Pleural Rosai-Dorfman disease complicated with renal clear cell carcinoma: a case report and literature review. [PDF]
Tang S, Yang X, Wang S, Xiao Q.
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A Rare Case of a Solid Variant Aneurysmal Bone Cyst of the Medial Sphenoid Bone: Clinical Features, Diagnostic Points, and Treatment. [PDF]
Yamashita S +11 more
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Pituitary apoplexy within a prolactin-secreting macroadenoma in a child: A rare clinical entity with radiological correlation. [PDF]
Mouhcine Y +9 more
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Spontaneous Regression of Rosai-Dorfman Disease Presenting as a Thigh Mass With Vascular Involvement: A Case Report. [PDF]
Bouhani M +5 more
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A rare case of Erdheim Chester disease. [PDF]
Oualladi FE +6 more
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Unveiling Langerhans cell histiocytosis presenting as hidradenitis suppurativa: A case report and systematic review. [PDF]
Mohammadzadeh I +5 more
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SLC29A3 Pathogenic Variants Resulting in Dural Based Fibroinflammatory Mass Lesions and H Syndrome Treated With Cobimetinib: A Case Report. [PDF]
Banks SA +16 more
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Sinus histiocytosis with massive lymphadenopathy: A “massive” misnomer
Diagnostic Cytopathology, 2014Sinus histiocytosis with massive lymphadenopathy also known as Rosai–Dorfman disease is a rare, benign, histiocytic disorder of unknown origin characterized by lymphadenopathy. Since its original description by Rosai and Dorfman in 1969, small number of cases has been reported; hence no specific diagnostic criteria and treatment guidelines have been ...
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Sinus Histiocytosis with Massive Lymphadenopathy
Annals of Otology, Rhinology & Laryngology, 1989Sinus histiocytosis with massive lymphadenopathy is a lymphoreticular disorder of obscure pathogenesis with extranodal lesions and a variable clinical course. Clinical manifestations are most often in the head and neck, with 97% of patients showing cervical lymphadenopathy and a significant but lesser number having lesional infiltrates in the upper ...
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