Cruz Antonio Augusto V, Leite Lívio Viana de Oliveira, Chahud Fernando, Neder Luciano, Tone Luiz Gonzaga, Valera Elvis Terci, Elias Jorge
Department of Ophthalmology, Otorhinolaryngology, and Head and Neck, School of Medicine of Ribeirão Preto, University of São Paulo, Brazil.
Ophthalmic Plast Reconstr Surg. 2004 Nov;20(6):473-6. doi: 10.1097/01.iop.0000144935.03795.0f.
We describe a rare case of sinonasal T-cell lymphoma in an 11-year-old boy who presented with a right acute orbit characterized by proptosis, eyelid edema and erythema, limitation of eye movements, and excruciating pain on the right side of his face. Orbital computed tomography showed progressive right extraocular muscle enlargement. One biopsy specimen showed extensive tissue necrosis and an infiltrate of atypical cells with pleomorphic nuclei within the walls of blood vessels. Immunohistochemical studies demonstrated that these cells were positive for leucocyte common antigen (CD45), CD3 cytoplasmic, CD45RO, and terminal deoxynucleotidyl transferase and negative for CD20, CD57, CD56, CD99 and Epstein-Barr virus. Chemotherapy for T-cell non-Hodgkin lymphoma was initiated, but the patient's status deteriorated and the child died of respiratory insufficiency, sepsis, and central nervous system infection.
我们描述了一例罕见的鼻窦T细胞淋巴瘤病例,患者为一名11岁男孩,表现为右侧急性眼眶病变,其特征为眼球突出、眼睑水肿和红斑、眼球运动受限以及右侧面部剧痛。眼眶计算机断层扫描显示右侧眼外肌逐渐增大。一份活检标本显示广泛的组织坏死以及血管壁内有非典型细胞核的细胞浸润。免疫组织化学研究表明,这些细胞对白血细胞共同抗原(CD45)、CD3胞质、CD45RO和末端脱氧核苷酸转移酶呈阳性,而对CD20、CD57、CD56、CD99和爱泼斯坦-巴尔病毒呈阴性。开始进行T细胞非霍奇金淋巴瘤的化疗,但患者病情恶化,最终死于呼吸功能不全、败血症和中枢神经系统感染。