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[肾周嗜铬细胞瘤]

[Peri-renal pheochromocytoma].

作者信息

Ochmański W, Kózka M, Krzywoń J, Kordas W, Lejman W, Polakiewicz J

机构信息

I Katedry i Kliniki Chorób Wewnetrznych Collegium Medicum Uniwersytetu Jagiellońskiego w Krakowie.

出版信息

Przegl Lek. 1998;55(6):349-51.

PMID:9857714
Abstract

Presented is a case of pheochromocytoma with an ectopic or extrarenal localisation in a 47 year old female farmer. The patient was admitted to the 1st Chair and Clinic of Internal Disease, Jagiellonian University Collegium Medicum due to a three year history of hypertension. The bouts of hypertension were characterised by sudden increases of blood pressure to 250/150 mmHg, which occurred after physical exertion but particularly during the night. On physical examination no abnormalities were detected. Laboratory analysis revealed no changes apart from mild hyperglycemia. 24 hour vanillymandelic acid excretion was normal on two successive accounts, but on a third analysis was raised. Fundus examination revealed bilateral hypertensive and diabetic angiopathy. Abdominal ultrasound revealed a tumor in the region of the pancreas with an echogenicity similar to that of the liver. Abdominal CT scan revealed normal suprarenal glands bilaterally. A smooth walled tumor of 55 mm diameter was visualized below the head of the pancreas. Its structure was not uniform with degenerating features. The tumor adhered to the descending and transverse part of duodenum, compressing the vena cava inferior and was in close proximity to the abdominal aorta. After surgical consultation the patient was transferred to the II Clinic of General Surgery Jagiellonian University Collegium Medicum where after pretreatment with alpha and beta blockers, ACE inhibitors, diuretics and Insulin CHOS the patient underwent surgery. Posterior to the duodenum, inferior to the head of the pancreas, between the aorta and vena cava inferior was a polycystic tumor of 80 mm diameter, which was evacuated in its entirety. Histopathology revealed a paraganglioma with an appearance of pheochromocytoma. On a three month follow up visit the patient was without symptoms. Her blood pressure and glycemia were normal despite being without treatment.

摘要

本文介绍了一例47岁女性农民患有的异位或肾外嗜铬细胞瘤病例。该患者因三年高血压病史入住雅盖隆大学医学院第一内科教研室及诊所。高血压发作的特点是血压突然升至250/150 mmHg,发作于体力活动后,尤其是夜间。体格检查未发现异常。实验室分析除轻度高血糖外无其他变化。连续两次24小时香草扁桃酸排泄量正常,但第三次分析升高。眼底检查显示双侧高血压和糖尿病性血管病变。腹部超声显示胰腺区域有一个肿瘤,其回声与肝脏相似。腹部CT扫描显示双侧肾上腺正常。在胰头下方可见一个直径55 mm的壁光滑肿瘤。其结构不均匀,有退行性特征。肿瘤附着于十二指肠降部和横部,压迫下腔静脉,且紧邻腹主动脉。经外科会诊后,患者被转至雅盖隆大学医学院普通外科第二诊所,在使用α和β受体阻滞剂、ACE抑制剂、利尿剂和胰岛素CHO进行预处理后接受手术。在十二指肠后方、胰头下方、主动脉和下腔静脉之间有一个直径80 mm的多囊性肿瘤,已将其完整切除。组织病理学显示为副神经节瘤,具有嗜铬细胞瘤的外观。在三个月的随访中,患者无症状。尽管未接受治疗,但其血压和血糖正常。

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