Zobrazeno 1 - 10
of 1 221
pro vyhledávání: '"kaposiform hemangioendothelioma"'
Publikováno v:
Vascular Health and Risk Management, Vol Volume 20, Pp 251-254 (2024)
Nan Dang,1 Yunqing Ren2 1Shanghai Children’s Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China; 2Children’s Hospital of Zhejiang University School of Medicine, Hangzhou, People’s Republic of Chi
Externí odkaz:
https://doaj.org/article/6175055f061247d4910d25bd9fbc9e88
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-5 (2024)
Abstract Background Kaposiform hemangioendothelioma (KHE) is a rare neoplasm of vascular origin. It may involve skin, bone, connective tissue, and parenchymal organs, and it is difficult to make a definite diagnosis in the early stage because Kasabac
Externí odkaz:
https://doaj.org/article/0dd6143c446d4f75a95f243814735506
Publikováno v:
Journal of Biological Engineering, Vol 18, Iss 1, Pp 1-12 (2024)
Abstract Background Kaposiform hemangioendothelioma (KHE) is a rare intermediate vascular tumor with unclear pathogenesis. Recently, three dimensional (3D) cell spheroids and organoids have played an indispensable role in the study of many diseases,
Externí odkaz:
https://doaj.org/article/85587c4c839b402ca8da34b67601fed2
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Externí odkaz:
https://doaj.org/article/4cdaa0f5e97e4245828bc913be0e9a97
Autor:
Miaomiao Li, Xusheng Wang, Rosalind Kieran, Zheng Wei Sun, Yubin Gong, Hongzhao Lei, Bin Sun, Li Xiao, Yanlin Wang, Song Wang, Zhiyu Li, Luying Wang, Renrong Lv, Feng Xue, Jianfeng Ge, Changxian Dong, Ran Huo
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundKaposiform hemangioendothelioma (KHE) is a rare vascular tumor with a high risk of mortality. Few studies with large samples of KHE have been reported. KHE may develop into the Kasabach–Merritt phenomenon (KMP), which is characterized by
Externí odkaz:
https://doaj.org/article/20a4b113b67147c7a98d51d09e2cf9bd
Autor:
Lingke Liu, Weizhong Gu, Liping Teng, Yiping Xu, Fei Zheng, Minfei Hu, Meiping Lu, Xuefeng Xu
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Kaposiform hemangioendothelioma (KHE) is a rare vascular neoplasm affecting infants or young children. KHE includes a spectrum of lesions, ranging from small and superficial tumors to large and invasive lesions with Kasabach-Merri
Externí odkaz:
https://doaj.org/article/940d1dacc3d24ec6842b79b62abe6164
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28802- (2024)
The coexistence of kaposiform hemangioendothelioma (KHE) and capillary malformation (CM) is quite rare, and few relevant studies can be found to confirm whether this phenomenon is accidental. We diagnosed and treated two such patients, revealing inte
Externí odkaz:
https://doaj.org/article/1753c932253f470fa5a66181e50fae90
Autor:
Alexa Bello, Mir B. Alikhan, Aparna Subramaniam, Zenab I. Yusuf, Bruce Brockstein, Vinod Ravi
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Kaposiform hemangioendothelioma (KHE), a rare form of vascular neoplasm, is typically seen in children. In this paper, we report a unique case of KHE replacing bone marrow tissue mimicking myeloproliferative neoplasm with additional involvement in th
Externí odkaz:
https://doaj.org/article/ca671d0456104a77bfac7cf5262d5e25
Autor:
Margarida Morgado, MD, Filipe Barros Alves, MD, Sofia Pedrosa, MD, Maria Garcia, MD, Sílvia Costa Dias, MD, António J. Madureira, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 9, Pp 3152-3156 (2023)
Kaposiform hemangioendothelioma is a rare, locally aggressive or borderline vascular tumor that typically affects infants. It presents as a purpuric cutaneous lesion and may be associated with life-threatening coagulation disorders, such as the Kasab
Externí odkaz:
https://doaj.org/article/c02d785a303d43ceb9b95bf7808ac619
Publikováno v:
Journal of Interventional Medicine, Vol 6, Iss 3, Pp 130-133 (2023)
An infant with Kasabach-Merritt Phenomenon (KMP) presented with a giant subcutaneous mass in the right lower limb, severe hypofibrinogenemia, and thrombocytopenia. Glucocorticoids, along with supportive treatments including transfusion of blood produ
Externí odkaz:
https://doaj.org/article/3f15ca4f5c1b4c49a34b8d3ef9bed8ba