Bronchoscopic diagnosis of Langerhans cell histiocytosis and lymphangioleiomyomatosis
โ Scribed by Sergio Harari; Olga Torre; Roberto Cassandro; Angelo M. Taveira-DaSilva; Joel Moss
- Book ID
- 119359280
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 347 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0954-6111
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๐ SIMILAR VOLUMES
## SUMMARY Langerhans cell histiocytosis is a rare condition that can affect any organ of the body. Patients of all ages may present to the dermatologist and it is important to make the diagnosis as quickly as possible, because time from presentation to diagnosis is of prognostic importance in adul
## BACKGROUND. The objective of this descriptive analysis of a large cohort of patients with Langerhans cell histiocytosis (LCH) was to add to the understanding of the natural history, management, and outcome of this disease. ## METHODS. Three hundred fourteen Mayo Clinic patients with histolog