Literature DB >> 26840078

Gardner Fibroma: Clinical and Histopathologic Implications of Germline APC Mutation Association.

Nathan A Dahl1, Amy Sheil, Sarah Knapke, James I Geller.   

Abstract

The proportion and clinical characteristics of Gardner fibromas (GAFs) that are sporadic versus familial adenomatous polyposis (FAP)-associated have not been clearly established. We report on 7 patients diagnosed with GAF who underwent APC sequencing and duplication/deletion testing. Three (43%) were found to have underlying APC germline perturbations consistent with FAP; these patients had multifocal (1) or large; unresectable (2) GAFs. The 4 patients with negative APC testing each had a single resectable GAF. β-catenin reactivity was noted in all FAP-associated GAFs and in 1/4 APC wild-type cases. FAP-associated GAFs may be less common than sporadic GAFs and can demonstrate clinically distinct features.

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Year:  2016        PMID: 26840078     DOI: 10.1097/MPH.0000000000000493

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  5 in total

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3.  Gardner fibroma with localized hypertrichosis without adenomatous polyposis coli gene mutation.

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Journal:  Chin Med J (Engl)       Date:  2019-09-05       Impact factor: 2.628

Review 4.  Nonmalignant Features Associated with Inherited Colorectal Cancer Syndromes-Clues for Diagnosis.

Authors:  Diana Haimov; Sari Lieberman; Sergi Castellvi-Bel; Maartje Nielsen; Yael Goldberg
Journal:  Cancers (Basel)       Date:  2022-01-26       Impact factor: 6.639

5.  From Gardner fibroma diagnosis to constitutional APC mutation detection: a one-way street.

Authors:  Claudia Santoro; Teresa Giugliano; Delfina Bifano; Carolina D'Anna; Vittoria D'Onofrio; Silverio Perrotta
Journal:  Clin Case Rep       Date:  2017-08-10
  5 in total

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