Sinus Histocytosis with Splenomegaly in Children- A Rare Case Report

Autor:	Soma Halder, Ekhlasur Rahman, Kuntal Roy, Syed Khairul Amin, Fabia Hannan Mone
Rok vydání:	2019
Předmět:	medicine.medical_specialty medicine.anatomical_structure business.industry Rare case medicine General Medicine Radiology business Sinus (anatomy)
Zdroj:	Anwer Khan Modern Medical College Journal. 10:176-178
ISSN:	2304-5701 2221-836X
DOI:	10.3329/akmmcj.v10i2.44132
Popis:	Sinus Histiocytosis/Rosai-Dorfman Disease (RDD) are benign, rare proliferative disorder caused by over production and accumulation of specific type of white blood cell (Phagocytic Histiocyte) in the lymph nodes of the body. Here, lymphadenopathy mostly painless and commonly found in the neck (cervical) but may occur in other areas of the body such as skin, lung, central nervous system, kidney (less than 5%). Predominantly it affects the young age group of children, adolescents or young adults. In spite of spontaneous remissions, treatment strategies can be different according to involvement and severity (RDD- Seldom life threatening disease). Anwer Khan Modern Medical College Journal Vol. 10, No. 2: July 2019, P 176-178
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7a94b7ab954fad566745c1f0f8acbfbb https://doi.org/10.3329/akmmcj.v10i2.44132 Zobrazit plný text záznamu