Langerhans cell histiocytosis natural history
Langerhans cell histiocytosis Microchapters |
Differentiating Langerhans cell histiocytosis from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Langerhans cell histiocytosis natural history On the Web |
American Roentgen Ray Society Images of Langerhans cell histiocytosis natural history |
Directions to Hospitals Treating Langerhans cell histiocytosis |
Risk calculators and risk factors for Langerhans cell histiocytosis natural history |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Haytham Allaham, M.D. [2]
Overview
The clinical course of Langerhans cell histiocytosis may range from a unifocal disease that spontaneously regress to a rapidly progressive disease with multi-system involvement. Common complications of Langerhans cell histiocytosis include pulmonary fibrosis, pathological bone fractures, and central diabetes insipidus. Depending on the extent of the tumor at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as excellent.
Natural History
- The clinical course of Langerhans cell histiocytosis may range from a unifocal disease that spontaneously regress to a rapidly progressive disease with multi-system involvement.[1]
Complications
- Pulmonary fibrosis
- Pulmonary hypertension
- Pathological bone fractures
- Anemia
- Recurrent bleeding
- Recurrent infections
- Central diabetes insipidus
Prognosis
- Depending on the extent of the tumor at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as excellent.[2][3][1][4][5][6]
- The 5-year survival rate of patients with unifocal Langerhans cell histiocytosis is approximately 99%.
- The 5-year survival rate of patients with multifocal unisystem Langerhans cell histiocytosis is approximately 97%.
- The 5-year survival rate of patients with multifocal multisystem Langerhans cell histiocytosis (with risk of organ failure) is approximately 77%.
- The table below lists prognostic factors for Langerhans cell histiocytosis patients:
Prognostic Factor | Description |
---|---|
Age |
|
Organ involvement |
|
Response to treatment |
|
Cellular markers |
|
References
- ↑ 1.0 1.1 1.2 DiCaprio MR, Roberts TT (2014). "Diagnosis and Management of Langerhans Cell Histiocytosis". J Am Acad Orthop Surg. 22 (10): 643–652. doi:10.5435/JAAOS-22-10-643. PMID 25281259.
- ↑ 2.0 2.1 Komp DM, El Mahdi A, Starling KA, Easley J, Vietti TJ, Berry DH; et al. (1980). "Quality of survival in histiocytosis X: a Southwest Oncology Group study". Med Pediatr Oncol. 8 (1): 35–40. PMID 6969347.
- ↑ 3.0 3.1 Langerhans Cell Histiocytosis Treatment (PDQ®): Health Professional Version. National Cancer Institute (2015) http://www.cancer.gov/types/langerhans/hp/langerhans-treatment-pdq Accessed on February, 3 2016
- ↑ 4.0 4.1 Harmon CM, Brown N (2015). "Langerhans Cell Histiocytosis: A Clinicopathologic Review and Molecular Pathogenetic Update". Arch Pathol Lab Med. 139 (10): 1211–4. doi:10.5858/arpa.2015-0199-RA. PMID 26414464.
- ↑ 5.0 5.1 Langerhans cell histiocytosis. Wikipedia (2015) https://en.wikipedia.org/wiki/Langerhans_cell_histiocytosis Accessed on February, 2 2016
- ↑ 6.0 6.1 Langerhans cell histiocytosis. Radiopeadia (2015) http://radiopaedia.org/articles/langerhans-cell-histiocytosis Accessed on February, 3 2016