Lymphangioma (patient information): Difference between revisions
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==What causes Lymphangioma?== | ==What causes Lymphangioma?== | ||
There are no known direct causes for lymphangioma. | |||
Cystic hygroma usually presents in syndromes such as [[Turner syndrome]] and [[Down syndrome]]. Therefore it is thought that the lymphatic malformations can arise from gene mutations, occuring as missing or deleted part of chromosomes.[2] | |||
Acquired lymphangioma circumscriptum occur as a sequele of chronic lymphatic obstruction such as after surgery, infections or radiotherapy | |||
==Who is at highest risk?== | ==Who is at highest risk?== | ||
Revision as of 14:12, 18 October 2018
For the WikiDoc page on this topic, click here
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Lymphangioma |
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Lymphangioma On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Lymphangioma is abnormality of lymph vessels.
What are the symptoms of Lymphangioma?
- The majority of patients with lymphangioma are asymptomatic.
- As the mass increases in size, lymphangioma patients may develop site-specific symptoms, such as:
- Dysphagia
- Difficulty breathing
- Constipation
- Failure to thrive
What causes Lymphangioma?
There are no known direct causes for lymphangioma. Cystic hygroma usually presents in syndromes such as Turner syndrome and Down syndrome. Therefore it is thought that the lymphatic malformations can arise from gene mutations, occuring as missing or deleted part of chromosomes.[2] Acquired lymphangioma circumscriptum occur as a sequele of chronic lymphatic obstruction such as after surgery, infections or radiotherapy
Who is at highest risk?
Diagnosis
When to seek urgent medical care?
Treatment options
Where to find medical care for Lymphangioma?
Directions to Hospitals Treating Lymphangioma