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Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report

Mixed connective tissue disorder (MCTD) is a multisystem disease with overlapping features of other autoimmune diseases, such as systemic lupus erythematosus (SLE), myositis, rheumatoid arthritis, and scleroderma. MCTD presents with a distinctive antibody in serum known as U1-ribonucleoprotein (RNP)...

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Autores principales: Naqvi, Syeda, Talib, Vikash, Aijaz, Razia, Ali, Zeeshan, Bashir, Shehroz, Ahmad, Syed Masroor, Naveed, Shabnam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498117/
https://www.ncbi.nlm.nih.gov/pubmed/28690947
http://dx.doi.org/10.7759/cureus.1313
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author Naqvi, Syeda
Talib, Vikash
Aijaz, Razia
Ali, Zeeshan
Bashir, Shehroz
Ahmad, Syed Masroor
Naveed, Shabnam
author_facet Naqvi, Syeda
Talib, Vikash
Aijaz, Razia
Ali, Zeeshan
Bashir, Shehroz
Ahmad, Syed Masroor
Naveed, Shabnam
author_sort Naqvi, Syeda
collection PubMed
description Mixed connective tissue disorder (MCTD) is a multisystem disease with overlapping features of other autoimmune diseases, such as systemic lupus erythematosus (SLE), myositis, rheumatoid arthritis, and scleroderma. MCTD presents with a distinctive antibody in serum known as U1-ribonucleoprotein (RNP). MCTD is quite rare as compared to other connective tissue disorders like SLE, systemic sclerosis, dermatomyositis, and polymyositis. We describe a case of MCTD in a young Asian female of 30 year old. This case highlights rare co-existence of polyneuropathy and autoamputation in MCTD disorder. Trigeminal neuralgia and cranial nerve involvements have been previously reported in MCTD but the findings of polyneuropathy and autoamputation are extremely rare.
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spelling pubmed-54981172017-07-07 Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report Naqvi, Syeda Talib, Vikash Aijaz, Razia Ali, Zeeshan Bashir, Shehroz Ahmad, Syed Masroor Naveed, Shabnam Cureus Rheumatology Mixed connective tissue disorder (MCTD) is a multisystem disease with overlapping features of other autoimmune diseases, such as systemic lupus erythematosus (SLE), myositis, rheumatoid arthritis, and scleroderma. MCTD presents with a distinctive antibody in serum known as U1-ribonucleoprotein (RNP). MCTD is quite rare as compared to other connective tissue disorders like SLE, systemic sclerosis, dermatomyositis, and polymyositis. We describe a case of MCTD in a young Asian female of 30 year old. This case highlights rare co-existence of polyneuropathy and autoamputation in MCTD disorder. Trigeminal neuralgia and cranial nerve involvements have been previously reported in MCTD but the findings of polyneuropathy and autoamputation are extremely rare. Cureus 2017-06-05 /pmc/articles/PMC5498117/ /pubmed/28690947 http://dx.doi.org/10.7759/cureus.1313 Text en Copyright © 2017, Naqvi et al. http://creativecommons.org/licenses/by/3.0/ 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 author and source are credited.
spellingShingle Rheumatology
Naqvi, Syeda
Talib, Vikash
Aijaz, Razia
Ali, Zeeshan
Bashir, Shehroz
Ahmad, Syed Masroor
Naveed, Shabnam
Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report
title Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report
title_full Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report
title_fullStr Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report
title_full_unstemmed Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report
title_short Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report
title_sort autoamputation and polyneuropathy in mixed connective tissue disorder: a case report
topic Rheumatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498117/
https://www.ncbi.nlm.nih.gov/pubmed/28690947
http://dx.doi.org/10.7759/cureus.1313
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