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模拟牙源性病变的骨内肌纤维瘤。

Intraosseous myofibroma simulating an odontogenic lesion.

作者信息

Souza Denis P, Loureiro Caio C S, Rejas Roberto A G, Sousa Suzana O M, Raitz Ricardo

机构信息

Department of Oral and Maxillofacial Surgery, School of Dentistry, University of São Paulo, São Paulo, Brazil.

出版信息

J Oral Sci. 2009 Jun;51(2):307-11. doi: 10.2334/josnusd.51.307.

Abstract

Myofibroma is a rare benign nodular tumor of the soft tissues, bones, or internal organs, and may affect both children and adults. It is mostly found in the head and neck region, although uncommon in the jaw bones, where only a few lesions have been described. Radiographically, it may appear as a well-defined unilocular radiolucent entity simulating a cystic or odontogenic lesion. Histopathologic findings alone may be insufficient for a final diagnosis, and immunostaining for markers such as vimentin, alpha-smooth muscle actin, desmin and S-100 may be required. Intraosseous myofibroma is a diagnostic challenge and requires careful histopathologic, immunohistochemical and radiographic correlation. The present article describes a conservatively treated intraosseous myofibroma that occurred in a 7-year-old girl. The clinical, radiographic, histopathologic and immunohistochemical features are discussed.

摘要

肌纤维瘤是一种罕见的软组织、骨骼或内脏良性结节性肿瘤,可累及儿童和成人。它大多见于头颈部区域,尽管在颌骨中并不常见,仅有少数病例报道。在影像学上,它可能表现为边界清晰的单房性透射性病变,类似囊肿或牙源性病变。仅靠组织病理学检查结果可能不足以做出最终诊断,可能需要对波形蛋白、α-平滑肌肌动蛋白、结蛋白和S-100等标志物进行免疫染色。骨内肌纤维瘤的诊断具有挑战性,需要仔细的组织病理学、免疫组织化学和影像学相互印证。本文描述了一例发生在一名7岁女孩身上的经保守治疗的骨内肌纤维瘤。并对其临床、影像学、组织病理学和免疫组织化学特征进行了讨论。

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