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一名5岁儿童的下颌肿胀——下颌肌纤维瘤

Mandibular swelling in a 5-year-old child--mandibular myofibroma.

作者信息

Rai Birendra, Ludusan Evodia, McGovern Brianán, Sharif Farhana

机构信息

Department of Pediatrics, Midland Regional Hospital, Westmeath, Ireland.

Department of Histopathology, Our Lady's Children's Hospital, Dublin, Ireland.

出版信息

BMJ Case Rep. 2014 Sep 1;2014:bcr2014203977. doi: 10.1136/bcr-2014-203977.

Abstract

A 5-year-old girl of African descent presented with a history of progressive painless swelling on the right side of the jaw since the past 2-3 months. Orthopantomogram showed a radiolucent lesion near the angle of the mandible. Subsequent CT scan revealed a 2 cm×2 cm radiolucent lesion with intense periosteal reaction surrounding the lesion and destruction of the overlying cortex. Radiological perplexity aroused regarding the possibility of eosinophilic granuloma or some other malignant lesion. Incisional biopsy performed and microscopy showed spindle cell tumor. Immunohistochemistry confirmed it as myofibroma. Myofibroma is a rare benign tumour involving mesenchyme. Involvement of the mandible is rare. Radiological presentation with strong periosteal reaction is a rarity and has rarely been reported in the medical literature. We conclude that intraosseous myofibroma can sometimes have strong periosteal reaction and careful radiological evaluation is a prerequisite for accurate diagnosis and to avoid unnecessary aggressive therapy.

摘要

一名5岁非洲裔女孩,在过去2至3个月里,右侧颌部出现进行性无痛肿胀。全景曲面断层片显示下颌角附近有一透光性病变。随后的CT扫描显示一个2厘米×2厘米的透光性病变,病变周围有强烈的骨膜反应,覆盖其上的皮质有破坏。对于嗜酸性肉芽肿或其他一些恶性病变的可能性,引发了放射学上的困惑。进行了切开活检,显微镜检查显示为梭形细胞瘤。免疫组织化学证实为肌纤维瘤。肌纤维瘤是一种罕见的涉及间充质的良性肿瘤。下颌骨受累罕见。伴有强烈骨膜反应的放射学表现很罕见,医学文献中鲜有报道。我们得出结论,骨内肌纤维瘤有时可伴有强烈骨膜反应,仔细的放射学评估是准确诊断和避免不必要的积极治疗的先决条件。

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