Literature DB >> 22150579

Familial multiple pilomatrixomas as a presentation of attenuated adenomatosis polyposis coli.

Joshua Trufant1, Wayne Kurz, Amylynne Frankel, Viswanathan Muthusamy, Wendy McKinnon, Marc Greenblatt, Alex Lazar, Deborah Cook, Marcus Bosenberg.   

Abstract

Pilomatrixomas are benign follicular tumors that occur most commonly in children. Rare multiple or familial pilomatrixomas have been associated with myotonic dystrophy and other disorders. Although sporadic pilomatrixomas and hybrid cutaneous cysts with pilomatrixoma-like features have been observed in some kindreds with Gardner syndrome, an autosomal dominant form of familial adenomatous polyposis, no definitive association has been made with multiple or familial pilomatrixomas. Here we describe two siblings with multiple pilomatrixomas who were also found to have a family history of colonic adenocarcinoma. Genetic testing revealed a mutation in the 5' portion of the adenomatous polyposis coli (APC) gene, in a region associated with an attenuated APC phenotype. These findings show that multiple pilomatrixomas may be the presenting symptom of patients with APC gene mutations.
Copyright © 2011 John Wiley & Sons A/S.

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Year:  2011        PMID: 22150579     DOI: 10.1111/j.1600-0560.2011.01836.x

Source DB:  PubMed          Journal:  J Cutan Pathol        ISSN: 0303-6987            Impact factor:   1.587


  6 in total

1.  Orthokeratinized Odontogenic Cyst with an Associated Keratocystic Odontogenic Tumor Component and Ghost Cell Keratinization and Calcifications in a Patient with Gardner Syndrome.

Authors:  Prokopios P Argyris; Ioannis G Koutlas
Journal:  Head Neck Pathol       Date:  2016-08-08

2.  Burkitt-like lymphoma in a pediatric patient with familial adenomatous polyposis.

Authors:  Katie M Strobel; Jacquelyn N Crane; Kathryn L Bradford; Yalda Naeini; William A May; Vivian Y Chang
Journal:  Cancer Genet       Date:  2019-09-04

Review 3.  Current Diagnosis and Treatment Options for Cutaneous Adnexal Neoplasms with Follicular Differentiation.

Authors:  Iga Płachta; Marcin Kleibert; Anna M Czarnecka; Mateusz Spałek; Anna Szumera-Ciećkiewicz; Piotr Rutkowski
Journal:  Int J Mol Sci       Date:  2021-04-30       Impact factor: 5.923

4.  Childhood neuroendocrine tumours: a descriptive study revealing clues for genetic predisposition.

Authors:  I J Diets; I D Nagtegaal; J Loeffen; I de Blaauw; E Waanders; N Hoogerbrugge; M C J Jongmans
Journal:  Br J Cancer       Date:  2016-12-13       Impact factor: 7.640

5.  Mutation analysis of multiple pilomatricomas in a patient with myotonic dystrophy type 1 suggests a DM1-associated hypermutation phenotype.

Authors:  Albert Rübben; Renate Ursula Wahl; Thomas Eggermann; Edgar Dahl; Nadina Ortiz-Brüchle; Claudio Cacchi
Journal:  PLoS One       Date:  2020-03-10       Impact factor: 3.240

6.  No Evidence of Abnormal Expression of Beta-Catenin and Bcl-2 Proteins in Pilomatricoma as One Clinical Feature of Tetrasomy 9p Syndrome.

Authors:  Chariyawan Charalsawadi; Sasipong Trongnit; Kanoot Jaruthamsophon; Juthamas Wirojanan; Somchit Jaruratanasirikul; Anupong Nitiruangjaras; Pornprot Limprasert
Journal:  Int J Pediatr       Date:  2021-12-15
  6 in total

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