Abstract
Hirschsprung’s disease (congenital megacolon) is a congenital disorder of the intestine. It is caused by incomplete migration of neural crest cells destined to become the nervous system of the distal intestine. The resultant aganglionic bowel is unable to relax, thus causing a functional obstruction. The consequences of this disease can be severe and even life threatening. Fortunately, advancements in surgical techniques and perioperative care have significantly reduced mortality rates. Furthermore, minimally invasive surgical approaches for uncomplicated cases are becoming increasingly common. This chapter provides a concise overview of Hirschsprung’s disease, including etiology, genetic associations, diagnostic workup, and treatment. The core surgical principles and procedures that were originally described for Hirschsprung’s disease will be briefly summarized. We then describe a minimally invasive surgical technique being used today to treat short-segment disease, the laparoscopic-assisted transanal pull-through. The chapter concludes with a review of the main complications and long-term issues.
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Cheek, R., Salesi, L., Scholz, S. (2017). Laparoscopic-Assisted Pull-Through for Hirschsprung’s Disease. In: Walsh, D., Ponsky, T., Bruns, N. (eds) The SAGES Manual of Pediatric Minimally Invasive Surgery. Springer, Cham. https://doi.org/10.1007/978-3-319-43642-5_36
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DOI: https://doi.org/10.1007/978-3-319-43642-5_36
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