J Korean Child Neurol Soc.  2009 Nov;17(2):226-230.

A Case of Radiologically Suspected Mesenteric Plexiform Neurofibromas in a Patient with Type I Neurofibromatosis

Affiliations
  • 1Department of Pediatrics, School of Medicine, Chonnam National University, Gwangju, Korea. yjwoo@chonnam.ac.kr

Abstract

Neurofibromatosis type I(NF-1) is an autosomal dominant neurocutaneous syndrome characterized by cafe-au-lait spots, optic glioma, skeletal dysplasia, and iris hamartoma. Mesenteric plexiform neurofibromas(PNF) have been rarely reported in NF-1, especially in children. We report a case of radiologically suspected mesenteric PNF along the celiac axis in an 8-year-old boy who had cafe-au-lait spots and a family history of maternal NF-1.

Keyword

Neurofibromatosis Type 1; Neurofibroma; Plexiform

MeSH Terms

Axis, Cervical Vertebra
Cafe-au-Lait Spots
Child
Hamartoma
Humans
Iris
Neurocutaneous Syndromes
Neurofibroma
Neurofibroma, Plexiform
Neurofibromatoses
Neurofibromatosis 1
Optic Nerve Glioma
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