Paravertebral and Retroperitoneal Vascular Tumour with Kasab
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Vascular anomalies include a spectrum of disorders from simple lesions to life-threatening entities. Kasabach-Merritt phenomenon is characterized by vascular tumour and consumptive coagulopathy with life-threatening thrombocytopenia, prolonged prothrombin time , and activated partial thromboplastin time , hypofibrinogenemia, and the presence of D-dimer and fibrin split products. Kaposiform hemangioendothelioma (KHE) is the responsible lesion most of the time. Mortality rate is around 10%–37%. Here, we describe a 3-year-old boy with unusual localization of extensive vascular lesions involving spinal vertebrae from T11 to L5 that caused fatal consumptive coagulopathy.....

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578750/
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