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Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report

Amyloidosis is a group of heterogeneous diseases characterized by pathological deposition of proteinaceous substance extracellularly in various tissues. The clinical presentation depends on the site of amyloid deposition, with predominant involvement of mesenchymal elements and cutaneous findings in...

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Autores principales: Vyas, Kapil, Morgaonkar, Manjaree, Gupta, Savera, Jain, Suresh Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817453/
https://www.ncbi.nlm.nih.gov/pubmed/27057028
http://dx.doi.org/10.4103/0019-5154.177767
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author Vyas, Kapil
Morgaonkar, Manjaree
Gupta, Savera
Jain, Suresh Kumar
author_facet Vyas, Kapil
Morgaonkar, Manjaree
Gupta, Savera
Jain, Suresh Kumar
author_sort Vyas, Kapil
collection PubMed
description Amyloidosis is a group of heterogeneous diseases characterized by pathological deposition of proteinaceous substance extracellularly in various tissues. The clinical presentation depends on the site of amyloid deposition, with predominant involvement of mesenchymal elements and cutaneous findings in 30–40% of patients in case of primary systemic amyloidosis. We present a case of idiopathic primary systemic amyloidosis presenting with an unusual finding of nodulo-ulcerative lesion over tongue along with multiple skin-colored nodules, mimicking squamous cell carcinoma of tongue with secondary cutaneous metastasis, as well as lacking the classical presentation of purpura, macroglossia, waxy papules, and plaques.
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spelling pubmed-48174532016-04-07 Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report Vyas, Kapil Morgaonkar, Manjaree Gupta, Savera Jain, Suresh Kumar Indian J Dermatol Case Report Amyloidosis is a group of heterogeneous diseases characterized by pathological deposition of proteinaceous substance extracellularly in various tissues. The clinical presentation depends on the site of amyloid deposition, with predominant involvement of mesenchymal elements and cutaneous findings in 30–40% of patients in case of primary systemic amyloidosis. We present a case of idiopathic primary systemic amyloidosis presenting with an unusual finding of nodulo-ulcerative lesion over tongue along with multiple skin-colored nodules, mimicking squamous cell carcinoma of tongue with secondary cutaneous metastasis, as well as lacking the classical presentation of purpura, macroglossia, waxy papules, and plaques. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4817453/ /pubmed/27057028 http://dx.doi.org/10.4103/0019-5154.177767 Text en Copyright: © 2016 Indian Journal of Dermatology 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Vyas, Kapil
Morgaonkar, Manjaree
Gupta, Savera
Jain, Suresh Kumar
Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report
title Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report
title_full Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report
title_fullStr Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report
title_full_unstemmed Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report
title_short Primary Systemic Amyloidosis with Unusual Dermatological Manifestations: A Rare Case Report
title_sort primary systemic amyloidosis with unusual dermatological manifestations: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817453/
https://www.ncbi.nlm.nih.gov/pubmed/27057028
http://dx.doi.org/10.4103/0019-5154.177767
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