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Brooke-Spiegler Syndrome: A Rare Entity

Brooke-Spiegler syndrome (BSS) is a rare autosomal dominant disorder characterized by the presence of various adnexal tumors including multiple cylindromas, trichoepitheliomas and spiradenomas. A 35-year-old female presented with multiple asymptomatic nodular lesions over face and scalp since the ag...

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Autores principales: Manchanda, Kajal, Bansal, Manish, Bhayana, Aakash Amar, Pandey, SS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358935/
https://www.ncbi.nlm.nih.gov/pubmed/22628987
http://dx.doi.org/10.4103/0974-7753.96084
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author Manchanda, Kajal
Bansal, Manish
Bhayana, Aakash Amar
Pandey, SS
author_facet Manchanda, Kajal
Bansal, Manish
Bhayana, Aakash Amar
Pandey, SS
author_sort Manchanda, Kajal
collection PubMed
description Brooke-Spiegler syndrome (BSS) is a rare autosomal dominant disorder characterized by the presence of various adnexal tumors including multiple cylindromas, trichoepitheliomas and spiradenomas. A 35-year-old female presented with multiple asymptomatic nodular lesions over face and scalp since the age of 5 years. There were no complaints suggestive of systemic involvement. Her son, elder sister, younger sister, father, father's sister, and grandmother had history of similar lesions. On examination, there were multiple asymptomatic skin-colored firm papulonodular lesions measuring from 2 to 8 mm in diameter, with smooth surface mainly affecting central part of face. Scalp showed pinkish, firm, smooth-surfaced, dome-shaped nodules measuring about 1 to 3 cm in size. Histopathological examination was consistent with trichoepitheliomas for the facial lesions and cylindromas for the scalp lesions. The diagnosis of BSS was thus confirmed.
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spelling pubmed-33589352012-05-24 Brooke-Spiegler Syndrome: A Rare Entity Manchanda, Kajal Bansal, Manish Bhayana, Aakash Amar Pandey, SS Int J Trichology Case Report Brooke-Spiegler syndrome (BSS) is a rare autosomal dominant disorder characterized by the presence of various adnexal tumors including multiple cylindromas, trichoepitheliomas and spiradenomas. A 35-year-old female presented with multiple asymptomatic nodular lesions over face and scalp since the age of 5 years. There were no complaints suggestive of systemic involvement. Her son, elder sister, younger sister, father, father's sister, and grandmother had history of similar lesions. On examination, there were multiple asymptomatic skin-colored firm papulonodular lesions measuring from 2 to 8 mm in diameter, with smooth surface mainly affecting central part of face. Scalp showed pinkish, firm, smooth-surfaced, dome-shaped nodules measuring about 1 to 3 cm in size. Histopathological examination was consistent with trichoepitheliomas for the facial lesions and cylindromas for the scalp lesions. The diagnosis of BSS was thus confirmed. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3358935/ /pubmed/22628987 http://dx.doi.org/10.4103/0974-7753.96084 Text en Copyright: © International Journal of Trichology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Manchanda, Kajal
Bansal, Manish
Bhayana, Aakash Amar
Pandey, SS
Brooke-Spiegler Syndrome: A Rare Entity
title Brooke-Spiegler Syndrome: A Rare Entity
title_full Brooke-Spiegler Syndrome: A Rare Entity
title_fullStr Brooke-Spiegler Syndrome: A Rare Entity
title_full_unstemmed Brooke-Spiegler Syndrome: A Rare Entity
title_short Brooke-Spiegler Syndrome: A Rare Entity
title_sort brooke-spiegler syndrome: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358935/
https://www.ncbi.nlm.nih.gov/pubmed/22628987
http://dx.doi.org/10.4103/0974-7753.96084
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