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肾上腺嗜铬细胞瘤嗜铬反应阳性。This pheochromocytoma demonstrates the chromaffin reaction.

病理及随访证实5例为恶性嗜铬细胞瘤。Of them 5 cases were confirmed as malignant pheochromocytoma.

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乳癌转移至混合嗜铬性细胞瘤更是少见。Breast cancer metastasizing to composite pheochromocytoma is still rarer.

目的提高肾上腺嗜铬细胞瘤的诊断与治疗水平。Objective To improve the diagnosis and treatment of adrenal pheochromocytoma.

乳癌与混合嗜铬性细胞瘤同时存在很少见。Synchronous presentation of breast cancer and composite pheochromocytoma is quite rare.

目的分析亚临床嗜铬细胞瘤的临床特点。Objective To analyze the clinical features of patients with subclinical pheochromocytoma.

目的探讨肾上腺嗜铬细胞瘤的诊断和治疗。Objective To identify the key of the diagnosis and treatment of adrenal pheochromocytoma.

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检测尿儿茶酚胺和VMA诊断嗜铬细胞瘤。Objective To measure urinary catecholamines and VMA by HPLC-ECD for diagnosis of pheochromocytoma.

目的提高对恶性嗜铬细胞瘤的诊治水平。Objective To review the experience with the diagnosis and treatment of malignant pheochromocytoma.

比较后腹腔镜和开放性行肾上腺切除术治疗嗜铬细胞瘤的临床疗效。We compared the clinical outcomes of retroperitoneoscopic and open adrenalectomy for pheochromocytoma.

结论恶性嗜铬细胞瘤经手术切除后，症状可以长期缓解。CONCLUSIONS Surgical excision of malignant pheochromocytoma can achieve long term remission of symptoms.

本研究拟建立人嗜铬细胞瘤细胞的原代培养方法。The study is to establish a method of separating and primarily culturing of human pheochromocytoma cells.

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我们报告一13岁嗜铬细胞瘤男孩在四年内并发反覆中风。We report a13-year-old boy with pheochromocytoma complicated with repeated stroke attacks during four years.

目的探讨小儿特殊嗜铬细胞瘤的临床特点及治疗。Objective To evaluate the clinical characteristics and treatment of rare types of pheochromocytoma in children.

目的探讨儿茶酚胺替代法在嗜铬细胞瘤围手术期的应用。Objective To probe into the application of catecholamine substitution therapy in perioperation of pheochromocytoma.

肾上腺增生、肾上腺腺瘤和嗜铬细胞瘤是较常见引起肾上腺源性高血压的病因。Adrenal Hyperplasia, adrenal adenoma and pheochromocytoma are the more common cause of adrenal-derived hypertension.

术后诊断隐匿型嗜铬细胞瘤14例，无功能嗜铬细胞瘤14例。Postoperative diagnosis was latent pheochromocytoma in 14 cases and nonfunctioning pheochromocytoma in another 14 cases.

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对于恶性者，CT图像上缺乏特征性表现，易误诊为其他恶性肿瘤。Malignant ectopic pheochromocytoma is apt to be misdiagnosed as other malignant tumors for lack of characteristic CT signs.

方法回顾分析4例肾上腺皮髓质混合性病变资料。Methods The clinical data of 4 cases of coexisting primary aldosteronism and pheochromocytoma were retrospectively analyzed.

目的探讨原发性腹膜后肾上腺外嗜铬细胞瘤的诊断和治疗经验。Objective To investigate the experience in diagnosis and treatment of primary retroperitoneal external adrenal pheochromocytoma.