Literature DB >> 1259448

Malignant atrophic papulosis (Degros disease). A report of two cases with clinical and histological studies.

S A Muller, M Landry.   

Abstract

Two women had malignant atrophic papulosis that affected the skin only. Immunologic studies showed normal amounts of serum immunoglobulins and complement and normal delayed hypersensitivity skin test results. Fibrinolysis autografts showed complete loss of fibrinolysis within the lesions but normal fibrinolysis in uninvolved skin. Histopathologic studies showed moderate inflammatory infiltration consisting of lymphocytes in addition to the typical cone-shaped regions of necrobiosis. Large amounts of mucin also were seen. Endovasculitis, thrombosis, and perivascular lymphocytic inflammation were noted in the subcutaneous arterioles of the lesions in only one of the patients. Enzyme histochemical studies showed oxidative enzymes, although in reduced amounts, in the epidermal and dermal cells of the affected skin. Electron microscopic studies of lesions showed paromyxovirus-like inclusions in endothelial cells and fibroblasts. The possibility of an unusual viral causation should be examined further.

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Year:  1976        PMID: 1259448     DOI: 10.1001/archderm.112.3.357

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  2 in total

1.  An atypical paediatric case of malignant atrophic papulosis (Köhlmeier-Degos disease).

Authors:  A Barabino; F Pesce; R Gatti; P Colotto; F Nobili; R Colacino; A Giampalmo
Journal:  Eur J Pediatr       Date:  1990-04       Impact factor: 3.183

2.  Lethal systemic degos disease with prominent cardio-pulmonary involvement.

Authors:  Yaghoobi Notash Ali; Mazoochy Hamed; Nikoo Azita
Journal:  Indian J Dermatol       Date:  2011 Sep-Oct       Impact factor: 1.494

  2 in total

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