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Pili Torti: A Feature of Numerous Congenital and Acquired Conditions

Pili torti is a rare condition characterized by the presence of the hair shaft, which is flattened at irregular intervals and twisted 180° along its long axis. It is a form of hair shaft disorder with increased fragility. The condition is classified into inherited and acquired. Inherited forms may b...

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Autores principales: Hoffmann, Aleksandra, Waśkiel-Burnat, Anna, Żółkiewicz, Jakub, Blicharz, Leszek, Rakowska, Adriana, Goldust, Mohamad, Olszewska, Małgorzata, Rudnicka, Lidia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432236/
https://www.ncbi.nlm.nih.gov/pubmed/34501349
http://dx.doi.org/10.3390/jcm10173901
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author Hoffmann, Aleksandra
Waśkiel-Burnat, Anna
Żółkiewicz, Jakub
Blicharz, Leszek
Rakowska, Adriana
Goldust, Mohamad
Olszewska, Małgorzata
Rudnicka, Lidia
author_facet Hoffmann, Aleksandra
Waśkiel-Burnat, Anna
Żółkiewicz, Jakub
Blicharz, Leszek
Rakowska, Adriana
Goldust, Mohamad
Olszewska, Małgorzata
Rudnicka, Lidia
author_sort Hoffmann, Aleksandra
collection PubMed
description Pili torti is a rare condition characterized by the presence of the hair shaft, which is flattened at irregular intervals and twisted 180° along its long axis. It is a form of hair shaft disorder with increased fragility. The condition is classified into inherited and acquired. Inherited forms may be either isolated or associated with numerous genetic diseases or syndromes (e.g., Menkes disease, Björnstad syndrome, Netherton syndrome, and Bazex-Dupré-Christol syndrome). Moreover, pili torti may be a feature of various ectodermal dysplasias (such as Rapp-Hodgkin syndrome and Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome). Acquired pili torti was described in numerous forms of alopecia (e.g., lichen planopilaris, discoid lupus erythematosus, dissecting cellulitis, folliculitis decalvans, alopecia areata) as well as neoplastic and systemic diseases (such as cutaneous T-cell lymphoma, scalp metastasis of breast cancer, anorexia nervosa, malnutrition, cataracts, and chronic graft-vs.-host disease). The condition may also be induced by several drugs (epidermal growth factor receptor inhibitors, oral retinoids, sodium valproate, and carbamide perhydrate). The diagnosis of pili torti is based on trichoscopic or microscopic examination. As pili torti is a marker of numerous congenital and acquired disorders, in every case, the search for the signs of underlying conditions is recommended.
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spelling pubmed-84322362021-09-11 Pili Torti: A Feature of Numerous Congenital and Acquired Conditions Hoffmann, Aleksandra Waśkiel-Burnat, Anna Żółkiewicz, Jakub Blicharz, Leszek Rakowska, Adriana Goldust, Mohamad Olszewska, Małgorzata Rudnicka, Lidia J Clin Med Review Pili torti is a rare condition characterized by the presence of the hair shaft, which is flattened at irregular intervals and twisted 180° along its long axis. It is a form of hair shaft disorder with increased fragility. The condition is classified into inherited and acquired. Inherited forms may be either isolated or associated with numerous genetic diseases or syndromes (e.g., Menkes disease, Björnstad syndrome, Netherton syndrome, and Bazex-Dupré-Christol syndrome). Moreover, pili torti may be a feature of various ectodermal dysplasias (such as Rapp-Hodgkin syndrome and Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome). Acquired pili torti was described in numerous forms of alopecia (e.g., lichen planopilaris, discoid lupus erythematosus, dissecting cellulitis, folliculitis decalvans, alopecia areata) as well as neoplastic and systemic diseases (such as cutaneous T-cell lymphoma, scalp metastasis of breast cancer, anorexia nervosa, malnutrition, cataracts, and chronic graft-vs.-host disease). The condition may also be induced by several drugs (epidermal growth factor receptor inhibitors, oral retinoids, sodium valproate, and carbamide perhydrate). The diagnosis of pili torti is based on trichoscopic or microscopic examination. As pili torti is a marker of numerous congenital and acquired disorders, in every case, the search for the signs of underlying conditions is recommended. MDPI 2021-08-30 /pmc/articles/PMC8432236/ /pubmed/34501349 http://dx.doi.org/10.3390/jcm10173901 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hoffmann, Aleksandra
Waśkiel-Burnat, Anna
Żółkiewicz, Jakub
Blicharz, Leszek
Rakowska, Adriana
Goldust, Mohamad
Olszewska, Małgorzata
Rudnicka, Lidia
Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
title Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
title_full Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
title_fullStr Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
title_full_unstemmed Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
title_short Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
title_sort pili torti: a feature of numerous congenital and acquired conditions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432236/
https://www.ncbi.nlm.nih.gov/pubmed/34501349
http://dx.doi.org/10.3390/jcm10173901
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