Department of Neurosurgery, University Hospital Center Osijek, 31000 Osijek, Croatia.
Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Medicina (Kaunas). 2024 Jul 25;60(8):1203. doi: 10.3390/medicina60081203.
: Schwannomas (Schs) are benign tumor masses that rarely occur intra-abdominally and rarely reach larger diameters. When present, they occur as rare solitary nerve sheath tumors of peri-neural Schwann cells. Schwannoma mostly affects the nerves of the extremities, trunk, or the head and neck region. They are more common in female patients, mostly among patients between the third and fifth decade. They occur spontaneously but could also be found in association with a group of genetic autosomal dominant disorders called type 2. When present intra-abdominally, schwannomas grow slowly without significant clinical signs and symptoms. Clinical importance is presented in cases of occupying intra-abdominal space and impingement of surrounding structures, which causes intermittent pain. Only 0.5-5% of all retroperitoneal tumors are schwannomas and their malignant transformation is very rare. : The authors present a case of a large intra-abdominal schwannoma in a 70-year-old female patient. She underwent CT scanning due to refractory left-sided subcostal pain, which revealed a large tumor mass in the left-sided hemiabdomen. Preoperative cytologic biopsy confirmed Sch. The patient underwent an MRI scan upon admission to our department, which revealed the origin of the tumor at the left-sided L3 level and intra-abdominal tumor spreading with the largest diameter of 25 cm. The patient underwent multidisciplinary surgical excision, confirmed by MRI scan in a period of five months postoperatively. : Its rare presentation leads to the necessity to adequately evaluate such patients, especially to avoid any hidden diagnosis which might lead to further complications. The goal of a multidisciplinary approach should be emphasized as maintaining a good postsurgical condition without neurological deficits.
神经鞘瘤(Schwannomas,Schs)是一种良性肿瘤,很少发生在腹腔内,也很少长到较大的直径。当发生时,它们是罕见的、单发的、神经鞘 Schwann 细胞来源的肿瘤。神经鞘瘤主要影响四肢、躯干或头颈部的神经。它们在女性患者中更为常见,主要发生在 30 至 50 岁的患者中。它们是自发性的,但也可能与一组称为 2 型的常染色体显性遗传疾病有关。当发生在腹腔内时,神经鞘瘤生长缓慢,没有明显的临床症状和体征。当它们占据腹腔空间并压迫周围结构时,会引起间歇性疼痛,此时才具有临床重要性。只有 0.5%至 5%的腹膜后肿瘤是神经鞘瘤,其恶性转化非常罕见。
作者报告了一例 70 岁女性患者的巨大腹腔内神经鞘瘤。她因左侧肋弓下难治性疼痛接受 CT 扫描,发现左侧半腹部有一个大的肿瘤肿块。术前细胞学活检证实为 Sch。患者入院后进行了 MRI 扫描,显示肿瘤起源于左侧 L3 水平,并在腹腔内扩散,最大直径为 25 厘米。患者接受了多学科手术切除,术后五个月的 MRI 扫描证实了这一点。
其罕见的表现导致需要充分评估此类患者,特别是要避免任何可能导致进一步并发症的隐匿性诊断。多学科方法的目标应该是强调保持良好的术后状态,而不出现神经功能缺陷。