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Total resection of a giant retroperitoneal and mediastinal ganglioneuroma—case report and systematic review of the literature

机译:巨型腹膜瘤和纵隔甘露甘露瘤的总切除术 - 病例报告和对文献的系统审查

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摘要

Abstract Background Ganglioneuromas (GNs) are extremely rare, slowly growing, benign tumors that can arise from Schwann cells, ganglion cells, and neuronal or fibrous tissues. Due to their origin from the sympathetic neural crest, they show neuroendocrine potential; however, most are reported to be hormonally inactive. Nevertheless, complete surgical removal is recommended for symptom control or for the prevention of potential malignant degeneration. Case Report A 30-year-old female was referred to our oncologic center due to a giant retroperitoneal and mediastinal mass detected in computed tomography (CT) scans. The initial symptoms were transient nausea, diarrhea, and crampy abdominal pain. There was a positive family history including 5 first- and second-degree relatives. Presurgical biopsy revealed a benign ganglioneuroma. Total resection (TR) of a 35 × 25 × 25 cm, 2550-g tumor was obtained successfully via laparotomy combined with thoracotomy and partial incision of the diaphragm. Histopathological analysis confirmed the diagnosis. Surgically challenging aspects were the bilateral tumor invasion from the retroperitoneum into the mediastinum through the aortic hiatus with the need of a bilateral 2-cavity procedure, as well as the tumor-related displacement of the abdominal aorta, the mesenteric vessels, and the inferior vena cava. Due to their anatomic course through the tumor mass, the lumbar aortic vessels needed to be partially resected. Postoperative functioning was excellent without any sign of neurologic deficit. Conclusion Here, we present the largest case of a TR of a GN with retroperitoneal and mediastinal expansion. On review of the literature, this is the largest reported GN resected and was performed safely. Additionally, we present the first systematic literature review for large GN (> 10 cm) as well as for resected tumors growing from the abdominal cavity into the thoracic cavity.
机译:摘要背景神经核瘤(GNS)非常罕见,慢慢生长,可以从施旺细胞,神经节细胞和神经元或纤维组织产生的良性肿瘤。由于他们的起源来自同情神经嵴,他们表现出神经内分泌潜力;然而,据报道,大多数是激素不活跃的。尽管如此,建议症状控制或预防潜在的恶性退化来完全外科去除。案例报告由于在计算机断层扫描(CT)扫描中检测到巨型腹膜后腹膜和纵隔物质,将一名30岁女性提到了我们的肿瘤中心。初始症状是短暂的恶心,腹泻和痉挛性腹痛。有一个积极的家庭历史,包括5个第一和二级亲属。预设活检显示出一种良性甘草瘤。通过剖腹手术结合胸廓切开术和隔膜部分切口成功地获得35×25×25cm,2550g肿瘤的总切除术(TR)。组织病理学分析证实了诊断。手术挑战性方面是通过主动脉内部的双侧肿瘤侵入血型血管侵入含有双侧2腔手术的主动脉内容,以及腹膜主动脉,肠系膜和下腔内的肿瘤相关位移静脉。由于它们通过肿瘤质量解剖学过程,腰主动脉血管需要部分切除。术后功能优异而没有任何神经系统缺陷的迹象。结论在此,我们呈现了腹膜腹膜和纵隔膨胀的GN TR的最大案例。在审查文献中,这是据最大的报告的GN切除并安全地进行。此外,我们介绍了大型GN(> 10cm)的第一个系统文献回顾,以及切除从腹腔生长到胸腔的肿瘤。

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