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起源于迷走神经鞘瘤的血管肉瘤——病例报告及文献综述

Angiosarcoma Arising in a Vagal Schwannoma - Report and Literature Review.

作者信息

Shaikh Zeeshan Ali, Khyani Iqbal A Muhammad, Diwan Asad, Naseem Paras, Abbas Hasan

机构信息

Department of Otorhinolaryngology, Shaheed Mohtarma Benazir Bhutto Medical College and Lyari General Hospital, Karachi, Pakistan.

Department of Pathology, Aga Khan University Hospital, Karachi, Pakistan.

出版信息

Turk Arch Otorhinolaryngol. 2024 Oct 23;62(2):72-76. doi: 10.4274/tao.2024.2023-6-2.

Abstract

Schwannoma and angiosarcoma are rare occurrences. Angiosarcoma's occurrence in a preexisting schwannoma is a very rare event with only fifteen cases reported in the literature. We report the sixteenth case of angiosarcoma arising in a schwannoma, a 30-year-old male patient with a long-standing (15 years) history of right neck lump. The lump measured around 10x7 cm at the time of presentation and all cranial nerves were intact. We performed a fiberoptic laryngoscopy and a computed tomography scan of the head and neck with contrast. Our provisional diagnosis was a parapharyngeal space neoplasm, most likely a salivary gland malignancy. The tumor was excised surgically. On histopathology it contained two distinct tissue architectures representing a schwannoma and epithelioid angiosarcoma, also confirmed on immunohistochemistry. Literature review of these limited cases implicates a poor prognosis of the disease. The pathogenesis is uncertain, but the theories put forward suggest chronic vascular stasis or vascular endothelial proliferation as possible etiologies. The main takeaway of our report is to consider the potential of malignancy in long standing cases of schwannomas. Prompt surgical treatment should be offered, and the patient and their family be counselled for postoperative adjuvant treatment for better prognosis.

摘要

神经鞘瘤和血管肉瘤均较为罕见。血管肉瘤发生于既往存在的神经鞘瘤中是极为罕见的事件,文献中仅报道了15例。我们报告第16例发生于神经鞘瘤的血管肉瘤,患者为一名30岁男性,有右侧颈部肿块长达15年的病史。就诊时肿块大小约为10×7厘米,所有颅神经均完整。我们进行了纤维喉镜检查以及头颈部增强计算机断层扫描。我们的初步诊断是咽旁间隙肿瘤,很可能是涎腺恶性肿瘤。肿瘤通过手术切除。组织病理学检查显示其包含两种不同的组织结构,分别代表神经鞘瘤和上皮样血管肉瘤,免疫组织化学检查也证实了这一点。对这些有限病例的文献回顾表明该疾病预后不良。发病机制尚不确定,但提出的理论认为慢性血管淤滞或血管内皮增殖可能是病因。我们报告的主要要点是,对于长期存在的神经鞘瘤病例要考虑其恶变的可能性。应及时进行手术治疗,并向患者及其家属提供术后辅助治疗的咨询,以获得更好的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751a/11572335/90fe4ed793d3/TurkArchOtorhinolaryngol-62-72-figure-1.jpg

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