Autor: |
Farkaš D, Švajdler Ml M, Fröhlichová L, Šprláková J, Iannaccone SF, Szép Z, Nyitrayová O |
Jazyk: |
čeština |
Zdroj: |
Ceskoslovenska patologie [Cesk Patol] 2015; Vol. 51 (2), pp. 89-93. |
Abstrakt: |
Epidermolysis bullosa represents a group of mechanobullous diseases which are most commonly genetically determined. We describe the case of a 15-day-old female newborn with congenital epidermolysis bullosa which was inflicted on aproximately 1/3 of her skin surface, who died because of incorrigible sepsis with multiorgan failure. The main topic of our report is a description of an unusual pulmonary finding of massive alveolar filling with foamy macrophages after amnion fluid aspiration, which contained a excessive amount of desquamated epidermal cells. Introduced case shows outstanding discrepancy of negative clinical finding on one side and massive histopathological finding on the other. |
Databáze: |
MEDLINE |
Externí odkaz: |
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