Saito Atsushi, Ninomiya Atsuhiko, Ishida Tomohisa, Inoue Tomoo, Inoue Takashi, Suzuki Shinsuke, Ezura Masayuki, Uenohara Hiroshi
Department of Neurosurgery, Sendai Medical Center, Sendai, Miyagi, Japan.
Department of Neurosurgery, Sendai Medical Center, Sendai, Miyagi, Japan.
World Neurosurg. 2019 Feb;122:116-122. doi: 10.1016/j.wneu.2018.10.132. Epub 2018 Nov 1.
There are few case reports of primary leiomyosarcoma originating from the dura mater. We herein report a case of primary dural leiomyosarcoma that presented with repeated intracranial hemorrhage.
A 62-year-old man presented with a 4-year history of a temporo-occipital bump. He showed a disturbance with reading words. The sudden onset of occipitalgia occurred 13 days after the onset. Computed tomography revealed a left temporal subcortical hematoma and thin subacute subdural hematoma associated with a temporal osteolytic mass lesion extending into the subcutaneous layer. The hematoma and tumorous mass lesion were removed. The subcutaneous tumor mass penetrating the skull bone originated from the dura mater and extended into the transverse sinus. No invasion into the cortical surface was observed. The lesion adjacent to the transverse sinus was not resected, and the remnant lesion was irradiated with local radiation therapy of 60 Gy. A left subdural hematoma and intrasylvian subarachnoid hemorrhage occurred 3 months after the first surgery, and a second removal was performed. Temporal subcortical hemorrhage repeatedly occurred 2 months after the second surgery, and the patient died.
In the present case, primary dural leiomyosarcoma may have invaded the dural sinus and repeated intracranial hemorrhage occurred due to a venous circulatory disturbance. The aggressive clinical course observed is rare. A clearer understanding of the route of invasion and a careful evaluation after primary treatment are needed in order to avoid hemorrhagic complications.
原发性硬脑膜平滑肌肉瘤的病例报告较少。我们在此报告一例原发性硬脑膜平滑肌肉瘤,该病例表现为反复颅内出血。
一名62岁男性,有4年颞枕部肿块病史。他出现阅读文字障碍。发病13天后突然出现枕部疼痛。计算机断层扫描显示左侧颞叶皮质下血肿和薄的亚急性硬膜下血肿,伴有一个延伸至皮下层的颞骨溶骨性肿块病变。血肿和肿瘤性肿块病变被切除。穿透颅骨的皮下肿瘤肿块起源于硬脑膜并延伸至横窦。未观察到侵犯皮质表面。未切除与横窦相邻的病变,残余病变接受了60 Gy的局部放射治疗。首次手术后3个月发生左侧硬膜下血肿和大脑外侧裂蛛网膜下腔出血,进行了第二次切除。第二次手术后2个月颞叶皮质下出血反复发生,患者死亡。
在本病例中,原发性硬脑膜平滑肌肉瘤可能侵犯了硬脑膜窦,由于静脉循环障碍导致反复颅内出血。观察到的侵袭性临床病程较为罕见。为避免出血并发症,需要更清楚地了解侵袭途径并在初次治疗后进行仔细评估。