Abdelouahed K, Laghmari M, Tachfouti S, Cherkaoui W, Khorassani M, M'Seffer F Alaoui, Mohcine Z
Service Ophtalmologie A, Rabat, Maroc.
J Fr Ophtalmol. 2005 Feb;28(2):197-200. doi: 10.1016/s0181-5512(05)81043-5.
The authors report a case of an 6-year-old pediatric patient with a history of acute onset of proptosis of his right eye. He was admitted at hospital 6 months ago for proptosis concomitant with orbital trauma. Computed tomography scan demonstrated a mass involving the right orbit, right maxillary sinus, and zygoma with endocranial extension.
Incisional biopsy of the mass revealed after of histopathologic and immuno-histochemical evaluation a T-cell lymphoblastic lymphoma. Systemic examination and bone marrow aspirate show a acute lymphoblastic leukemia. The patient was treated with LMT96 Protocol. A complete Remission was observed after 13 months of follow up.
Primary T-cell lymphoblastic lymphoma of the orbit is a rare entity in any age group, but it is very rare in children. When tumors occurs in the orbit, it presents a challenging diagnosis problem, especially in pediatric patients.
作者报告了一例6岁儿科患者,有右眼急性眼球突出病史。他于6个月前因眼球突出伴眼眶外伤入院。计算机断层扫描显示一个肿块累及右眼眶、右上颌窦和颧骨,并向颅内延伸。
对肿块进行切开活检,经组织病理学和免疫组织化学评估后显示为T细胞淋巴母细胞淋巴瘤。全身检查和骨髓穿刺显示为急性淋巴细胞白血病。该患者接受了LMT96方案治疗。随访13个月后观察到完全缓解。
眼眶原发性T细胞淋巴母细胞淋巴瘤在任何年龄组中都是一种罕见的疾病,但在儿童中极为罕见。当肿瘤发生在眼眶时,会带来具有挑战性的诊断问题,尤其是在儿科患者中。