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Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report

AL amyloidosis is a complication of B-cell dyscrasias and multiple myeloma, manifest as deposition of antibody fragments in many different organs, including the skin. We describe a rare case of this systemic disease which presented with isolated scalp alopecia. Further investigation led to the diagn...

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Autores principales: Sutherland, Rory A, Crawford, Richard I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501649/
https://www.ncbi.nlm.nih.gov/pubmed/31105951
http://dx.doi.org/10.1177/2050313X19847783
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author Sutherland, Rory A
Crawford, Richard I
author_facet Sutherland, Rory A
Crawford, Richard I
author_sort Sutherland, Rory A
collection PubMed
description AL amyloidosis is a complication of B-cell dyscrasias and multiple myeloma, manifest as deposition of antibody fragments in many different organs, including the skin. We describe a rare case of this systemic disease which presented with isolated scalp alopecia. Further investigation led to the diagnosis of an occult plasma-cell dyscrasia, showing the benefit of including systemic amyloidosis in the differential diagnosis of alopecia. The biopsy finding of cutaneous amyloidosis should prompt further workup to exclude an underlying pathology.
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spelling pubmed-65016492019-05-17 Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report Sutherland, Rory A Crawford, Richard I SAGE Open Med Case Rep JCMS Case Report AL amyloidosis is a complication of B-cell dyscrasias and multiple myeloma, manifest as deposition of antibody fragments in many different organs, including the skin. We describe a rare case of this systemic disease which presented with isolated scalp alopecia. Further investigation led to the diagnosis of an occult plasma-cell dyscrasia, showing the benefit of including systemic amyloidosis in the differential diagnosis of alopecia. The biopsy finding of cutaneous amyloidosis should prompt further workup to exclude an underlying pathology. SAGE Publications 2019-05-02 /pmc/articles/PMC6501649/ /pubmed/31105951 http://dx.doi.org/10.1177/2050313X19847783 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle JCMS Case Report
Sutherland, Rory A
Crawford, Richard I
Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
title Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
title_full Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
title_fullStr Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
title_full_unstemmed Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
title_short Scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: A case report
title_sort scalp biopsy identifies systemic amyloidosis presenting as isolated telogen effluvium: a case report
topic JCMS Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501649/
https://www.ncbi.nlm.nih.gov/pubmed/31105951
http://dx.doi.org/10.1177/2050313X19847783
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