Mikami Takeshi, Niwa Jun, Kubota Tsukasa, Chiba Masahiko
Department of Neurosurgery, Hakodate Municipal Hospital, Japan.
No Shinkei Geka. 2003 Aug;31(8):905-9.
A 55-year-old woman first underwent total thyroidectomy in 1973, and the histopathology was medullary thyroid carcinoma. There was no familial history of endocrine neoplasm. She remained asymptomatic for the next 19 years. Neck and tracheal recurrence was treated with tracheal stent and radiation, in 1997. On July 1998, she presented with headache. Magnetic resonance imaging revealed a gadolinium enhanced mass in the left inferior temporal gyrus. Angiogram revealed a marked tumor stain feeding from the middle and inferior temporal artery. The tumor was successfully excised via a temporal craniotomy. Histopathological sections of the resected specimen confirmed the diagnosis, it demonstrated the medullary pattern that was composed of vascular stroma and clumps of cells. Immunocytochemistry, using carcino-embryonic antigen and calcitonin showed a strongly positive reaction, and MIB-1 was 5.4%. The patient subsequently underwent a course of whole brain radiotherapy, a total of 30 Gy/10 fr. She remains asymptomatic 14 months after treatment. Brain metastasis from medullary carcinoma of the thyroid is extremely rare and it does not usually occur distant spread. Thyroid carcinoma with brain metastasis tends to be identified in patients with older age, larger primary tumor, more frequent evidence of extrathyroidal invasion, and more aggressive histologies. The number of medullary thyroid carcinoma with brain metastasis is small and there has been little evidence from benefit of therapy. Neither is it clear wether radiation therapy is beneficial also is not clear. In this case, surgical resection and radiation therapy was effective against recurrence of other lesion.
一名55岁女性于1973年首次接受全甲状腺切除术,组织病理学检查为甲状腺髓样癌。无内分泌肿瘤家族史。在接下来的19年里她一直无症状。1997年,颈部和气管复发采用气管支架和放疗进行治疗。1998年7月,她出现头痛。磁共振成像显示左侧颞下回有钆增强肿块。血管造影显示有明显的肿瘤染色,由颞中动脉和颞下动脉供血。通过颞部开颅手术成功切除肿瘤。切除标本的组织病理学切片证实了诊断,显示由血管间质和成簇细胞组成的髓样结构。使用癌胚抗原和降钙素的免疫细胞化学显示强烈阳性反应,MIB - 1为5.4%。患者随后接受了全脑放疗疗程,共30 Gy/10次。治疗后14个月她仍无症状。甲状腺髓样癌脑转移极为罕见,通常不会发生远处转移。甲状腺癌脑转移多见于年龄较大、原发肿瘤较大、甲状腺外侵犯证据更频繁以及组织学更具侵袭性的患者。甲状腺髓样癌脑转移的病例数较少,几乎没有证据表明治疗有益。放疗是否有益也不清楚。在本病例中,手术切除和放疗对其他病变的复发有效。