scholarly journals HISTOCYTOPATHOLOGICAL DIAGNOSIS OF ROSAI-DORFMAN DISEASE: CASE REPORT AND LITERATURE REVIEW

2021 ◽  
Author(s):  
Zephania Abraham ◽  
Zerd Francis ◽  
Advera Ngaiza ◽  
Aveline Kahinga ◽  
Faustine Bukanu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Sinus Histiocytosis ◽  
Unknown Etiology ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Disease Case

Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self-limiting disease of the cells of macrophage-histiocyte family is of unknown etiology and presents with massive lymphadenopathy. We are hereby reporting a case of RDD presenting with massive bilateral cervical and submandibular lymphadenopathy, diagnosed by histocytopathology.

scholarly journals Treatment of sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease): Report of a case and literature review

2001 ◽  
Vol 69 (1) ◽  
pp. 67-71 ◽  
Author(s):  
Alessandro Pulsoni ◽  
Gabriel Anghel ◽  
Paolo Falcucci ◽  
Roberta Matera ◽  
Edoardo Pescarmona ◽  
...  
Keyword(s):  
Literature Review ◽  
Sinus Histiocytosis ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease

scholarly journals Cytodiagnosis of Rosai–Dorfman disease masquerading as lymphoma: A case report with brief review of literature

2018 ◽  
Vol 10 (04) ◽  
pp. 460-463
Author(s):  
Manjari Kishore ◽  
Prajwala Gupta ◽  
Arvind Ahuja ◽  
Minakshi Bhardwaj
Keyword(s):  
Case Report ◽  
Sinus Histiocytosis ◽  
Male Child ◽  
Differential Diagnoses ◽  
Review Of Literature ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Cytological Features

ABSTRACTRosai–Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy (SHML) is a self-limiting, benign histiocytic disorder. We report a case of RDD mimicking lymphoma clinically and cytologically in a 3-year-old male child. The present case highlights the importance of cytology in the diagnosis of RDD along with cytological features of other differential diagnoses.

Rosai–Dorfman Disease (Sinus Histiocytosis with Massive Lymphadenopathy) of the Pancreas: Second Case Report

2008 ◽  
Vol 13 (4) ◽  
pp. 806-809 ◽  
Author(s):  
Sean P. Zivin ◽  
Mohammed Atieh ◽  
Michael Mosier ◽  
Gladell P. Paner ◽  
Gerard V. Aranha
Keyword(s):  
Case Report ◽  
Sinus Histiocytosis ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease

Isolated intracranial Rosai-Dorfman disease: Case report and literature review

1998 ◽  
Vol 48 (5) ◽  
pp. 396-402 ◽  
Author(s):  
Hsuan-Ying Huang ◽  
Chao-Cheng Huang ◽  
Cheun-Chung Lui ◽  
Han-Jung Chen ◽  
Wei-Jen Chen
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rosai Dorfman Disease ◽  
Disease Case

scholarly journals Primary Rosai-Dorfman Disease in 39-Year-Old Woman With Osseous Tibial Lesion Manifestion: A Case Report and Literature Review

2021 ◽  
Vol 6 (4) ◽  
pp. 247301142110600
Author(s):  
Jasmin Mansoori ◽  
Olivia Fisher ◽  
Ivana O. Akinyeye ◽  
Michael A. Sobolevsky ◽  
Robert H. Quinn
Keyword(s):  
Case Report ◽  
Osteolytic Lesion ◽  
Magnetic Resonance Images ◽  
Unknown Etiology ◽  
Medial Malleolus ◽  
Ankle Pain ◽  
Plain Radiographs ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Physical Mass

Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with <10% bone involvement. The report is of a case seen at the authors’ hospital of a patient presenting with several months’ onset unspecified nontraumatic ankle pain. There was no physical mass or lymphadenopathy appreciated on examination. Plain radiographs and magnetic resonance images demonstrated an osteolytic lesion at the medial malleolus. Biopsy revealed the diagnosis of intraosseous manifestation of Rosai-Dorfman disease.

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