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儿童期异步嗜铬细胞瘤

Asynchronous pheochromocytoma in childhood.

作者信息

Vary J, Lebel M, Grose J H, Dionne L

出版信息

Can J Surg. 1984 May;27(3):262-4, 273.

PMID:6722673
Abstract

A case of asynchronous pheochromocytoma in a 13-year-old boy is reported. Two years elapsed between excision of the right adrenal gland and the appearance of another tumour in the contralateral gland. Selective central venous sampling for plasma catecholamine measurement and adrenal phlebography were of diagnostic value. Excision of the tumour with partial adrenalectomy was the preferred surgical treatment in the remaining contralateral adrenal; no clinical or biochemical abnormalities were observed 2 years after removal of the second pheochromocytoma. This case stresses the importance of a closer follow-up in children for early detection of a second pheochromocytoma.

摘要

报告了一例13岁男孩的非同步性嗜铬细胞瘤病例。右侧肾上腺切除与对侧肾上腺出现另一肿瘤之间间隔了两年。用于血浆儿茶酚胺测量的选择性中心静脉采样和肾上腺静脉造影具有诊断价值。在对侧剩余肾上腺进行肿瘤切除并部分肾上腺切除术是首选的手术治疗方法;切除第二个嗜铬细胞瘤两年后未观察到临床或生化异常。该病例强调了对儿童进行密切随访以早期发现第二个嗜铬细胞瘤的重要性。

相似文献

1
Asynchronous pheochromocytoma in childhood.儿童期异步嗜铬细胞瘤
Can J Surg. 1984 May;27(3):262-4, 273.
2
[Scintigraphic diagnosis of multiple pheochromocytomas in childhood with 131I-m-benzylguanidine].
Monatsschr Kinderheilkd. 1984 Oct;132(10):791-6.
3
Preoperative localization of pheochromocytoma.嗜铬细胞瘤的术前定位
Acta Radiol Diagn (Stockh). 1973 Sep;14(5):545-60. doi: 10.1177/028418517301400507.
4
Partial adrenalectomy for pheochromocytoma with maintenance of adrenocortical function.
J Clin Endocrinol Metab. 1989 Nov;69(5):1078-81. doi: 10.1210/jcem-69-5-1078.
5
Button sequestrum of the tibia and pheochromocytoma.胫骨纽扣状死骨与嗜铬细胞瘤
Padiatr Padol. 1992;27(2):51-2.
6
[Surgery of adrenal medulla].[肾上腺髓质手术]
Chirurg. 1969 Jul;40(7):304-8.
7
[Malignant pheochromocytoma of the adrenal gland. Diagnosis 14 years after an incidental discovery of a contralateral pheochromocytoma].[肾上腺恶性嗜铬细胞瘤。对侧嗜铬细胞瘤偶然发现14年后的诊断]
Ann Chir. 1994;48(2):206-9.
8
Coexistence of aldosteronoma and pheochromocytoma in an adrenal gland.肾上腺中醛固酮瘤与嗜铬细胞瘤并存。
J Surg Oncol. 1985 Jan;28(1):75-8. doi: 10.1002/jso.2930280118.
9
[Severe arterial hypertension and pheochromocytoma in childhood. Case report and review of the literature].
Arch Mal Coeur Vaiss. 2000 May;93(5):627-30.
10
[Surgical treatment of pheochromocytoma].
Med Klin. 1973 Nov 2;68(44):1423-6.

引用本文的文献

1
Phaeochromocytoma: report of three cases.
Pediatr Nephrol. 1987 Jan;1(1):46-9. doi: 10.1007/BF00866884.
2
Long-term evaluation following resection of apparently benign pheochromocytoma(s)/paraganglioma(s).明显良性嗜铬细胞瘤/副神经节瘤切除术后的长期评估
World J Surg. 1990 May-Jun;14(3):325-9. doi: 10.1007/BF01658516.