Results 191 to 200 of about 18,833 (224)
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Pediatric Dermatology, 1995
Abstract: Eosinophilic pannicuiitis is a pooriy defined entity with variabie ciinicai features. We report a case of rapidiy eniarging, asymptomatic subcutaneous scalp nodules in a 6‐year‐old biack boy with atopic dermatitis. The noduies resolved spontaneously over two to three days.
C P, Samlaska +2 more
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Abstract: Eosinophilic pannicuiitis is a pooriy defined entity with variabie ciinicai features. We report a case of rapidiy eniarging, asymptomatic subcutaneous scalp nodules in a 6‐year‐old biack boy with atopic dermatitis. The noduies resolved spontaneously over two to three days.
C P, Samlaska +2 more
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Southern Medical Journal, 1989
We have reviewed the case of a young man with an omental mass diagnosed as mesenteric panniculitis. The clinical history, physical findings, and laboratory and radiologic studies were typical of this disorder. The diagnosis was suggested by CT scan, and confirmed on surgical biopsy.
D W, Monahan, W K, Poston, G J, Brown
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We have reviewed the case of a young man with an omental mass diagnosed as mesenteric panniculitis. The clinical history, physical findings, and laboratory and radiologic studies were typical of this disorder. The diagnosis was suggested by CT scan, and confirmed on surgical biopsy.
D W, Monahan, W K, Poston, G J, Brown
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Journal of the American Academy of Dermatology, 2004
Neutrophilic (lobular) panniculitis (NP) is a very rare condition that belongs to the group of neutrophilic dermatoses. We report the case of a patient with NP and review the relevant literature. NP appears as a subcutaneous nodular eruption. Histology shows a lobular neutrophilic infiltrate.
Claudine, Sutra-Loubet +3 more
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Neutrophilic (lobular) panniculitis (NP) is a very rare condition that belongs to the group of neutrophilic dermatoses. We report the case of a patient with NP and review the relevant literature. NP appears as a subcutaneous nodular eruption. Histology shows a lobular neutrophilic infiltrate.
Claudine, Sutra-Loubet +3 more
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Journal of Cutaneous Pathology, 2007
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.
Eun Ji, Kwon +4 more
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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.
Eun Ji, Kwon +4 more
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The Journal of Dermatology, 1993
AbstractA 39‐year‐old obese female patient with borderline diabetes mellitus who developed multiple, tender, and hard nodules on the lower abdominal wall is described. The histological features were characterized by mixed panniculitis, showing massive eosinophilic infiltration and fibrosis in the septae and many foam cells in the parenchymal area of ...
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AbstractA 39‐year‐old obese female patient with borderline diabetes mellitus who developed multiple, tender, and hard nodules on the lower abdominal wall is described. The histological features were characterized by mixed panniculitis, showing massive eosinophilic infiltration and fibrosis in the septae and many foam cells in the parenchymal area of ...
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Journal of Urology, 1993
Panniculitis is an inflammatory condition of adipose tissue that is mainly seen subcutaneously or intra-abdominally. There have been rare case reports of retroperitoneal involvement but no reported cases of perinephric panniculitis. To our knowledge we report the first documented case of perinephric panniculitis.
S D, Rockoff, J H, Vitenson, R J, Irwin
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Panniculitis is an inflammatory condition of adipose tissue that is mainly seen subcutaneously or intra-abdominally. There have been rare case reports of retroperitoneal involvement but no reported cases of perinephric panniculitis. To our knowledge we report the first documented case of perinephric panniculitis.
S D, Rockoff, J H, Vitenson, R J, Irwin
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Povidone panniculitis. Polyvinylpyrrolidone panniculitis.
Archives of dermatology, 1980Multiple subcutaneous nodules and recurrent flu-like episodes developed in a 60-year-old woman after she had received local intramuscular injections of procaine povidone for a seven-year period. A skin biopsy specimen showed distinctive gray-blue material in the histiocytes in sections stained with hematoxylin-eosin. Povidone is an inert substance that
S, Kossard, R I, Ecker, C H, Dicken
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