Results 51 to 60 of about 900 (120)
Sirolimus for Pediatric Cervicofacial Lymphatic Malformation: A Systematic Review and Meta‐Analysis
Objective This study is a systematic review and meta‐analysis of the efficacy and safety of sirolimus in the management of pediatric cervicofacial lymphatic malformations (LMs). Data Sources EMBASE, Medline, Scopus, and Cochrane databases were searched, along with the reference list of all included articles.
Yasmine Kamhieh +5 more
wiley +1 more source
How we use angiopoietin‐2 in the diagnosis and management of vascular anomalies
Abstract The diagnosis of vascular anomalies remains challenging due to significant clinical heterogeneity and uncertain etiology. Evaluation using biopsy and/or genetic testing for somatic variants is invasive, expensive, and prone to sampling error. There is great need for noninvasive and easily measured blood laboratory biomarkers that can aid not ...
Elissa R. Engel +2 more
wiley +1 more source
Successful Treatment of Mild Pediatric Kasabach-Merritt Phenomenon with Propranolol Monotherapy
Kasabach-Merritt phenomenon (KMP) is relatively rare in childhood and adolescents with high mortality rate because of its hemorrhagic complications and unresponsiveness to treatments such as corticosteroids, vincristine, intravascular embolization, and ...
Worawut Choeyprasert +2 more
doaj +1 more source
Very rare mediastinal location of Kaposiform haemangioendothelioma: A case report and a brief review of the previously published cases [PDF]
Kaposiform haemangioendothelioma (KHE) is a rare, locally invasive vascular tumour that is commonly associated with the Kasabach-Merritt phenomenon (KMP).
Đuričić Slaviša M. +3 more
doaj
Kaposiform hemangioendothelioma: current knowledge and future perspectives
Kaposiform hemangioendothelioma (KHE) is a rare vascular neoplasm with high morbidity and mortality. The initiating mechanism during the pathogenesis of KHE has yet to be discovered.
Yi Ji +4 more
doaj +1 more source
Background Angiosarcoma is a rapidly proliferating vascular tumor that originates in endothelial cells of vessels. Rarely, it can be associated with consumptive coagulopathy due to disseminated intravascular coagulation eventually leading to ...
Ahmad Talha Tariq +3 more
doaj +1 more source
Kasabach–Merritt Phenomenon Associated with Congenital Hydrocephalus: A Case Report
Background: Kasabach–Merritt phenomenon (KMP) is a rare condition characterized by thrombocytopenia and consumptive coagulopathy in the setting of rapidly expanding vascular tumors.
Kritika Goel +3 more
doaj +1 more source
Kasabach-Merritt Phenomenon (KMP) is a life-threatening consumptive coagulopathy that commonly occurs in infants and young children. It is a combination of an enlarging vascular lesion, thrombocytopenia, microangiopathic haemolytic anaemia, and ...
Hafiz Khalid Pervaiz +4 more
doaj +1 more source
Kaposiform hemangioendothelioma (KHE) is a locally aggressive vascular tumor that may be complicated by Kasabach-Merritt phenomenon (KMP), a profound thrombocytopenia resulting from platelet trapping within a vascular tumor, either KHE or tufted angioma (
Grecia V. Vivas-Colmenares +4 more
doaj +1 more source
Kasabach-Merritt phenomenon (KMP) is characterized by vascular tumour and consumptive coagulopathy with life-threatening thrombocytopenia, prolonged prothrombin time and partial thromboplastin time, hypofibrinogenemia, and the presence of high fibrin ...
Gonca Keskindemirci +7 more
doaj +1 more source

