Skip segment Hirschsprung's disease: report of two rare cases and management

Purpose Skip segment Hirschsprung's disease (SS-HSCR) is defined as the occurrence of a segment of ganglionated intestine surrounded proximally and distally by aganglionosis. The presence of the skip intestinal segment often leads to clinical misdiagnosis, missed diagnosis or inadequate resection of the lesions. The purpose was to describe two new cases of SS-HSCR with the aim of proposing questions regarding the diagnosis and treatment of this rare disease. Methods We reported two cases of infants with SS-HSCR that were admitted to our institution within the last 3 years. Results One patient had a skip segment of ganglionated intestine in the ascending colon. In the other patient, there were no ganglionic cells in the rectum and appendix, but ganglionic cells were visible in the proximal ascending colon. The entire colons in the both cases were finally resected, and a pull-through operation was performed. Conclusion Multipoint biopsy should be performed when the biopsy results are inconsistent with clinical manifestations. Intraoperative laparoscopic identification of the transition zone may be necessary when TCA is suspected. Multisegment biopsy is needed to as a preventative measure for SS-HSCR if TCA is indicated during surgery. Further study is required to determine the optimal length and method of retention of segments.

Automated summary

The article describes two cases of SS-HSCR, highlighting key issues in the diagnosis and treatment of this rare disease, including multipoint biopsy, laparoscopic identification of the transition zone, and multisegment biopsy as a preventative measure. Further research is needed to determine the optimal length and method of retention of segments.