Lymphangioma: Difference between revisions
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A '''lymphangioma''' is [[benign tumor]] of the [[lymphatic system]], usually due to a congenital malformation. It must not be confused with a malignant [[lymphangiosarcoma]]. | |||
They may bleed, or their cells may die and support an infection. They may block body functions based on their location, so they should be removed. | |||
Surgery has been the mainstay of removing lymphangiomas, but [[sclerotherapy]] with [[bleomycin]] has been reported as successful. <ref>{{citation | |||
| url = http://www.jpma.org.pk/full_article_text.php?article_id=2188 | |||
| title = Giant unresectable Lymphangioma of the trunk managed via intra-tumour injections of bleomycin | |||
| journal = Journal of Pakistan Medical Association | |||
| author = Umair Khalid, Saulat Hasnain Fatimi, Taimur Saleem}}</ref> | |||
==References== | |||
{{reflist}} | |||
Revision as of 17:48, 1 July 2010
A lymphangioma is benign tumor of the lymphatic system, usually due to a congenital malformation. It must not be confused with a malignant lymphangiosarcoma.
They may bleed, or their cells may die and support an infection. They may block body functions based on their location, so they should be removed.
Surgery has been the mainstay of removing lymphangiomas, but sclerotherapy with bleomycin has been reported as successful. [1]
References
- ↑ Umair Khalid, Saulat Hasnain Fatimi, Taimur Saleem, "Giant unresectable Lymphangioma of the trunk managed via intra-tumour injections of bleomycin", Journal of Pakistan Medical Association