首页> 美国卫生研究院文献>Journal of Endourology Case Reports >Laparoscopic Unilateral Total and Contralateral Subtotal Adrenalectomy for Bilateral Adrenocorticotropic Hormone-Secreting Pheochromocytoma: Report of a Rare Case
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Laparoscopic Unilateral Total and Contralateral Subtotal Adrenalectomy for Bilateral Adrenocorticotropic Hormone-Secreting Pheochromocytoma: Report of a Rare Case

机译:腹腔镜单侧全肾对侧全肾切除术治疗双侧促肾上腺皮质激素性嗜铬细胞瘤:罕见病例报告

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摘要

>Background: Bilateral adrenal tumors are not common in clinical practice, but are an important source of ectopic adrenocorticotropic hormone (ACTH) secretion. Standard operative management for bilateral pheochromocytomas might dictate the removal of the involved adrenal gland and the removal of the contralateral adrenal gland. We present a case of bilateral ACTH-secreting pheochromocytoma treated with staged laparoscopic unilateral total and contralateral subtotal adrenalectomy.>Case Presentation: A 58-year-old male with elevated hyperglycemia and general fatigue was hospitalized for pneumonia. CT incidentally revealed bilateral adrenal tumor. Biochemical examination was significant for elevated urinary metanephrine and normetanephrines, and plasma catecholamine level. CT scan of the head, neck, thorax, and pelvis was normal. Under the clinical diagnosis of ACTH-dependent pheochromocytoma, laparoscopic right total adrenalectomy was performed. As endocrinologic examination showed residual ACTH-dependent pheochromocytoma after surgery, laparoscopic left subtotal adrenalectomy was performed. Pathology analysis revealed pheochromocytoma with stained ACTH lesions in both adrenal tumors.>Conclusion: This is a rare case of ACTH-secreting bilateral pheochromocytoma effectively treated with staged laparoscopic unilateral total and contralateral subtotal adrenalectomy, in which the production of ACTH was confirmed by immunohistochemical staining.
机译:>背景:双侧肾上腺肿瘤在临床实践中并不常见,但却是异位促肾上腺皮质激素(ACTH)分泌的重要来源。双侧嗜铬细胞瘤的标准手术治疗可能要求切除受累肾上腺和对侧肾上腺。我们报道了一例经分期腹腔镜单侧全侧和对侧次全肾上腺切除术治疗的双侧分泌ACTH的嗜铬细胞瘤。>病例报告:一名58岁高血糖和全身疲劳升高的男性因肺炎住院。 CT偶然发现双侧肾上腺肿瘤。生化检查对于尿中肾上腺素和去甲肾上腺素的升高以及血浆儿茶酚胺水平具有重要意义。头部,颈部,胸部和骨盆的CT扫描正常。在ACTH依赖型嗜铬细胞瘤的临床诊断下,进行了腹腔镜右全肾上腺切除术。由于内分泌检查显示术后残留有ACTH依赖的嗜铬细胞瘤,因此进行了腹腔镜左全肾上腺切除术。病理分析显示,在两个肾上腺肿瘤中,嗜铬细胞瘤均带有染色的ACTH病变。免疫组化染色证实了ACTH。

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