Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama

Tuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and extracutaneous hamartomas. The diagnosis is based on the association of major and minor criteria, defined by a consensus conference updated in 2012. The clinical examination of the skin is crucial becaus...

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Main Authors: Marine Cascarino, Stéphanie Leclerc-Mercier
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Dermatopathology
Subjects:
Online Access:https://www.mdpi.com/2296-3529/8/3/29
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spelling doaj-7c4e4fbdbe10442e9f8f340e3cfb93352021-09-25T23:58:26ZengMDPI AGDermatopathology2296-35292021-07-0182923625210.3390/dermatopathology8030029Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A PanoramaMarine Cascarino0Stéphanie Leclerc-Mercier1Department of Pathology, Paris Saint-Joseph Hospital Group, 75014 Paris, FranceReference Center for Genodermatoses (MAGEC Center), Department of Pathology, Necker-Enfants Malades Hospital, Paris Centre University, 75015 Paris, FranceTuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and extracutaneous hamartomas. The diagnosis is based on the association of major and minor criteria, defined by a consensus conference updated in 2012. The clinical examination of the skin is crucial because seven diagnostic criteria are dermatological: four major (hypomelanotic macules, angiofibroma or fibrous cephalic plaques, ungual fibromas, shagreen patches) and three minor criteria (confetti skin lesions, dental enamel pits, intraoral fibromas). Skin biopsy is commonly performed to assert the diagnosis of TSC when the clinical aspect is atypical. Histopathology of TSC cutaneous lesions have been poorly reported until now. In this article, we review the histologic features described in the literature and share our experience of TSC skin biopsies in our pediatric hospital specialized in genetic disorders. Both hypomelanotic lesions and cutaneous hamartomas (angiofibroma/fibrous cephalic plaques, ungual fibromas, shagreen patches) are discussed, including the recent entity called folliculocystic and collagen hamartoma, with a special emphasis on helpful clues for TSC in such lesions.https://www.mdpi.com/2296-3529/8/3/29tuberous sclerosis complexhypomelanotic lesionsconfetti skin lesionsshagreen patchangiofibromacutaneous hamartoma
collection DOAJ
language English
format Article
sources DOAJ
author Marine Cascarino
Stéphanie Leclerc-Mercier
spellingShingle Marine Cascarino
Stéphanie Leclerc-Mercier
Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama
Dermatopathology
tuberous sclerosis complex
hypomelanotic lesions
confetti skin lesions
shagreen patch
angiofibroma
cutaneous hamartoma
author_facet Marine Cascarino
Stéphanie Leclerc-Mercier
author_sort Marine Cascarino
title Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama
title_short Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama
title_full Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama
title_fullStr Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama
title_full_unstemmed Histological Patterns of Skin Lesions in Tuberous Sclerosis Complex: A Panorama
title_sort histological patterns of skin lesions in tuberous sclerosis complex: a panorama
publisher MDPI AG
series Dermatopathology
issn 2296-3529
publishDate 2021-07-01
description Tuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and extracutaneous hamartomas. The diagnosis is based on the association of major and minor criteria, defined by a consensus conference updated in 2012. The clinical examination of the skin is crucial because seven diagnostic criteria are dermatological: four major (hypomelanotic macules, angiofibroma or fibrous cephalic plaques, ungual fibromas, shagreen patches) and three minor criteria (confetti skin lesions, dental enamel pits, intraoral fibromas). Skin biopsy is commonly performed to assert the diagnosis of TSC when the clinical aspect is atypical. Histopathology of TSC cutaneous lesions have been poorly reported until now. In this article, we review the histologic features described in the literature and share our experience of TSC skin biopsies in our pediatric hospital specialized in genetic disorders. Both hypomelanotic lesions and cutaneous hamartomas (angiofibroma/fibrous cephalic plaques, ungual fibromas, shagreen patches) are discussed, including the recent entity called folliculocystic and collagen hamartoma, with a special emphasis on helpful clues for TSC in such lesions.
topic tuberous sclerosis complex
hypomelanotic lesions
confetti skin lesions
shagreen patch
angiofibroma
cutaneous hamartoma
url https://www.mdpi.com/2296-3529/8/3/29
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