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下颌骨婴儿纤维肉瘤:病例报告

Infantile fibrosarcoma in the mandible: case report.

作者信息

Bang G, Baardsen R, Gilhuus-Moe O

机构信息

Department of Oral Pathology, University of Bergen, Norway.

出版信息

J Oral Pathol Med. 1989 Jul;18(6):339-43. doi: 10.1111/j.1600-0714.1989.tb01563.x.

DOI:10.1111/j.1600-0714.1989.tb01563.x
PMID:2810132
Abstract

A case of an infantile fibrosarcoma in the mandible is described. The primary tumor was seen in a 2.5 yr-old boy. In spite of repeated surgical interventions the tumor recurred five times during a 15-yr period, but no metastases have been observed. The difficulty in arriving at a correct histopathologic diagnosis on an unusual tumor in the oral region is demonstrated by the fact that 16 consulted pathologists suggested a long list of different tumors. The treatment of choice seems to be radical surgery. The patient has remained well and without recurrence for the last 7 yr.

摘要

本文描述了一例下颌骨婴儿纤维肉瘤病例。原发肿瘤见于一名2.5岁男孩。尽管反复进行手术干预,但在15年期间肿瘤复发了5次,但未观察到转移。16位会诊病理学家提出了一长串不同肿瘤的诊断,这表明对口腔区域不常见肿瘤做出正确的组织病理学诊断存在困难。首选的治疗方法似乎是根治性手术。在过去7年里,患者情况良好,未出现复发。

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Infantile fibrosarcoma in the mandible: case report.下颌骨婴儿纤维肉瘤:病例报告
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Ameloblastic Fibrosarcoma of the mandible evolving from a prior Ameloblastic Fibroma after two years: an unusual finding.下颌骨成釉细胞纤维肉瘤由两年前的成釉细胞纤维瘤演变而来:一项罕见发现。
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