ライフサイエンスコーパス: vitritis

1 required pars plana vitrectomy for worsening vitritis.

2 t of pediatric retinal degenerations exhibit vitritis.

3 arked vitritis, as opposed to 2 with minimal vitritis.

4 etinal lesions but manifested vasculitis and vitritis.

5 e diagnosed cytologically with granulomatous vitritis.

6 but not identified in any of the 3 eyes with vitritis.

7 anterior chamber inflammation, hypopyon, and vitritis.

8 ith outer retinal infiltrates at the time of vitritis.

9 lammation and refractory glaucoma then dense vitritis.

10 ripheral retina in both eyes with associated vitritis.

11 tment due to bilateral retinochoroiditis and vitritis.

12 hing and/or occlusion, and more than minimal vitritis.

13 retina-choroid-sclera complex, suggestive of vitritis.

14 d vitreoretinal lymphoma or biopsy-confirmed vitritis.

15 Common findings in FUS eyes included vitritis (100%), posterior subcapsular cataract (96%), s

16 34.19%) followed by reduced vision (21.94%), vitritis (12.9%) and choroiditis (7.74%).

17 owed intraocular inflammation: 24% with only vitritis, 16% with only anterior chamber reaction, and 6

18 n 14 of 17 eyes, the first presenting a mild vitritis 5 days following injection.

19 n=13), endophthalmitis (9.1%, n=12), sterile vitritis (7.6%, n=10), vitreous hemorrhage (6.8%, n=9),

20 uding anterior chamber flare (ROR = 1410.5), vitritis (853.3), retinal vasculitis (352.2), infectious

21 With obvious vitritis, a localized subretinal abscess was also found

22 OR = 4.75; P < .001), retinochoroiditis with vitritis/AC inflammation (OR = 2.85; P < .001), presumed

23 ilateral involvement, retinochoroiditis with vitritis/AC inflammation, and zone 1 lesions are major r

24 The difference in total inflammation and vitritis among groups S, S-Dex, and S-MTX is significant

25 The uveitis was posterior, with a 2+ vitritis and a large yellowish lesion involving the macu

26 unilateral anterior uveitis with or without vitritis and either: 1) heterochromia or 2) unilateral d

27 tly by intraocular lymphomatous involvement (vitritis and retinal infiltration), whereas optic nerve

28 e series of 3 patients with mild to moderate vitritis and retinal vasculitis without definite birdsho

29 In all, 90% of eyes had vitritis and/or macula-involving chorioretinitis.

30 eral anterior uveitis, keratic precipitates, vitritis, and absence of posterior synechiae, but the cl

31 Isolated anterior uveitis, vitritis, and choroidal mass are described in 3 patients

32 ad retinal vasculitis, low-grade to moderate vitritis, and hypocyanescent lesions on indocyanine gree

33 The combination of retinitis, vitritis, and optic disc edema without optic nerve enhan

34 Subretinal granulomatous mass/scar, vitritis, and scotoma were the most common ophthalmologi

35 The level of vitritis appears to act as a strong index of likelihood

36 gnosis, 15 were obtained in eyes with marked vitritis, as opposed to 2 with minimal vitritis.

37 of the right eye showed anterior uveitis and vitritis associated with large paravascular haemorrhages

38 to moderate pain and predominantly moderate vitritis, associated with granulomatous keratic precipit

39 All eyes had some degree of vitritis (average 1.8+; range 0.5+ to 4+).

40 B-scan of the right eye revealed vitritis, choroidal abscess, retinal detachment, and scl

41 Anterior uveitis, cataract, vitritis, cystoid macular edema, epiretinal membrane, an

42 jected with ganciclovir-loaded microspheres, vitritis decreased from days 3 to 14, and retinitis and

43 vascularization (ROR 1169, 95% CI 426-3205), vitritis, dry age-related macular degeneration, and cyst

