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Meningeal hemangiopericytoma only diagnosed at the time of late bone metastasis.

机译:脑膜血管周细胞瘤仅在骨转移晚期才被诊断出。

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摘要

Hemangiopericytoma is a rare neoplasm. Primary meningeal hemangiopericytomas account for 1 to 7% of all meningeal tumors. In the literature, meningeal hemangiopericytomas are mainly case reports, which confirm an aggressive behavior with a high rate of local recurrence and extracranial metastasis. Metastasis can be seen many years after initial surgical excision of the primary tumor, and the most common sites include the bone, liver and lung. We present a pathological study of four meningeal hemangiopericytomas with bone metastases. All patients are male with a mean age of 46.5 years. Metastases only involved bone. Three out of four lesions were initially misdiagnosed as meningiomas. Only one case was initially correctly diagnosed as meningeal hemangiopericytoma. All patients underwent surgery with complete resection. Only the patient immediately diagnosed with meningeal hemangiopericytoma received postoperative radiation therapy. Three patients had bone metastases without local recurrence including the one who received radiation therapy. One patient recurred locally after 7 years, and bone metastasis was found at the same time. Our cases confirm that meningeal hemangiopericytomas are a separate entity and have a high recurrence rate despite complete surgical resection, with extracranial metastases, mainly to bone, even after long intervals.
机译:血管周细胞瘤是一种罕见的肿瘤。原发性脑膜血管周细胞瘤占所有脑膜肿瘤的1%至7%。在文献中,脑膜血管内皮细胞瘤主要是病例报道,证实了侵袭性行为具有较高的局部复发率和颅外转移率。最初手术切除原发肿瘤后许多年即可见转移,最常见的部位包括骨,肝和肺。我们提出了四个具有骨转移的脑膜血管周细胞瘤的病理学研究。所有患者均为男性,平均年龄为46.5岁。转移仅涉及骨骼。最初,四分之三的病变被误诊为脑膜瘤。最初只有一例被正确诊断为脑膜血管周细胞瘤。所有患者均接受了完全切除术。仅立即诊断为脑膜血管周细胞瘤的患者接受术后放射治疗。三名患者发生了骨转移而无局部复发,其中一名接受了放射治疗。一名患者在7年后局部复发,并且同时发现了骨转移。我们的病例证实脑膜血管周细胞瘤是一个单独的实体,尽管进行了彻底的手术切除,但复发率很高,即使经过很长的间隔,颅外转移也主要发生在骨上。

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