Baig Iyza, Webb Ashley, Crowell Eric L, Supsupin Emilio P, Adesina Ore-Ofe O
Ruiz Department of Ophthalmology and Visual Science, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, TX, USA.
Robert Cizik Eye Clinic, Houston, TX, USA.
Eur J Ophthalmol. 2020 Mar;30(2):NP41-NP46. doi: 10.1177/1120672119842998. Epub 2019 Apr 25.
To describe a rare case of Burkitt lymphoma metastatic to the cavernous sinus that was initially diagnosed as Tolosa-Hunt syndrome.
A 31-year-old confirmed and treatment-compliant HIV-positive Hispanic male acutely developed diplopia, ptosis, numbness in the V1 distribution, and complete external ophthalmoplegia in the right eye over 1 week. Imaging showed a mass-like lesion within the right cavernous sinus without other intracranial abnormalities. He was started on broad-spectrum antibiotics and antifungals without improvement. Inflammatory and infectious workup was negative. A presumed diagnosis of Tolosa-Hunt syndrome was made based on clinical and radiographic findings, as well as the absence of another etiology to explain the patient's presentation. He was then started on high-dose oral steroids with improvement of orbital pain only. Shortly after being discharged on steroids, the patient returned to the hospital with severe abdominal pain. Computed tomography of the abdomen showed perforated ileitis with aneurysmal dilation of the ileum and marked wall thickening concerning for a mass lesion. Positron emission tomography-computed tomography showed an uptake in the terminal ileum and right cavernous sinus consistent with metastatic Burkitt lymphoma, matching with pathology. After several cycles of chemotherapy, symptoms improved, and he regained full ocular motility in the affected eye. However, the patient ultimately died due to peritonitis and pyelonephritis.
Burkitt lymphoma metastatic to the cavernous sinus was diagnosed after an initial diagnosis of Tolosa-Hunt syndrome. Tolosa-Hunt syndrome is a diagnosis of exclusion and should only be made after ruling out other pathologies.
描述一例罕见的转移性至海绵窦的伯基特淋巴瘤,该病例最初被诊断为托洛萨-亨特综合征。
一名31岁确诊且依从治疗的HIV阳性西班牙裔男性,在1周内急性出现复视、上睑下垂、V1分布区麻木以及右眼完全性眼球外肌麻痹。影像学检查显示右侧海绵窦内有一个肿块样病变,无其他颅内异常。给予广谱抗生素和抗真菌药物治疗后病情无改善。炎症和感染相关检查均为阴性。根据临床和影像学表现以及无其他病因可解释患者的症状,初步诊断为托洛萨-亨特综合征。随后开始给予高剂量口服类固醇治疗,仅眼眶疼痛有所改善。在出院接受类固醇治疗后不久,患者因严重腹痛再次入院。腹部计算机断层扫描显示回肠穿孔性炎症伴回肠动脉瘤样扩张以及肠壁明显增厚,怀疑有肿块病变。正电子发射断层扫描-计算机断层扫描显示回肠末端和右侧海绵窦有摄取,与转移性伯基特淋巴瘤相符,病理检查也证实了这一点。经过几个周期的化疗后,症状有所改善,患眼恢复了完全的眼球运动。然而,患者最终因腹膜炎和肾盂肾炎死亡。
在最初诊断为托洛萨-亨特综合征后,确诊为转移性至海绵窦的伯基特淋巴瘤。托洛萨-亨特综合征是一种排除性诊断,只有在排除其他病理情况后才能做出诊断。