Hans F J, Reinges M H T, Nolte K, Reipke P, Krings T
Department of Neurosurgery, University Hospital of the University of Technology, Aachen, Germany.
Neuroradiology. 2005 Jul;47(7):539-42. doi: 10.1007/s00234-005-1394-4. Epub 2005 Jun 7.
This case demonstrates the rare finding of a primary malignant lymphoma of the frontobasis and ethmoidal cells in a patient presenting with progressive loss of vision. Computed tomography and MRI demonstrated a homogenously enhancing tumour with extensive bony destructions of the skull base. After transsphenoidal biopsy, histology revealed a highly malignant primary B-cell lymphoma. The patient was further treated with immunochemotherapy. Tissue diagnosis is, therefore, crucial before a definitive therapy is instituted.
该病例展示了一名视力逐渐丧失患者罕见的额筛窦原发性恶性淋巴瘤。计算机断层扫描和磁共振成像显示肿瘤均匀强化,伴有广泛的颅底骨质破坏。经蝶窦活检后,组织学检查显示为高度恶性的原发性B细胞淋巴瘤。该患者进一步接受了免疫化疗。因此,在确定治疗方案之前,组织诊断至关重要。