Multiple keratoacanthomas of Ferguson‐Smith type

We report a case of a 41‐year‐old male patient with no family history, presented with extensive multiple keratoacanthomas with disfiguring scars. The diagnosis of a sporadic form of Ferguson‐Smith syndrome was made. Treatment with acitretin showed a marked response. Recognizing this syndrome is cruc...

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Detalles Bibliográficos
Autores principales: Litaiem, Noureddine, Khammouma, Ferdaous, Mrad, Malek, Bacha, Takwa, Belhadj Kacem, Linda, Zeglaoui, Faten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552544/
https://www.ncbi.nlm.nih.gov/pubmed/36245454
http://dx.doi.org/10.1002/ccr3.6429
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author Litaiem, Noureddine
Khammouma, Ferdaous
Mrad, Malek
Bacha, Takwa
Belhadj Kacem, Linda
Zeglaoui, Faten
author_facet Litaiem, Noureddine
Khammouma, Ferdaous
Mrad, Malek
Bacha, Takwa
Belhadj Kacem, Linda
Zeglaoui, Faten
author_sort Litaiem, Noureddine
collection PubMed
description We report a case of a 41‐year‐old male patient with no family history, presented with extensive multiple keratoacanthomas with disfiguring scars. The diagnosis of a sporadic form of Ferguson‐Smith syndrome was made. Treatment with acitretin showed a marked response. Recognizing this syndrome is crucial. Early treatment helps avoid scar formation.
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spelling pubmed-95525442022-10-14 Multiple keratoacanthomas of Ferguson‐Smith type Litaiem, Noureddine Khammouma, Ferdaous Mrad, Malek Bacha, Takwa Belhadj Kacem, Linda Zeglaoui, Faten Clin Case Rep Case Report We report a case of a 41‐year‐old male patient with no family history, presented with extensive multiple keratoacanthomas with disfiguring scars. The diagnosis of a sporadic form of Ferguson‐Smith syndrome was made. Treatment with acitretin showed a marked response. Recognizing this syndrome is crucial. Early treatment helps avoid scar formation. John Wiley and Sons Inc. 2022-10-11 /pmc/articles/PMC9552544/ /pubmed/36245454 http://dx.doi.org/10.1002/ccr3.6429 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Litaiem, Noureddine
Khammouma, Ferdaous
Mrad, Malek
Bacha, Takwa
Belhadj Kacem, Linda
Zeglaoui, Faten
Multiple keratoacanthomas of Ferguson‐Smith type
title Multiple keratoacanthomas of Ferguson‐Smith type
title_full Multiple keratoacanthomas of Ferguson‐Smith type
title_fullStr Multiple keratoacanthomas of Ferguson‐Smith type
title_full_unstemmed Multiple keratoacanthomas of Ferguson‐Smith type
title_short Multiple keratoacanthomas of Ferguson‐Smith type
title_sort multiple keratoacanthomas of ferguson‐smith type
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552544/
https://www.ncbi.nlm.nih.gov/pubmed/36245454
http://dx.doi.org/10.1002/ccr3.6429
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AT belhadjkacemlinda multiplekeratoacanthomasoffergusonsmithtype
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