Zobrazeno 1 - 10
of 166
pro vyhledávání: '"sialoblastoma"'
Autor:
Ran Yang, Yong Zhan, Yi Li, Shu-Yang Dai, Shi-Wei He, Chun-Jing Ye, Ling-Du Meng, De-Qian Chen, Chen-Bin Dong, Lian Chen, Gong Chen, Kui-Ran Dong, Kai Li, Shan Zheng, Jun Li, Wei Yao, Rui Dong
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Sialoblastoma (SBL) is an infrequent embryonal malignant tumor originating from the salivary gland, resembling primitive salivary gland anlage, whereas hepatoblastoma (HB) is the most common pediatric liver malignancy. The simultaneous occurrence of
Externí odkaz:
https://doaj.org/article/fd638952143f42bb94769fbcd9421b1c
Publikováno v:
Children, Vol 10, Iss 4, p 628 (2023)
Sialoblastoma is an extremely rare embryonal tumor derived from salivary gland primordial cells. Treatment usually consists of surgery alone; however, in some cases, chemotherapy is required and is administered with good response. We present a case o
Externí odkaz:
https://doaj.org/article/95a7630b9cbf4db8a17a3d4718db64fa
Akademický článek
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Akademický článek
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Autor:
Lin Xu, Yumin Zhong
Publikováno v:
Iranian Journal of Radiology. 18
Sialoblastoma is a rare salivary gland tumor, diagnosed in the neonatal period or during infancy. Hepatoblastoma accounts for less than 1% of all pediatric malignancies. The co-occurrence of these two tumors is extremely uncommon. Here, we report a c
Akademický článek
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Autor:
Maria Elena Errico, Stefano Lucà, Andrea Ronchi, Immacolata Cozzolino, Pierluigi Mariani, Luigi Laino, Renato Franco, Vittoria Donofrio
Publikováno v:
Minerva dental and oral science.
Background The occurrence of a head and neck tumoral mass at birth or shortly afterwards may cause concern and the differential diagnosis may be complex. Sialoblastoma is a rare epithelial tumor of the salivary glands of uncertain malignant potential
Autor:
A. San Roman, C. Lagues, K. Albarenque, C. Schauvinhold, M. T. G. de Dávila, M. Rodríguez-Zubieta, D. Steinberg, D. Russo, A. Etchegaray, G. Podesta, Mar Varela
Publikováno v:
Case Reports in Pathology
Case Reports in Pathology, Vol 2021 (2021)
Case Reports in Pathology, Vol 2021 (2021)
We report a case of a newborn with two synchronous tumors—sialoblastoma and hepatoblastoma—diagnosed at 20 weeks of gestation by magnetic resonance imaging (MRI) and ultrasonography (US). The aim of this study was to describe the management of th
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology
Frontiers in Oncology
Objective: Salivary rare basaloid lesions, including cribriform type basal cell adenoma (cBCA), BCA with incomplete capsule (iBCA), sialoblastoma (SB), and intercalated duct hyperplasia (IDH), could easily be misdiagnosed as adenoid cystic carcinoma
Autor:
Linda Granowetter, Margaret Brandwein-Gensler, Rachel Kessel, Kanwal Majeed Farooqi, Deepa Manwani
Publikováno v:
Rare Tumors, Vol 3, Iss 2, Pp e13-e13 (2011)
Sialoblastoma is a rare salivary neoplasm which presents either congenitally or during early infancy. It was originally considered a benign neoplasm, however a number of reported cases have documented locoregional recurrence and distant metastases. C
Externí odkaz:
https://doaj.org/article/387ca3be0d4a4a11b2ba8206247efb56