chester disease
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2022 ◽  
Vol 17 (3) ◽  
pp. 784-789
Author(s):  
Jing Liu ◽  
Limin Gao ◽  
Huaxia Pu ◽  
Wenzhang He ◽  
Liqing Peng

2022 ◽  
Vol 17 (3) ◽  
pp. 525-530
Author(s):  
Rene Epunza Kanza ◽  
Olivier Houle ◽  
Pierre-Luc Simard ◽  
Jonathan St-Gelais ◽  
Catherine Raymond

2022 ◽  
Author(s):  
Ryo Konishi ◽  
Takuya Morinishi ◽  
Koji Takaori ◽  
Yuta Iwamoto ◽  
Makiko Kondo ◽  
...  

Author(s):  
Jithma P. Abeykoon ◽  
Terra L. Lasho ◽  
Surendra Dasari ◽  
Karen L. Rech ◽  
Wasantha K. Ranatunga ◽  
...  

2021 ◽  
Vol 15 (1) ◽  
pp. 77-82
Author(s):  
Aleksandar Popovic ◽  
Christopher Curtiss ◽  
Timothy A. Damron

Background: Erdheim-chester disease (ECD) is a rare non-Langerhans histiocytosis of unknown etiology, which typically presents with bilateral symmetric osteosclerosis and multi-organ involvement. Lesions may be intraosseous or extraosseous and involve the heart, pulmonary system, CNS, and skin in order of decreasing likelihood. Objective: The objective of this study is to discuss a case of erdheim-chester disease and conduct a review of the literature. Case: We describe a rare case of erdheim-chester in an asymptomatic 37-year-old male who was diagnosed after suffering a right ulnar injury. Subsequent evaluation revealed a solitary radiolucent ulnar lesion without multi-system involvement. Results & Conclusion: The case is unique in its solitary distribution, lytic radiographic appearance, and asymptomatic presentation preceding pathologic fracture. This presentation may simulate multiple other bone lesions.


Hematology ◽  
2021 ◽  
Vol 27 (1) ◽  
pp. 65-69
Author(s):  
Antonio Adolfo Guerra Soares Brandão ◽  
André Ramires Neder Abdo ◽  
Luís Alberto de Pádua Covas Lage ◽  
Giancarlo Fatobene ◽  
Juliana Pereira ◽  
...  

Cureus ◽  
2021 ◽  
Author(s):  
Yasser Ghazi S Alarimah ◽  
Khalid Athal H Alanazi ◽  
Nouf H Alshammari ◽  
Hanadi A Fatani ◽  
Nader F Aldajani

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