Foster William J, Harbour J William, Holekamp Nancy M, Shah Gaurav K, Thomas Matthew A
Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, and Barnes Retina Institute, St. Louis, Missouri 63110, USA.
Am J Ophthalmol. 2003 Sep;136(3):471-6. doi: 10.1016/s0002-9394(03)00244-7.
To determine the safety of pars plana vitrectomy in eyes containing a treated posterior uveal melanoma.
Interventional case series.
Retrospective case series of patients with posterior uveal melanoma who underwent pars plana vitrectomy. Complications, vitreous cytology, local tumor control, and metastasis were assessed.
Nine patients met study criteria. Tumors were treated with (125)I plaque radiotherapy (seven patients) or transpupillary thermotherapy (two patients). Vitrectomy was performed for vitreous hemorrhage (five patients), macular pucker (two patients), macular hole (one patient), and rhegmatogenous retinal detachment (one patient). Vitrectomy was performed at a mean of 24.7 months (range, 7-47 months) after melanoma treatment. Dispersion of tumor cells at vitrectomy was not observed in any patients. Melanoma cells were detected in the vitreous aspirate in one of seven cases examined cytologically. This patient had intratumoral and vitreous hemorrhage before plaque radiotherapy, underwent combined vitrectomy/cataract extraction, and developed intraocular tumor dissemination 56 months after vitrectomy. No other patients developed intraocular tumor dissemination. At mean follow-up of 24 months (range, 3-63 months) after vitrectomy, none of the nine patients developed systemic metastasis.
Pars plana vitrectomy rarely may lead to intraocular tumor dissemination, although the risk of this complication is probably low if the tumor has been treated and has responded to therapy before vitrectomy. Vitrectomy should be approached with caution if a vitreous hemorrhage is present, especially if the hemorrhage occurred before tumor treatment, as this may seed tumor cells into the vitreous cavity.
确定在已治疗的后葡萄膜黑色素瘤眼中进行玻璃体切除术的安全性。
干预性病例系列。
对接受玻璃体切除术的后葡萄膜黑色素瘤患者进行回顾性病例系列研究。评估并发症、玻璃体细胞学检查、局部肿瘤控制和转移情况。
9例患者符合研究标准。肿瘤采用碘(125)粒子敷贴放疗(7例患者)或经瞳孔温热疗法(2例患者)治疗。因玻璃体出血(5例患者)、黄斑皱襞(2例患者)、黄斑裂孔(1例患者)和孔源性视网膜脱离(1例患者)而行玻璃体切除术。玻璃体切除术在黑色素瘤治疗后平均24.7个月(范围7 - 47个月)进行。所有患者在玻璃体切除术中均未观察到肿瘤细胞扩散。在7例接受细胞学检查的病例中,有1例在玻璃体抽吸物中检测到黑色素瘤细胞。该患者在粒子敷贴放疗前有瘤内和玻璃体出血,接受了玻璃体切除术/白内障摘除联合手术,并在玻璃体切除术后56个月发生眼内肿瘤播散。其他患者均未发生眼内肿瘤播散。玻璃体切除术后平均随访24个月(范围3 - 63个月),9例患者均未发生全身转移。
尽管如果肿瘤在玻璃体切除术之前已接受治疗且对治疗有反应,这种并发症的风险可能较低,但玻璃体切除术仍可能很少导致眼内肿瘤播散。如果存在玻璃体出血,尤其是在肿瘤治疗前发生出血时,进行玻璃体切除术应谨慎,因为这可能会将肿瘤细胞播散到玻璃体腔中。