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首页> 外文期刊>The Journal of craniofacial surgery >Metastatic Follicular Thyroid Carcinoma Masquerading as Olfactory Neuroblastoma: With Skull-Base, Cranium, Paranasal Sinus, Lung, and Diffuse Bone Metastases
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Metastatic Follicular Thyroid Carcinoma Masquerading as Olfactory Neuroblastoma: With Skull-Base, Cranium, Paranasal Sinus, Lung, and Diffuse Bone Metastases

机译:伪装成嗅神经母细胞瘤的转移性滤泡性甲状腺癌:颅底,颅骨,鼻旁窦,肺和弥漫性骨转移。

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摘要

Skull-base metastasis is rarely reported in thyroid carcinoma. We are presenting an unusual interesting case mimicking metastatic renal cell carcinoma with intense clear cell morphology, the thyroid origin of which was detected via positron emission tomography/computerized tomography scan proposed by the oncology council, while we were monitoring the subject with the initial diagnosis of paranasal sinus tumor. A mass was detected in the left nasal cavity in the endoscopic examination of the 68-year-old female patient referred by the ophthalmology clinic with the preliminary diagnosis of retro-orbital tumor upon being admitted with proptosis. A soft tissue lesion at a size of 68 x 39 x 53 mm located intracranially was detected by the brain computerized tomography. The biopsy taken and the immunohistochemical results were not satisfactory. Intense fluorodeoxyglucose involvement was observed in both lobes of the thyroid gland at positron emission tomography/computerized tomography taken with the recommendation of the council. Moreover, hypermetabolic nodules were seen in both lung parenchyma areas, whereas intense hypermetabolic lytic lesions were observed in the skeletal system. Thyroglobulin and thyroid transcription factor 1 stains displayed a strong staining on paraffin block. On the basis of these characteristics, the case was regarded as compatible metastatic follicular thyroid carcinoma, with skull-base, cranial, retro-orbital, paranasal sinus, lung, and bone metastases. This case showed us that multidisciplinary work and assessment of the oncology council play a highly critical role in making the diagnosis and guiding the treatment.
机译:甲状腺癌很少报道颅底转移。我们正在提出一个异常有趣的案例,该案例模仿具有强烈透明细胞形态的转移性肾细胞癌,该肿瘤的甲状腺起源是通过肿瘤学委员会提议的正电子发射断层扫描/计算机断层扫描来检测的,而我们正在监测该患者的初步诊断鼻旁窦肿瘤。经眼科门诊转诊的68岁女性患者经鼻内镜检查,初步诊断出眼眶后肿瘤,在内镜检查中发现左鼻腔有肿块。通过脑部计算机断层摄影术检测到位于颅内的大小为68 x 39 x 53 mm的软组织病变。活检和免疫组织化学结果均不令人满意。在理事会的建议下,在正电子发射断层扫描/计算机断层扫描中,在甲状腺的两个肺叶均观察到强烈的氟脱氧葡萄糖参与。此外,在两个肺实质区域都观察到了代谢亢进的结节,而在骨骼系统中则观察到了强烈的代谢亢进的溶解性病变。甲状腺球蛋白和甲状腺转录因子1染色在石蜡块上显示出强烈的染色。基于这些特征,该病例被认为是相容性转移性滤泡性甲状腺癌,有颅底,颅骨,眶后,鼻旁窦,肺和骨转移。这个案例告诉我们,肿瘤学委员会的多学科工作和评估在做出诊断和指导治疗中起着至关重要的作用。

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