上颚侵袭性复发性多形性腺瘤1例并文献复习

E.N. Nokaneng
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引用次数: 0

摘要

多形性腺瘤(PA)是一种唾液腺肿瘤,其显微特征是结构多形性而不是细胞多形性。肿瘤也有手指状突起进入假包膜,这在临床上归因于与肿瘤相关的高复发率。血管和神经侵犯已被报道,被认为是肿瘤的不典型特征。文献回顾表明,肿瘤侵袭骨而不发生恶性转化是非常罕见的。一位28岁的女性被诊断为上颚的侵袭性复发性PA,需要整体切除左上颌骨。计算机断层扫描显示一个均匀的,明确的,多室病变,从上颌骨的前部延伸到后部。组织学分析未发现病变有任何恶性转化。虽然骨侵蚀是这种病变的一个已知特征,但骨侵犯是不典型的。本病例为罕见的侵袭性复发性多形性腺瘤。
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Invasive recurrent pleomorphic adenoma of the palate: A case report and literature review

Pleomorphic adenoma (PA) is a salivary gland tumour characterised microscopically by architectural rather than cellular pleomorphism. The neoplasm also has finger-like projections into the pseudocapsule, which clinically has attributed to the high recurrence rate associated with the neoplasm. Vascular and neural invasion have been reported and are regarded as atypical features of the neoplasm. Review of the literature suggests that invasion of bone without malignant transformation by the neoplasm is very rare.

A 28-year-old female was diagnosed with an invasive recurrent PA of the palate, which required en-bloc resection of the left maxilla. The computed tomography scan showed a homogeneous, well-defined, multilocular lesion which extended from the anterior to the posterior of the maxilla. The histological analysis did not report any malignant transformation of the lesion. Although bone erosion is a known feature of this lesion, bone invasion is atypical. This case represents a rare occurrence of an invasive recurrent pleomorphic adenoma.

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来源期刊
Oral and Maxillofacial Surgery Cases
Oral and Maxillofacial Surgery Cases Medicine-Otorhinolaryngology
CiteScore
0.60
自引率
0.00%
发文量
43
审稿时长
69 days
期刊介绍: Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.
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