2015
DOI: 10.1111/his.12749
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Simultaneous juvenile polyposis syndrome and neurofibromatosis type 1 – Response to Letter to the Editor

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Cited by 1 publication
(2 citation statements)
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“…In cases where multiple true juvenile polyps in an NF1 patient are suggested with limited clinical information and biopsy specimens, the coexistence of NF1 and juvenile polyposis should be considered 3 even though this situation is extremely rare. 2 In conclusion, we presented a case of surgical resection for a polyp that may be the same as those reported by Agaimy et al 1 in the present report. The lesion was both a mucosal and submucosal inflammatory polyp composed of stromal proliferation, which was overall similar to IFPs rather than to juvenile polyps or hyperplastic polyps.…”
Section: Discussionsupporting
confidence: 88%
See 1 more Smart Citation
“…In cases where multiple true juvenile polyps in an NF1 patient are suggested with limited clinical information and biopsy specimens, the coexistence of NF1 and juvenile polyposis should be considered 3 even though this situation is extremely rare. 2 In conclusion, we presented a case of surgical resection for a polyp that may be the same as those reported by Agaimy et al 1 in the present report. The lesion was both a mucosal and submucosal inflammatory polyp composed of stromal proliferation, which was overall similar to IFPs rather than to juvenile polyps or hyperplastic polyps.…”
Section: Discussionsupporting
confidence: 88%
“…Agaimy et al 1,2 and Brosens et al 3 reported inflammatory polyps of the gastrointestinal (GI) tract in patients with neurofibromatosis type 1 (NF1). Agaimy et al 1 reported 4 cases of lesions specific to NF1, while Brosens et al 3 considered the possibility of incidentally coexisting true juvenile polyps in NF1 patients.…”
Section: Introductionmentioning
confidence: 99%