Results 171 to 180 of about 1,868 (215)
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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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Sinus histiocytosis with massive lymphadenopathy: skeletal involvement

Pediatric Radiology, 1985
A 9-year-old girl with known sinus histiocytosis with massive lymphadenopathy (SHML) has been followed since infancy. At age six, she developed swelling and pain in several joints. Subsequently, bone lesions were identified by scintigraphy and radiographs. Biopsy of the bone showed typical features of SHML. Bone lesions in this disease are rare.
M S, Puczynski, T C, Demos, C R, Suarez
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[Sinus histiocytosis with massive lymphadenopathy].

Harefuah, 1984
A case of sinus histiocytosis with massive lymphadenopathy in a boy of 13 with multiple subcutaneous tumor-like formations 0.5 to 2.5 cm in diameter is described. The general condition of the patient was not changed despite the 7-month course of the disease. Mild anemia and increased ESR were observed.
Z, Estrov   +3 more
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Sinus histiocytosis with massive lymphadenopathy.

Archives of otolaryngology (Chicago, Ill. : 1960), 1979
Sinus histiocytosis with massive lymphadenopathy (SHML) is a newly recognized, distinct, pseudolymphomatous benign entity with very characteristic microscopic features. Most patients are children or young adults with massive painless cervical adenopathy, although other node groups and extranodal sites often are involved.
E, Foucar, J, Rosai, R F, Dorfman
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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 (Rosai–Dorfman disease)

International Journal of Pediatric Otorhinolaryngology, 1998
Sinus histiocytosis with massive lymphadenopathy (SHML) is a distinct clinicopathological entity described by Rosai and Dorfman and differentiated by other childhood histiocytoses by its distinct characteristics. This is a rare pathology and should be kept in mind for differential diagnosis of neck masses, especially in childhood.
O F, Unal, S, Köybaşi, S, Kaya
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[Sinus histiocytosis with massive lymphadenopathy].

Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology, 2011
To explore the therapeutic strategy of sinus histiocytosis with massive lymphadenopathy (SHML).The six patients with SHML were treated with different therapeutic strategies.Two of six patients were treated with radiation therapy and chemical therapy resulting in tumor lessened markedly.
Youzhong, Li   +3 more
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Sinus histiocytosis with massive lymphadenopathy simulating subacute thyroiditis

Human Pathology, 1986
A white woman who had sinus histiocytosis with massive lymphoadenopathy (SHML) presented with a painful goiter and tender cervical lymph nodes. She had biochemical evidence of hypothyroidism but remained clinically euthyroid. Histologic examination confirmed SHML in the thyroid and cervical lymph nodes. The disease remitted spontaneously.
D F, Larkin   +3 more
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Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease)

Pediatric Radiology, 1990
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a unique disease of unknown etiology with a childhood predilection. Reports have established the worldwide distribution of the disorder. Although peripheral lymphadenopathy is the most common mode of presentation, numerous studies and individual case reports have established ...
W H, McAlister, T, Herman, L P, Dehner
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