Title of article
Large Neurofibroma of the Anorectal Canal: A Case Report
Author/Authors
Ghahramani، Leila نويسنده Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , , Izadpanah، Ahmad نويسنده Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , , Bananzadeh، Ali Mohammad نويسنده Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , , Akrami، Majid نويسنده Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , , Bahrami، Faranak نويسنده Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , , Hosseini، Seyed Vahid نويسنده ,
Issue Information
فصلنامه با شماره پیاپی 0 سال 2011
Pages
5
From page
43
To page
47
Abstract
Neurofibromatosis type 1, also known as von Recklinghausen disease, is an
autosomal dominant disorder with an incidence of 1 per 4000. Neurofibromas are benign,
heterogeneous tumors arising from the connective tissue of peripheral nerve sheaths,
especially the endoneurium. Visceral involvement in disseminated neurofibromatosis
is rare. Neurofibroma occurs most frequently in the stomach and jejunum, but the colon
and anorectal canal may also be involved. Gastrointestinal neurofibromas may lead to
bleeding, obstruction, intussusception, protein-losing enteropathy and bowel perforation.
We present a case of diffuse involvement of the anorectal area by a huge neurofibroma,
with pelvic pain, watery diarrhea and urgency.
Journal title
Middle East Journal of Cancer (MEJC)
Serial Year
2011
Journal title
Middle East Journal of Cancer (MEJC)
Record number
655358
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