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Unusual facial lesions in H syndrome
H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological featur...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291265/ https://www.ncbi.nlm.nih.gov/pubmed/35865784 http://dx.doi.org/10.1002/ccr3.6098 |
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author | Rekik, Mariem Bahloul, Emna Ben Rejeb, Mohamed Sellami, Khadija Charfi, Slim Chouk, Hamza Boudaouara, Tahya Turki, Hamida |
author_facet | Rekik, Mariem Bahloul, Emna Ben Rejeb, Mohamed Sellami, Khadija Charfi, Slim Chouk, Hamza Boudaouara, Tahya Turki, Hamida |
author_sort | Rekik, Mariem |
collection | PubMed |
description | H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. |
format | Online Article Text |
id | pubmed-9291265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92912652022-07-20 Unusual facial lesions in H syndrome Rekik, Mariem Bahloul, Emna Ben Rejeb, Mohamed Sellami, Khadija Charfi, Slim Chouk, Hamza Boudaouara, Tahya Turki, Hamida Clin Case Rep Case Report H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. John Wiley and Sons Inc. 2022-07-18 /pmc/articles/PMC9291265/ /pubmed/35865784 http://dx.doi.org/10.1002/ccr3.6098 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Rekik, Mariem Bahloul, Emna Ben Rejeb, Mohamed Sellami, Khadija Charfi, Slim Chouk, Hamza Boudaouara, Tahya Turki, Hamida Unusual facial lesions in H syndrome |
title | Unusual facial lesions in H syndrome |
title_full | Unusual facial lesions in H syndrome |
title_fullStr | Unusual facial lesions in H syndrome |
title_full_unstemmed | Unusual facial lesions in H syndrome |
title_short | Unusual facial lesions in H syndrome |
title_sort | unusual facial lesions in h syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291265/ https://www.ncbi.nlm.nih.gov/pubmed/35865784 http://dx.doi.org/10.1002/ccr3.6098 |
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