Lanfranchi Elena, Fairplay Tracy, Tedeschi Roberto
Department of Medicine and Health Science "Vincenzo Tiberio", University of Molise, "Cardarelli Hospital", 86100 Campobasso, Italy; Department of Biomedical and Neuromotor Sciences, Alma Mater Studiorum, University of Bologna, Bologna, Italy; Studio Lanfranchi, Private Practice, Bologna, Italy.
Studio Fairplay - Functional Rehabilitation of the Upper Extremity, Private Practice, Bologna, Italy.
Int J Surg Case Rep. 2023 Sep;110:108664. doi: 10.1016/j.ijscr.2023.108664. Epub 2023 Aug 16.
Schwannomas, or neurilemmomas, are rare benign nerve sheath tumors primarily originating from peripheral nerves. Brachial plexus schwannomas, constituting approximately 5 % of cases, present a diagnostic and surgical challenge due to their rarity and the complex anatomy of the brachial plexus.
We present the case of a 51-year-old man who visited our physiotherapy clinic with a two-year history of intermittent pain and tingling in the fourth and fifth metacarpals of his non-dominant hand (Numeric Pain Rating Scale 2/10). The pain was nocturnal and resistant to various treatments. Physical examination did not reveal "red flag" symptoms. Considering the persistent and atypical nature of the symptoms, further diagnostic investigations, including an ultrasound of the supraclavicular region, were recommended.
Our case report emphasizes the importance of considering brachial plexus schwannomas in patients with prolonged and unconventional symptoms in the fourth and fifth digits, accompanied by supraclavicular swelling and a positive Tinel's sign. Comprehensive diagnostic evaluation is crucial to confirm or rule out a schwannoma in the supraclavicular area. The rarity of such tumors and the intricate brachial plexus anatomy require meticulous diagnostic and surgical approaches.
This case adds to the growing understanding of brachial plexus schwannomas and their diagnostic complexities. Our report underscores the significance of recognizing these tumors in patients with distinct symptomatology and highlights the need for detailed diagnostic assessments and surgical planning.
施万细胞瘤,又称神经鞘瘤,是罕见的良性神经鞘肿瘤,主要起源于周围神经。臂丛神经施万细胞瘤约占病例的5%,因其罕见性以及臂丛神经复杂的解剖结构,在诊断和手术方面具有挑战性。
我们报告一例51岁男性患者,其因非优势手第四和第五掌骨间歇性疼痛和刺痛两年前来我院理疗门诊就诊(数字疼痛评分量表为2/10)。疼痛为夜间发作,对各种治疗均无效。体格检查未发现“危险信号”症状。考虑到症状持续且不典型,建议进行进一步的诊断性检查,包括锁骨上区域超声检查。
我们的病例报告强调,对于第四和第五指出现长期非典型症状、伴有锁骨上肿胀和Tinel征阳性的患者,应考虑臂丛神经施万细胞瘤。全面的诊断评估对于确认或排除锁骨上区域的施万细胞瘤至关重要。此类肿瘤的罕见性以及臂丛神经复杂的解剖结构需要细致的诊断和手术方法。
本病例增进了对臂丛神经施万细胞瘤及其诊断复杂性的认识。我们的报告强调了在有明显症状的患者中识别这些肿瘤的重要性,并突出了进行详细诊断评估和手术规划的必要性。