Neonatal Solitary Intestinal Myofibromatosis

Authors

  • Rachida Laamiri Department of pediatric surgery Fattouma Bourguiba University Hospital Monastir, Tunisia
  • Nahla Kechiche Department of pediatric surgery Fattouma Bourguiba University Hospital Monastir, Tunisia
  • Meriem Braiki Department of pediatric surgery Fattouma Bourguiba University Hospital- Monastir, Tunisia
  • Rim Hadhri Department of Anatomy and pathologic cytology Fattouma Bourguiba University Hospital-Monastir, Tunisia
  • Lassaad Sahnoun Department of pediatric surgery Fattouma Bourguiba University Hospital- Monastir, Tunisia
  • Mongi Mekki Department of pediatric surgery Fattouma Bourguiba University Hospital- Monastir, Tunisia
  • Mohsen Belghith Department of pediatric surgery Fattouma Bourguiba University Hospital- Monastir, Tunisia
  • Abdellatif Nouri Department of pediatric surgery Fattouma Bourguiba University Hospital- Monastir, Tunisia

DOI:

https://doi.org/10.21699/jns.v7i1.676

Keywords:

Solitary intestinal fibromatosis, Neonatal intestinal obstruction, Pediatrics

Abstract

Solitary intestinal myofibromatosis (SIF) is a very rare condition affecting the pediatric population and carries good prognosis following adequate management based on segmental resection. We describe a rare case who presented with features of neonatal intestinal obstruction due to a solitary stenosing fibrotic lesion originating from the ileum and compatible with SIF.

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Published

2018-01-05

How to Cite

1.
Laamiri R, Kechiche N, Braiki M, Hadhri R, Sahnoun L, Mekki M, Belghith M, Nouri A. Neonatal Solitary Intestinal Myofibromatosis. J Neonatal Surg [Internet]. 2018Jan.5 [cited 2021Jan.15];7(1):7. Available from: https://jneonatalsurg.com/ojs/index.php/jns/article/view/370

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