Salunke Abhijeet Ashok, Chen Yongsheng, Tan Jun Hao, Chen Xi, Foo Tun-Lin, Gartner Louise Elizabeth, Puhaindran Mark Edward
Division of Musculoskeletal Oncology, National University Hospital, Singapore ; Pramukhswami Medical College & MS Patel Cancer Centre, Karamsad, Gujarat, India.
Department of Orthopaedic Surgery, National University Hospital, Singapore.
Singapore Med J. 2015 Oct;56(10):555-7. doi: 10.11622/smedj.2015151.
Schwannomas that arise within the muscle plane are called intramuscular schwannomas. The low incidence of these tumours and the lack of specific clinical features make preoperative diagnosis difficult. Herein, we report our experience with intramuscular schwannomas. We present details of the clinical presentation, radiological diagnosis and management of these tumours.
Between January 2011 and December 2013, 29 patients were diagnosed and treated for histologically proven schwannoma at the National University Hospital, Singapore. Among these 29 patients, eight (five male, three female) had intramuscular schwannomas.
The mean age of the eight patients was 40 (range 27-57) years. The most common presenting feature was a palpable mass. The mean interval between surgical treatment and the onset of clinical symptoms was 17.1 (range 4-72) months. Six of the eight tumours (75.0%) were located in the lower limb, while 2 (25.0%) were located in the upper limb. None of the patients had any preoperative neurological deficits. Tinel's sign was present in one patient. Magnetic resonance (MR) imaging showed that the findings of split-fat sign, low signal margin and fascicular sign were present in all patients. The entry and exit sign was observed in 4 (50.0%) patients, a hyperintense rim was observed in 7 (87.5%) patients and the target sign was observed in 5 (62.5%) patients. All patients underwent microsurgical excision of the tumour and none developed any postoperative neurological deficits.
Intramuscular schwannomas demonstrate the findings of split-fat sign, low signal margin and fascicular sign on MR imaging. These findings are useful for the radiological diagnosis of intramuscular schwannoma.
发生于肌层内的施万瘤称为肌内施万瘤。这些肿瘤发病率低且缺乏特异性临床特征,使得术前诊断困难。在此,我们报告我们对肌内施万瘤的诊治经验。我们展示了这些肿瘤的临床表现、影像学诊断及治疗细节。
2011年1月至2013年12月期间,新加坡国立大学医院对29例经组织学证实为施万瘤的患者进行了诊断和治疗。在这29例患者中,8例(5例男性,3例女性)患有肌内施万瘤。
8例患者的平均年龄为40岁(范围27 - 57岁)。最常见的表现是可触及肿块。手术治疗与临床症状出现的平均间隔时间为17.1个月(范围4 - 72个月)。8例肿瘤中有6例(75.0%)位于下肢,2例(25.0%)位于上肢。所有患者术前均无神经功能缺损。1例患者出现Tinel征阳性。磁共振(MR)成像显示,所有患者均出现脂肪分离征、低信号边缘和束状征。4例(50.0%)患者观察到出入征,7例(87.5%)患者观察到高信号环,5例(62.5%)患者观察到靶征。所有患者均接受了肿瘤显微手术切除,术后均未出现神经功能缺损。
肌内施万瘤在MR成像上表现为脂肪分离征、低信号边缘和束状征。这些表现有助于肌内施万瘤的影像学诊断。