Epidermal nevus syndrome

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Epidermal nevus syndrome (also known as "Feuerstein and Mims syndrome,"[1][2] and "Solomon's syndrome"[1]:775[3]) was first described in 1968, and consists of extensive epidermal nevi with abnormalities of the CNS, skeleton, skin, cardiovascular system, genitourinary system, and eyes.[2]:634 However, since the syndrome's first description, a broader concept for the "epidermal nevus" syndrome has been proposed, with at least six types being described[4][1]:776:

See also

References

  1. ↑ 1.0 1.1 1.2 Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
  2. ↑ 2.0 2.1 James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  3. ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. 
  4. ↑ Happle, R. "Epidermal nevus syndrome." Semin Dermatol. 1995;14:111.
Tumors: Skin neoplasm, Epidermis (C44.L12–L38/D23.L53-83, 173/216)
Tumor
  • Forms
    • Aberrant
    • Cicatricial
    • Cystic
    • Fibroepithelioma of Pinkus
    • Infltrative
    • Micronodular
    • Nodular
    • Pigmented
    • Polypoid
    • Pore-like
    • Rodent ulcer
    • Superficial
  • Nevoid basal cell carcinoma syndrome
Ungrouped
Benign
tumors
  • Generalized eruptive
  • Keratoacanthoma centrifugum marginatum
  • Multiple
  • Solitary
Other
Epidermal nevus
Other nevus
Ungrouped

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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