Langerhans cell histiocytosis natural history: Difference between revisions
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==Overview== | ==Overview== | ||
==Natural History== | ==Natural History== | ||
* The clinical course of Langerhans cell histiocytosis may range from a disease that spontaneously regress to a rapidly progressive disease with multi-system involvement. | |||
==Complications== | ==Complications== | ||
* Common complications of Langerhans cell histiocytosis include: | |||
:* Pulmonary fibrosis | |||
:* Pulmonary hypertension | |||
:* Pathological bone fractures | |||
==Prognosis== | ==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. | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 16:00, 4 February 2016
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Differentiating Langerhans cell histiocytosis from other Diseases |
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Langerhans cell histiocytosis natural history On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Haytham Allaham, M.D. [2]
Overview
Natural History
- The clinical course of Langerhans cell histiocytosis may range from a disease that spontaneously regress to a rapidly progressive disease with multi-system involvement.
Complications
- Common complications of Langerhans cell histiocytosis include:
- Pulmonary fibrosis
- Pulmonary hypertension
- Pathological bone fractures
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.