Musculoskeletal imaging features of non-Langerhans cell histiocytoses

Choraria, Anika; Andrei, Vanghelita; Rajakulasingam, Ramanan; Saifuddin, Asif

doi:10.1007/s00256-021-03765-0

Cited by 6 publications

(4 citation statements)

References 59 publications

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“…Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is a rare histiocytic proliferative disorder, characterized by massive painless lymphadenopathy. [1][2][3] Extranodal disease may occur in any organs as in association with nodal involvement or a primary process. 1 Bone involvement is uncommon, with the skull, tibia, and femur being the most commonly involved sites.…”

Section: Figurementioning

confidence: 99%

“…1 Bone involvement is uncommon, with the skull, tibia, and femur being the most commonly involved sites. [1][2][3] Rosai-Dorfman disease usually shows increased FDG uptake. [4][5][6][7][8][9][10][11][12][13][14] Therefore, FDG PET/CT is useful for defining disease extent and guiding biopsy.…”

Section: Figurementioning

confidence: 99%

“…Rosai-Dorfman disease was proved by pathology. Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is a rare histiocytic proliferative disorder, characterized by massive painless lymphadenopathy 1–3 . Extranodal disease may occur in any organs as in association with nodal involvement or a primary process 1 .…”

mentioning

confidence: 99%

“…Extranodal disease may occur in any organs as in association with nodal involvement or a primary process 1 . Bone involvement is uncommon, with the skull, tibia, and femur being the most commonly involved sites 1–3 . Rosai-Dorfman disease usually shows increased FDG uptake 4–14 .…”

mentioning

confidence: 99%

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