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Radiological feature of skip-segment Hirschsprung’s disease
  1. Jia-liang Zhou,
  2. Xiao-chun Zhu,
  3. Yuan-long Fang,
  4. Song Tian,
  5. Wu-ping Ge
  1. Department of Neonatal Surgery, Guangdong Women and Children Hospital, Guangzhou, China
  1. Correspondence to Dr Wu-ping Ge, Department of Neonatal surgery, Guangdong Women and Children Hospital, Guangzhou, China; gewuping{at}

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A term neonate was hospitalised for progressive abdominal distension and delayed meconium passage on his third day of birth. Plain abdominal radiograph revealed no gas in the distal colon. Constrast enema study revealed narrow rectosigmoid and descending colon with a transitional zone at the left transverse colon (figure 1). Rectal biopsy was performed, which showed an absence of ganglion cells in the lamina propria. Diagnosed with long-segment Hirschsprung disease (HD), the patient was managed with rectal irrigations at home. At the age of 3 months, he underwent laparoscopic transanal pull-through procedure. At laparoscopy, the distal colon was collapsed with a classic …

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  • Contributors J-lZ: idea for the article, literature review, writing, editing of the article and images. W-pG: performed the surgery. X-cZ: revision of the article. Y-lF and ST: clinician responsible for the patient.

  • Funding This study was funded by Medical Scientific Research Foundation of Guangdong Province, China (A2017304) and Science and Technology Planning Project of Guangdong Province of China (2017ZC0315).

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Patient consent for publication Obtained.