Anetoderma
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(Redirected from Jadassohn–Pellizzari anetoderma)
Lua error in Module:Infobox at line 235: malformed pattern (missing ']'). 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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tag; name "Bolognia" defined multiple times with different content - ↑ 2.0 2.1 Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). Page 1027. McGraw-Hill. ISBN 0-07-138076-0.
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