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自发性破裂嗜铬细胞瘤:一例罕见病例报告及文献复习

Spontaneous ruptured pheochromocytoma: an unusual case report and literature review.

作者信息

Jee Ye Seob

机构信息

Department of Surgery, Dankook University Hospital, Dankook University College of Medicine, Cheonan, Korea.

出版信息

Ann Surg Treat Res. 2017 Sep;93(3):170-172. doi: 10.4174/astr.2017.93.3.170. Epub 2017 Aug 30.

DOI:10.4174/astr.2017.93.3.170
PMID:28932734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5597542/
Abstract

Ruptured pheochromocytoma is a rare disease. Its mortality rate is up to 31%-50%. Proper management of ruptured pheochromocytoma remains unclear. A 44-year-old male patient visited our Emergency Department and presented with abrupt onset of left flank pain. His blood pressure was 190/140 mmHg with purse rate of 130 beats/min. CT scan showed 8.1 × 5.6-cm-sized heterogeneously mass with rupture on the left retroperitoneal space and active bleeding. His symptom of abdominal pain was aggravated. Follow-up laboratory analysis revealed elevated WBC count and decreased hemoglobin 2 hours after admission. Emergency laparotomy was performed. We resected the ruptured left retroperitoneal mass and hemostasis. Pathologic exams revealed adrenal pheochromocytoma with rupture. Although our patient was alive, according to literature review, mortality rate of emergency operation without medical management is higher than elective operation after blood pressure control with either medical or interventional methods such as transcatheter arterial embolization.

摘要

嗜铬细胞瘤破裂是一种罕见疾病。其死亡率高达31% - 50%。嗜铬细胞瘤破裂的恰当处理方法仍不明确。一名44岁男性患者就诊于我院急诊科,表现为突发左侧腰痛。其血压为190/140 mmHg,心率为130次/分钟。CT扫描显示左腹膜后间隙有一个大小为8.1×5.6 cm的不均匀肿块,伴有破裂及活动性出血。他的腹痛症状加重。入院2小时后的后续实验室分析显示白细胞计数升高,血红蛋白降低。遂进行了急诊剖腹手术。我们切除了破裂的左腹膜后肿块并进行了止血。病理检查显示为肾上腺嗜铬细胞瘤伴破裂。尽管我们的患者存活了下来,但根据文献综述,未进行药物治疗的急诊手术死亡率高于在通过药物或诸如经导管动脉栓塞等介入方法控制血压后进行的择期手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3af7/5597542/423a14699c06/astr-93-170-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3af7/5597542/423a14699c06/astr-93-170-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3af7/5597542/423a14699c06/astr-93-170-g001.jpg

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引用本文的文献

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Cureus. 2023 Mar 29;15(3):e36890. doi: 10.7759/cureus.36890. eCollection 2023 Mar.
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Minimally Invasive Management of Hemorrhagic Pheochromocytoma-A Rare Case Report.嗜铬细胞瘤出血的微创治疗——1例罕见病例报告
Surg J (N Y). 2023 Mar 26;9(1):e52-e57. doi: 10.1055/s-0043-1762554. eCollection 2023 Jan.
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Non-surgically treated case of nonfunctioning ruptured adrenal adenoma in a patient on hemodialysis.血液透析患者非手术治疗无功能性破裂肾上腺腺瘤病例。

本文引用的文献

1
Arterial embolization for ruptured adrenal pheochromocytoma.动脉栓塞治疗破裂的肾上腺嗜铬细胞瘤。
Curr Oncol. 2010 Nov;17(6):65-70. doi: 10.3747/co.v17i6.597.
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Phaeochromocytoma.嗜铬细胞瘤
Lancet. 2005;366(9486):665-75. doi: 10.1016/S0140-6736(05)67139-5.
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Spontaneous rupture of adrenal pheochromocytoma: review and analysis of prognostic factors.肾上腺嗜铬细胞瘤自发性破裂:预后因素的综述与分析
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Spontaneous rupture of adrenal pheochromocytoma: a case report.肾上腺嗜铬细胞瘤自发性破裂:一例报告
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