Wiethölter S, Steube D, Stotz H P
Neurologische Klinik Bad Neustadt/Saale.
Zentralbl Neurochir. 1998;59(3):166-70.
The syndrome of intra-vitreous bleeding in association with subarachnoid hemorrhage (SAH) was first described by the French ophthalmologist Albert Terson. In the last 10 years, 31 articles describing 202 cases of Terson's syndrome (TS) were published. Only 3 out of the 31 were printed in non-ophthalmological journals. The findings of our prospective study underline the fact that too little attention is paid to TS in the early treatment of patients with SAH. Between 1/95 and 8/97, 89 patients with spontaneous SAH (7% of all admissions) were transferred to our hospital for post acute phase rehabilitation. Out of these, 13 patients (19 eyes) could be diagnosed with TS. This corresponds to an incidence of 14.6% of all patients with SAH (previous studies: 2-27%). However, only one patient had been correctly diagnosed with TS in the referring clinic. Early recognition of TS is of high importance since diminuation of visual acuity even to functional blindness, complicated in the bilateral case, can hamper the rehabilitative process considerably. Moreover, complications can lead to significant and irreversible damage, i.e. proliferative vitreo-retinopathy (PVR), retinal breaks, traction amotio, and cataract. Suspicion of TS is raised in either cooperative patients complaining of compromised visual acuity or in patients where funduscopy shows vitreous opacity. According to our results, visual evoked potentials (VEP) have only a limited role in diagnosis because of their low sensitivity. Not infrequently, however, VEP may point to accompanying optic nerve atrophy, thereby suggesting conservative treatment. Absolute indications for surgical interventions are PVR and its sequelae; relative indications are subjective visual impairment, impediment of rehabilitation, or lack of spontaneous resorption of the hemorrhage. The surgical procedure of choice is the pars plana vitrectomy (PPV). Rare complications of this operation are retinal damage, endophthalmitis, and reoccurrence of hemorrhage.
玻璃体内出血合并蛛网膜下腔出血(SAH)综合征最早由法国眼科医生阿尔贝·特尔松描述。在过去10年中,发表了31篇描述202例特尔松综合征(TS)的文章。31篇文章中只有3篇发表在非眼科期刊上。我们前瞻性研究的结果强调了一个事实,即在SAH患者的早期治疗中,对TS的关注太少。在1995年1月至1997年8月期间,89例自发性SAH患者(占所有入院患者的7%)被转至我院进行急性期后康复治疗。其中,13例患者(19只眼)被诊断为TS。这相当于所有SAH患者中的发病率为14.6%(以往研究:2%-27%)。然而,在转诊诊所中只有1例患者被正确诊断为TS。早期识别TS非常重要,因为视力下降甚至导致功能性失明,在双侧病例中情况更复杂,会严重妨碍康复进程。此外,并发症可导致严重且不可逆转的损害,即增殖性玻璃体视网膜病变(PVR)、视网膜裂孔、牵拉性视网膜脱离和白内障。对于主诉视力受损的合作患者或眼底检查显示玻璃体混浊的患者,应怀疑患有TS。根据我们的结果,视觉诱发电位(VEP)在诊断中的作用有限,因为其敏感性较低。然而,VEP常常可提示伴有视神经萎缩,从而建议采取保守治疗。手术干预的绝对指征是PVR及其后遗症;相对指征是主观视力损害、康复障碍或出血未自发吸收。首选的手术方法是玻璃体切除术(PPV)。该手术罕见的并发症有视网膜损伤、眼内炎和出血复发。