Objective To observe the clinical manifestation and ophthalmoscopic image characteristics of uveal metastatic carcinoma. Methods Thirty-six uveal metastatic carcinoma patients (43 eyes) were enrolled in this study. The patients included 21 males and 15 females. The patientsprime; ages ranged from 28 to 71 years, with a mean age of (47.3plusmn;10.2) years. Seven patients had bilateral carcinoma and 29 patients had unilateral carcinoma. There were 30 patients with lung cancer, three patients with breast cancer, one patient with gastric cancer and two patients without primary tumors. There were 20 patients with known primary cancer, 16 patients visited the Department of Ophthalmology first. All the patients were examined documenting visual acuity, intraocular pressure, slit-lamp microscopy and mydriatic fundus examination. Meanwhile, 22 patients (26 eyes) were examined using B-type ultrasound and/or color Doppler flow imaging (CDFI). Twelve patients (12 eyes) were examined using fundus fluorescein angiography (FFA) and/or indocyanine green angiography (ICGA). Seventeen patients (22 eyes) were examined using MRI and/or CT. The clinical manifestation and ophthalmoscopic image characteristics of uveal metastatic carcinoma patients were observed. Results Among 43 eyes, four lesions were in the iris, three lesions in the ciliary body and 32 lesions were in the choroid. Fundus examination showed an isolated mass in 26 eyes and more than two masses in nine eyes. Metastatic tumors of the iris and ciliary body often showed irregular cauliflower-like mass with gray-white or meat-red color and abundant vessels. The choroidal metastasis usually demonstrated flat rounded or irregular intraocular masses with gray-yellow or gray-white color in the posterior pole. B-type ultrasound showed ill-defined, flat, and irregular-shaped masses with uneven internal reflectivity. CDFI showed rich blood flow within the tumor. FFA and (or) ICGA showed pinpoint and mottled leaks against hyperfluorescence background. MRI revealed low or middle signal using T1WI and low signal intensity using T2WI. Conclusions The uveal metastatic carcinoma usually occurs in one eye with an isolated mass. Most of them show a flat gray-yellow mass in posterior choroids and have the primary cancer sites of the lung. FFA and/or ICGA show pinpoint and mottled leaks against hyperfluorescence background. B-type ultrasound and (or) CDFI show ill-defined, flat, and irregular-shaped mass with rich blood flow within the tumor. MRI reveals low signal intensity on T2WI.
Objective To evaluate the influence of histopathological invasion on the survival prognosis of patients with unilateral retinoblastoma. Methods Seventyseven patients with unilateral retinoblastoma who were treated by primary enucleation were followed up after treatment. The patients were followed up for a median period of 49 months (range from 1 week to 89 months). The survival data were collected by follow-up appointment, telephone or letter. The Kaplan-Meier method was used to calculate the cumulative survival rate and curve comparison was done with the log-rank test including the degree of the optic nerve invasion, choroidal invasion, choroidal invasion with or without optic nerve invasion, as well as the anterior segment involvement or not. Results The two years survival rate was 88.31%. The survival rate of the group with tumor involvement in the cut end of optic nerve was 16.67%, and significantly lower than other groups with optic nerve involvement (chi;2=19.51, 18.42, 18.42, 14.39; P=0.000 0).The survival rate of the group with massive choroidal invasion and scleral involvement was 60.00% and significantly lower than the group without choroidal involvement (chi;2=7.69，P=0.005 5). The survival rate of the group with optic nerve involvement and massive choroidal invasion was 75.00%, and the survival rate of the group with optic nerve involvement and scleral or orbital invasion was 60.00%. The survival rate of those two groups were significantly lower respectively than the group only with optic nerve invasion（chi;2=4.25, P=0.039 3;chi;2=7.59, P=0.005 9）.There was no significant difference of survival rate between groups with or without anterior segments involvement (chi;2=0.05，P=0.823 5).Conclusions The risk factors for RB death include the surgical marginal involvement of optic nerve, massive choroidal invasion combined with optic nerve and scleral involvement. The anterior segment involvement has no effect on prognosis of patients with unilateral retinoblastoma.