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Analysis of imaging characteristics of primary malignant bone tumors in children

机译:儿童原发性恶性骨肿瘤的影像学特征分析

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摘要

The present study aimed to investigate the imaging characteristics of primary malignant bone tumors in children. The imaging results of 34 children with primary malignant bone tumors confirmed by histopathological diagnosis between March 2008 and January 2014 were retrospectively analyzed. In total, 25 patients had osteosarcoma, with radiography and computed tomography (CT) showing osteolytic bone destruction or/and osteoblastic bone sclerosis, an aggressive periosteal reaction, a soft-tissue mass and cancerous bone. The tumors appeared as mixed magnetic resonance imaging (MRI) signals that were inhomogeneously enhanced. A total of 5 patients presented with Ewing sarcoma, with radiography and CT showing invasive bone destruction and a soft-tissue mass. Of the 5 cases, 2 showed a laminar periosteal reaction. The tumors were shown to have mixed low signal on T1-weighted images (T1WI) and high signal on T2-weighted images (T2WI); 1 case showed marked inhomogeneous enhancement. Another 3 patients exhibited chondrosarcoma. Of these cases, 1 was adjacent to the cortex of the proximal tibia, and presented with local cortical bone destruction and a soft-tissue mass containing scattered punctate and amorphous calcifications. MRI revealed mixed low T1 signal and high T2 signals. Another case was located in the medullary cavity of the distal femur, with radiography revealing a localized periosteal reaction. The tumor appeared with mixed MRI signals, and with involvement of the epiphysis and epiphyseal plates. Radiography and CT of the third case showed bone destruction in the right pubic ramus, with patchy punctate, cambered calcifications in the soft-tissue mass. MRI of the soft-tissue mass revealed isointensity on T1WI and heterogeneous hyperintensity on T2WI. Ossifications and the septum appeared as low T1WI and T2WI. Of the 34 patients, 1 patient presented with lymphoma involving the T12, L1 and L2 vertebrae. CT showed vertebral bone destruction, a soft-tissue mass and a compression fracture of L1. MRI showed a soft-tissue mass with low T1 signal and high T2 signal and marked inhomogeneous enhancement. Overall, osteosarcoma was the most common primary malignant bone tumor, followed by Ewing sarcoma, chondrosarcoma and lymphoma. Osteoblastic or osteolytic bone destruction, an invasive periosteal reaction, soft-tissue masses, a tumor matrix and inhomogeneous enhancement were important imaging features of malignant bone tumors.
机译:本研究旨在调查儿童原发性恶性骨肿瘤的影像学特征。回顾性分析2008年3月至2014年1月经病理组织学确诊的34例原发性恶性骨肿瘤患儿的影像学结果。共有25例骨肉瘤患者,放射线照相和计算机断层扫描(CT)显示溶骨性破坏或/和成骨性骨硬化,侵袭性骨膜反应,软组织肿块和癌骨。肿瘤表现为不均匀增强的混合磁共振成像(MRI)信号。共有5例表现为尤因肉瘤的患者,放射线照相和CT扫描显示侵入性骨破坏和软组织肿块。在5例中,有2例显示出层状骨膜反应。肿瘤在T1加权图像(T1WI)上混合了低信号,在T2加权图像(T2WI)上混合了高信号。 1例表现出明显的不均匀增强。另外3例表现为软骨肉瘤。在这些病例中,有1例邻近胫骨近端皮质,并表现为局部皮质骨破坏和软组织肿块,其中包括散乱的点状和无定形钙化。 MRI显示混合的低T1信号和高T2信号。另一例位于股骨远端的髓腔内,X线片显示局部骨膜反应。肿瘤表现为混合的MRI信号,并累及骨physi和骨phy板。第三例的X线摄片和CT检查显示右耻骨支有骨破坏,软组织肿块中有斑点状点状,弯曲的钙化。 MRI的软组织肿块显示T1WI上的等强度和T2WI上的异质性高强度。骨化和中隔表现为低T1WI和T2WI。在这34例患者中,有1例患者出现了涉及T12,L1和L2椎骨的淋巴瘤。 CT显示椎骨破坏,软组织肿块和L1压缩性骨折。 MRI显示软组织肿块,T1信号低,T2信号高,增强明显不均匀。总体而言,骨肉瘤是最常见的原发性恶性骨肿瘤,其次是尤因肉瘤,软骨肉瘤和淋巴瘤。成骨细胞或溶骨性骨破坏,侵入性骨膜反应,软组织肿块,肿瘤基质和不均匀增强是恶性骨肿瘤的重要影像学特征。

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