Total colonic aganglionosis initially diagnosed in an adolescent

• Published in: Gastroenterology (New York, N.Y. 1943) Vol. 87; no. 6; p. 1364
• Main Authors: Lefebvre, M P, Leape, L L, Pohl, D A, Safaii, H, Grand, R J
• Format: Journal Article
• Language: English
• Published: United States 01-12-1984
• Subjects: Abdomen; Child; Colectomy; Colon - innervation; Colon, Sigmoid - innervation; Constipation - etiology; Female; Hirschsprung Disease - pathology; Hirschsprung Disease - surgery; Humans; Ileum - innervation; Pain - etiology
• ISSN: 0016-5085
• DOI: 10.1016/0016-5085(84)90205-1

A 12-yr-old girl was admitted for evaluation of a 5-wk history of increasing abdominal pain. She also reported a history of constipation since birth requiring chronic laxative use. Occasional bouts of abdominal distention and vomiting resulted in dehydration necessitating hospitalization. Two previous laparotomies had identified an apparent obstructing angulation of the ascending colon. Rectal biopsy specimens obtained on this admission failed to reveal any ganglion cells. Sequential biopsy specimens of the entire colon obtained at laparotomy also failed to reveal any ganglion cells. Ganglion cells were found in the distal ileum. A total colectomy was performed. Three previously reported cases of total colonic aganglionosis initially diagnosed in older patients are reviewed. Similarities included nonspecific radiographic findings, a history of constipation since birth, and initial laparotomies revealing spurious causes of bowel obstruction.