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我们从1971年12月至1980年11月9年中,收治嗜铬细胞瘤5例,均经病理检验证实,现报告如下,并加讨论。临床资料本组病人全部为男性,年龄最小14岁,最大45岁;5例均发生于肾上腺,左侧2例,右侧3例。但其中一例除肾上腺之外,在腹主动脉旁的嗜铬体(Zuckerkandle)发生巨大肿瘤。1例右腋有鸽蛋大淋巴结转移,经病理检验,属恶性嗜铬细胞瘤。一、临床表现:5例病程由3个月至10年不等,3例呈阵发性高血压,伴有明显
From December 1971 to November 9th, 1980, we treated 5 cases of pheochromocytoma, which were confirmed by pathological examination. The present report is as follows and discussed. Clinical data All patients in this group were males, youngest 14 years old, maximum 45 years old; 5 cases occurred in the adrenal glands, left 2 cases, right 3 cases. However, in one case, except for the adrenal gland, there was a huge tumor in the chromite body near the abdominal aorta (Zuckerkandle). In one case, there was a large lymph node metastasis in the right iliac crest. According to pathological examination, it was a malignant pheochromocytoma. First, the clinical manifestations: 5 cases of course ranging from 3 months to 10 years, 3 cases of paroxysmal hypertension, accompanied by obvious