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对存档于某口腔医学科室的59例颌骨骨肉瘤进行的回顾性临床病理研究。

A retrospective clinicopathological study of 59 osteogenic sarcoma of jaw bone archived in a stomatology unit.

作者信息

Ajura A J, Lau S H

机构信息

Stomatology Unit, Cancer Research Centre, Institute for Medical Research, 50588 Jalan Pahang, Kuala Lumpur, Malaysia.

出版信息

Malays J Pathol. 2010 Jun;32(1):27-34.

Abstract

OBJECTIVES

To determine the clinicopathological features of osteogenic sarcomas of the mandible and maxilla.

MATERIALS AND METHODS

A retrospective study was carried out on all osteosarcoma from the jaw diagnosed in the Stomatology Unit, Institute for Medical Research, Kuala Lumpur from 1967 to 2008. All data regarding the age at presentation, gender, race, clinical presentation, radiographical findings and diagnoses were retrieved from computerized records.

RESULTS

There were 59 cases (36 males and 23 females) with ages ranging from 7 to 68 years. The patients comprised 28 Malays, 16 Chinese, 2 Indians and 13 of other ethnicity. Forty cases involved the mandible and 19 the maxilla. The main complaint was painless or painful bony swelling. Nine cases presented with numbness of the associated region. Four patients had history of prior radiotherapy. The radiographic findings which varied from radiolucent to radiopaque lesions were mentioned in only 26 cases. Histologically, the majority (30) were osteoblastic, 19 chondroblastic, 6 fibroblastic and 4 telangiectatic in type. No small cell type osteosarcoma was identified.

CONCLUSION

Osteogenic sarcoma of the jaws is a rare malignant bone tumour. Over 40 years, there were only 59 cases diagnosed by our institution and to date this is the first report of jaw osteosarcoma in Malaysia.

摘要

目的

确定下颌骨和上颌骨骨肉瘤的临床病理特征。

材料与方法

对1967年至2008年在吉隆坡医学研究所口腔病科诊断的所有颌骨骨肉瘤进行回顾性研究。从计算机记录中检索所有关于就诊年龄、性别、种族、临床表现、影像学检查结果和诊断的数据。

结果

共59例(男性36例,女性23例),年龄7至68岁。患者包括28名马来人、16名中国人、2名印度人和13名其他种族。40例累及下颌骨,19例累及上颌骨。主要症状为无痛或疼痛性骨肿胀。9例伴有相关区域麻木。4例患者有既往放疗史。仅26例提及影像学检查结果,表现为从透射性到不透射性的病变。组织学上,大多数(30例)为成骨细胞型,19例为软骨母细胞型,6例为纤维母细胞型,4例为毛细血管扩张型。未发现小细胞型骨肉瘤。

结论

颌骨骨肉瘤是一种罕见的恶性骨肿瘤。40多年来,我们机构仅诊断出59例,迄今为止,这是马来西亚颌骨骨肉瘤的首例报告。

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