scholarly journals Extranodal intraosseous Rosai–Dorfman disease in the lower jaw: a case report and review of the literature

2018 ◽  
Vol 8 (2) ◽  
pp. 34-38
Author(s):  
X. Yang ◽  
S. R. Gvetadze ◽  
K. D. Ilkaev ◽  
M. Lv ◽  
J. Sun ◽  
...  
Keyword(s):  
Case Report ◽  
Review Of The Literature ◽  
Lower Jaw ◽  
Rosai Dorfman Disease

Rosai–Dorfman disease presenting as mediastinal lymphadenopathy: case report and review of the literature

2013 ◽  
Vol 33 (2) ◽  
pp. 120-123 ◽  
Author(s):  
Nazan Cobanoglu ◽  
Nilufer Galip ◽  
Ceyhun Dalkan ◽  
Cem Comunoglu ◽  
Nerin Bahceciler
Keyword(s):  
Case Report ◽  
Mediastinal Lymphadenopathy ◽  
Review Of The Literature ◽  
Rosai Dorfman Disease

Extranodal Rosai-Dorfman Disease Involving Colon A Case Report with Review of the Literature

2010 ◽  
Vol 3 (3) ◽  
pp. 128 ◽  
Author(s):  
Haiying Chen ◽  
Jianlan Sun ◽  
Lalarukh Aftab ◽  
Amy Sands ◽  
◽  
...  
Keyword(s):  
Case Report ◽  
Review Of The Literature ◽  
Rosai Dorfman Disease

scholarly journals Isolated Intracranial Rosai-Dorfman Disease Mimicking Suprasellar Meningioma: Case Report with Review of the Literature

2008 ◽  
Vol 36 (5) ◽  
pp. 1134-1139 ◽  
Author(s):  
S Swan ◽  
X Teng ◽  
R Zhan ◽  
J Yu ◽  
J Gu ◽  
...  
Keyword(s):  
Case Report ◽  
Lymph Nodes ◽  
Definitive Diagnosis ◽  
Review Of The Literature ◽  
Radiological Features ◽  
Rosai Dorfman Disease

Rosai-Dorfman disease (RDD) is an idiopathic histiocytic proliferation affecting the lymph nodes. Isolated intracranial RDD is rare and usually appears as a well-defined, dural-based lesion without lymphadenopathy. The clinical and radiological features of intracranial RDD are similar to meningioma. Histopathology and immunohistochemistry are essential for a definitive diagnosis. This is a report of a 43-year old male with isolated intracranial RDD, which manifested as a suprasellar meningioma. The clinical, radiological and pathological aspects of the disease are discussed within the context of a review of previously reported cases.

scholarly journals Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature

2018 ◽  
Vol 11 (1) ◽  
pp. 55-62 ◽  
Author(s):  
Amer A. Lardhi ◽  
Abdullah K. Al-Mutairi ◽  
Mohammed H. Al-Qahtani ◽  
Atheer K. Al-Mutairi
Keyword(s):  
Case Report ◽  
Hemolytic Anemia ◽  
Autoimmune Hemolytic Anemia ◽  
Female Child ◽  
Infectious Agents ◽  
Review Of The Literature ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Generalized Lymphadenopathy

Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented with fever, pallor, and generalized lymphadenopathy complicated by the development of autoimmune hemolytic anemia. A review of the literature of this condition is also provided.

scholarly journals Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature

2016 ◽  
Vol 16 (1) ◽  
Author(s):  
Francesco di Dio ◽  
Ilaria Mariotti ◽  
Elena Coccolini ◽  
Patrizia Bruzzi ◽  
Barbara Predieri ◽  
...  
Keyword(s):  
Case Report ◽  
Unusual Presentation ◽  
Review Of The Literature ◽  
Italian Child ◽  
Rosai Dorfman Disease
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