Manjila S, Ray A, Hu Y, Cai DX, Cohen ML, Cohen AR:
Embryonal tumor with abundant neuropil and true rosettes (ETANTR): two illustrative cases and review of the literature.
Not exact matches
About 60 percent of rhabdomyosarcoma patients have
tumors of the
embryonal subtype, and about 25 percent have the alveolar subtype.
When researchers screened a library of more than 200 drugs and related compounds for activity against
embryonal subtype
tumor cells from three patients, the most promising results involved drugs that increased oxidative stress in
tumor cells.
Embryonal rhabdomyosarcoma included far more genomic alterations than alveolar subtype
tumors.
Research led by Mark Hatley, MD, PhD, of St. Jude Oncology, has shown that certain
embryonal rhabdomyosarcoma
tumors arise from early endothelial cells instead.
Pineal region
tumors: This group of
tumors includes germ cell
tumors, germinomas, non-germinomatous germ cell
tumors,
embryonal cell
tumor, yolk sac
tumors, teratomas (immature vs. mature), pinealoblastomas, and pineocytomas.
Beckwith - Wiedemann syndrome (BWS) is a disorder of prenatal overgrowth and affected patients frequently have
embryonal malignancies such as Wilms»
tumor (WT).
In vivo imaging of
tumor - propagating cells, regional
tumor heterogeneity, and dynamic cell movements in
embryonal rhabdomyosarcoma.