Eosinophilic panniculitis: a new form of local reaction with specific immunotherapy.

Allergy

University of Kirikkale, School of Medicine, Süleyman Demirel Research Hospital, Allergic Diseases Department, Kirikkale 71100, Turkey.

Published: November 2009

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http://dx.doi.org/10.1111/j.1398-9995.2009.02114.xDOI Listing

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Background: Cytophagic histiocytic panniculitis (CHP) is a rare panniculitis associated with systemic features characterized by the infiltration of subcutaneous adipose tissue by benign-appearing T lymphocytes and phagocytic histiocytes, mimicking hemophagocytic lymphohistiocytosis (HLH) and subcutaneous panniculitis-like T-cell lymphoma (SPTCL).

Purpose: To establish the clinicopathological features and response to treatment of CHP and evaluate the prognosis of patients and guide therapy based on the current state of knowledge.

Material And Methods: Clinical, laboratory, histopathological, and outcome data of 12 patients with CHP were retrospectively collected between 2009 and 2022.

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