首页> 外文期刊>Acta Radiologica >Imaging of rare appendicular non-acral soft-tissue chondromas in adults with histopathologic correlation
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Imaging of rare appendicular non-acral soft-tissue chondromas in adults with histopathologic correlation

机译:具有组织病理学相关性的成人稀有附奇非腺软组织软组织软组织乳腺癌的成像

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Background Soft-tissue chondroma (STC) is a rare benign soft tissue tumor that arises primarily in acral extra-skeletal locations. Occasionally, STCs may arise in more proximal non-acral locations, accompanied by non-classic features that label them as indeterminate lesions and pose diagnostic challenge for both radiologists and pathologists alike. Purpose To explicate the potential of diagnostic imaging in the identification and characterization of appendicular non-acral STCs with emphasis on their morphologic magnetic resonance imaging (MRI) enhancement. Material and Methods Our clinical database records were searched for patients with histologically proven primary soft-tissue chondroid lesions over a five-year period. Two musculoskeletal (MSK) trained radiologists evaluated the imaging studies and an MSK pathologist revised the pathological findings. Results The study included six cases of appendicular non-acral STCs (mean age?=?40.5 years). The mean size of the tumors was 5.6?cm, with four localized to the knee region, one in the thigh, and one in the sternoclavicular region. All cases showed high signal intensity matrix with low-signal intensity septa on T2-weighted MRI and post-contrast marginal/septal enhancement. The lesions were lobulated and lacked host tissue reaction except for one showing subjacent mild soft-tissue edema. Histologically, the cases lacked overt features of malignancy although one was originally misdiagnosed as chondrosarcoma. Conclusion Non-acral STCs are benign cartilaginous tumors that may pose a diagnostic challenge, both radiologically and pathologically. Collaborative imaging and pathologic workup is needed for better characterization of non-aggression of these lesions, and to avoid diagnostic pitfalls and unnecessary radical resections.
机译:背景技术软组织软组织软组织(STC)是一种稀有的良性软组织肿瘤,主要是轴上的超骨骼位置。偶尔,STC可能在更近端的非轴上出现,伴随着非经典特征,使它们标记为不确定的病变和辐射学家和病理学家的诊断挑战。目的突出诊断成像在鉴定和表征中具有强调其形态磁共振成像(MRI)增强的潜在诊断成像。材料和方法我们的临床数据库记录被搜查了在五年期间的组织学过验证的原发性软组织软组织软组织病变的患者。训练有素的放射科学家的两次肌肉骨骼(MSK)评估了成像研究和MSK病理学家修订了病理发现。结果该研究包括六例附奇非急性STC(平均年龄?= 40.5岁)。肿瘤的平均尺寸为5.6?cm,用四个局部化到膝关节区域,在大腿中,一个在胸椎管区域中的一个。所有病例均显示出高信号强度矩阵,具有低信号强度隔膜,T2加权MRI和对比度后边际/隔膜增强。除了显示亚平和轻度软组织水肿之外,病变被裂解并缺乏宿主组织反应。组织学上,这种情况缺乏恶性肿瘤的明显特征,尽管一个人最初被误诊为嗜胞菌。结论非锐利STC是良性软骨肿瘤,可在发光和病理学上进行诊断挑战。需要协作成像和病理处理,以便更好地表征这些病变的非侵略性,并避免诊断陷阱和不必要的根治切除。

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