Author(s): Woodcock RJ Jr, Mandell JW, Lipper MH
Sinus histiocytosis with massive lymphadenopathy (SHML) is an uncommon disorder that typically manifests as systemic symptoms and lymphadenopathy. Extranodal, intracranial disease is uncommon. The authors report on a 15-year-old adolescent girl who had a suprasellar mass at magnetic resonance imaging. Biopsy results demonstrated lymphophagocytosis consistent with a diagnosis of SHML. The clinical, radiologic, and histologic aspects of the disease are discussed.
Referred From: https://www.ncbi.nlm.nih.gov/pubmed/10580957
Author(s): Kutlubay Z, Bairamov O, Sevim A, Demirkesen C, Mat MC
Author(s): Wang F, Qiao G, Lou X, Song X, Chen W
Author(s): Rotondo F, Munoz DG, Hegele RG, Gray B, Khatun N, et al.
Author(s): Wan S, Teng X, Zhan R, Yu J, Gu J, et al.
Author(s): Kelly WF, Bradey N, Scoones D
Author(s): Ng HK, Poon WS
Author(s): Adeleye AO, Amir G, Fraifeld S, Shoshan Y, Umansky F, et al.
Author(s): Wu M, Anderson AE, Kahn LB
Author(s): Foucar E, Rosai J, Dorfman R
Author(s): Foucar E, Rosai J, Dorfman RF, Brynes RK
Author(s): Kattner KA, Stroink AR, Roth TC, Lee JM
Author(s): Sharma MS, Padua MD, Jha AN
Author(s): Purav P, Ganapathy K, Mallikarjuna VS, Annapurneswari S, Kalyanaraman S, et al.
Author(s): Sachdev R, Setia N, Jain S
Author(s): Deshayes E, Le Berre JP, Jouanneau E, Vasiljevic A, Raverot G, et al.
Author(s): Konishi E, Ibayashi N, Yamamoto S, Scheithauer BW
Author(s): Andriko JA, Morrison A, Colegial CH, Davis BJ, Jones RV
Author(s): Deodhare SS, Ang LC, Bilbao JM
