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Nonmyxoid mediastinal lipoblastoma in a 2-year-old girl: Case report with US CT and MRI findings

机译:2岁女孩的非粘液性纵隔脂肪母细胞瘤:USCT和MRI表现的病例报告

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摘要

Lipoblastomas are rare, benign tumors of mesenchymal origin that contain adipose tissue. They usually develop in the soft tissues of an extremity in infants, children, and young adolescents. We report the case of a 22-month old girl referred to our staff for swelling in the supraclavicular fossa, which was observed when the child cried. The ulstrasonographic examination revealed a mass in the anterosuperior portion of the mediastinum that extended into the right supraclacular fossa. The lesion was weakly hyperechoic with clear-cut margins and did not appear to invade surrounding tissues. On CT, it appeared inhomogeneously hypodense with denitometric characteristics of adipose tissue. On MRI, it was hyperintense on both T1- and T2-weighted sequences and reduced signal intensity in FAT SAT sequences. In light of the imaging features and predominant adipose tissue component, the mass was diagnosed as a mediastinal lipoblastoma, and this diagnosis was confirmed by surgical histology.
机译:脂肪母细胞瘤是间质起源的罕见良性肿瘤,其中含有脂肪组织。它们通常在婴儿,儿童和青少年的四肢软组织中发育。我们报告了一例22个月大的女孩因锁骨锁骨上窝肿胀而转诊给我们的工作人员的情况,该儿童在哭泣时被观察到。超声检查发现纵隔前上部分有肿块,延伸到右锁骨上窝。病变为弱回声,边缘清晰,似乎未侵及周围组织。在CT上,它表现出脂肪组织反硝化特征的不均匀低密度。在MRI上,它在T1和T2加权序列上都很强烈,并且在FAT SAT序列中信号强度降低。根据影像学特征和主要的脂肪组织成分,将该肿块诊断为纵隔脂肪母细胞瘤,并通过手术组织学证实了该诊断。

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