pheochromocytoma

management of catecholamine substitution therapy in perioperation of pheochromocytoma (report of 15 cases)

儿茶酚胺替代法在嗜铬细胞瘤围手术期应用（附15例报告）

Changes of dopamine and noradrenalin in CVF before and after intracranial transplantation of autologous adrenal medulla Expression of Adrenomedullin and Its Receptor mRNA in the Tissues of Normal Adrenal Medulla and Pheochromocytoma △

自体肾上腺髓质脑内移植术前后脑室液多巴胺、去甲基肾上腺素含量的变化肾上腺髓质素及受体在肾上腺和嗜铬细胞瘤中的表达

Conditions with the lowest incidence were adrenocortical carcinoma, pheochromocytoma, and pituitary adenomas.

其次为肾上腺皮质癌 、 嗜铬细胞瘤 、 垂体腺瘤.

the incidence of malignant ectopic pheochromocytoma was rather high reaching 13% and the accuracy of ct diagnosis was 87% in this series.

与肾上腺髓质嗜铬细胞瘤相比较，异位嗜铬细胞中恶性肿瘤者较多。CT诊断正确率为87%。

Selective adrenal arteriography was more sensitive than ultrasound, CT, etc in diagnosing adrenal pheochromocytoma.

并指出选择性肾上腺动脉造影对诊断肾上腺嗜铬细胞瘤较B超、CT，有较高的特异性。

Results: The patients include adrenocortical cancer in 4 cases, 6 cases of metastasis tumor, 18 cases of adrenal adenoma, pheochromocytoma in 25 cases, adrenal cyst in 7 cases, adrenal hyperplasia in 3 cases and adrenal tubercle in 1 case.

结果：其中肾上腺皮质癌4例，转移癌6例，肾上腺腺瘤18例，嗜铬细胞瘤25例，肾上腺囊肿7例，肾上腺皮质增生肥大3例，肾上腺结核1例。

The patient was a female, 29 years old, with 7 tumor, ie. acidophilic adenoma of pituitary gland, parathyroid adenoma, multiple pancreatic islet cell tumor, biliteral pheochromocytoma, thyroid adenoma, as well as biliteral renal carcinoma, and neurofibroma in mediastinum.

患者女性，29岁，同时患有垂体腺瘤、甲状旁腺腺瘤、多发性胰岛细胞瘤、双侧肾上腺嗜铬细胞瘤、甲状腺腺瘤、双侧肾癌及纵膈神经纤维瘤等7种10个肿瘤。

objective to probe into the application of catecholamine substitution therapy in perioperation of pheochromocytoma.

目的探讨儿茶酚胺替代法在嗜铬细胞瘤围手术期的应用。

effects of pancuronium on nicotinic acetylcholine receptors in pheochromocytoma cells

泮库溴铵对肾上腺嗜铬细胞乙酰胆碱受体的作用

Objective : To explore the diagnosis and treatment of extra-adrenal pheochromocytoma.

目的: 探讨肾上腺外嗜铬细胞瘤的诊治特点.

Result : Hemodynamic insufflation and tumor manipulation in the laparoscopic excision of pheochromocytoma.

血流动力学摘要:目的: 总结腹腔镜嗜铬细胞瘤切除术的麻醉方法.

Conclusion ( 1) Atypical pheochromocytoma has high tendency to malignance.

结论（1）特殊类型嗜铬细胞瘤恶性率高。

Giant nonfunctional pheochromocytoma of adrenal: one case report

巨大无功能性肾上腺嗜铬细胞瘤1例

Expression significance of apoptosis related bak gene protein in adrenal pheochromocytoma

肾上腺嗜铬细胞瘤凋亡相关基因bak蛋白表达的意义

Objective To investigate the protective effect of gross saponin tribulus terrestris ( GSTT) on the apoptosis of pheochromocytoma cells ( PC12 cells) induced by H2O2 and its mechanisms.

目的：探讨蒺藜总皂苷（GSTT）对过氧化氢（H2O2）诱导大鼠肾上腺嗜铬细胞瘤细胞（PC12）凋亡的保护作用及其机制。

Conclusion Pheochromocytoma associated with other endocrine disorders in MEN may manifest itself as the main clinical symptom or most frequently as an occult tumor.

结论在MEN病人中，嗜铬细胞瘤可能以主要临床表现与其它内分泌疾病相关，但更多的情况下是以无症状肿瘤的形式与其它内分泌疾病共存。

a case of pheochromocytoma that manifests first as erythrocytosis

以红细胞增多为首发症状的嗜铬细胞瘤一例

Clinical significant of blood glucose and Regitine test in the pheochromocytoma's diagnoses

血糖浓度和立其丁试验在诊断嗜铬细胞瘤中的临床意义

Objective To elevate the perioperative security of pheochromocytoma cases.

摘要目的提高嗜铬细胞瘤患者围手术期治疗的安全性.

If pheochromocytoma occurs, it is usually bilateral an anterior abdominal approach is preferred for the operation.

如有嗜铬细胞瘤, 通常为双侧性,最好行前腹腔开腹法.

Objective : To evaluate the diagnostic value of MRI and DSA in the large adrenal pheochromocytoma.

目的: 评估较大肾上腺嗜铬细胞瘤的MRI及DSA的诊断价值.

Abstract: Purpose : To evaluate the surgical method of pheochromocytoma.

文摘: 目的: 提高嗜铬细胞瘤手术治疗水平.

Pheochromocytoma ( Report of 23 Cases with Review of Literature)

嗜铬细胞瘤（23例报告及文献复习）

Endocrine hypertension comprised 59.70% of primary aldosteronism, 38.06% of pheochromocytoma, and there were 3 in-patients suffered from cushing syndrome.

在内分泌性高血压中，原发性醛固酮增多症占59.70%，嗜铬细胞瘤占38.06%，柯兴综合症3例。

Results: All 22 cases succeeded uneventfully. The pathologic study confirm that 14 cases were adrenal adenoma ( 10 primary aldosteronism, 4 adrenocortical adenoma), 6 cases pheochromocytoma, 2 cases adrenal cysts.

结果：22例全部成功，术后病理检查证实：肾上腺皮质腺瘤14例（原发性醛固酮增多症10例，皮质醇腺瘤4例），嗜铬细胞瘤6例，肾上腺囊肿2例。

Pheochromocytoma is a neoplasm of neural crest origin arising in the adrenal medulla.

嗜铬细胞瘤是发起于肾上腺髓质神经嵴起源点的一种赘生物.

PHEOCHROMOCYTOMA OF THE BLADDER Results The average time of operation was 41 minutes. No hematorrhea and vesical perforation happened.

结果手术时间平均41min，未发生大出血及膀胱穿孔。

Methods: HR, SBP, DBP, MAP, CVP of28 patients with pheochromocytoma treated with esmolol during anesthesia induction and operation were analysed.

方法分析28例嗜铬细胞瘤手术病人在麻醉诱导期和术中使用艾司洛尔后HR、SBP、DBP、MAP、CVP的变化。

This staining, particularly for chromogranin A, may be useful in distinguishing pheochromocytoma from adrenal cortical carcinoma.

该染色, 尤其是嗜铬粒蛋白A染色, 有可能在区分嗜铬细胞瘤与肾上腺皮质癌方面有用.

Nine cases of adrenal pheochromocytoma ( AP ) were confirmed by surgery and pathology.

讨论了9例经手术及病理证实的,原发性肾上腺嗜 铬 细胞瘤的选择性肾上腺动脉 造影 诊断价值.