نتایج جستجو برای: rosai

تعداد نتایج: 804  

Journal: :An International Journal Clinical Rhinology 2015

Journal: :Haematology Journal of Bangladesh 2020

Journal: :Herz Kardiovaskuläre Erkrankungen 2006

Journal: :Annals of International medical and Dental Research 2017

2016
Md. Taufiq Abul Khair Ferdousy Begum Shabnam Akhter Md. Shamim Farooq Mohammed Kamal

Background. Rosai-Dorfman disease (RDD) is a benign histiocytic proliferative disorder of unknown etiology. This rare condition commonly causes massive cervical lymphadenopathy. Intracranial RDD without any nodal involvement is extremely rare. Case Report. A young Bangladeshi male complained of bilateral complete blindness with left sided deafness for about three years. There was no lymphadenop...

2016
Han Chen Haiyan Zhou Zhi Song

Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease (RDD), is an uncommon benign histioproliferative disorder with systemic symptoms and lymphadenopathy. Mostly affecting lymph nodes, RDD typically presents as substantial painless bilateral cervical lymphadenopathy associated with fever, leukocytosis, anemia, polyclonal hypergammaglobulinemia, and increased ery...

Journal: :The Journal of the Association of Physicians of India 2016
Harshit Jain Nikhil Gupta Jalees Fatima Ritu Karoli Vaibhav Shukla

Rosai Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy (SHML) is a rare disorder that typically manifests as lymphadenopathy and systemic symptoms.The authors report a 56 year old man who presented with massive generalised lymphadenopathy with haemolytic anaemia. Histopathological examination demonstrated lymphophagocytosis (emperipolesis) consistent with a diagnosis of...

2010
Munenori Ide Takayuki Asao Takatomo Yoshida Junko Hirato Tatsuo Shimura Nobuhiro Morinaga Yoshinori Shitara Masatoshi Ishizaki Hiroyuki Kuwano

Rosai-Dorfman disease (RDD) was formerly known as "sinus histiocytosis with massive lymphadenopathy", and cases involving the gastrointestinal tract are rare. We present a case of pure extranodal RDD, resected as a polypoid lesion in colonoscopic study. The patient was a 62-year old woman with a history of sigmoidectomy for unexplained peritonitis. Microscopic study of the polypoid lesion showe...

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