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REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY

Remittent idiopathic necrotizing acrocyanosis is a very rare condition characterized by persistent systemic cyanotic or erythrocyanotic discoloration of hands and feet. It is associated with pain, tenderness of fingers and toes and may present as ulceration or gangrene of extremities. It is aggravat...

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Autores principales: Das, Sudip, Roy, Alok Kumar, Maiti, Arunasis
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856383/
https://www.ncbi.nlm.nih.gov/pubmed/20418987
http://dx.doi.org/10.4103/0019-5154.60362
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author Das, Sudip
Roy, Alok Kumar
Maiti, Arunasis
author_facet Das, Sudip
Roy, Alok Kumar
Maiti, Arunasis
author_sort Das, Sudip
collection PubMed
description Remittent idiopathic necrotizing acrocyanosis is a very rare condition characterized by persistent systemic cyanotic or erythrocyanotic discoloration of hands and feet. It is associated with pain, tenderness of fingers and toes and may present as ulceration or gangrene of extremities. It is aggravated with cold exposure but persists even in summer. Acrocyanosis is not due to any systemic disease; peripheral arteriolar constriction with secondary vasodilatation due to disordered vascular tone of unknown etiology has been postulated. It responds to peripheral vasodilator drug but usually needs continuous long term therapy along with avoidance of cold exposure. We report the case of a 53-year-old male farmer with remittent necrotizing acrocyanosis.
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spelling pubmed-28563832010-04-25 REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY Das, Sudip Roy, Alok Kumar Maiti, Arunasis Indian J Dermatol Case Report Remittent idiopathic necrotizing acrocyanosis is a very rare condition characterized by persistent systemic cyanotic or erythrocyanotic discoloration of hands and feet. It is associated with pain, tenderness of fingers and toes and may present as ulceration or gangrene of extremities. It is aggravated with cold exposure but persists even in summer. Acrocyanosis is not due to any systemic disease; peripheral arteriolar constriction with secondary vasodilatation due to disordered vascular tone of unknown etiology has been postulated. It responds to peripheral vasodilator drug but usually needs continuous long term therapy along with avoidance of cold exposure. We report the case of a 53-year-old male farmer with remittent necrotizing acrocyanosis. Medknow Publications 2010 /pmc/articles/PMC2856383/ /pubmed/20418987 http://dx.doi.org/10.4103/0019-5154.60362 Text en © Indian Journal of Dermatology http://creativecommons.org/licenses/by/2.0/ 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 work is properly cited.
spellingShingle Case Report
Das, Sudip
Roy, Alok Kumar
Maiti, Arunasis
REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY
title REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY
title_full REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY
title_fullStr REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY
title_full_unstemmed REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY
title_short REMITTENT IDIOPATHIC NECROTIZING ACROCYANOSIS - A RARE ENTITY
title_sort remittent idiopathic necrotizing acrocyanosis - a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856383/
https://www.ncbi.nlm.nih.gov/pubmed/20418987
http://dx.doi.org/10.4103/0019-5154.60362
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