Literature DB >> 6175330

Acrokeratoelastoidosis.

A S Highet, A Rook, J R Anderson.   

Abstract

A case of acrokeratoelastoidosis (AKE) is reported. A review of the literature has established that at least three clinicopathological entities have been reported under this term. Two of the entities show a combination of hyperkeratosis with fragmentation of dermal elastic tissue, which justifies the designation AKE. The first, for which the term familial AKE is perhaps appropriate, though many cases have been sporadic, begins in childhood or early adult life, and there is no evidence that trauma or light exposure are factors in its production. The second is a more variable clinical syndrome occurring in middle or late adult life, and both physical trauma and light exposure appear to be concerned in its induction. The third syndrome to be reported under the designation AKE shows no abnormality of elastic tissue and appears to be a separate entity.

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Year:  1982        PMID: 6175330     DOI: 10.1111/j.1365-2133.1982.tb01733.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  3 in total

1.  Pseudo-ainhum, angiodysplasia and focal acral hyperkeratosis.

Authors:  R M Graham; M P James
Journal:  J R Soc Med       Date:  1985       Impact factor: 5.344

2.  Acrokeratoelastoidosis.

Authors:  Kinjal D Rambhia; Uday S Khopkar
Journal:  Indian Dermatol Online J       Date:  2015 Nov-Dec

3.  A sporadic case of unilateral acrokeratoelastoidosis in Saudi Arabia: a case report.

Authors:  Hassan S AlKahtani; Ahmed A AlHumidi; Abdullah H Al-Hargan; Ahmed A Al-Sayed
Journal:  J Med Case Rep       Date:  2014-05-08
  3 in total

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