CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES

Cytophagic histiocytic panniculitis (CHP) was first described in 1980 by Winkelmann as a chronic histiocytic disease of the subcutaneous adipose tissue, which is characterized clinically by tender erythematous nodules, recurrent high fever, malaise, jaundice, organomegaly, serosal effusions, pancyto...

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Autores principales: Manoj, Jayasree, Kaliyadan, Feroze, Unni, Manoj, Dharmaratnam, A D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132910/
https://www.ncbi.nlm.nih.gov/pubmed/21772594
http://dx.doi.org/10.4103/0019-5154.82487
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author Manoj, Jayasree
Kaliyadan, Feroze
Unni, Manoj
Dharmaratnam, A D
author_facet Manoj, Jayasree
Kaliyadan, Feroze
Unni, Manoj
Dharmaratnam, A D
author_sort Manoj, Jayasree
collection PubMed
description Cytophagic histiocytic panniculitis (CHP) was first described in 1980 by Winkelmann as a chronic histiocytic disease of the subcutaneous adipose tissue, which is characterized clinically by tender erythematous nodules, recurrent high fever, malaise, jaundice, organomegaly, serosal effusions, pancytopenia, hepatic dysfunction, and coagulatory abnormalities. CHP may occur either isolated or as part of cutaneous manifestations of hemophagocytic syndrome. Here, we report two different presentations of CHP.
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spelling pubmed-31329102011-07-19 CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES Manoj, Jayasree Kaliyadan, Feroze Unni, Manoj Dharmaratnam, A D Indian J Dermatol Case Report Cytophagic histiocytic panniculitis (CHP) was first described in 1980 by Winkelmann as a chronic histiocytic disease of the subcutaneous adipose tissue, which is characterized clinically by tender erythematous nodules, recurrent high fever, malaise, jaundice, organomegaly, serosal effusions, pancytopenia, hepatic dysfunction, and coagulatory abnormalities. CHP may occur either isolated or as part of cutaneous manifestations of hemophagocytic syndrome. Here, we report two different presentations of CHP. Medknow Publications 2011 /pmc/articles/PMC3132910/ /pubmed/21772594 http://dx.doi.org/10.4103/0019-5154.82487 Text en © 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Manoj, Jayasree
Kaliyadan, Feroze
Unni, Manoj
Dharmaratnam, A D
CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES
title CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES
title_full CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES
title_fullStr CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES
title_full_unstemmed CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES
title_short CYTOPHAGIC HISTIOCYTIC PANNICULITIS: REPORT OF TWO CASES
title_sort cytophagic histiocytic panniculitis: report of two cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132910/
https://www.ncbi.nlm.nih.gov/pubmed/21772594
http://dx.doi.org/10.4103/0019-5154.82487
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AT kaliyadanferoze cytophagichistiocyticpanniculitisreportoftwocases
AT unnimanoj cytophagichistiocyticpanniculitisreportoftwocases
AT dharmaratnamad cytophagichistiocyticpanniculitisreportoftwocases

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