Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association

We report a rare case of systemic lupus erythematosus presenting initially with cutaneous manifestations of linear IgA bullous dermatosis. Later the patient developed renal abnormalities due to thrombotic microangiopathy and lupus nephritis with inflammatory necrotizing vasculitis. Paucity of immune...

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Autores principales: Malipatel, R., Gnanapriya, V., Manocha, A., Inchara, Y. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309391/
https://www.ncbi.nlm.nih.gov/pubmed/30647502
http://dx.doi.org/10.4103/ijn.IJN_200_17
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author Malipatel, R.
Gnanapriya, V.
Manocha, A.
Inchara, Y. K.
author_facet Malipatel, R.
Gnanapriya, V.
Manocha, A.
Inchara, Y. K.
author_sort Malipatel, R.
collection PubMed
description We report a rare case of systemic lupus erythematosus presenting initially with cutaneous manifestations of linear IgA bullous dermatosis. Later the patient developed renal abnormalities due to thrombotic microangiopathy and lupus nephritis with inflammatory necrotizing vasculitis. Paucity of immune deposits was observed on Immunofluorescence. This association of SLE with these cutaneous and renal lesions is rarely reported in the literature.
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spelling pubmed-63093912019-01-15 Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association Malipatel, R. Gnanapriya, V. Manocha, A. Inchara, Y. K. Indian J Nephrol Case Report We report a rare case of systemic lupus erythematosus presenting initially with cutaneous manifestations of linear IgA bullous dermatosis. Later the patient developed renal abnormalities due to thrombotic microangiopathy and lupus nephritis with inflammatory necrotizing vasculitis. Paucity of immune deposits was observed on Immunofluorescence. This association of SLE with these cutaneous and renal lesions is rarely reported in the literature. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6309391/ /pubmed/30647502 http://dx.doi.org/10.4103/ijn.IJN_200_17 Text en Copyright: © 2018 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Malipatel, R.
Gnanapriya, V.
Manocha, A.
Inchara, Y. K.
Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association
title Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association
title_full Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association
title_fullStr Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association
title_full_unstemmed Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association
title_short Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association
title_sort systemic lupus erythematosus with linear iga bullous dermatosis and renal vascular lesions: an extremely rare association
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309391/
https://www.ncbi.nlm.nih.gov/pubmed/30647502
http://dx.doi.org/10.4103/ijn.IJN_200_17
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