Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses
Systemic amyloidosis is a rare disease that can be rapidly progressive due to widespread organ involvement. There are well-described renal, cardiac, pulmonary, neurological, and dermatologic findings. Here, we outline one patient’s experience with the condition from presentation to making the diagno...
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2016-03-01
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Series: | International Journal of Women's Dermatology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2352647515000684 |
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doaj-00e7aa178e4a4ca2bb783b4f43cb0ddc2020-11-25T01:58:49ZengElsevierInternational Journal of Women's Dermatology2352-64752016-03-01211822Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymosesAndrew Kelsey, MD0Diane H. Smith, MD1Joyce Meng, MD2Michael Murphy, MD3Marti J. Rothe, MD4Department of Dermatology, University of Connecticut Health Center, Farmington, ConnecticutDepartment of Dermatology, University of Connecticut Health Center, Farmington, ConnecticutDepartment of Dermatology, University of Connecticut Health Center, Farmington, ConnecticutDepartment of Dermatology, University of Connecticut Health Center, Farmington, ConnecticutCorresponding Author.; Department of Dermatology, University of Connecticut Health Center, Farmington, ConnecticutSystemic amyloidosis is a rare disease that can be rapidly progressive due to widespread organ involvement. There are well-described renal, cardiac, pulmonary, neurological, and dermatologic findings. Here, we outline one patient’s experience with the condition from presentation to making the diagnosis. She presented with pathognomonic dermatologic findings including pinch purpura and ecchymoses found in the skin folds. Key words: apple-green birefringence, amyloid, amyloidosis, Congo red, inframammary erosions, periorbital ecchymoses, pinch purpura, plasma-cell dyscrasia, serum protein electrophoresishttp://www.sciencedirect.com/science/article/pii/S2352647515000684 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrew Kelsey, MD Diane H. Smith, MD Joyce Meng, MD Michael Murphy, MD Marti J. Rothe, MD |
spellingShingle |
Andrew Kelsey, MD Diane H. Smith, MD Joyce Meng, MD Michael Murphy, MD Marti J. Rothe, MD Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses International Journal of Women's Dermatology |
author_facet |
Andrew Kelsey, MD Diane H. Smith, MD Joyce Meng, MD Michael Murphy, MD Marti J. Rothe, MD |
author_sort |
Andrew Kelsey, MD |
title |
Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses |
title_short |
Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses |
title_full |
Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses |
title_fullStr |
Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses |
title_full_unstemmed |
Amyloidosis: A story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses |
title_sort |
amyloidosis: a story of how inframammary erosions eclipsed inconspicuous periorbital ecchymoses |
publisher |
Elsevier |
series |
International Journal of Women's Dermatology |
issn |
2352-6475 |
publishDate |
2016-03-01 |
description |
Systemic amyloidosis is a rare disease that can be rapidly progressive due to widespread organ involvement. There are well-described renal, cardiac, pulmonary, neurological, and dermatologic findings. Here, we outline one patient’s experience with the condition from presentation to making the diagnosis. She presented with pathognomonic dermatologic findings including pinch purpura and ecchymoses found in the skin folds. Key words: apple-green birefringence, amyloid, amyloidosis, Congo red, inframammary erosions, periorbital ecchymoses, pinch purpura, plasma-cell dyscrasia, serum protein electrophoresis |
url |
http://www.sciencedirect.com/science/article/pii/S2352647515000684 |
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