Medical College, Aga Khan University, Karachi, Pakistan.
Section of Histopathology, Department of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
J Med Case Rep. 2023 Dec 11;17(1):538. doi: 10.1186/s13256-023-04234-z.
Schwannomas are solitary well-circumscribed encapsulated benign tumors that exhibit Schwann cell differentiation, and arise directly from myelinated peripheral or central nerves. Although they are usually asymptomatic and found incidentally, schwannomas can cause symptoms due to compression of nearby structures which, depending on the location, can make clinical presentations widely variable. Despite their rarity, schwannomas have been documented in a number of locations including the limbs, cerebellopontine angle, posterior mediastinum, and, far more infrequently, the lungs.
In this article, we report an incidental finding of an intrapulmonary schwannoma in a 59-year-old Pakistani woman who was grossly asymptomatic upon presentation to the cardiothoracic surgery clinic. An [F]fluorodeoxyglucose positron emission tomography/computed tomography scan revealed a lobulated soft-tissue lesion measuring 23 mm × 23 mm in the lower lobe of the right lung. A computed tomography-guided core biopsy of the mass was performed, which revealed a benign spindle cell lesion based on histopathological examination and immunohistochemical staining. The mass was surgically resected via a right lower lobectomy, and subsequently confirmed to be an encapsulated neoplastic lesion composed of well-differentiated Schwann cells. There were no short- or long-term complications, morbidities, or recurrences based on 1-year follow-up.
This report underscores the predominantly asymptomatic nature of schwannomas and reemphasizes the efficacy of surgical resection as a safe and curative procedure for a tumor of this nature. Albeit very rare, intrapulmonary schwannomas can be considered a differential diagnosis when encountering solitary asymptomatic pulmonary nodules or masses.
神经鞘瘤是一种孤立的、边界清楚的包膜良性肿瘤,表现出施万细胞分化,直接起源于有髓鞘的周围或中枢神经。虽然它们通常是无症状的,是偶然发现的,但神经鞘瘤可以因压迫附近结构而引起症状,根据位置的不同,临床表现可能会有很大差异。尽管它们很罕见,但神经鞘瘤已在许多部位被记录,包括四肢、桥小脑角、后纵隔,以及更为罕见的肺部。
本文报道了一例 59 岁巴基斯坦女性肺部神经鞘瘤的偶然发现,该患者在就诊心胸外科诊所时几乎没有任何症状。氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描显示右肺下叶有一个 23mm×23mm 的分叶状软组织病变。对该肿块进行了计算机断层扫描引导下的核心活检,根据组织病理学检查和免疫组织化学染色显示为良性梭形细胞病变。该肿块通过右下肺叶切除术进行了手术切除,随后证实为由分化良好的施万细胞组成的包膜性肿瘤。根据 1 年的随访,没有出现短期或长期并发症、发病率或复发。
本报告强调了神经鞘瘤主要是无症状的性质,并再次强调了手术切除作为这种性质肿瘤的一种安全和有效的治疗方法。尽管非常罕见,但当遇到孤立的无症状性肺结节或肿块时,肺部神经鞘瘤可以被视为鉴别诊断。