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甲状腺原发性平滑肌肉瘤

Primary leiomyosarcoma of the thyroid gland.

作者信息

Iida Y, Katoh R, Yoshioka M, Oyama T, Kawaoi A

机构信息

Second Department of Pathology, Yamanashi Medical University, Japan.

出版信息

Acta Pathol Jpn. 1993 Jan-Feb;43(1-2):71-5. doi: 10.1111/j.1440-1827.1993.tb02917.x.

Abstract

A primary leiomyosarcoma of the thyroid gland in a 72 year old Japanese woman is described. This is the second case reported in the English literature. The patient presented with a 7 month history of a gradually expanding tumor in the right neck. The surgical specimen taken by thyroid lobectomy revealed a relatively well demarcated tumor, 2 x 2 x 3 cm in size, confined to the right lobe. Histologically, the tumor showed a classical leiomyosarcomatous appearance of interlacing fascicles of spindle-shaped cells with occasional blunt-ended nuclei and a high frequency of mitotic figures. Immunohistochemistry of the tumor cells clearly showed smooth muscle differentiation; the cells were positive for desmin, muscle-specific actin and vimentin and negative for cytokeratin, epithelial membrane antigen, carcinoembryonic antigen, thyroglobulin and calcitonin. The patient was free of disease for 3 years and 11 months without further treatment when evidence of multiple bone metastases appeared on bone scintigraphy. She died of pneumonia 4 years and 3 months after the lobectomy.

摘要

本文描述了一名72岁日本女性的原发性甲状腺平滑肌肉瘤。这是英文文献中报道的第二例病例。患者有右侧颈部逐渐增大的肿块,病程7个月。甲状腺叶切除术获取的手术标本显示肿瘤边界相对清晰,大小为2×2×3 cm,局限于右叶。组织学上,肿瘤呈现典型的平滑肌肉瘤外观,由梭形细胞交织成束状,偶见钝端核,有较高的有丝分裂象频率。肿瘤细胞的免疫组化结果明确显示平滑肌分化;细胞结蛋白、肌特异性肌动蛋白和波形蛋白呈阳性,细胞角蛋白、上皮膜抗原、癌胚抗原、甲状腺球蛋白和降钙素呈阴性。患者未经进一步治疗,无病生存3年11个月,之后骨闪烁显像显示有多发骨转移迹象。肺叶切除术后4年3个月,患者死于肺炎。

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