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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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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. |
format | Online Article Text |
id | pubmed-6501649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sutherlandrorya scalpbiopsyidentifiessystemicamyloidosispresentingasisolatedtelogeneffluviumacasereport AT crawfordrichardi scalpbiopsyidentifiessystemicamyloidosispresentingasisolatedtelogeneffluviumacasereport |