Gündüz Ahmet Kaan, Mirzayev Ibadulla, Kuzu Işınsu, Gahramanli Zarifakhanim, Mirzayeva Leyla
Department of Ophthalmology, Ankara University Faculty of Medicine, Ankara, Turkey.
Private Eye Clinic, Ankara, Turkey.
Orbit. 2024 Apr;43(2):253-257. doi: 10.1080/01676830.2022.2114501. Epub 2022 Aug 29.
A 71-year-old male presented with painless and slowly progressive proptosis of the right eye. The patient had no history of cancer and was in good health. Orbital magnetic resonance imaging showed a well-demarcated, slightly lobulated intraconal orbital mass hypo-isointense on T1- weighted and isointense on T2-weighted images, demonstrating contrast enhancement in the right orbit. The lesion had a central cavitary region. An anterior orbitotomy with lower lid crease incision was performed and the lesion was excised in toto. Histopathologic examination revealed diffuse infiltration of monomorphic population of small lymphoid cells. Immunohistochemical staining demonstrated diffuse and strong positivity for CD20, CD5, and cyclin D1. Histopathological and immunohistochemical findings were consistent with mantle cell lymphoma. Positron emission tomography-computed tomography did not show systemic involvement. The patient underwent orbital external beam radiotherapy (36 Gy). There was no recurrence and/or systemic involvement at 2.5 years follow-up.
一名71岁男性因右眼无痛性、渐进性眼球突出就诊。患者无癌症病史,身体健康。眼眶磁共振成像显示眶内有一界限清楚、略呈分叶状的肿块,位于肌锥内,T1加权像呈略低信号,T2加权像呈等信号,右侧眼眶有强化表现。病变有中央空洞区。采用下睑皱襞切口行前路眼眶切开术,将病变完整切除。组织病理学检查显示小淋巴细胞单形性弥漫浸润。免疫组化染色显示CD20、CD5和细胞周期蛋白D1弥漫强阳性。组织病理学和免疫组化结果符合套细胞淋巴瘤。正电子发射断层扫描-计算机断层扫描未显示全身受累。患者接受了眼眶外照射放疗(36 Gy)。随访2.5年无复发和/或全身受累。