Репозиторий Университета

Scleromyxedema as a systemic disease of glycosaminoglycan accumulation


  • Radenska-Lopovok S.
  • Volkova P.
  • Gorodetsky V.
  • Egorova O.
  • Ananyeva L.
Дата публикации:01.01.2018
Журнал: Arkhiv Patologii
БД: Scopus
Ссылка: Scopus

Аннтотация

© 2018 Media Sphera Publishing Group. All rights reserved. Scleromyxedema is a rare mucinosis with a primary skin lesion due to diffuse mucin deposition, sclerosis, and lichenoid eruptions in the absence of hypothyroidism. The paper describes scleromyxedema cases and gives recommendations for the histological diagnosis of the disease by histochemical reactions to detect acid and neutral glycosaminoglycans.


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