Costa acrokeratoelastoidosis: a rare case


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The paper considers the etiopathogenetic factors of Costa acrokeratoelastoidosis that is a type of focal palmoplantar keratoderma with predominantly autosomal dominant inheritance and is accompanied by an elastic tissue lesion. It gives clinical and morphological criteria for verifying this pathology: childhood or adolescence diseases; focal palmoplantar keratoderma that is manifested by thickening of the stratum corneum of the palms and soles, by multiple ochroleucous horny papules, hyperhidrosis, as well as by histological changes characteristic of Costa acrokeratoelastoidosis (hyperkeratosis, acanthosis, granulosis of the epidermis and elastorrhexis) in the reticular dermis. The paper describes a rare sporadic case of non-hereditary Costa acrokeratoelastodosis. Its differential diagnosis is performed with focal acral hyperkeratosis and Devergie’s disease. The authors show the important diagnostic role of a histopathological examination of papular elements with the mandatory use of histochemical staining of elastic fibers

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作者简介

M. Tlish

Kuban State Medical University

Email: marina@netzkom.ru
MD Krasnodar

N. Sycheva

Kuban State Medical University

Email: marina@netzkom.ru
Candidate of Medical Sciences Krasnodar

M. Kartashevskaya

Kuban State Medical University

Email: marina@netzkom.ru
Candidate of Medical Sciences Krasnodar

M. Shavilova

Kuban State Medical University

Email: marina@netzkom.ru
Krasnodar

F. Psavok

Kuban State Medical University

Email: marina@netzkom.ru
Candidate of Medical Sciences Krasnodar

参考

  1. Скрипкин Ю.К., Бутов Ю.С. Клиническая дерматовенерология: руководство для врачей. Т. II / М.: ГЭОТАР-Медиа, 2009; с. 757-8
  2. Costa O. Akrokerato-elastoidosis (a hitherto undescribed skin disease) // Dermatologica. - 1953; 107 (3): 164-8.
  3. Marques L., Trope B., Pina J. et al. Inverse papularacrokeratosis of Oswaldo Costa: a case report // J. Clin. Aesthetic Dermatol. - 2010; 3 (6): 51-3.
  4. AlKahtani H., AlHumidi A., Al-Hargan A. et al. A sporadic case of unilateral acrokeratoelastoidosis in Saudi Arabia: a case report // J. Med. Case Rep. - 2014; 8: 143. doi: 10.1186/1752-1947-8-143.
  5. Turchetto C., Giovanna P., Cabrera H. et al. Acroqueratoelastoidosis de Costa // Arch. Argent. Dermatol. - 2013; 63 (4): 153-6.
  6. Lanssens S., Suys E. Acrokerato-elastoidose van Costa of focaleacralehyperkeratose? // Nederlands Tijdschrift voor Dermatologie en venereology. - 2012; 9 (22): 561-2.
  7. Цветкова Г.М., Мордовцева В.В., Вавилов А.М. и др. Патоморфология болезней кожи. Руководство для врачей / М.: Медицина; 2003
  8. Lopes J., de Almeida H. Jr., da Cunha Filho R. et al. Ultrastructure of acrokeratoelastoidosis // J. Eur. Acad. Dermatol. Venereol. - 2018; 32 (5): 165-7. doi: 10.1111/jdv.14660.
  9. Zanini M. Focal acral hyperkeratosis: case report and discussion on marginal keratodermas // Ann. Bras. Dermatol. - 2006; 81 (5 Supl. 3): 293-6.
  10. Duman H., Oguz Topal I., Cakir C. Acrokeratoelastoidosis and focal acral hyperkeratosis: Report of two cases // Our Dermatol. Online. - 2017; 8 (3): 293-5. doi: 10.7241/ourd.20173.84.
  11. Александрова А.К., Смольянникова В.А., Тертычный А.С. Себорейный кератоз и вульгарные бородавки у пациента с вульгарным ихтиозом // Кубанский научный медицинский вестник. - 2014; 4: 150-3

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