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Sinus histiocytosis with massive lymphadenopathy (Rosai‐Dorfman disease)

Histopathology, 1989
A child of 11 years with a solitary involvement of the right radius by sinus histiocytosis with massive lymphadenopathy (Rosai‐Dorfman disease) is presented. The literature of bone involvement in this condition is reviewed.
I M, Nawroz, D, Wilson-Storey
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Sinus Histiocytosis with Massive Lymphadenopathy

Annals of Otology, Rhinology & Laryngology, 1989
Sinus 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 ...
N, Sneige, J G, Batsakis
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SINUS HISTIOCYTOSIS WITH MASSIVE LYMPHADENOPATHY

Acta Paediatrica, 1977
Abstract Brostrøm, K. and Baandrup, U. (University Department of Paediatrics and University Institute of Pathology, Kommunehospitalet, Aarhus, Denmark). Sinus histiocytosis with massive lymphadenopathy. Acta Paediatr Scand, 66:257, 1977.—The present case report brings to attention an unusual form of massive benign lymphadenopathy which can simulate ...
K, Brostrom, U, Baandrup
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Sinus Histiocytosis with Massive Lymphadenopathy

Clinical Nuclear Medicine, 1987
Gallium uptake corresponding to the extent of the disease in a patient with histologically proven sinus histiocytosis with massive lymphadenopathy (SHML) is reported. Computerized tomography confirmed the presence of bilateral retrobulbar masses, involvement of both lateral recti, erosion of the bony orbital floor with encroachment of tumor into the ...
B, Pastakia, S H, Weiss
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Sinus histiocytosis with massive lymphadenopathy

Archives of Orthopaedic and Trauma Surgery, 1993
A 64-year-old female patient has been suffering from sinus histiocytosis with massive lymphadenopathy (SHML) for 2 years. After 12 months of illness, the patient developed swelling and pain in various skeletal regions. Scintigraphic, radiological and CT imaging revealed multiple osseous lesions.
M, Lehnert   +3 more
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Sinus Histiocytosis With Massive Lymphadenopathy

Archives of Dermatology, 1988
In the present issue of theArchives, Suster et al 1 describe a 72-year-old woman with large soft-tissue masses that spontaneously disappeared over a period of several weeks. In spite of the absence of lymphadenopathy, the authors cautiously suggest the diagnosis sinus histiocytosis with massive lymphadenopathy (SHML) (Rosai-Dorfman disease), based ...
Elise A. Olsen   +2 more
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Sinus histiocytosis with massive lymphadenopathy: A “massive” misnomer

Diagnostic Cytopathology, 2014
Sinus 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 ...
Divesh, Sardana   +2 more
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Brucellosis and sinus histiocytosis with massive lymphadenopathy

The American Journal of Medicine, 1989
S inus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a benign pseudolymphomatous entity with distinct clinical and pathologic features [l-3]. This disorder, usually occurring during the first two decades of life, is manifested by massive, painless cervical lymphadenopathy in association with fever, leukocytosis ...
J D, Yao   +3 more
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Sinus Histiocytosis With Massive Lymphadenopathy

Archives of Pediatrics & Adolescent Medicine, 1995
I am writing in reference to Case 1 of the Pathological Cases of the Month in the July issue of theArchives.1The clinical and pathologic data in this infant support the diagnosis of sinus histiocytosis with massive lymphadenopathy, Rosai-Dorfman disease.
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