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颅骨底部巨大动脉瘤样骨囊肿采用地舒单抗治疗。

Massive aneurysmal bone cyst of the skull base treated with denosumab.

机构信息

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

Head Neck. 2018 Dec;40(12):E107-E113. doi: 10.1002/hed.25438. Epub 2018 Nov 26.

Abstract

BACKGROUND

Aneurysmal bone cysts are rare, benign expansile tumors most commonly involving long bones and vertebrae in patients younger than age 20. Skull base involvement is rare. Aneurysmal bone cysts shares radiological and histological features with other bone tumors, posing a diagnostic challenge.

METHODS/RESULTS: We report the case of a 32-year-old man who presented with facial pain, epistaxis, and cranial neuropathies secondary to a massive tumor of the maxillary sinus and anterior skull base. The tumor was originally misdiagnosed as osteosarcoma. However, genomic analysis revealed a rearrangement in the USP6 gene, elucidating a diagnosis of primary aneurysmal bone cysts. The patient was treated with denosumab. Within 5 months, the patient was asymptomatic with CT showing ossification of the tumor.

CONCLUSIONS

This case highlights (1) the utility of genomic analysis in aggressive bone tumors when the diagnosis is unclear and (2) the effectiveness of denosumab as a treatment for aneurysmal bone cysts when surgical resection is unfavorable.

摘要

背景

动脉瘤样骨囊肿是一种罕见的良性膨胀性肿瘤,最常发生于 20 岁以下的长骨和椎体。颅底受累较为罕见。动脉瘤样骨囊肿在影像学和组织学上与其他骨肿瘤具有相似特征,因此诊断具有一定挑战性。

方法/结果:我们报告了 1 例 32 岁男性病例,其因上颌窦和前颅底的巨大肿瘤导致面部疼痛、鼻出血和颅神经病变。该肿瘤最初被误诊为骨肉瘤。然而,基因组分析显示 USP6 基因发生重排,明确诊断为原发性动脉瘤样骨囊肿。患者接受地舒单抗治疗。在 5 个月内,患者无症状,CT 显示肿瘤骨化。

结论

该病例强调了(1)当诊断不明确时,基因组分析在侵袭性骨肿瘤中的应用价值,以及(2)当手术切除不利时,地舒单抗作为动脉瘤样骨囊肿治疗方法的有效性。

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