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[嗜铬细胞瘤的罕见钙化:一例报告]

[Uncommon calcification of a pheochromocytoma: a case report].

作者信息

Kojima Y, Nakamura M, Koide T, Sonoda T, Haruna Y, Mishima M, Kuzuya T

机构信息

Department of Urology, Osaka University Medical School.

出版信息

Hinyokika Kiyo. 1989 Sep;35(9):1555-9.

PMID:2683660
Abstract

A 62-year-old man with a 2-year history of hypertension was referred for evaluation of severe back pain, but his blood pressure was normal during his hospital stay. Plain radiography and excretory urography demonstrated central and eggshell-like calcification in the left suprarenal area. Computed tomographic scan confirmed similar shapes for the left adrenal calcifications. Laboratory examination revealed that the urinary normetanephrine was elevated. Left adrenal venography showed that the mass was in the middle to lower portion of the left adrenal gland. The most likely diagnosis was, calcified pheochromocytoma. The left adrenal tumor was removed surgically through a thoracolumbar incision on September 19, 1985. The blood pressure rose to 186/102 mmHg at the time of tumor manipulation. The tumor was a markedly hard mass, which was 3.5 x 3.5 x 3.0 cm and weighed 20 g. The histopathologic diagnosis was calcified pheochromocytoma. The patient remained symptomless after the operation.

摘要

一名有2年高血压病史的62岁男性因严重背痛前来接受评估,但住院期间其血压正常。X线平片和排泄性尿路造影显示左肾上腺区有中央及蛋壳样钙化。计算机断层扫描证实左肾上腺钙化呈类似形态。实验室检查显示尿去甲肾上腺素升高。左肾上腺静脉造影显示肿块位于左肾上腺中下部。最可能的诊断是钙化性嗜铬细胞瘤。1985年9月19日经胸腰段切口手术切除左肾上腺肿瘤。肿瘤操作时血压升至186/102 mmHg。肿瘤为明显坚硬的肿块,大小为3.5×3.5×3.0 cm,重20 g。组织病理学诊断为钙化性嗜铬细胞瘤。术后患者无症状。

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1
[Uncommon calcification of a pheochromocytoma: a case report].[嗜铬细胞瘤的罕见钙化:一例报告]
Hinyokika Kiyo. 1989 Sep;35(9):1555-9.
2
[Embolization for massive retroperitoneal hemorrhage from adrenal pheochromocytoma: a case report].[肾上腺嗜铬细胞瘤致大量腹膜后出血的栓塞治疗:一例报告]
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Peripartum hypertension from pheochromocytoma: a rare and challenging entity.嗜铬细胞瘤所致围产期高血压:一种罕见且具有挑战性的病症。
Am J Hypertens. 2005 Oct;18(10):1306-12. doi: 10.1016/j.amjhyper.2005.04.021.
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[Postural ventricular tachycardia in patients with pheochromocytoma].[嗜铬细胞瘤患者的体位性室性心动过速]
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[Hereditary pheochromocytoma--a family affected by von Hippel-Lindau disease].[遗传性嗜铬细胞瘤——一个受冯·希佩尔-林道病影响的家族]
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Steroid-induced crisis and rhabdomyolysis in a patient with pheochromocytoma: a case report and review.类固醇诱导的危象和横纹肌溶解症在嗜铬细胞瘤患者中的表现:病例报告及文献复习。
Int J Cardiol. 2011 Jan 21;146(2):e41-5. doi: 10.1016/j.ijcard.2008.12.183. Epub 2009 Feb 1.
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[A case of cystic pheochromocytoma].
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[A case of pheochromocytoma associated with von Recklinghausen's disease].[1例与冯·雷克林霍增氏病相关的嗜铬细胞瘤病例]
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A case of pheochromocytoma presenting as low back pain.一例以腰痛为表现的嗜铬细胞瘤病例。
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[Pheochromocytoma associated with neurofibromatosis 1: a report of two cases].[与1型神经纤维瘤病相关的嗜铬细胞瘤:两例报告]
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