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Juvenile‐like (inflammatory/hyperplastic) mucosal polyps of the gastrointestinal tract in neurofibromatosis type 1
Author(s) -
Agaimy Abbas,
Schaefer IngaMarie,
Kotzina Leopoldina,
Knolle Jürgen,
Baumann Irith,
Ströbel Philipp,
Vieth Michael
Publication year - 2014
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/his.12325
Subject(s) - neurofibromatosis , medicine , neurofibroma , pathology , gastroenterology , gastrointestinal tract , ganglioneuroma , inflammatory bowel disease , hyperplasia , hyperplastic polyp , colonoscopy , disease , colorectal cancer , cancer , biology , genetics , cell culture , neuroblastoma
Aims Diffuse neurofibromatosis/ganglioneuromatosis, solitary/plexiform neurofibroma, periampullary carcinoids and gastrointestinal stromal tumour ( GIST ) are the main gastrointestinal manifestations of neurofibromatosis type 1 ( NF ‐1, von Recklinghausen disease). Inflammatory (juvenile‐like) polyps have not been recognised to date as specific gastrointestinal ( GI ) manifestations of NF ‐1. Methods and results We describe four males aged 23–65 years with NF ‐1 and inflammatory (juvenile‐like) gastrointestinal polyps, and review the literature for similar cases. Two patients had single polyps (sigmoid colon and antrum, respectively), one had two polyps (left colon), and one had three polyps (distal oesophagus and colon). Histological appearances were variable, ranging from juvenile‐like to granulation tissue‐rich, predominantly inflammatory and hyperplastic. Three lesions showed obliterative vasculopathic changes. None had neurofibromatous or ganglioneuromatous polyps. A review of the literature disclosed 11 similar cases. Most patients presented with severe gastrointestinal symptoms and/or anaemia. Conclusions NF ‐1‐associated inflammatory polyps probably represent specific GI manifestations of this disorder, and should be considered, particularly in patients with GI symptoms. They should be distinguished from inflammatory fibroid polyps and from juvenile‐like changes associated with ganglioneuroma/ganglioneuromatosis and neurofibroma/neurofibromatosis. Their aetiology remains obscure, but different mechanisms, including NF ‐1 inactivation, NF ‐1‐associated vasculopathy, and localised mucosal prolapse/damage caused by motility disorders, might be involved.