Langerhans' Cell Histiocytosis
Langerhans' Cell Histiocytosis
Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. The disease has gone by several names, including Hand–Schüller–Christian disease, Abt-Letterer-Siwe disease, and histiocytosis X, until it was renamed in 1985.
Langerhans’ Cell Histiocytosis
Chris Restrepo
http://radiology.med.sc.edu/
Histiocytic Disorders Diagnosis and Treatment
http://www.mcw.edu
Case Study
Kenneth Clark, MD
http://neuro.pathology.pitt.edu
Case Study
Lananh Nguyen, M.D
http://neuro.pathology.pitt.edu
The Pediatric Central Skull Base
Gary L. Hedlund, D.O.
http://medicine.utah.edu/
Periodontal And Periapical Diseases
http://student.ahc.umn.edu
Pituitary Tumors
Jerome M. Volk III, HO V
http://www.medschool.lsuhsc.edu
Diseases of WBCs, Lymph Nodes, Spleen, Thymus
http://faculty.ccc.edu
Brainstem glioma
http://neuroradiology.rad.jhmi.edu/education/brainreview2.ppt
Monocyte/Macrophage Disorders
http://www.atsu.edu
Interstitial Lung Disease
http://medicine.med.unc.edu
Latest 100 Published articles of Langerhans' Cell Histiocytosis
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