ライフサイエンスコーパス: fibroma

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1 eratotic epithelium overlying a large dermal fibroma.

2 d leiomyoma, benign inflammatory nodule, and fibroma.

3 me has shed light on the etiology of cardiac fibromas.

4 ubset of histotypes such as rhabdomyomas and fibromas.

5 with papillary fibroelastomas, 18 (6%) with fibromas, 12 (4%) with lipomas, 28 (9%) with other benig

6 atients were identified: 106 rhabdomyoma, 25 fibroma, 14 myxoma, 6 vascular, 4 teratoma, 3 lipoma, an

7 neoplasms, 7 patients had benign histology (fibroma-5, rhabdomyoma-1, and pheochromocytoma-1) and 21

8 d 1 relative also showing multiple sclerotic fibromas, a cutaneous manifestation of PTEN (phosphatase

9 ecific translocations (eg, cemento-ossifying fibroma and myxoid chondrosarcoma) and the association o

10 ties such as ameloblastomas, carcinomas, and fibromas and clinically may resemble localized periodont

11 low signal intensity on T2-weighted images, fibromas and fibrothecomas display a relatively specific

12 All fibromas and fibrothecomas showed homogeneous low signal

13 ther features include such tumors as ovarian fibromas and medulloblastomas.

14 ted that patients who underwent resection of fibromas and myxomas had superior survival characteristi

15 were benign (rhabdomyoma, myxoma, teratoma, fibroma, and hemangioma).

16 l cell carcinomas, medulloblastomas, ovarian fibromas, and a variety of developmental defects.

17 manifestations include gingival enlargement, fibromas, and dental enamel pitting.

18 fibroblast-like angiofibroma and periungual fibroma cells than in fibroblasts from normal-appearing

19 nd uninfected fibroblasts indicated that the fibroma component was not required for productive infect

20 tumors (myxomas, lipomas, rhabdomyomas, and fibromas) have provided insight into fundamental mechani

21 sion for VT associated with rhabdomyomas and fibromas in selected patients is an important and effect

22 ve instability and focal soft tissue tumors (fibromas, lipomas, etc).

23 ture teratoma (n = 3); hydrosalpinx (n = 2); fibroma (n = 1); and benign Brenner tumor (n = 1).

24 in 4 countries had the following diagnoses: fibroma (n = 30), rhabdomyoma (n = 14), malignant tumor

25 clude ganglion cysts, giant-cell cancers and fibromas of the tendon sheath, epidermal inclusion cysts

26 Here, we show that ossifying fibroma (OF) contains a stem cell population that resemb

27 1 female patients with histologically proved fibromas or fibrothecomas were reviewed, and morphologic

28 s and extracolonic lesions including desmoid fibromas, osteomas, epidermoid cysts, and congenital hyp

29 iminated in 18 of these 20, including all 13 fibroma patients.

30 s diagnosed with desmoid tumor, desmoplastic fibroma, periosteal desmoid tumor, osteofibrous dysplasi

31 The peripheral ossifying fibroma (POF), one of the most common gingival lesions,

32 ls from 10 angiofibromas and five periungual fibromas produced higher levels of monocyte chemoattract

33 pical adenomas and carcinomas, ossifying jaw fibromas, renal tumours and uterine benign and malignant

34 Dermal hyperneury and multiple sclerotic fibromas should be added to the list of cutaneous manife

35 57) whereas those who underwent resection of fibromas (SMR 11.17, P=0.002), papillary fibroelastomas

36 re conserved in the capping enzymes of Shope fibroma virus, molluscum contagiosum virus, and African

37 nd the percentage of low signal intensity in fibromas was not significantly different from that in fi

38 In addition, the occurrence of desmoid fibromas was strongly enhanced by p53 deficiency.

39 Patients with large fibromas were the highest-risk group, with VT occurring

40 d no influence on the development of desmoid fibromas, whereas the combination of piroxicam and diflu

41 kin hamartomas (angiofibromas and periungual fibromas) with normal-appearing skin of the same patient

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