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手术切除导致糖尿病的中纵隔副神经节瘤。

Surgical resection of a middle mediastinal paraganglioma that caused diabetes.

作者信息

Miura Kentaro, Kobayashi Nobutaka, Satomi Hidetoshi

机构信息

Department of Thoracic Surgery, Japanese Red Cross Society Nagano Hospital, 5-22-1 Wakasato, Nagano, 380-8582, Japan.

Department of Pathology, Japanese Red Cross Society Nagano Hospital, Nagano, Japan.

出版信息

Surg Case Rep. 2020 Sep 30;6(1):241. doi: 10.1186/s40792-020-00983-x.

Abstract

BACKGROUND

Paragangliomas are rare neuroendocrine tumors originating from chromaffin cells of extra-adrenal origin. Ninety percent of adrenergic tumors originate in the adrenal medulla and are known as pheochromocytomas; the remaining 10% are extra-adrenal and are called paragangliomas. Mediastinum paragangliomas is rare and commonly originate from the posterior mediastinum, while those originating from the middle posterior are quite rare. Some paragangliomas secrete catecholamines, leading to symptoms such as hypertension, tachycardia, and diabetes.

CASE PRESENTATION

A 76-year-old woman visited our hospital for the treatment and further evaluation of diabetes. Her hemoglobin A1c levels had risen to 11.0%. To investigate the cause of her diabetes, a contrast-enhanced chest computed tomography scan was performed, revealing a ring-enhancing tumor (30 × 30 mm) in the middle mediastinum. The surgical resection was performed via video-assisted thoracic surgery. Surgery was performed using a vessel-sealing device; however, bleeding was persistent from the surrounding tissue. Total bleeding was 400 g. Blood pressure fluctuations and arrhythmia did not occur during the operation. The patient's uncontrolled diabetes was cured after the surgery, and the tumor was diagnosed as a functional paraganglioma.

CONCLUSIONS

We encountered a rare case of functional paraganglioma located in the middle mediastinum. Functional paragangliomas should be considered as a potential cause of uncontrolled diabetes, and a whole-body CT scan should be performed to investigate this possible cause.

摘要

背景

副神经节瘤是起源于肾上腺外嗜铬细胞的罕见神经内分泌肿瘤。90%的肾上腺能肿瘤起源于肾上腺髓质,称为嗜铬细胞瘤;其余10%为肾上腺外肿瘤,称为副神经节瘤。纵隔副神经节瘤罕见,通常起源于后纵隔,而起源于中后部的则极为罕见。一些副神经节瘤分泌儿茶酚胺,导致高血压、心动过速和糖尿病等症状。

病例介绍

一名76岁女性因糖尿病治疗及进一步评估就诊于我院。她的糖化血红蛋白水平已升至11.0%。为探究其糖尿病病因,进行了胸部增强计算机断层扫描,结果显示中纵隔有一个环形强化肿瘤(30×30mm)。通过电视辅助胸腔镜手术进行了手术切除。手术使用了血管闭合装置;然而,周围组织持续出血。总出血量为400克。术中未出现血压波动和心律失常。术后患者失控的糖尿病得到治愈,肿瘤被诊断为功能性副神经节瘤。

结论

我们遇到了一例罕见的位于中纵隔的功能性副神经节瘤病例。功能性副神经节瘤应被视为糖尿病失控的潜在原因,应进行全身CT扫描以探究这一可能病因。

原文中“Total bleeding was 400 g.”这里的“g”可能有误,根据语境推测可能是“ml”(毫升),但按照要求未作修改。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae2f/7527386/c8569161de5d/40792_2020_983_Fig1_HTML.jpg

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