scholarly journals Concurrent Langerhans Cell Histiocytosis and Autoimmune Hepatitis: A Case and Review of the Literature

Cureus ◽  
2020 ◽  
Author(s):  
Ahmed Ahmed ◽  
Hasan Ali ◽  
Mark Galan ◽  
Jie-gen Jiang ◽  
Vivek Lingiah
2010 ◽  
Vol 2010 ◽  
pp. 1-3 ◽  
Author(s):  
Harpreet Singh ◽  
Satnam Kaur ◽  
P. Yuvarajan ◽  
Nishant Jain ◽  
Lalit Maini

The radiological diagnosis of osteolytic lesions of the long bones in pediatric population constitutes a challenge when the case history and clinical data are uncharacteristic. We believe that the description of few clinically and histologically proven cases to verify the existence of radiological signs useful for diagnosis may be of interest. Here, we describe a case of Langerhans' cell histiocytosis (LCH) presenting as unifocal eosinophilic granuloma of femur along with a brief review of the literature.


Oncotarget ◽  
2018 ◽  
Vol 9 (31) ◽  
pp. 22236-22240 ◽  
Author(s):  
Anne Heisig ◽  
Jan Sörensen ◽  
Stefanie-Yvonne Zimmermann ◽  
Stefan Schöning ◽  
Dirk Schwabe ◽  
...  

Thyroid ◽  
2001 ◽  
Vol 11 (7) ◽  
pp. 697-705 ◽  
Author(s):  
Robert J. Behrens ◽  
Angelique W. Levi ◽  
William H. Westra ◽  
Deepa Dutta ◽  
David S. Cooper

2007 ◽  
Vol 2 (Suppl 1) ◽  
pp. S24
Author(s):  
K Mueller ◽  
M Trippel ◽  
A Berlis ◽  
W Janzarik ◽  
B Volk

2018 ◽  
Vol 2018 ◽  
pp. 1-5 ◽  
Author(s):  
Rashid AL Umairi ◽  
Danielle Blunt ◽  
Wedad Hana ◽  
Matthew Cheung ◽  
Anastasia Oikonomou

Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare nonmalignant lymphohistiocytic proliferative disorder. We report a patient with RDD who presented with multiple skin lesions, pulmonary involvement, and CT manifestations mimicking Langerhans cell histiocytosis, which improved after initiation of corticosteroid treatment.


Sign in / Sign up

Export Citation Format

Share Document