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一例下颌骨及颅底尤因肉瘤病例。

A case of Ewing's sarcoma in the mandible and the skull base.

作者信息

Kalcioğlu M Tayyar, Oncel Semih, Miman Murat Cem, Erdem Tamer, Mizrak Bülent

机构信息

Department of Otolaryngology, Medicine Faculty of Inönü University, Malatya, Turkey.

出版信息

Kulak Burun Bogaz Ihtis Derg. 2003 Nov;11(5):144-7.

Abstract

A thirteen-year-old boy with Ewing's sarcoma was presented. The treatment was considerably delayed because of the initial diagnostic difficulties due to its insidious presentation and the unwillingness of the child's parents to further investigations and treatment. During a three-year delay, the tumor turned out to be a gross painful mass from a painless lesion. Cranial computed tomography and magnetic resonance imaging with contrast showed a destructive lesion extensively involving the right mandible and the skull base, with invasion to the intracranial space. Facial and intratemporal portions of the mass were removed totally, but the intracranial extension could not be totally excised because of cavernous sinus involvement. Histologic and immunohistochemical findings were consistent with the diagnosis of Ewing's sarcoma. The patient received systemic chemotherapy and radiotherapy following surgery. A month after radiation therapy, radiologic investigations showed a lung mass suggestive of metastasis. He died two days after hospitalization, from an intracranial hemorrhage associated with the intracranial mass.

摘要

本文报告了一名13岁患有尤因肉瘤的男孩。由于该病起病隐匿,最初诊断困难,且患儿父母不愿进一步检查和治疗,导致治疗显著延迟。在三年的延迟期内,肿瘤从无痛性病变发展为明显疼痛的肿块。头颅计算机断层扫描和增强磁共振成像显示,有一个破坏性病变广泛累及右下颌骨和颅底,并侵入颅内空间。肿块的面部和颞内部分被完全切除,但由于海绵窦受累,颅内延伸部分无法完全切除。组织学和免疫组化结果与尤因肉瘤的诊断一致。患者术后接受了全身化疗和放疗。放疗一个月后,影像学检查显示肺部有一个提示转移的肿块。他在住院两天后死于与颅内肿块相关的颅内出血。

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