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Erschienen in: Pediatric Surgery International 11/2010

01.11.2010 | Original Article

Skip segment Hirschsprung’s disease: a systematic review

verfasst von: Anne-Marie O’Donnell, Prem Puri

Erschienen in: Pediatric Surgery International | Ausgabe 11/2010

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Abstract

Purpose

Hirschsprung’s disease is characterised by the congenital absence of ganglion cells beginning in the distal rectum and extending proximally for varying distances. ‘Zonal aganglionosis’ is a phenomenon involving a zone of aganglionosis occurring within normally innervated intestine. ‘Skip segment’ Hirschsprung’s disease (SSHD) involves a ‘skip area’ of normally ganglionated intestine, surrounded proximally and distally by aganglionosis. While Hirschsprung’s disease is believed to be the result of incomplete craniocaudal migration of neural crest-derived cells, the occurence of SSHD has no clear embryological explanation. The aim of this study was to perform a systematic review of SSHD, reported in the literature between 1954 and 2009, in order to determine the clinical characteristics of this rare entity and its significance.

Methods

The first reported case of SSHD was published in 1954. A systematic review of SSHD cases in the literature, from 1954 to 2009, was carried out using the electronic database ‘Pubmed’. Detailed information was recorded regarding the age, gender, presenting symptoms and location of the skip segment in each patient.

Results

24 cases of SSHD have been reported in the literature to date. 18/24 (75%) of these cases were males and 6/24 (25%) were females. Of these, 22/24 (92%) were cases of total colonic aganglionosis (TCA), and 2/24 (8%) were rectosigmoid Hirschsprung’s disease. Of the 22 TCA cases, 9 (41%) had a skip segment in the transverse colon, 6 (27%) in the ascending colon, 2 (9%) in the caecum and 5 (23%) had multiple skip segments. In both rectosigmoid Hirschsprung’s disease cases, the skip segment was in the sigmoid colon. Overall, the length of the skip segment was variable, with the entire transverse colon ganglionated in some cases.

Conclusion

SSHD occurs predominantly in patients with TCA. The existence of a skip area of normally innervated colon in TCA may influence surgical management, enabling surgeons to preserve and use the ganglionated skip area during pull-through operations.
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Metadaten
Titel
Skip segment Hirschsprung’s disease: a systematic review
verfasst von
Anne-Marie O’Donnell
Prem Puri
Publikationsdatum
01.11.2010
Verlag
Springer-Verlag
Erschienen in
Pediatric Surgery International / Ausgabe 11/2010
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-010-2692-4

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