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Multiple milia formation in blistering diseases

BACKGROUND: Milia are superficial keratinous cysts seen as pearly white, dome-shaped lesions 1–2 mm in diameter. Milia are associated with diseases that cause subepidermal blistering, such as hereditary forms of epidermolysis bullosa, epidermolysis bullosa acquisita, bullous pemphigoid, bullous lich...

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Autores principales: Patsatsi, Aikaterini, Uy, Cybill Dianne C., Murrell, Dedee F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330451/
https://www.ncbi.nlm.nih.gov/pubmed/32637544
http://dx.doi.org/10.1016/j.ijwd.2020.03.045
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author Patsatsi, Aikaterini
Uy, Cybill Dianne C.
Murrell, Dedee F.
author_facet Patsatsi, Aikaterini
Uy, Cybill Dianne C.
Murrell, Dedee F.
author_sort Patsatsi, Aikaterini
collection PubMed
description BACKGROUND: Milia are superficial keratinous cysts seen as pearly white, dome-shaped lesions 1–2 mm in diameter. Milia are associated with diseases that cause subepidermal blistering, such as hereditary forms of epidermolysis bullosa, epidermolysis bullosa acquisita, bullous pemphigoid, bullous lichen planus, and porphyria cutanea tarda. Multiple eruptive milia are rare and more extensive in number than primary milia. OBJECTIVE: The aim of this study was to search the literature for cases of blistering diseases with multiple milia formation, especially in areas of the skin where there was no evidence of blistering or trauma, and review the interpretations of their pathogenesis. METHODS: We performed a literature search with the terms multiple milia and bullous diseases, pemphigoid, and pemphigus. RESULTS: Very few studies have investigated the origin of milia. Primary milia are thought to originate from the sebaceous collar of vellus hairs, and secondary milia are believed to derive from eccrine ducts more commonly than from overlying epidermis, hair follicles, or sebaceous ducts. Milia secondary to blisters or trauma are speculated to be produced through the regeneration process of disrupted sweat glands or hair follicles. Immunological predisposition, aberrant interaction between the hemidesmosomes, and the extracellular matrix components beneath the hemidesmosomes have been described with regard to the formation of numerous milia during recovery. Multiple milia could be a primary manifestation of dystrophic epidermolysis bullosa in skin areas without evidence of blistering. CONCLUSION: The exact etiology of multiple milia remains unknown. Immunological predisposition and improper interaction between hemidesmosomes and extracellular matrix components are speculated to play a role in the formation of milia during recovery of bullous lesions in blistering diseases. Still, further studies on the triggering mechanisms of keratinocyte dysfunction in cases of multiple milia formation without evidence of prior blistering are needed.
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spelling pubmed-73304512020-07-06 Multiple milia formation in blistering diseases Patsatsi, Aikaterini Uy, Cybill Dianne C. Murrell, Dedee F. Int J Womens Dermatol Article BACKGROUND: Milia are superficial keratinous cysts seen as pearly white, dome-shaped lesions 1–2 mm in diameter. Milia are associated with diseases that cause subepidermal blistering, such as hereditary forms of epidermolysis bullosa, epidermolysis bullosa acquisita, bullous pemphigoid, bullous lichen planus, and porphyria cutanea tarda. Multiple eruptive milia are rare and more extensive in number than primary milia. OBJECTIVE: The aim of this study was to search the literature for cases of blistering diseases with multiple milia formation, especially in areas of the skin where there was no evidence of blistering or trauma, and review the interpretations of their pathogenesis. METHODS: We performed a literature search with the terms multiple milia and bullous diseases, pemphigoid, and pemphigus. RESULTS: Very few studies have investigated the origin of milia. Primary milia are thought to originate from the sebaceous collar of vellus hairs, and secondary milia are believed to derive from eccrine ducts more commonly than from overlying epidermis, hair follicles, or sebaceous ducts. Milia secondary to blisters or trauma are speculated to be produced through the regeneration process of disrupted sweat glands or hair follicles. Immunological predisposition, aberrant interaction between the hemidesmosomes, and the extracellular matrix components beneath the hemidesmosomes have been described with regard to the formation of numerous milia during recovery. Multiple milia could be a primary manifestation of dystrophic epidermolysis bullosa in skin areas without evidence of blistering. CONCLUSION: The exact etiology of multiple milia remains unknown. Immunological predisposition and improper interaction between hemidesmosomes and extracellular matrix components are speculated to play a role in the formation of milia during recovery of bullous lesions in blistering diseases. Still, further studies on the triggering mechanisms of keratinocyte dysfunction in cases of multiple milia formation without evidence of prior blistering are needed. Elsevier 2020-04-01 /pmc/articles/PMC7330451/ /pubmed/32637544 http://dx.doi.org/10.1016/j.ijwd.2020.03.045 Text en © 2020 Published by Elsevier Inc. on behalf of Women's Dermatologic Society. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Patsatsi, Aikaterini
Uy, Cybill Dianne C.
Murrell, Dedee F.
Multiple milia formation in blistering diseases
title Multiple milia formation in blistering diseases
title_full Multiple milia formation in blistering diseases
title_fullStr Multiple milia formation in blistering diseases
title_full_unstemmed Multiple milia formation in blistering diseases
title_short Multiple milia formation in blistering diseases
title_sort multiple milia formation in blistering diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330451/
https://www.ncbi.nlm.nih.gov/pubmed/32637544
http://dx.doi.org/10.1016/j.ijwd.2020.03.045
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