Parapharyngeal space hemangiopericytoma treated with surgery and postoperative radiation--a case report.

Muhammad Mohsin Fareed, Abdullah Suleiman Mazaed Al Amro, Rashad Akasha, Mansour Al Assiry, Mushabbab Al Asiri, Mutahir Tonio, Yasser Bayoumi
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引用次数: 15

Abstract

Hemangiopericytoma (HPC) is a rare tumor of uncertain malignant potential arising from mesenchymal cells with pericytic differentiation. It accounts for 3-5% of soft tissue sarcomas and 1% of vascular tumors. It usually presents in 5th to 6th decade of life. Most common sites are limbs, pelvis and head and neck. About 20% of all hemangiopericytomas are seen in head and neck, mostly in adults. Usually it presents in orbit, nasal cavity, oral cavity, jaw, parotid gland, parapharyngeal space, masticator space and jugular foramen. Long term follow up is important because of imprecise nature of the histological criteria for prediction of biologic behavior.We report herein a case of HPC in 66-year-old man, who presented in our department with headache, nasal obstruction and dysphagia. A neck computer tomography scan and magnetic resonance imaging showed a large left parapharyngeal mass bulging into nasopharynx and oropharynx with extension to pharyngeal mucosal surface and causing narrowing of airways and total obstruction of left posterior nostril. Angiography showed a highly vascular neoplasm. Initially he was managed as a case of schwannoma and embolization was done but with no response. An attempt to do complete surgical resection was made, but due to its critical position, it was not possible. During surgery, highly vascularised tumor was found. The histopathologic examination revealed a vascular tumor consistent with hemangiopericytoma G-II. The patient had normal postoperative course of healing and was given adjuvant radiation. He is on regular follow up without signs of recurrence or metastases.In summary, parapharyngeal space is a rare site of presentation for hemangiopericytoma which is highly vascular tumor, requiring extensive work up including magnetic resonance imaging, computed tomography scan and angiography. Complete surgical excision should be attempted. Postoperative radiation is indicated in cases of incomplete resection.

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咽旁间隙血管外皮细胞瘤手术及术后放疗1例报告。
摘要血管外皮细胞瘤(HPC)是一种罕见的恶性肿瘤,发生于间充质细胞并呈周细胞分化。占软组织肉瘤的3-5%,占血管肿瘤的1%。它通常出现在生命的第五到第六个十年。最常见的部位是四肢、骨盆和头颈部。约20%的血管外皮细胞瘤见于头颈部,多见于成人。通常表现在眼眶、鼻腔、口腔、颌骨、腮腺、咽旁间隙、咀嚼间隙和颈静脉孔。长期随访很重要,因为预测生物学行为的组织学标准不精确。我们在此报告一个66岁男性HPC病例,他在我科表现为头痛、鼻塞和吞咽困难。颈部计算机断层扫描和磁共振成像显示左侧咽旁肿物向鼻咽和口咽膨出,并延伸至咽粘膜表面,引起气道狭窄和左侧后鼻孔完全阻塞。血管造影显示为高度血管性肿瘤。最初,他作为一个神经鞘瘤病例进行了治疗,并进行了栓塞治疗,但没有反应。试图做完全的手术切除,但由于其关键位置,这是不可能的。手术中发现高度血管化的肿瘤。组织病理学检查显示为血管肿瘤,符合G-II型血管外皮细胞瘤。患者术后愈合过程正常,给予辅助放疗。他正在定期随访,没有复发或转移的迹象。总之,咽旁间隙是一种罕见的血管外皮细胞瘤的表现部位,它是一种高度血管性的肿瘤,需要广泛的检查,包括磁共振成像、计算机断层扫描和血管造影。应尝试完全手术切除。术后放疗适用于不完全切除的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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