| Descriptor English: | Malignant Atrophic Papulosis | ||||||
| Descriptor Spanish: |
Papulosis Atrófica Maligna
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| Descriptor Portuguese: | Papulose Atrófica Maligna | ||||||
| Descriptor French: | Papulose atrophiante maligne | ||||||
| Entry term(s): |
Atrophic Papuloses, Malignant Atrophic Papulosis, Malignant Degos Disease Degos Syndrome Degos's Malignant Atrophic Papulosis Disease, Degos Disease, Kohlmeier-Degos Erythrokeratoderma en cocardes Kohlmeier-Degos Disease Malignant Atrophic Papuloses Papuloses, Malignant Atrophic Papulosis, Malignant Atrophic Syndrome, Degos |
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| Tree number(s): |
C14.907.137.520 C14.907.940.530 C17.800.862.457 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D054853 | ||||||
| Scope note: | Variously described as a vasculopathy, endovasculitis, or occlusive arteriopathy, this condition occurs in a benign cutaneous form and a lethal multiorgan systemic variant. It is characterized by a narrowing and occlusion of the lumen of small to medium-sized blood vessels, leading to ischemia and infarction in the involved organ systems. The etiology and pathophysiology are unknown. |
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| Annotation: | malignant does not refer to neoplasm; do not confuse with the neoplasm ACANTHOMA, DEGOS see ACANTHOMA |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2008 |
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| History Note: | 2008 |
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| DeCS ID: | 52617 | ||||||
| Unique ID: | D054853 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2008/01/01 | ||||||
| Date of Entry: | 2007/07/09 | ||||||
| Revision Date: | 2012/07/03 |
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Malignant Atrophic Papulosis
- Preferred
| Concept UI |
M0508347 |
| Scope note | Variously described as a vasculopathy, endovasculitis, or occlusive arteriopathy, this condition occurs in a benign cutaneous form and a lethal multiorgan systemic variant. It is characterized by a narrowing and occlusion of the lumen of small to medium-sized blood vessels, leading to ischemia and infarction in the involved organ systems. The etiology and pathophysiology are unknown. |
| Preferred term | Malignant Atrophic Papulosis |
| Entry term(s) |
Atrophic Papuloses, Malignant Atrophic Papulosis, Malignant Degos Disease Degos Syndrome Degos's Malignant Atrophic Papulosis Disease, Degos Disease, Kohlmeier-Degos Erythrokeratoderma en cocardes Kohlmeier-Degos Disease Malignant Atrophic Papuloses Papuloses, Malignant Atrophic Papulosis, Malignant Atrophic Syndrome, Degos |
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