Anetoderma
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(Redirected from Schweninger–Buzzi anetoderma)
| Anetoderma | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | L90.9 (ILDS L90.910) |
| DiseasesDB | 29805 |
| Patient UK | Anetoderma |
Anetoderma (also known as "Anetoderma maculosa,"[1] "Anetoderma maculosa cutis,"[1] "Atrophia maculosa cutis,"[1] and "Macular atrophy"[2]) is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue.[2] Anetoderma comes in three types:
- Primary anetoderma
- Jadassohn–Pellizzari anetoderma is a benign condition with focal loss of dermal elastic tissue.[3] Jadassohn-Pellizzari is one of two major classifications of primary anetoderma, the other being Schweninger–Buzzi anetoderma. The difference between the two is that Jadassohn–Pellizzari anetoderma is preceded by inflammatory lesions.[1]
- Schweninger–Buzzi anetoderma is a cutaneous condition characterized by loss of dermal elastic tissue.[1]
- Secondary anetoderma
- Familial anetoderma
See also
References
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