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Amyloïdosis, sarcoidosis and systemic lupus erythematosus

The occurrence of renal and multiple organ Amyloïdosis is currently considered exceptional in the course of systemic lupus erythematosus. We report a case of a concomitant SLE and Amyloïdosis in a 57 year old female patient with hypothyroidism history, who presented with erythema nodosum, fever, art...

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Autores principales: Rezgui, Amel, Hassine, Imene Ben, Karmani, Monia, Fredj, Fatma Ben, Laouani, Chadia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992389/
https://www.ncbi.nlm.nih.gov/pubmed/27583087
http://dx.doi.org/10.11604/pamj.2016.24.23.8853
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author Rezgui, Amel
Hassine, Imene Ben
Karmani, Monia
Fredj, Fatma Ben
Laouani, Chadia
author_facet Rezgui, Amel
Hassine, Imene Ben
Karmani, Monia
Fredj, Fatma Ben
Laouani, Chadia
author_sort Rezgui, Amel
collection PubMed
description The occurrence of renal and multiple organ Amyloïdosis is currently considered exceptional in the course of systemic lupus erythematosus. We report a case of a concomitant SLE and Amyloïdosis in a 57 year old female patient with hypothyroidism history, who presented with erythema nodosum, fever, arthralgia and sicca syndrome. Biological findings showed an inflammatory syndrome, renal failure, proteinuria (1g / 24h), positive auto antibodies and anti DNA. Lung radiology revealed medistinal lymphadenopathy, pleural nodules, ground glass infiltrates and pleuritis. Bronchial biopsy showed non specific inflammation. The salivary gland biopsy showed amyloïd deposits. This case report reminds us that lupus and Amyloïdosis association, although exceptional remains possible. The occurrence of Lofgren syndrome in this situation make the originality of this report.
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spelling pubmed-49923892016-08-31 Amyloïdosis, sarcoidosis and systemic lupus erythematosus Rezgui, Amel Hassine, Imene Ben Karmani, Monia Fredj, Fatma Ben Laouani, Chadia Pan Afr Med J Case Report The occurrence of renal and multiple organ Amyloïdosis is currently considered exceptional in the course of systemic lupus erythematosus. We report a case of a concomitant SLE and Amyloïdosis in a 57 year old female patient with hypothyroidism history, who presented with erythema nodosum, fever, arthralgia and sicca syndrome. Biological findings showed an inflammatory syndrome, renal failure, proteinuria (1g / 24h), positive auto antibodies and anti DNA. Lung radiology revealed medistinal lymphadenopathy, pleural nodules, ground glass infiltrates and pleuritis. Bronchial biopsy showed non specific inflammation. The salivary gland biopsy showed amyloïd deposits. This case report reminds us that lupus and Amyloïdosis association, although exceptional remains possible. The occurrence of Lofgren syndrome in this situation make the originality of this report. The African Field Epidemiology Network 2016-05-06 /pmc/articles/PMC4992389/ /pubmed/27583087 http://dx.doi.org/10.11604/pamj.2016.24.23.8853 Text en © Amel Rezgui et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rezgui, Amel
Hassine, Imene Ben
Karmani, Monia
Fredj, Fatma Ben
Laouani, Chadia
Amyloïdosis, sarcoidosis and systemic lupus erythematosus
title Amyloïdosis, sarcoidosis and systemic lupus erythematosus
title_full Amyloïdosis, sarcoidosis and systemic lupus erythematosus
title_fullStr Amyloïdosis, sarcoidosis and systemic lupus erythematosus
title_full_unstemmed Amyloïdosis, sarcoidosis and systemic lupus erythematosus
title_short Amyloïdosis, sarcoidosis and systemic lupus erythematosus
title_sort amyloïdosis, sarcoidosis and systemic lupus erythematosus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992389/
https://www.ncbi.nlm.nih.gov/pubmed/27583087
http://dx.doi.org/10.11604/pamj.2016.24.23.8853
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