Tzikos Georgios, Menni Alexandra, Cheva Angeliki, Pliakos Ioannis, Tsakona Anastasia, Apostolidis Stilianos, Iakovou Ioannis, Michalopoulos Antonios, Papavramidis Theodosios
1st Propedeutic Department of Surgery, Aristotle University of Thessaloniki, AHEPA University Hospital, Thessaloniki, Greece.
Pathology Department, Faculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Front Surg. 2022 Feb 22;9:824076. doi: 10.3389/fsurg.2022.824076. eCollection 2022.
Composite paragangliomas consist of two components, paraganglioma and ganglioneuroma, representing a rare subgroup of paragangliomas. The purpose of the study is to describe a case of composite paraganglioma of the celiac trunk and a brief review of the existing literature.
A 64-year-old female patient with a history of epigastric abdominal pain and a 51 mm-diameter tumor found in a Computerized Tomography of the abdomen was admitted to our surgical department for further evaluation and treatment. After a brief preoperative surgical assessment, the patient underwent a mini-laparotomy for the excision of this tumor. After having the results of the pathology report, a comprehensive review of the international literature was carried out by applying the appropriate search terms.
As it was found intraoperatively, the tumor was located at the cephalad aspect of the common hepatic artery, over the portal vein and the inferior vena cava. A negative-margin resection was achieved and the tumor was sent for pathology analysis. The final pathology report revealed a composite paraganglioma, with α paraganglioma and a ganglioneuroma component. Seventeen cases of extra-adrenal composite paraganglioma have been reported in the international literature so far. This case was the first one found in the area of the celiac trunk.
Composite paragangliomas comprise rare and potentially malignant tumors with variable prognosis. Establishing their diagnosis promptly is of vital significance. Due to the first-described location of the composite paraganglioma in our case, the differential diagnosis of tumors in this area should also include composite paragangliomas.
复合性副神经节瘤由副神经节瘤和神经节神经瘤两个成分组成,是副神经节瘤中一个罕见的亚组。本研究的目的是描述一例腹腔干复合性副神经节瘤病例,并对现有文献进行简要回顾。
一名64岁女性患者,有上腹部疼痛病史,腹部计算机断层扫描发现一个直径51毫米的肿瘤,入住我院外科进行进一步评估和治疗。经过简短的术前手术评估,患者接受了小切口剖腹术以切除该肿瘤。在获得病理报告结果后,通过应用适当的检索词对国际文献进行了全面回顾。
术中发现肿瘤位于肝总动脉头侧,覆盖门静脉和下腔静脉。实现了切缘阴性切除,并将肿瘤送去进行病理分析。最终病理报告显示为复合性副神经节瘤,包含α副神经节瘤和神经节神经瘤成分。迄今为止,国际文献中已报道了17例肾上腺外复合性副神经节瘤。该病例是在腹腔干区域发现的首例。
复合性副神经节瘤是罕见的、具有潜在恶性的肿瘤,预后不一。及时确立其诊断至关重要。由于我们病例中复合性副神经节瘤的首次描述位置,该区域肿瘤的鉴别诊断也应包括复合性副神经节瘤。