Kasabach-Merritt phenomenon

Important
It is possible that the main title of the report Kasabach-Merritt phenomenonis not the name you expected.

Synonyms

KMS
hemangioma thrombocytopenia syndrome
thrombocytopenia-hemangioma syndrome

Disorder Subdivisions

None

General Discussion

Kasabach-Merritt phenomenon is a rare association of profound thrombocytopenia associated 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.

Resources

NIH/National Heart, Lung and Blood Institute
31 Center Drive MSC 2480
Building 31A Rm 4A16
Bethesda
MD
20892-2480
Tel: (301)592-8573
Fax: (240)629-3246
nhlbiinfo@rover.nhlbi.nih.gov
http://www.nhlbi.nih.gov/

Hemangioma Support System
c/o Cynthia Schumerth
1484 Sand Acres Drive
DePere
WI
54115
Tel: (920)336-9399MUMS (Mothers United for Moral Support, Inc) National Parent-to-Parent Network
150 Custer Court
Green Bay
WI
54301-1243
USA
Tel: (920)336-5333
Fax: (920)339-0995
800: (877)336-5333
mums@netnet.net
http://www.netnet.net/mums/

Madisons Foundation
PO Box 241956
Los Angeles
CA
90024
Tel: (310)264-0826
Fax: (310)264-4766
getinfo@madisonsfoundation.org
http://www.madisonsfoundation.org

National Organization of Vascular Anomalies
PO Box 0358
Findlay
OH
45840-0358
Khall@mail.novanews.org
http://www.novanews.org

For a Complete Report:

This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html

The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.

It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report

This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.

For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org

Last Updated: 5/8/2008
Copyright 1994, 1998, 2008 National Organization for Rare Disorders, Inc.

WebMD Medical Reference from the National Organization of Rare Disorders

Last Updated: May 08, 2008

This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.