Premium
Poststeroid panniculitis
Author(s) -
Kwon Eun Ji,
Emanuel Patrick O.,
Gribetz Canin H.,
Mudgil Adarsh V.,
Phelps Robert G.
Publication year - 2007
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1111/j.1600-0560.2007.00738.x
Subject(s) - panniculitis , medicine , differential diagnosis , pathology , erythema , dermatology , biopsy
Poststeroid panniculitis (PSP) is a rare complication of systemic corticosteroid therapy. Clinically, erythematous nodules and indurated plaques develop on the cheeks of children within days or weeks following rapid systemic steroid tapering or cessation. The clinical differential diagnosis of childhood cheek erythema is broad. However, PSP can be identified by clinical history and, if necessary, with a biopsy. Histologically, PSP presents as lobular panniculitis with a mixed inflammatory infiltrates without vasculitis. Needle‐shaped clefts within adipocytes are characteristic. The histological differential diagnosis of adipocytes containing needle‐shaped crystals is limited. We describe a case of poststeroid panniculitis and discuss the clinicopathological features and pertinent differential diagnoses.