Imaizumi M, Fujita K, Ojika T, Kondo D, Watanabe H, Nishimura M, Abe T, Nagasaka T
Department of Thoracic Surgery, Nagoya University School of Medicine, Japan.
Nihon Kyobu Shikkan Gakkai Zasshi. 1991 Oct;29(10):1287-91.
Paraganglioma is a tumor arising from the extra-adrenal paraganglion system and is rarely observed in the mediastinum. The authors experienced a case of nonfunctioning paraganglioma of the upper posterior mediastinum. The patient was a 40-year-old female in whom abnormal shadows were noted in chest X-ray films taken in March, 1989. She was examined at our hospital with a diagnosis of mediastinal tumor in June of the same year. CT of the chest revealed a tumor in the upper posterior mediastinum and it was shown to be hypervascular by a DSA study. Urinary hormone levels were normal. The tumor was resected in May, 1990. The tumor, measuring 6.8 X 4.0 X 3.5 cm, was encapsulated, appeared dark red and had relatively clear borders. A histopathologic diagnosis of paraganglioma was made. The patient remains disease-free at present, 6 months after operation. Problems concerning diagnosis and treatment of mediastinal paraganglioma were evaluated with a review of cases reported in Japan.
副神经节瘤是一种起源于肾上腺外副神经节系统的肿瘤,很少见于纵隔。作者遇到一例上后纵隔无功能性副神经节瘤。患者为40岁女性,1989年3月胸部X线片发现异常阴影。同年6月因纵隔肿瘤诊断入我院检查。胸部CT显示上后纵隔有一肿瘤,数字减影血管造影(DSA)检查显示该肿瘤血运丰富。尿激素水平正常。1990年5月切除肿瘤。肿瘤大小为6.8×4.0×3.5cm,有包膜,呈暗红色,边界相对清晰。病理组织学诊断为副神经节瘤。术后6个月,患者目前无疾病复发。通过回顾日本报道的病例,对纵隔副神经节瘤的诊断和治疗问题进行了评估。