ライフサイエンスコーパス: ganglioneuroma

1 ate activated AKT as a tumorigenic driver in ganglioneuroma.

2 al nerve sheath tumor (PNST) that arose in a ganglioneuroma.

3 ude neuroblastoma, ganglioneuroblastoma, and ganglioneuroma.

4 tomas, musculoskeletal anomalies and mucosal ganglioneuromas.

5 ing from immature malignant tumors to benign ganglioneuromas.

6 distal colonic aganglionosis and intestinal ganglioneuromas.

7 he disease course and clinical management of ganglioneuromas.

8 Patients who had >/=1 ganglioneuroma (29% vs 2%; P < .001) or presented with p

9 onal cell vitronectin was detected in 7 of 9 ganglioneuromas, 5 of 8 peripheral ganglia, and 14 of 21

10 The child was diagnosed with ganglioneuroma and embryonal rhabdomyosarcoma (ERMS) at

11 ies that could reduce the size and extent of ganglioneuroma and therefore limit surgical morbidity.

12 kemias, osteosarcomas, Ewing's sarcomas, and ganglioneuromas and in normal tissues.

13 Ganglioneuromas and occasional neuroblastomas formed in

14 chromocytoma and malignant PNST arising in a ganglioneuroma appear to be nonspecific.

15 Most ganglioneuromas are asymptomatic and found incidentally.

16 Ganglioneuromas are rare tumors derived from neural cres

17 f mTOR inhibitors as a means to shrink large ganglioneuromas before resection in order to reduce surg

18 retroperitoneal, intra-abdominal, and pelvic ganglioneuromas between January 1, 2000, and January 1,

19 t an AKT-mTOR-S6 pathway was active in human ganglioneuroma but not neuroblastoma samples.

20 Homozygotes did not develop gastrointestinal ganglioneuromas, but displayed ganglioneuromas of the ad

21 patients with malignant PNST that arose in a ganglioneuroma, contrast-enhanced CT showed a large, mar

22 wnstream AKT target, mTOR, in zebrafish with ganglioneuroma effectively reduced the tumor burden.

23 ected identical band shifts in the leukemia, ganglioneuroma, ERMS, and normal tissues, consistent wit

24 Ganglioneuroma (GN) is a rare benign tumor arising from

25 Most ganglioneuromas have indolent disease courses and rarely

26 al tumors, histologically identical to human ganglioneuromas, in their sympathetic nervous systems an

27 Retroperitoneal ganglioneuroma is a rare bening tumor, generally asympto

28 trointestinal ganglioneuromas, but displayed ganglioneuromas of the adrenal medulla, enlargement of t

29 and adrenal chromaffin cells, together with ganglioneuromas of the gastrointestinal tract and other

30 is syndrome associated with gastrointestinal ganglioneuromas of unknown etiology.

31 Findings in cases of ganglioneuroma-pheochromocytoma and malignant PNST arisi

32 CT findings in two patients with ganglioneuroma-pheochromocytoma included central necrosi

33 nine patients with ganglioneuroma, two with ganglioneuroma-pheochromocytoma, and two with malignant

34 NBL, 12 ganglioneuroblastoma (GNBL), and 20 ganglioneuroma samples in a multivariate model.

35 In most ganglioneuroma samples, a low percentage of tumor cells

36 Diagnosis of ganglioneuroma should be considered when typical CT or M

37 median follow-up of 1.9 years, with 92.2% of ganglioneuromas stable in size.

38 REPORT: We present a case of retroperitoneal ganglioneuroma that mimicked renal mass on imaging.

39 In nine patients with ganglioneuroma, the mass ranged in size from 2 x 4 x 4 c

40 ed of imaging findings in nine patients with ganglioneuroma, two with ganglioneuroma-pheochromocytoma

41 Surgery is the only effective therapy for ganglioneuroma, which may be challenging due to the loca

42 athetic nervous system were found to develop ganglioneuroma without progression to neuroblastoma.