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Orbital Pheochromocytoma Metastasis in 2 Patients With Known Pheochromocytoma

机译:2例患有嗜尼计量细胞瘤的2名患者的轨道嗜铬细胞瘤转移

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摘要

Two patients with previously diagnosed pheochromocytoma presented with facial pain and ptosis. Imaging revealed orbital lesions. Both patients were referred for surgical evaluation of the orbital mass. Surgical excision was performed for both. Pathology confirmed metastatic pheochromocytoma. Pheochromocytomas commonly metastasize to bone, liver, and other tissues. Five cases of metastasis to orbital bone have been previously described. These 2 cases are unique in that the metastases were not hormonally active, presented soon after initial diagnosis, and were treated palliatively with surgical excision. Previous treatment of orbital bony metastasis used radiotherapy. These cases demonstrate that surgical resection is a viable treatment option in these situations. Orbital metastasis of pheochromocytomas should be considered with the appropriate clinical presentation. These are the first documented cases of intraorbital metastasis, separate from the bony walls. Previously, orbital bony wall metastases were treated with radiation. Surgical excision is a viable option for treatment of such metastases.
机译:两名患有先前诊断的嗜铬细胞瘤的患者,呈现面部疼痛和皮下。成像显示出轨道病变。两种患者都被称为眶肿块的外科评估。对两者进行手术切除。病理学证实了转移性噬菌体细胞瘤。 Pheochromocytomas通常转移到骨,肝脏和其他组织。先前已经描述了五种转移的转移患者。这2例是独一无二的,因为在初步诊断后不久呈现出嗅觉活跃的转移,并且用手术切除持有姑息性。先前治疗眶骨转移使用放射疗法。这些病例表明,手术切除在这些情况下是一种可行的治疗选择。应考虑使用适当的临床介绍来考虑嗜铬细胞瘤的轨道转移。这些是胎肾炎性转移的第一个记录病例,与骨壁分开。以前,用辐射处理轨道骨壁转移。手术切除是治疗此类转移的可行选择。

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