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Adrenal Pheochromocytoma with Multiple Neurofibromatosis on the Trunk

机译:肾上腺嗜铬细胞瘤伴躯干多发性神经纤维瘤病

摘要

We report a case of adrenal pheochromocytoma in a patient with neurofibromatosis type 1 (NF1). A 65-year-old female patient was admitted to our hospital for examination of a right adrenal mass. The adrenal tumor was incidentally discovered by abdominal computed tomography during examination for hypertension in another hospital. She had large multiple neurofibromatous lesions and café-au-lait spots on the trunk. We thought that it was difficult to make a skin incision on normal skin. Serum and urinary catecholamines were markedly increased. Magnetic resonance imaging revealed a solid round tumor 3 cm in diameter, located in the right adrenal gland. Laparoscopic right adrenalectomy was performed. Serum and urinary catecholamines returned to the normal range on post-operative day 10. Laparoscopic surgery may be a good option for NF1 patients with pheochromocytoma, especially those who had multiple neurofibromatosis on the trunk.
机译:我们报告了1型神经纤维瘤病(NF1)患者肾上腺嗜铬细胞瘤的情况。一名65岁的女性患者被收治到我们医院检查右肾上腺肿块。在另一家医院检查高血压时,通过腹部计算机断层扫描偶然发现了肾上腺肿瘤。她的躯干上有多个神经纤维瘤的大病变和咖啡色斑点。我们认为很难在正常皮肤上切开皮肤。血清和尿儿茶酚胺明显增加。磁共振成像显示直径3厘米的实心圆形肿瘤,位于右肾上腺。进行腹腔镜右肾上腺切除术。术后第10天血清和尿儿茶酚胺恢复正常。腹腔镜手术对于患有嗜铬细胞瘤的NF1患者,尤其是躯干多发性神经纤维瘤的患者,可能是一个很好的选择。

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