Zobrazeno 1 - 10
of 73
pro vyhledávání: '"KASABACH MERRIT SYNDROME"'
Autor:
Frontiers Production Office
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Externí odkaz:
https://doaj.org/article/ec2040d4d17c44679480e4358e83bfc4
Akademický článek
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Publikováno v:
Frontiers in Pediatrics, Vol 9 (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 transar
Externí odkaz:
https://doaj.org/article/190c8da1eaad4d7d85d17fca62e503db
Autor:
Matteo Chinello, Daniela Di Carlo, Francesca Olivieri, Rita Balter, Massimiliano De Bortoli, Virginia Vitale, Ada Zaccaron, Elisa Bonetti, Alice Parisi, Simone Cesaro
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 10, Iss 1, Pp e2018043-e2018043 (2018)
Background: Kaposiform Hemangioendothelioma (KHE) is a rare vascular tumour of the infancy and of the first decade of life. It is locally aggressive and potentially life threatening when associated to consumptive coagulopathy, known as Kasabach-Merri
Externí odkaz:
https://doaj.org/article/cc13d3b545d44e8d8ca250df330e3307
Autor:
Wang, Huaijie, Guo, Zhengtuan
Publikováno v:
Frontiers in Pediatrics
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 transar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3af753ca213d3860fbe7388be98aacd6
https://doi.org/10.3389/fped.2022.846207
https://doi.org/10.3389/fped.2022.846207
Publikováno v:
International Journal of Scientific Research and Management. 8:382-386
Kasabach-Merritt syndrome is a rare disorder of the newborn or very young child which combines a rapidly expanding red-purple vascular tumor and a hematological syndrome dominated by major thrombocytopenia and more moderate consumption of fibrinogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7adce62bdd748ed3b58019572389b2f
https://doi.org/10.18535/ijsrm/v8i08.mp01
https://doi.org/10.18535/ijsrm/v8i08.mp01
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 19, Iss 4, Pp 233-235 (2014)
We report the identification of Kaposiform hemangioendothelioma of the cecum presenting as colocolic intussusception in a 4-month-old boy without Kasabach-Merrit syndrome. To our knowledge this is the first reported case in the literature of such a p
Externí odkaz:
https://doaj.org/article/87cc240bf70b4c9599d6fc3907e17d23
Publikováno v:
Frontiers in Pediatrics, Vol 9 (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 transar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baffb6feab1fe27b871417ca4ec4cb1b
https://pubmed.ncbi.nlm.nih.gov/35795336
https://pubmed.ncbi.nlm.nih.gov/35795336
Autor:
V. Archana, S. Sundari
The most common paediatric neoplasm is haemangioma, which is a vascular lesion caused by excessive blood vessel proliferation. Haemangioma are congenital lesions that commonly affect newborns infants and children. They are generally benign and often
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0de0ee241c518976ef51639cc0b8b885
https://doi.org/10.9734/bpi/hmmr/v12/2137f
https://doi.org/10.9734/bpi/hmmr/v12/2137f
Autor:
M. Valdés Mas, M. L. Ortiz Sánchez, J. L. Rodrigo Agudo, M. Miras López, J. A. Pons Miñano, F. Carballo Álvarez
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 100, Iss 8, Pp 511-513 (2008)
El hemangioma hepático es el tumor benigno más frecuente del hígado. La gran mayoría de ellos son de pequeño tamaño, asintomáticos y con un pronóstico excelente. En raras ocasiones son de mayor tamaño y pueden estar asociados a una coagulopa
Externí odkaz:
https://doaj.org/article/36c16d396c3d4cbf8973c07836ec232d