malignant atrophic papulosis

ma·lig·nant a·troph·ic pa·pu·lo·sis

[MIM*602248] a cutaneovisceral syndrome characterized by pathognomonic umbilicated porcelain-white papules with elevated telangiectatic anular borders, followed by the development of intestinal ulcers that perforate, causing peritonitis; arterioles in the lesions are occluded by thrombosis without inflammatory cells, leading to infarction, progressive neurological disability, and death. Synonym(s): Degos disease, Degos syndrome

malignant atrophic papulosis

A rare, often multisystem disease affecting small blood vessels of the skin, gastrointestinal and genitourinary tracts, central and peripheral nervous systems, heart, lungs, eyes, pancreas, adrenals, and kidneys, which is characterised by proliferation of the vascular intima and thrombosis, and infarction of the regions supplied by the involved arteries.
Clinical patterns
• Malignant systemic form—affects multiple organs and typically causes death within 2 years of presentation due to focal necrosis and perforation of the gastrointestinal tract.
• Benign cutaneous form—limited to the skin.
Management
MAP has been consistently resistant to treatments, including corticosteroids, MTX, sulfonamides, tacrolimus, warfarin, etc.

Degos,

Robert, French dermatologist, 1904-1987. Degos acanthoma - obsolete term for clear cell acanthoma.Degos disease - a cutaneovisceral syndrome characterized by pathognomonic umbilicated porcelain-white papules followed by peritonitis, progressive neurological disability, and death. Synonym(s): Degos syndrome; malignant atrophic papulosisDegos syndrome - Synonym(s): Degos diseaseKohlmeier-Degos syndrome - see under Kohlmeier

单词	malignant atrophic papulosis
释义	DictionarySeepapulosis malignant atrophic papulosis ma·lig·nant a·troph·ic pa·pu·lo·sis [MIM602248] a cutaneovisceral syndrome characterized by pathognomonic umbilicated porcelain-white papules with elevated telangiectatic anular borders, followed by the development of intestinal ulcers that perforate, causing peritonitis; arterioles in the lesions are occluded by thrombosis without inflammatory cells, leading to infarction, progressive neurological disability, and death. Synonym(s): Degos disease, Degos syndrome malignant atrophic papulosis A rare, often multisystem disease affecting small blood vessels of the skin, gastrointestinal and genitourinary tracts, central and peripheral nervous systems, heart, lungs, eyes, pancreas, adrenals, and kidneys, which is characterised by proliferation of the vascular intima and thrombosis, and infarction of the regions supplied by the involved arteries. Clinical patterns • Malignant systemic form—affects multiple organs and typically causes death within 2 years of presentation due to focal necrosis and perforation of the gastrointestinal tract. • Benign cutaneous form—limited to the skin. Management MAP has been consistently resistant to treatments, including corticosteroids, MTX, sulfonamides, tacrolimus, warfarin, etc. Degos, Robert, French dermatologist, 1904-1987. Degos acanthoma* - obsolete term for clear cell acanthoma.Degos disease - a cutaneovisceral syndrome characterized by pathognomonic umbilicated porcelain-white papules followed by peritonitis, progressive neurological disability, and death. Synonym(s): Degos syndrome; malignant atrophic papulosisDegos syndrome - Synonym(s): Degos diseaseKohlmeier-Degos syndrome - see under Kohlmeier
随便看	convulse with convulse with (something) convulsible convulsing convulsing with convulsion convulsional convulsionary convulsionist convulsions convulsive convulsive disorder convulsive equivalent convulsive ergotism convulsive foal syndrome convulsively convulsiveness convulsive reflex convulsive seizure convulsive shock therapy convulsive state convulsive syncope convulsive therapy convulsive tic convulsive uraemia