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Childhood undifferentiated embryonal liver sarcoma: clinical features and immunohistochemistry analysis.

机译:儿童未分化胚胎肝肉瘤:临床特征和免疫组化分析。

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摘要

PURPOSE: The aim of the study was to report on 3 cases of childhood undifferentiated embryonal liver sarcoma (UELS) and to highlight the clinical features, laboratory findings, diagnosis, and management of this rare disease. METHODS: The patients' age, sex, clinical features, laboratory findings, pathologic results, and therapy were reviewed. Immunohistochemistry analysis was performed on the resected mass sections. RESULTS: In this study, 2 cases were female (aged 8 and 12 years) and 1 was male (aged 9 years). The causes of hospitalization were mainly abdominal pain, mass, or fever. An elevated erythrocyte sedimentation rate was noted in 2 available cases, and alpha fetoprotein (AFP) was within the normal range. Imaging findings indicated a well-defined heterogeneous large mass in the right lobe. Histopathologic evaluation of the mass confirmed the diagnosis of UELS. Immunohistochemical staining showed that vimentin and CD68 antigen were positive in all samples, whereas desmin was positive in one sample. Surgery with chemotherapy was performed in 2 cases. CONCLUSION: The diagnosis of UELS depends mainly on the pathologic findings. Undifferentiated embryonal liver sarcoma should be included in the differential diagnosis of mass in the liver, especially with well-defined heterogeneous imaging findings and normal AFP. Diagnosis and management should be made early as UELS is a potentially treatable tumor.
机译:目的:本研究的目的是报告3例儿童未分化的胚胎肝肉瘤(UELS),并强调该罕见病的临床特征,实验室检查结果,诊断和治疗。方法:回顾了患者的年龄,性别,临床特征,实验室检查结果,病理结果和治疗方法。对切​​除的肿块切片进行免疫组织化学分析。结果:本研究中,女性2例(8岁和12岁),男性1例(9岁)。住院的原因主要是腹痛,肿块或发烧。在2例可用病例中发现了较高的红细胞沉降率,并且甲胎蛋白(AFP)处于正常范围内。影像学检查结果表明右叶有明确的异质大块。肿块的组织病理学评估证实了UELS的诊断。免疫组织化学染色显示波形蛋白和CD68抗原在所有样品中均为阳性,而结蛋白在一个样品中为阳性。 2例行化疗手术。结论:UELS的诊断主要取决于病理结果。未分化的胚胎肝肉瘤应包括在肝脏肿块的鉴别诊断中,尤其是具有明确的异质成像表现和正常AFP的患者。由于UELS是一种可能可治疗的肿瘤,因此应及早进行诊断和处理。

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