儿童胸骨假瘤的声像图特征

Q3 Medicine
Samantha Gerrie, Mike Watson, Phil Morreau
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引用次数: 0

摘要

胸骨假瘤是一种重要但罕见的病变,被认为是一种可模拟肿瘤的炎性、非肿瘤性病变。本文旨在说明这种病变的影像学特征,以避免不必要的检查。本文回顾了2016年2月至2019年7月期间诊断为胸骨假瘤的四名患者的临床笔记和影像学特征。患者发病时的中位年龄为12.5个月。发病前症状持续时间的中位数为 3.5 天。一名患者的C反应蛋白轻度升高。胸片显示胸骨前软组织肿块,伴有或不伴有胸骨下骨质破坏。超声波检查显示胸骨前软组织肿块呈异质、低回声,内部血管多变,在胸骨骨化中心之间延伸。CT和MRI显示,病变呈增强的哑铃状,有胸骨前和胸骨后软组织成分。完全缓解的中位时间为 3 个月。一名患者进行了活组织检查,结果显示存在慢性炎症和纤维化。这些病变通常发生在幼儿身上,病史为1至2周,胸骨上出现2至4厘米的局灶性肿胀。病因不明,但可能是一种尚未确定的病原体。炎症标志物和培养物正常或轻度升高。重要的鉴别考虑因素包括胸骨骨髓炎或肿瘤性病因,如尤文肉瘤、横纹肌肉瘤、朗格汉斯细胞组织细胞增生症和婴儿纤维肉瘤。我们的建议是,这是一种 "不可触碰 "的病变,需要在外科门诊进行密切的短期随访,并进行超声检查,直至病变消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sonographic features of sternal pseudotumour in children

Introduction

Sternal pseudotumour is an important but rare entity thought to be an inflammatory, non-neoplastic lesion that can mimic tumours. The purpose of this paper was to illustrate the imaging features of this lesion to avoid unnecessary investigations.

Methods

The clinical notes and imaging features of four patients with a diagnosis of sternal pseudotumour were reviewed over a period from February 2016 to July 2019.

Results

All patients were afebrile with no history of trauma. The median age at presentation was 12.5 months. The median length of symptoms prior to presentation was 3.5 days. One patient had a mildly elevated C-reactive protein. Chest radiographs showed a pre-sternal soft-tissue mass, with or without osseous destruction of the subjacent sternum. Ultrasound showed a heterogeneous, hypoechoic pre-sternal soft-tissue mass with variable internal vascularity with extension between sternal ossification centres. CT and MRI showed an enhancing dumbbell-shaped lesion with a pre-sternal and retro-sternal soft-tissue component. The median time to complete resolution was 3 months. One patient had a biopsy that showed chronic inflammation and fibrosis.

Discussion

These lesions present in young children typically with a 1- to 2-week history of a focal 2- to 4-cm swelling over the sternum. The aetiology is unknown but may be on the basis of a yet-to-be identified pathogen. Inflammatory markers and cultures are normal or mildly elevated. Important differential considerations include sternal osteomyelitis or neoplastic causes such as Ewing sarcoma, rhabdomyosarcoma, Langerhans cell histiocytosis and infantile fibrosarcoma.

Conclusion

Sternal pseudotumor is a rare but important entity to be aware of to avoid unnecessary invasive biopsy or further investigations. Our suggestion is that this is a ‘Don't touch’ lesion that requires close short-interval follow-up at a surgical outpatient clinic and with ultrasound until resolution.

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来源期刊
Australasian Journal of Ultrasound in Medicine
Australasian Journal of Ultrasound in Medicine Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.90
自引率
0.00%
发文量
40
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