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颞下颌关节腱鞘弥漫型巨细胞瘤:一种罕见肿瘤的诊断与处理

Tenosynovial, diffuse type giant cell tumor of the temporomandibular joint, diagnosis and management of a rare tumor.

作者信息

Bredell Marius, Schucknecht Bernhard, Bode-Lesniewska Baete

机构信息

Department of Craniomaxillofacial and Oral Surgery, University Hospital Zurich, Frauenklinikstrasse 24, 8091 Zurich, Switzerland.

MRI Institute, Bahnhofplatz 3, 8001 Zurich, Switzerland.

出版信息

J Clin Med Res. 2015 Apr;7(4):262-6. doi: 10.14740/jocmr1872w. Epub 2015 Feb 9.

Abstract

The purpose of this paper was to describe a rare unusual case of primary mandibular condylar tenosynovial giant cell tumor of diffuse type with predominantly intraosseous growth and its management by resection and functional reconstruction with a vascularized costochondral graft. Clinical presentation was swelling in the right condylar area and limited mouth opening with radiological evidence of central bone destruction and magnetic resonance imaging showed central hemosiderin deposition. Fine needle aspiration did not lead to a diagnosis and an open biopsy had to be performed. Management consisted of tumor resection and reconstruction with a free vascularized costochondral graft. Tenosynovial diffuse type giant cell tumor of the temporomandibular joint is very rare. Complete resection leads to a low recurrence rate and reconstruction with a costochondral free vascularized flap leads to an excellent functional outcome.

摘要

本文旨在描述一例罕见的原发性下颌髁突弥漫型腱鞘巨细胞瘤,其主要呈骨内生长,并通过带血管肋软骨移植进行切除和功能重建。临床表现为右侧髁突区肿胀及张口受限,影像学检查显示中央骨质破坏,磁共振成像显示中央含铁血黄素沉积。细针穿刺抽吸未能明确诊断,故需进行切开活检。治疗包括肿瘤切除及带血管游离肋软骨移植重建。颞下颌关节弥漫型腱鞘巨细胞瘤非常罕见。完整切除可降低复发率,带血管肋软骨瓣重建可获得良好的功能效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d300/4330020/0cfcad108a64/jocmr-07-262-g001.jpg

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