Kiessling John W, Whitney Eric, Cathel Alessandra, Khan Yasir R, Mahato Deependra
Neurosurgery, Desert Regional Medical Center, Palm Springs, USA.
Cureus. 2020 Jun 27;12(6):e8856. doi: 10.7759/cureus.8856.
Primary non-Hodgkin's lymphoma of the bone remains an uncommon presentation of non-Hodgkin's lymphoma. Primary lymphoma of the cranial vault is exceptionally rare. Here, we present a 62-year-old immunocompetent male presenting with the rapid growth of a left parietal scalp lesion and new-onset seizure. In addition to his imaging, which showed an extracranial, cranial, and intracranial mass with bony destruction, sagittal sinus involvement, and parenchymal invasion, his diagnostic angiogram demonstrated extensive vascular supply from both the right and left external carotid branches. Intraoperatively, we confirmed a frank invasion of the posterior sagittal sinus. After subtotal resection followed by R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone therapy, the patient continues to be disease-free at the 10-month follow-up. We report here a case of primary cranial vault lymphoma that very closely mimicked meningioma in many ways, with positive angiography and intraoperatively confirmed venous sinus invasion.
原发性骨非霍奇金淋巴瘤仍然是非霍奇金淋巴瘤的一种罕见表现形式。原发性颅顶淋巴瘤极为罕见。在此,我们报告一例62岁免疫功能正常的男性,其表现为左侧顶叶头皮病变迅速生长并新发癫痫。除影像学检查显示有颅外、颅骨及颅内肿块伴骨质破坏、矢状窦受累及实质侵犯外,其诊断性血管造影显示来自左右颈外动脉分支的广泛血管供应。术中,我们证实后矢状窦有明显侵犯。在次全切除并接受R-CHOP(利妥昔单抗、环磷酰胺、阿霉素、长春新碱和泼尼松)治疗后,患者在10个月的随访中仍无疾病复发。我们在此报告一例原发性颅顶淋巴瘤,该病例在许多方面与脑膜瘤极为相似,血管造影呈阳性且术中证实有静脉窦侵犯。