Neuritis ossificans mimicking a malignancy in a child: case report and literature review.

IF 1.9 3区 医学 Q2 ORTHOPEDICS
Skeletal Radiology Pub Date : 2025-05-01 Epub Date: 2024-07-26 DOI:10.1007/s00256-024-04759-4
Valerie Weyns, Erik Seghers, Kristof Kempeneers, Jan Vandevenne, Eveleen Buelens, Koen Peers, Frank Weyns
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Abstract

We present the case of a child with neuritis ossificans after acute trauma, treated conservatively. The aim of the review is to compare several parameters in this disease. Emphasis is placed on the clinical-radiological features distinguishing neuritis ossificans from malignancy to avoid unnecessary biopsy and surgery.A literature review was performed. Only 18 cases were described. Except for one, all describe adults, and none had acute trauma. Nearly all were treated surgically.Our 13-year-old patient presented with posterior knee pain after trauma. MRI demonstrated a mass within the tibial nerve with oedema, some lymph nodes and increased avidity on 18fluoro-2-deoxyglucose-positron emission tomography. These findings can be reactive but also associated with malignancy. However, eggshell-like calcifications in the periphery of the mass were seen on CT. Biopsy and resection were proposed. Follow-up visits over the next weeks showed remarkable clinical improvement. Wait-and-scan was advised after international discussion. Follow-up imaging after 2 months showed resolution of the oedema and volume reduction of the mass, suggesting a benign pathology. Diagnosis of neuritis ossificans was proposed based on the clinical and radiological features. There was a favorable course with no complaints after two months. Imaging after seven months showed an almost complete regression.Neuritis ossificans should be considered within a painfull (mono)neuropathy. The initial inflammatory phase may mimic malignancy, misleading clinicians toward biopsy or surgery with the risk of nerve damage. As seen in our case, neuritis ossificans can be a self-limiting process. Therefore, conservative therapy should be considered with a wait-and-scan approach.

Abstract Image

模仿恶性肿瘤的儿童骨化性神经炎:病例报告和文献综述。
我们介绍了一例急性创伤后神经骨化性神经炎患儿的病例,该患儿接受了保守治疗。回顾性分析的目的是比较该疾病的几个参数。重点是区分骨化性神经炎和恶性肿瘤的临床放射学特征,以避免不必要的活检和手术。文献中仅描述了 18 个病例。除一例外,其他病例均为成人,且均无急性外伤。我们的患者 13 岁,外伤后出现膝关节后部疼痛。核磁共振成像显示胫神经内有肿块,伴有水肿、一些淋巴结和18氟-2-脱氧葡萄糖-正电子发射断层扫描的嗜性增高。这些结果可能是反应性的,但也可能与恶性肿瘤有关。然而,CT 显示肿块外围有蛋壳样钙化。建议进行活检和切除。接下来几周的随访显示临床症状明显好转。经国际讨论后,建议等待并扫描。2 个月后的随访造影显示水肿消退,肿块体积缩小,表明这是一种良性病变。根据临床和放射学特征,建议诊断为骨化性神经炎。两个月后,患者病情好转,没有任何不适。七个月后的影像学检查显示,该病几乎完全消退。最初的炎症期可能与恶性肿瘤相似,会误导临床医生进行活检或手术,从而有可能造成神经损伤。在我们的病例中,骨化性神经炎可能是一种自限性过程。因此,应考虑采取保守疗法,等待时机。
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来源期刊
Skeletal Radiology
Skeletal Radiology 医学-核医学
CiteScore
4.40
自引率
9.50%
发文量
253
审稿时长
3-8 weeks
期刊介绍: Skeletal Radiology provides a forum for the dissemination of current knowledge and information dealing with disorders of the musculoskeletal system including the spine. While emphasizing the radiological aspects of the many varied skeletal abnormalities, the journal also adopts an interdisciplinary approach, reflecting the membership of the International Skeletal Society. Thus, the anatomical, pathological, physiological, clinical, metabolic and epidemiological aspects of the many entities affecting the skeleton receive appropriate consideration. This is the Journal of the International Skeletal Society and the Official Journal of the Society of Skeletal Radiology and the Australasian Musculoskelelal Imaging Group.
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