The Rare Large Common Peroneal Nerve’s Schwannoma—A Case Report and Literature Review

IF 0.6 Q4 ONCOLOGY Case Reports in Oncological Medicine Pub Date : 2024-05-02 DOI:10.1155/2024/9397436
Rudiansyah Harahap, Nurmaliannysa Dwinandia Harahap
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Abstract

Schwannoma in the popliteal fossa is still rare, often diagnosed late because it grows slowly and has no symptoms. It is often misdiagnosed with connective tissue tumors or with neurological disorders originating in the spine or disorders of the peroneal nerve. Schwannoma within the common peroneal nerve is still rare in the popliteal fossa, with most tumor sizes around 2 cm in diameter due to their smaller size of nerve but can cause neurologic disturbance, especially when it is large. And over a long time, it can cause serious complaints like neurological deficits and make surgery difficult by leaving greater sequelae. There is no data yet showing the incidence of schwannoma in the common peroneal nerve. In this case, a 36-year-old woman, for 5 years, feels soreness in the popliteal fossa and pain in the right instep, suspected that a nerve was pinched, due to an abnormality in the spine. As time went on, there was a lump in the fold of the right knee, suspected to be a Baker’s cyst. As time went by, the complaint was burning pain in the right instep to the lateral ankle and distal right lower leg, disturbing sleep. Tinel’s sign was positive. The right instep has hypoesthesia and a slight drop in the foot. On radiological examination of the right knee, a circumferential mass appeared, measuring 5 cm×4 cm. The diagnosis is suspicious for a common peroneal nerve tumor. The encapsulated operation to remove the tumor was carried out with a size measuring 5 cm×4.5 cm×4 cm. The histopathological examination showed schwannoma. After surgery, the pain disappeared, hypoesthesia and a slight drop in the foot underwent physiotherapy, and stimulation with the result gradually improved. A thorough early examination includes correct and systematic anamnesis, physical examination, and neurological evaluation such as paraesthesia, hypoesthesia, and Tinel’s sign; also, additional examinations, such as radiographic, ultrasound, and MRI, are needed for early detection of schwannoma so that delays in diagnosis and surgery can be avoided to prevent neurological deficits.
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罕见的大腓总神经束瘤--病例报告和文献综述
腘窝处的许旺瘤仍很罕见,由于生长缓慢且无症状,通常诊断较晚。它经常被误诊为结缔组织肿瘤或源自脊柱的神经系统疾病或腓总神经疾病。腓总神经内的许旺瘤在腘窝中还是比较少见的,由于其神经体积较小,肿瘤大小大多在直径 2 厘米左右,但会引起神经功能紊乱,尤其是当肿瘤较大时。而且时间长了,会引起神经功能缺损等严重不适,并留下较大后遗症,给手术带来困难。目前还没有数据显示腓总神经裂孔瘤的发病率。在这个病例中,一名 36 岁的妇女 5 年来一直感到腘窝酸痛和右脚背疼痛,怀疑是脊柱异常导致的神经压迫。随着时间的推移,右膝盖褶皱处出现肿块,怀疑是贝克氏囊肿。随着时间的推移,患者主诉右脚背至外侧脚踝和右小腿远端有烧灼痛,影响睡眠。Tinel征阳性。右脚背感觉减退,足部轻微下垂。在对右膝盖进行放射检查时,发现了一个周缘肿块,大小为 5 厘米×4 厘米。诊断结果怀疑是腓总神经肿瘤。手术切除了肿瘤,肿瘤大小为 5 厘米×4.5 厘米×4 厘米。组织病理学检查显示为分裂瘤。术后,患者疼痛消失,感觉减退,足部轻微下垂,经过理疗和刺激,情况逐渐好转。全面的早期检查包括正确、系统的病史、体格检查和神经系统评估,如麻痹、感觉减退、Tinel's 征等;此外,还需要进行其他检查,如放射学、超声波和核磁共振成像,以便早期发现分裂瘤,从而避免延误诊断和手术,防止出现神经功能缺损。
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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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