妊娠期神经鞘肌瘤:病例报告

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Elena De Chiara, Valerio Gaetano Vellone, Jacopo Ferro, Chiara Trambaiolo Antonelli, Liliana Piro, Stefano Avanzini, Valentina Prono, Andrea Beccaria, Monica Muraca, Ramona Tallone
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引用次数: 0

摘要

神经鞘肌瘤(NSM)是一种罕见的良性周围神经鞘瘤,好发于青壮年。神经鞘肌瘤是一种无症状、生长缓慢的肿物,好发于上肢,下肢更为罕见。鉴于复发风险很高,建议进行完全切除术。据我们所知,目前还没有关于妊娠期 NMS 的演变和处理方法的描述。我们报告了首例妊娠期女孩复发性胫前腓肠肌挛缩症的病例及其在妊娠期间和妊娠后的随访和结果。NSM 很难通过临床或影像学诊断。最终诊断仍需通过组织病理学。众所周知,各种类型的良性和恶性皮肤肿瘤在妊娠期间会发生发展或变化。但我们的病例表明,妊娠并不会影响 NSM 的生长和演变。鉴于皮损的良性性质及其缓慢生长的趋势,在怀孕期间,可以通过超声波检查对 NSM 进行随访,并在分娩后推迟手术治疗。我们的病例强调了仔细监测和个体化决策的重要性,尤其是像 NSM 这样的罕见病例,因为有关良性病变进展的数据非常有限。我们的病例强调了在诸如 NSM 等罕见病例中进行仔细监测和针对性治疗的重要性,因为在这些病例中,良性病变进展的数据十分有限。考虑到病变的良性性质及其缓慢生长的趋势,可通过超声波检查对妊娠期 NSM 进行随访,并在分娩后推迟手术治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nerve Sheath Myxoma in Pregnancy: A Case Report.

Nerve sheath myxoma (NSM) is a rare benign peripheral nerve sheath tumor that affects young adults. NSMs are asymptomatic, slow-growing swellings located in the upper extremities, more rarely in the lower extremities. Given the high risk of recurrence, it is recommended to perform a complete exeresis. To our knowledge, the evolution and management of NMS during pregnancy have not been described yet. We report the first case of recurrent pretibial NSM in a pregnant girl and its follow-up and outcome during and after pregnancy. NSM is difficult to diagnose clinically or using imaging. The final diagnosis remains histopathological. It is known how various types of benign and malignant skin tumors can develop or change during pregnancy. With our case, however, we documented that pregnancy does not affect the growth and evolution of NSM. Given the benign nature of the lesions and their tendency to grow slowly, during pregnancy, follow-up of NSMs can be conducted through ultrasonography and surgical treatment postponed after delivery. Our case highlights the importance of careful monitoring and individualized decision making, especially in rare scenarios such as NSM, where data on the progression of benign lesions are limited. Our case highlights the importance of a careful monitoring and a tailored treatment in rare scenarios such as NSM, where data on the progression of benign lesions are limited. Considering the benign nature of the lesions and their tendency to grow slowly, follow-up of NSMs during pregnancy can be conducted through ultrasonography, and surgical treatment can be postponed after delivery.

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