Reactive perforating collagenosis
| Reactive perforating collagenosis | |
| ICD-10 | L87.1 (ILDS L87.100) |
|---|---|
| DiseasesDB | 31375 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Reactive perforating collagenosis is a rare, familial, nonpuritic skin disorder characterized by papules that grow in a diameter of 4 to 6mm and develop a central area of umbilication to which keratinous material is lodged.[1][2] The etiology of reactive perforating collagenosis is unknown.
See also
References
- ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Page 510. ISBN 0-7216-2921-0.
- ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
Template:Skin-appendage-stub Template:Cutaneous ketatosis, ulcer, atrophy, and necrobiosis