44 Chronic anterior uveitis, vitritis, early development of cataract, and the absence

45 One unresolved vitritis event, managed with observation, occurred in a

46 The median time to resolution of vitritis from the time of treatment was 89 days.

47 Studying vitritis in pediatric retinal degenerations may reveal w

48 In eyes injected with blank microspheres, vitritis increased from days 3 to 7, retinitis increased

49 ndings have included multifocal choroiditis, vitritis, intraretinal hemorrhages, iritis, keratic prec

50 cular inflammatory syndrome (immune recovery vitritis, IRV), which causes vision loss in AIDS patient

51 Paraneoplastic vitritis is primarily a disease of older age, with 67% o

52 3 [6%]), chorioretinal lesions (n = 2 [4%]), vitritis (n = 1 [2%]), and increased intraocular pressur

53 nosed with IRV if they developed symptomatic vitritis of >/=1+ severity associated with inactive CMV

54 d similar retinal lesions with no associated vitritis or anterior chamber cell in bilateral eyes, sug

55 ome measures included time to improvement in vitritis or chorioretinitis, systemic therapy modificati

56 e showed worsening cotton wool spots without vitritis or choroiditis.

57 idence interval [CI] 0.12-0.84; P < .01) and vitritis (OR = 0.32; 95% CI 0.11-0.91; P = .03).

58 signs of endophthalmitis, such as hypopyon, vitritis, or retinal periphlebitis, is important and ear

59 P < 0.002), posterior synechiae (P < 0.002), vitritis (P < 0.005), and chorioretinal scars (P < 0.02)

60 151 eyes [42.5%]), which was associated with vitritis (P = .005); cells in the anterior chamber (P =

61 Pro extrusion (P = 0.41), endophthalmitis or vitritis (P = 0.15), retinal detachments (P = 0.76), cys

62 n addition to peripheral retinal lesions and vitritis, papillitis was present in 95% of cases.

63 nal manifestations include anterior uveitis, vitritis, pars planitis, focal retinal vasculitis, a cha

64 cular manifestations include conjunctivitis, vitritis, post infectious optic neuropathy and a few cas

65 ange, 0%-12.5%; mean +/- SD, 4.6+/-4.6%) and vitritis (range, 0%-14.5%; mean +/- SD, 5.6+/-4.7%).

66 n, neovascularization, tractional membranes, vitritis, retinitis, and choroiditis.

67 Vitritis, retinitis, and optic neuritis were graded from

68 sociated with paraneoplastic optic neuritis, vitritis, retinitis, or a combination thereof, but few r

69 had the least total ocular inflammation and vitritis scores from days 3 to 14.

70 with a cytologic diagnosis of granulomatous vitritis seeking treatment from 2004 through 2018 were i

71 al fluconazole may be effective; however, if vitritis symptoms persist or progress, vitrectomy allows

72 ditis or very minimal endophthalmitis (i.e., vitritis), systemic treatment with oral fluconazole may

73 , hemodialysis, baseline vision, severity of vitritis, treatment strategies and complications.

74 and electroretinograms showed no evidence of vitritis, uveitis, or endophthalmitis after 1 week.

75 Eyes with baseline vitritis (vitreous haze score >/=+0.5, n = 45) had a pro

76 Vitritis was graded by the degree of vitreal haze.

77 Vitritis was observed in 9 of 23 eyes receiving VN.

78 segment involvement, increased reporting of vitritis was observed with brolucizumab (ROR = 1769.33),

79 Uncomplicated vitritis was reported in 6 eyes.

80 Vitritis was the most common presenting feature of lamin

81 Vitritis was the presenting feature (7 of 20 laminae, 35

82 Multifocal yellow-white lesions and vitritis were correlated with identification of the worm

83 d 3 eyes of 3 patients with biopsy-confirmed vitritis were evaluated.

84 with a cytologic diagnosis of granulomatous vitritis were identified, 8 of whom demonstrated systemi

85 tients with retinal vasculitis and low-grade vitritis with or without macular edema may have birdshot