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A case of giant malignant phaeochromocytoma

机译:一例巨恶性嗜铬细胞瘤

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Malignant phaeochromocytoma is defined as the presence of tumour deposits at sites that are normally devoid of chromaffin cells. We report on a 63-year-old man who had a giant malignant phaeochromocytoma of the right adrenal gland that encased the inferior vena cava. The urinary excretion rates of catecholamines and their metabolites were normal, except for normetanephrine, which was excreted at a higher rate than normal. The tumour was surgically unresectable by laparotomy. Postoperatively, the patient was given a 4-month trial of subcutaneous octreotide and intravenous meta-iodobenzylguanidine I 131. Occult lung secondary tumours were first detected by meta-iodobenzylguanidine scintigraphy after 2 years, and the patient died of bone and lung metastases 1 year later. Because phaeochromocytoma is rare, local experience in managing this disease is limited. This report alerts physicians of the methods of diagnosing and managing surgically unresectable malignant phaeochromocytoma.
机译:恶性嗜铬细胞瘤定义为在通常无嗜铬细胞的部位存在肿瘤沉积物。我们报道了一个63岁的男人,他的右肾上腺有巨大的恶性嗜铬细胞瘤,包裹着下腔静脉。儿茶酚胺及其代谢产物的尿排泄率正常,但去甲肾上腺素的排泄率高于正常水平。该肿瘤不能通过剖腹手术切除。术后对患者进行了为期4个月的皮下奥曲肽和静脉内间碘苄基胍I 131的试验。隐匿性肺继发性肿瘤在2年后首先通过间碘苄基胍闪烁显像法发现,并且该患者在1年后死于骨和肺转移。由于嗜铬细胞瘤很少,因此在控制这种疾病方面的本地经验有限。该报告提醒医生诊断和处理无法手术切除的恶性嗜铬细胞瘤的方法。

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