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一例罕见的蝶骨沙砾样骨化纤维瘤采用自体颗粒置换颅骨成形术进行重建。

A rare case of psammomatoid ossifying fibroma in the sphenoid bone reconstructed using autologous particulate exchange cranioplasty.

作者信息

Kasliwal Manish K, Rogers Gary F, Ramkissoon Shakti, Moses-Gardner Alexander, Kurek Kyle C, Smith Edward R

机构信息

Department of Neurosurgery, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Neurosurg Pediatr. 2011 Mar;7(3):238-43. doi: 10.3171/2010.12.PEDS10191.

Abstract

Psammomatoid ossifying fibroma (POF), a variant of ossifying fibroma, is a benign fibroosseous lesion typically arising within the nasal cavity, paranasal sinuses, and orbit. Cranial vault involvement is exceedingly rare, with very few cases reported in the literature. The authors report a case of POF in the neurocranium of an 11-year-old child, 4 years after chemotherapy and radiation therapy for acute lymphoblastic leukemia. This case is reported in view of its rarity, novelty of presentation, and the difficulty in diagnosis due to its radiological resemblance to aneurysmal bone cyst or monostotic cystic fibrous dysplasia, further aggravated by the clinical scenario. A novel technique of cranial reconstruction called autologous particulate exchange cranioplasty was used following tumor excision.

摘要

砂粒样骨化性纤维瘤(POF)是骨化性纤维瘤的一种变异型,是一种良性纤维骨性病变,通常发生于鼻腔、鼻窦和眼眶。累及颅顶极为罕见,文献报道的病例极少。作者报告了一例11岁儿童神经颅骨的POF病例,该患儿在接受急性淋巴细胞白血病化疗和放疗4年后发病。鉴于该病例的罕见性、表现的新颖性以及由于其影像学表现与动脉瘤样骨囊肿或单发性囊性纤维性骨发育不良相似而导致的诊断困难,再加上临床情况的复杂性,故予以报道。肿瘤切除后采用了一种名为自体颗粒置换颅骨成形术的新型颅骨重建技术。

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