Sadruddin Sarfaraz, Medeiros L Jeffrey, DeMonte Franco
Departments of Neurosurgery and Hematopathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
J Neurosurg Pediatr. 2010 Jan;5(1):94-7. doi: 10.3171/2009.7.PEDS09232.
The rare occurrence of T-cell lymphoblastic lymphoma as a primary tumor in the cavernous sinus is described. The patient, a 17-year-old girl, presented with right-sided ophthalmic and maxillary neuropathy and diplopia due to neuropathies of cranial nerves III and VI. An enhancing mass in the cavernous sinus was identified on MR imaging. Dexamethasone was prescribed but did not provide symptomatic relief. Rapid progression of symptoms led to open biopsy, and a diagnosis of T-cell lymphoblastic lymphoma was made. The patient promptly underwent aggressive chemotherapy in which a modified hyper-cyclophosphamide, vincristine, and dexamethasone without doxorubicin regimen with concurrent radiotherapy was used. The patient achieved complete remission and is currently completing the 2-year maintenance phase of chemotherapy.
本文描述了1例罕见的以海绵窦原发性肿瘤形式出现的T细胞淋巴母细胞淋巴瘤。患者为一名17岁女孩,因右侧动眼神经和展神经病变出现右侧眼神经和上颌神经病变及复视。磁共振成像显示海绵窦有一强化肿块。给予地塞米松治疗,但症状未缓解。症状迅速进展导致进行开放性活检,诊断为T细胞淋巴母细胞淋巴瘤。患者随即接受了积极化疗,采用了改良的不含阿霉素的环磷酰胺、长春新碱和地塞米松方案并同时进行放疗。患者达到完全缓解,目前正在完成化疗的2年维持期。