Results 131 to 140 of about 3,468 (180)
Some of the next articles are maybe not open access.
Radiology, 1987
A 26-year-old woman had an infiltrative renal lesion accompanied by massive regional lymphadenopathy. Biopsy of the renal mass and a coexistent orbital mass revealed identical histologic evidence of sinus histiocytosis. This unusual benign entity is uncommon in the kidney, but radiographically, it may closely simulate an infiltrative renal neoplasm ...
R E, Bechtold +3 more
openaire +2 more sources
A 26-year-old woman had an infiltrative renal lesion accompanied by massive regional lymphadenopathy. Biopsy of the renal mass and a coexistent orbital mass revealed identical histologic evidence of sinus histiocytosis. This unusual benign entity is uncommon in the kidney, but radiographically, it may closely simulate an infiltrative renal neoplasm ...
R E, Bechtold +3 more
openaire +2 more sources
Sinus Histiocytosis Clinically Limited to the Skin
Pediatric Dermatology, 1987Abstract: Sinus histiocytosis with massive lymphadenopathy is a rare clinicopalhologic entity thai affects mainly children and young adults. Although the lymph nodes are the most common sites of involvement, extranodal infiltrates may arise in the orbits, skin, upper respiratory tract, and bone, as well as other organs.
A P, Lazar +2 more
openaire +2 more sources
Sinus Histiocytosis Presenting as a Mediastinal Mass
Chest, 1984A 32-year-old man with a ten-year history of bilateral cervical adenopathy, parotid gland swelling, and a posterior mediastinal mass, presented with headaches. A CAT scan of the head revealed a suprasellar mass. Craniotomy and biopsy of this lesion led to a diagnosis of sinus histiocytosis.
M J, Friedman +5 more
openaire +2 more sources
Brucellosis and sinus histiocytosis with massive lymphadenopathy
The American Journal of Medicine, 1989S 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
openaire +2 more sources
Sinus histiocytosis with massive lymphadenopathy
Archives of Orthopaedic and Trauma Surgery, 1993A 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
openaire +2 more sources
Lymphadenitis with massive hemophagocytic sinus histiocytosis
Virchows Archiv B Cell Pathology, 1972Lymphadenitis with massive hemophagocytic sinus histiocytosis has been reported in patients with scleroma and in cervical lymph nodes of children without any known etiologic condition. Using electron microscopy, we conducted the present study on submandibular enlarged lymph nodes from a 6-year-old girl with this condition.
K, Lennert +3 more
openaire +2 more sources
Sinus histiocytosis: some radiologic observations
American Journal of Roentgenology, 1979Sinus histiocytosis with massive lymphadenopathy is an unusual disease characterized by prominent lymph node enlargement, especially in the cervical region. The clinical course is benign although prolonged, and no specific treatment is required. The etiology and pathogenesis are unknown.
M J, Siegel +2 more
openaire +2 more sources
Sinus Histiocytosis With Massive Lymphadenopathy
Archives of Dermatology, 1988In 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
openaire +2 more sources
Cutaneous Sinus Histiocytosis and Chronic Uveitis
Pediatric Dermatology, 2000Abstract: Sinus histiocytosis with massive lymphadenitis or Rosai–Dorfman disease (RDD) is a rare, benign, proliferative histiocytic disease of unknown origin. It predominately affects the lymph nodes The skin is the extranodal organ most frequently involved, although a few patients present with only lesions of the skin and soft tissues, without ...
J F, Silvestre, A, Aliaga
openaire +2 more sources
Orbital Involvement in 'Sinus' Histiocytosis
Archives of Ophthalmology, 1977Sinus histiocytosis is a newly recognized benign disease affecting mainly children and young adults and usually having a protracted clinical course that is relatively unaffected by therapy. This paper describes four additional patients who had orbital involvement initially and reviews the salient clinical and histopathologic features of this entity ...
D S, Friendly, R L, Font, N A, Rao
openaire +2 more sources

