Kyrle disease

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Kyrle disease
Classification and external resources
ICD-10 L87.0 (ILDS L87.000)
DiseasesDB 32593

Kyrle disease or hyperkeratosis follicularis et parafollicularis in cutem penetrans was first described in J. Kyrle in 1916, characterized by numerous up to cherry-sized hyperkeratotic, verrucous, clefted papules and nodules involving almost the entire skin.[1][2]

See also

References

  1. ↑ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). Page 685. McGraw-Hill. ISBN 0-07-138076-0.
  2. ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. 


Cutaneous keratosis, ulcer, atrophy, and necrobiosis (L82–L94, 700–701.5)
Epidermal thickening
Necrobiosis/granuloma
Necrobiotic/palisading
Foreign body granuloma
Other/ungrouped
Dermis/
localized CTD
Cutaneous lupus
erythematosus
Scleroderma/
Morphea
  • Localized scleroderma
    • Localized morphea
    • Morphea–lichen sclerosus et atrophicus overlap
    • Generalized morphea
    • Atrophoderma of Pasini and Pierini
    • Pansclerotic morphea
    • Morphea profunda
    • Linear scleroderma
Atrophic/
atrophoderma
Perforating
Skin ulcer
Other

M: INT, SF, LCT

anat/phys/devp

noco (i/b/d/q/u/r/p/m/k/v/f)/cong/tumr (n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)

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