A Rare Case Report on Kaposiform Hemangioendothelioma with Kasabach Meritt Syndrome
International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064


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Case Studies | Paediatrics | India | Volume 9 Issue 3, March 2020 | Popularity: 6.6 / 10


     

A Rare Case Report on Kaposiform Hemangioendothelioma with Kasabach Meritt Syndrome

Dr. Ajay Vaid, Dr. Amar Singh Thakur, Dr. Mohit Bajaj


Abstract: Tufted angioma and kaposiform hemangioendothelioma are rare vascular tumours that typically occurduring infancy or early childhood. Kasabach-Merritt syndrome is characterised by the combination of rapidly growing vascular tumour, life threatening thrombocytopenia, microangiopathic haemolytic anaemia and consumptive coagulopathy [1]. The blood clotting disorder results from platelets and other clotting factors of the blood being used up within the tumor. Here we report a newborn presenting with swelling left side of neck with bluish tinge on day 1 of life.


Keywords: Kasabach-Merritt syndrome KMS, Hemangioma, Thrombocytopenia, Hypofibrinogenemia


Edition: Volume 9 Issue 3, March 2020


Pages: 953 - 955



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Dr. Ajay Vaid, Dr. Amar Singh Thakur, Dr. Mohit Bajaj, "A Rare Case Report on Kaposiform Hemangioendothelioma with Kasabach Meritt Syndrome", International Journal of Science and Research (IJSR), Volume 9 Issue 3, March 2020, pp. 953-955, https://www.ijsr.net/getabstract.php?paperid=SR20316230339, DOI: https://www.doi.org/10.21275/SR20316230339

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