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下颌骨婴儿型纤维瘤病:伴有长期随访的病例报告。

Desmoid-type infantile fibromatosis of the mandible: case report with long-term follow-up.

机构信息

Oral and Maxillofacial Surgery, Eppendorf University Hospital, University of Hamburg, Martinistr. 52, 20246 Hamburg, Germany.

出版信息

In Vivo. 2010 Nov-Dec;24(6):877-81.

Abstract

A 6-year-old girl was referred to Eppendorf University Hospital because of a suspected malignant mandibular tumour. An osteolytic lesion was depicted on panoramic radiograph in the premolar region. The tumour was resected with covering skin and the defect was closed by primary intention. Histological investigation revealed fibromatosis. No local recurrence of infantile fibromatosis occurred during seven years of follow-up. The differential diagnosis of fibro-osseous lesion of the facial region is challenging. Especially in children, caution should be exercised in the treatment of benign lesions that resemble malignant conditions derived from connective tissue, with special reference to long-term follow-up.

摘要

一位 6 岁女孩因疑似恶性下颌肿瘤被转至埃彭多夫大学医院。全景片显示在臼齿区域有溶骨性病变。肿瘤连同覆盖的皮肤一起被切除,缺损直接缝合。组织学检查显示纤维瘤病。在七年的随访中,没有发生婴儿纤维瘤病的局部复发。面部纤维骨性病变的鉴别诊断具有挑战性。特别是在儿童中,对于类似于源自结缔组织的恶性情况的良性病变,在治疗时应特别注意长期随访。

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