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颌骨外颅面骨骨肉瘤

Osteosarcoma of extragnathic craniofacial bones.

作者信息

Nora F E, Unni K K, Pritchard D J, Dahlin D C

出版信息

Mayo Clin Proc. 1983 Apr;58(4):268-72.

PMID:6572774
Abstract

Osteosarcomas of extragnathic craniofacial bones--those bones of the skull excepting the jaw bones--are rare lesions, constituting fewer than 2% of all osteosarcomas. In our series of 21 patients (12 male and 9 female), the ages ranged from 6 to 77 years, and 10 patients were in the third or fourth decade of life. At least six patients had predisposing conditions: Paget's disease of bone in three and prior regional irradiation in three. Most of these tumors were high-grade lesions, and most were extensive when treated. There were 11 osteoblastic, 6 fibroblastic, and 1 small cell variant; 2 lesions had features resembling malignant fibrous histiocytoma. One tumor, originally interpreted as grade 4 osteosarcoma, was unavailable for variant classification. Surgical removal, irradiation, and chemotherapy were used in treatment, alone or in combination. Only two patients survived 5 years, and one of these patients died of her disease after 65 months. Almost half of our patients died within 1 year after diagnosis. The one long-term survivor (12 years) underwent a radical surgical procedure when her tumor was small; this was the only patient in this series who had a low-grade lesion. Because of the characteristics described, osteosarcoma of extragnathic craniofacial bones must be considered a distinct disease.

摘要

颌外颅面骨骨肉瘤——即除颌骨外的颅骨——是罕见病变,占所有骨肉瘤的比例不到2%。在我们的21例患者系列中(男性12例,女性9例),年龄范围为6至77岁,10例患者处于生命的第三个或第四个十年。至少6例患者有易感因素:3例患有骨Paget病,3例曾接受过局部放疗。这些肿瘤大多为高级别病变,治疗时大多已广泛扩散。有11例成骨细胞型、6例纤维母细胞型和1例小细胞型变体;2例病变具有类似恶性纤维组织细胞瘤的特征。1例最初被诊断为4级骨肉瘤的肿瘤无法进行变体分类。治疗采用手术切除、放疗和化疗,单独或联合使用。只有2例患者存活了5年,其中1例患者在65个月后死于该病。几乎一半的患者在诊断后1年内死亡。唯一的长期幸存者(12年)在肿瘤较小时接受了根治性手术;这是该系列中唯一一例低级别病变的患者。由于上述特征,颌外颅面骨骨肉瘤必须被视为一种独特的疾病。

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