Results 1 to 10 of about 1,028 (123)

Metastatic angiosarcoma and Kasabach-Merritt syndrome [PDF]

open access: yesRare Tumors, 2014
Angiosarcomas are exceedingly rare tumors that are often difficult to diagnose. Exceptionally unusual is the presentation of these tumors with Kasabach-Merritt Syndrome, a curious form of intratumoral coagulation that can be impossible to distinguish ...
Suleiman Massarweh   +4 more
doaj   +4 more sources

Kasabach-Merritt syndrome complicating a giant hemangioma of the liver: A case report [PDF]

open access: yesRadiology Case Reports, 2023
Liver hemangiomas are the most common benign tumors of the liver with a prevalence of 1%-20% according to autopsy series. They can in some cases reach measurable sized.
N. Amsiguine, MD   +6 more
doaj   +2 more sources

Kasabach–Merritt Syndrome, an underdiagnosed swollen leg in newborn with anemia and jaundice [PDF]

open access: yesClinical Case Reports, 2023
Key Clinical Message Kasabach–Merritt syndrome is a rare disease. Early recognition, timely transfer, and proper management are crucial in reducing bleeding complication and mortality.
Chariya Chap, Sakviseth Bin
doaj   +2 more sources

Transarterial Embolization in Neonatal Kasabach–Merritt Syndrome [PDF]

open access: yesFrontiers in Pediatrics, 2021
Background: Kasabach–Merritt syndrome (KMS) is characterized by large hemangiomas and persistent thrombocytopenia, which may result in visceral hemorrhage and disseminated intravascular coagulation. This study aimed to evaluate the value of transarterial
Yinghao Wang   +6 more
doaj   +2 more sources

Diffused hepatic angiosarcoma with Kasabach-Merritt syndrome-case report and literature review [PDF]

open access: yesBMC Gastroenterology, 2020
Background Hepatic angiosarcoma is a rare malignant tumor featured by highly aggressive behavior and poor prognosis. There are few reports about diffused hepatic angiosarcoma with Kasabach-Merritt syndrome till now.
Xing-mao Zhang   +3 more
doaj   +2 more sources

Kasabach-Merritt Syndrome in an Adult [PDF]

open access: yesTurkish Journal of Hematology, 2018
Kolar Vishwanath Vinod   +3 more
doaj   +4 more sources

Laparoscopic cholecystectomy for symptomatic cholecystolithiasis (CCL) in “Kasabach–Merritt syndrome” (KMS) (Kaposi-tumor like hemangioendothelioma with case-specific perioperative management) [PDF]

open access: yesInnovative Surgical Sciences, 2023
The Kasabach–Merritt syndrome (KMS) is characterized by the occurrence of hemangioendothelioma (giant hemangioma with thrombosis leading to thrombocytopenia), which can be associated with disseminated intravasal coagulation.
Arndt Stephan   +6 more
doaj   +2 more sources

Angiosarcoma associated with Kasabach–Merritt syndrome presenting with typical signs and symptoms of pulmonary tuberculosis: a case report [PDF]

open access: yesJournal of Medical Case Reports
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   +2 more sources

Successful treatment of an adult with Kasabach-Merritt syndrome using thalidomide, vincristine, and prednisone [PDF]

open access: yesJournal of International Medical Research, 2019
Objective Kasabach-Merritt syndrome is a rare disease that mainly occurs in infants and adolescents. It usually manifests as disseminated intravascular coagulation and severe bleeding, and is associated with high mortality. However, its low incidence and
Yue-Hua Huang   +4 more
doaj   +2 more sources

Propranolol in the preoperative treatment of Kasabach–Merritt syndrome: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2017
Background Kasabach–Merritt syndrome represents the association of hemangioma with thrombocytopenia and consumptive coagulopathy. We present a case of Kasabach–Merritt syndrome treatment with orally administered propranolol. Case presentation A 4.5-month-
Saša V. Radović   +2 more
doaj   +2 more sources

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