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颅底软骨黏液样纤维瘤:一种可能与脊索瘤和软骨肉瘤相混淆的肿瘤。三例报告并文献复习。

Chondromyxoid fibroma of the skull base: a tumor which may be confused with chordoma and chondrosarcoma. A report of three cases and review of the literature.

作者信息

Keel S B, Bhan A K, Liebsch N J, Rosenberg A E

机构信息

James Homer Wright Pathology Laboratories, Massachusetts General Hospital, Boston 02114, USA.

出版信息

Am J Surg Pathol. 1997 May;21(5):577-82. doi: 10.1097/00000478-199705000-00011.

Abstract

Three cases of chondromyxoid fibroma arising in the skull base are reported. The tumors arose in females 34, 65, and 66 (median 55) years of age. Two women presented with headaches, and one with nasal obstruction. Radiographic studies revealed that all three lesions were expansile soft tissue masses centered in the clivus, at least 4 cm in greatest diameter. One lesion involved primarily the clivus, the others extended from the clivus into the sphenoid and ethmoid sinuses. Two of the three cases were initially misdiagnosed as chordoma or chondrosarcoma. The initial treatment was curettage of gross disease in all three cases. One patient also received radiation therapy. One patient had local progression of disease, which was treated with surgery and radiation therapy. All patients are clinically free of disease 11 to 26 months following the most recent treatment. Chondromyxoid fibroma can and should be distinguished from chondrosarcoma and chordoma, two tumors which more commonly arise in the skull base and which have the potential to metastasize.

摘要

本文报告了3例发生于颅底的软骨黏液样纤维瘤。肿瘤发生于34岁、65岁和66岁(中位年龄55岁)的女性。2例女性表现为头痛,1例表现为鼻塞。影像学研究显示,所有3个病变均为以斜坡为中心的膨胀性软组织肿块,最大直径至少4 cm。1个病变主要累及斜坡,其他病变从斜坡延伸至蝶窦和筛窦。3例中有2例最初被误诊为脊索瘤或软骨肉瘤。所有3例的初始治疗均为刮除肉眼可见的病灶。1例患者还接受了放射治疗。1例患者疾病出现局部进展,接受了手术和放射治疗。所有患者在最近一次治疗后11至26个月临床无疾病。软骨黏液样纤维瘤能够且应该与软骨肉瘤和脊索瘤相鉴别,后两种肿瘤更常见于颅底且有转移的可能。

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