloric stenosis, gastrointestinal pathogens, acid reflux, and cow milk allergy, with no to little improvement in symptoms. Abdominal imaging showed bowel dilation with possible colonic obstruction while excluding malrotation. Exploratory laparotomy revealed abrupt reduction in caliber of the mid/distal transverse colon and extreme luminal narrowing, consistent with colonic stenosis. Extended right hemicolectomy and anastomosis resulted in returned bowel function and appropriate weight gain in follow-up. Though rare, CCS should be considered in cases of partial or subacute intestinal obstruction throughout the first year of life. Inconclusive clinical and imaging results may support exploratory laparotomy after excluding differential diagnoses.
先天性结肠狭窄(CCS)是肠梗阻的罕见病因,最常出现在新生儿期。我们报告一例迟发性CCS病例,并描述所遇到的诊断挑战。一名16周大的女性患者因肠梗阻症状出现持续生长发育迟缓。之前的检查包括针对幽门狭窄、胃肠道病原体、胃酸反流和牛奶过敏的检查,症状无改善或改善甚微。腹部影像学检查显示肠管扩张,可能存在结肠梗阻,同时排除了肠旋转不良。剖腹探查发现中/远段横结肠管径突然变窄,管腔极度狭窄,符合结肠狭窄表现。扩大右半结肠切除术及吻合术后,肠道功能恢复,随访中体重适当增加。尽管CCS罕见,但在生命的第一年出现部分或亚急性肠梗阻的病例中应考虑该病。在排除鉴别诊断后,不确定的临床和影像学结果可能支持剖腹探查。