Results 81 to 90 of about 1,455,846 (152)

Rapidly involuting congenital hemangioma associated with Kasabach-Merritt Syndrome

open access: yes, 2021
Background: Rapidly involuting congenital hemangioma (RICH) is a rare vascular tumor that is present at birth and involutes during the first year of life.
Rosalia Ballona*   +2 more
core   +1 more source

A case of Kasabach-Merritt Syndrome in a nine-month-old; a rare complication of haemangioma in the young

open access: yesJournal of the Pakistan Medical Association
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

The importance of early diagnosis and treatment of kaposiform hemangioendothelioma complicated by Kasabach-Merritt phenomenon

open access: yesDermatology Practical & Conceptual, 2015
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

Neonatal kaposiform hemangioendothelioma of the spleen associated with Kasabach-Merritt phenomenon

open access: yes, 2016
Kaposiform hemangioendothelioma is a rare locally aggressive vascular tumor that usually manifests during early childhood. Typically the lesion presents with skin, soft tissue and bone involvement and is characterized histologically by ill-defined ...
Shabtaie, Samuel A   +10 more
core   +1 more source

Hemangioma Esplénico no Adulto e Síndrome de Kasabach-Merritt [PDF]

open access: yes, 2011
The Kasabach Merritt syndrome is a rare disease that is characteristic of youth ages, that counts as an association of capillary hemangioma and thrombocytopenia.
Sousa, R.   +3 more
core  

Hemangioendotelioma kaposiforme con fenómeno de Kasabach-Merritt en una lactante:: reporte de caso y revisión de la literatura

open access: yes, 2023
Kaposiform hemangioendothelioma is an endothelial-derived cell neoplasm, with a variable clinical spectrum between benign and aggressive, rare in childhood and adolescence, associated with the Kasabach-Merritt phenomenon, which is a coagulopathy that can
Casas, C., Ortiz, Y., Lancheros, N.
core  

Kaposiform haemangioendothelioma and Kasabach-Merritt syndrome

open access: yes, 2008
Made available in DSpace on 2019-09-11T20:58:50Z (GMT). No. of bitstreams: 0 Previous issue date: 2008OBJETIVO: Descrever a apresentação e a evolução de um caso de hemangioendotelioma kaposiforme complicado por síndrome de Kasabach-Merritt.
Elias, Chelna Paolichi F.   +6 more
core   +1 more source

[Propranolol treatment in Kasabach-Merritt Syndrome secondary to congenital hepatic hemangioma. Clinical case]

open access: yes, 2021
Disponible en: https://www.sap.org.ar/docs/publicaciones/archivosarg/2021/v119n1a26.pdfAbstract in English, Spanish Hepatic hemangioma is the most common benign liver tumor.
Selzer, Erika., Malla, Ivone.
core   +1 more source

Kasabach–Merritt syndrome in an infant successfully treated with a combination of propranolol and methotrexate

open access: yes, 2018
Kasabach Merritt syndrome is a rare childhood vascular tumour,which develops bleeding as an acute complication. The underlying tumour is either a Kaposiform haemangioendothelioma or a tufted angioma.
Thulasi Weerasinghe   +2 more
core   +1 more source

Radiotherapy in Kasabach-Merritt syndrome

open access: yes, 1997
A male infant was born with a 1 x 3 cm reddish lesion under his umbilicus which enlarged within a month and was associated with consumptive coagulopathy. A diagnosis of Kasabach-Merritt syndrome (KMS) was made.
Arif Bülent Aras   +11 more
core   +1 more source

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