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[葡萄膜临床意外性恶性黑色素瘤。1981 - 1995年,埃尔朗根眼科病理实验室/D]

[Clinically unexpected malignant melanomas of the uvea. 1981-1995, Erlangen Ophthalmopathologic Laboratory/D].

作者信息

Mardin C Y, Küchle M, Naumann G O

机构信息

Augenklinik mit Poliklinik Erlangen, Universität Erlangen-Nürnberg.

出版信息

Klin Monbl Augenheilkd. 1997 Aug;211(2):118-21. doi: 10.1055/s-2008-1035107.

Abstract

PURPOSE

The aim of this study was to investigate the incidence of unexpected malignant uveal melanoma in the age of ultrasound diagnostics and to highlight the reasons for misdiagnosis.

PATIENTS AND METHODS

All eyes were surgically removed and histologic examination was performed between 1981 and 1995. The eyes were investigated for the incidence of uveal melanoma, and the history of the unexpected malignant melanoma of the uvea or ciliary body highlighted.

RESULTS

225 (18.7%) eyes with malignant melanoma out of 2583 enucleated eyes were found. Eight (3.6%) of 225 were clinically unexpected. The clinical misdiagnoses were secondary angle closure or open angle glaucoma (6), retinal detachment (5), iritis (1), scleritis (1), cataract (4) and an intraocular mass that was believed to be a metastasis of a colon carcinoma. Seven of eight eyes were blind, and one eye had light perception only. The longest follow up before enucleation was 13 years. On three eyes diagnostic ultrasound was reportedly performed without specific diagnosis of uveal melanoma. Surgery was performed on four eyes for reasons of uncontrollable intraocular pressure or retinal detachment up to five years before enucleation. Histologic diagnoses were 3 epitheloid-type, 2 spindel-type and 3 necrotic melanoma of the uvea. Four eyes showed scleral invasion by tumor cells and one eye an invasion into the episcleral space.

CONCLUSIONS

Even today the rate of unexpected uveal melanoma, according to our study is 3.6%. Therefore, all blind eyes without visualisation of the posterior pole should be examined with ultrasound in order to diagnose an uveal melanoma prior to enucleation.

摘要

目的

本研究旨在调查超声诊断时代意外性脉络膜恶性黑色素瘤的发生率,并强调误诊原因。

患者与方法

1981年至1995年间,所有眼球均经手术摘除并进行组织学检查。对这些眼球进行脉络膜黑色素瘤发生率的调查,并突出意外性脉络膜或睫状体恶性黑色素瘤的病史。

结果

在2583只摘除的眼球中,发现225只(18.7%)患有恶性黑色素瘤。225只中有8只(3.6%)在临床上属于意外情况。临床误诊包括继发性闭角型或开角型青光眼(6只)、视网膜脱离(5只)、虹膜炎(1只)、巩膜炎(1只)、白内障(4只)以及被认为是结肠癌转移的眼内肿物。8只眼中有7只失明,1只眼仅存光感。摘除眼球前最长随访时间为13年。据报道,3只眼进行了诊断性超声检查,但未明确诊断出脉络膜黑色素瘤。4只眼因眼压无法控制或视网膜脱离在摘除眼球前长达5年进行了手术。组织学诊断为3只眼为上皮样型、2只眼为梭形细胞型、3只眼为坏死性脉络膜黑色素瘤。4只眼显示肿瘤细胞侵犯巩膜,1只眼侵犯至巩膜上腔。

结论

根据我们的研究,即使在今天,意外性脉络膜黑色素瘤的发生率仍为3.6%。因此,所有无法看清后极部的盲眼都应进行超声检查,以便在摘除眼球前诊断脉络膜黑色素瘤。

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