Scleromyxedema as a systemic disease of glycosaminoglycan accumulation
Раденска-Лоповок С. Г., Волкова П., Городецкy В. Р., Егорова О. Н., Ананьева Л. П.
Архив патологии
Т. 80, Вып. 3, С. 53-58
Опубликовано: 2018
Тип ресурса: Статья
DOI:10.17116/patol201880353-58
Аннотация:
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. © 2018 Media Sphera Publishing Group. All rights reserved.
Ключевые слова:
Morphological diagnosis; Mucinoses; Scleroderma; Scleromyxedema
glycosaminoglycan; complication; human; lichenoid eruption; metabolism; scleromyxedema; skin disease; Glycosaminoglycans; Humans; Lichenoid Eruptions; Scleromyxedema; Skin Diseases
Язык текста: Русский
ISSN: 2309-1266
Раденска-Лоповок С. Г. Стефка Господинова 1951-
Волкова П.
Городецкy В. Р.
Егорова О. Н.
Ананьева Л. П.
Radenska-Lopovok S. G. Stefka Gospodinova 1951-
Volkova P.
Gorodetsky V. R.
Egorova O. N.
Ananyeva L. P.
Scleromyxedema as a systemic disease of glycosaminoglycan accumulation
Текст визуальный непосредственный
Архив патологии
Издательство Медиа Сфера
Т. 80, Вып. 3 С. 53-58
2018
Статья
Morphological diagnosis Mucinoses Scleroderma Scleromyxedema
glycosaminoglycan complication human lichenoid eruption metabolism scleromyxedema skin disease Glycosaminoglycans Humans Lichenoid Eruptions Scleromyxedema Skin Diseases
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. © 2018 Media Sphera Publishing Group. All rights reserved.