Neurological form of Erdheim-Chester disease : Case report and review of the literature

2014 ◽  
Vol 60 (6) ◽  
pp. 316-320 ◽  
Author(s):  
A. Perez ◽  
M. Crahes ◽  
A. Laquerrière ◽  
F. Proust ◽  
S. Derrey
1986 ◽  
Vol 80 (6) ◽  
pp. 1230-1236 ◽  
Author(s):  
Robin L. Miller ◽  
Leslie R. Sheeler ◽  
Thomas W. Bauer ◽  
Ronald M. Bukowski

2003 ◽  
Vol 45 (4) ◽  
pp. 241-245 ◽  
Author(s):  
Stefan Weidauer ◽  
Sebastian von Stuckrad-Barre ◽  
Edgar Dettmann ◽  
Friedhelm E. Zanella ◽  
Heinrich Lanfermann

2020 ◽  
Vol 83 (6) ◽  
pp. AB30
Author(s):  
Rita Pimenta ◽  
Manuel Gomes ◽  
Luis Soares-Almeida ◽  
Andre Oliveira ◽  
Paulo Leal-Filipe

2003 ◽  
Vol 169 (4) ◽  
pp. 1470-1471 ◽  
Author(s):  
EDWARD J. YUN ◽  
BENJAMIN M. YEH ◽  
ANNOEL P. YABES ◽  
FERGUS V. COAKLEY ◽  
CHRISTOPHER J. KANE

2005 ◽  
Vol 11 (6) ◽  
pp. 462-467 ◽  
Author(s):  
Penny J. Barnes ◽  
Annette Foyle ◽  
Kelly A. Dakin Hache ◽  
Richard G. B. Langley ◽  
Steven Burrell ◽  
...  

2020 ◽  
Vol 7 (1) ◽  
pp. 22
Author(s):  
Rémie Philippe Elia ◽  
ATALLAH Adnan ◽  
AKIKI Béatrice ◽  
WAKED Hani ◽  
ZEIDAN Marwan ◽  
...  

Erdheim Chester disease is a rare form of non-Langerhans histiocytosis with frequent BRAF V600E mutations. It is mainly characterized by multifocal osteosclerotic bone lesions with or without systemic involvement. The histologic image is consistent with a histiocytic proliferation of foamy cells in a polymorphic background. The main difference from the Langerhans histiocytosis is the immune profile with mainly S100, CD1a, and langerin negative. The overall prognosis is dependent on extraskeletal involvement. Herein, we present a typical presentation of Erdheim Chester disease with a review of the literature.


2018 ◽  
Vol 29 ◽  
Author(s):  
Mahtat El Mehdi ◽  
Safae Regragui ◽  
Hicham Eddou ◽  
Selim Jennane ◽  
Hicham El Maaroufi ◽  
...  

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