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Langerhans cell histiocytosis of the atlas in an adult
[Image: see text] Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a rare disorder (approximately 1:1,500,000 inhabitants) characterized by clonal proliferation and excess accumulation of pathologic Langerhans cells causing local or systemic effects. The exact etiology of L...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2899733/ https://ncbi.nlm.nih.gov/pubmed/19844749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00586-009-1172-9 |
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