Congenital Letterer-Siwe disease

dc.contributor.author	Plotski, A.
dc.contributor.author	Lupachik, E.
dc.contributor.author	Kononov, V,
dc.contributor.author	Sementkova, S.
dc.contributor.author	Smirnova, E.
dc.date.accessioned	2016-09-14T08:04:57Z
dc.date.available	2016-09-14T08:04:57Z
dc.date.issued	2013-01
dc.identifier.citation	Congenital Letterer-Siwe disease / A. Plotski, E. Lupachik, V. Kononov, S. Sementkova. E. Smirnova // Archives of Perinatal Medicine. – 2013. – Vol. 19, № 1. – Р. 55-57.	ru_RU
dc.identifier.uri	http://elib.grsmu.by/handle/files/760
dc.description	histiocytosis, congenital, pregnancy	ru_RU
dc.description.abstract	Langerhans' cells histiocytosis represent a group of rare disorders characterized by reactive infiltrates that usually are composed of varying proportions of histiocytes, lymphocytes, plasma cells, eosinophils, and neutrophils. Letterer-Siwe disease is the most severe form of histiocytoses. It commonly presents within the first year of life and, occasionally, in neonates. We present clinical and histopathological pictures in a neonate with unrecognized congenital Letterer-Siwe disease. The child died due to diffuse infiltration of lungs with histiocytic cells.	ru_RU
dc.language.iso	en	ru_RU
dc.title	Congenital Letterer-Siwe disease	ru_RU
dc.type	Article	ru_RU