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Hemangioma thrombocytopenia syndrome
Other Names for this Disease
- Kasabach Merritt phenomenon
- Kasabach Merritt syndrome
- Thrombocytopenia-hemangioma syndrome
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thrombocytopenia in association with two rare vascular tumors: kaposiform hemangioendotheliomas and tufted angiomas. The profound thrombocytopenia can cause life threatening bleeding and progress to a disseminated coagulopathy in patients with these tumors. The condition typically occurs in early infancy or childhood, although prenatal cases (diagnosed with the aid of ultrasonography), newborn presentations, and rare adult cases have been reported.Hemangioma thrombocytopenia syndrome is characterized by profound
Last updated: 10/19/2010
- Adams D. Kasabach-Merritt phenomenon. National Organization for Rare Disorders (NORD). 2008; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Kasabach-Merritt%20phenomenon. Accessed 10/19/2010.
- Vazquez MP. Kasabach-Merritt syndrome. Orphanet. 2006; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2330. Accessed 10/19/2010.
- Krafchik BR, Hendricks LK, Faguet GB, Kuthiala S. Kasabach-Merritt Syndrome. eMedicine. 2010; http://emedicine.medscape.com/article/202455-overview. Accessed 10/19/2010.
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- DermNet NZ is an online resource about skin diseases developed by the New Zealand Dermatological Society Incorporated. DermNet NZ provides information about this condition.
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- The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Hemangioma thrombocytopenia syndrome. Click on the link to go to OMIM and review these resources.
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- PubMed is a searchable database of medical literature and lists journal articles that discuss Hemangioma thrombocytopenia syndrome. Click on the link to view a sample search on this topic.