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Digitale Medien

Oncogenic osteomalacia (2000)

Sundaram, M. ; McCarthy, E. F.

Springer

Skeletal radiology 29 (2000), S. 117-124

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ISSN: 1432-2161

Schlagwort(e): Key words Osteomalacia ; Metabolic disease ; Hemangiopericytoma ; Fibrohistiocytic tumors ; Radiography ; MRI

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: Abstract The clinical, imaging, metabolic, histologic and biochemical aspects of oncogenic osteomalacia are reviewed. The bone and soft tissue tumor and tumor-like lesions associated with this paraneoplastic syndrome are discussed. The radiologist’s role in the diagnosis and evaluation of this entity is presented.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/s002560050581

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Digitale Medien

Metachronous multiple aneurysmal bone cysts (1997)

Sundaram, M. ; McDonald, Douglas J. ; Steigman, Carmen K. ; [weitere]

Springer

Skeletal radiology 26 (1997), S. 564-567

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ISSN: 1432-2161

Schlagwort(e): Key words Aneurysmal bone cysts ; Multiple ; Metachronous

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: Abstract We report on a 9-year-old boy with metachronous aneurysmal bone cysts involving the tibia and pubis respectively. The patient has been clinically and radiographically followed for 3 years.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/s002560050288

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Digitale Medien

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) presenting with skeletal lesions (1998)

Sundaram, M. ; deMello, Daphne ; Falbo, Stephanie ; [weitere]

Springer

Skeletal radiology 27 (1998), S. 115-117

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ISSN: 1432-2161

Schlagwort(e): Key words Sinus histiocytosis with massive lymphadenopathy (SHML) ; Clinical presentation ; Bone pain ; Bone lesions ; No treatment ; 1-year follow-up

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: Abstract A 2-year-old child presenting with bone pain and bone lesions was found to have sinus histiocytosis with massive lymphadenopathy (SHML). SHML presenting with skeletal symptoms is unusual. Management has been conservative and the child has been symptom free for 30 months, although the bone lesions have not completely regressed.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/s002560050349

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