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Undifferentiated embryonal sarcoma of the liver in an adult: Case report and literature review

机译:未分化的成年人肝脏胚胎肉瘤:案例报告和文献综述

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Undifferentiated embryonal sarcoma of the liver often presents in the childhood. Its occurrence rate in adults is extremely low. A 70-year-old woman suffered from right upper quadrant abdominal pain, fever, and body weight loss of 10 kg over half a year. Abdominal ultrasonography and computed tomography revealed one 9-cm tumor with a cystic component at S6/S7 of the liver. The tumor markers, such as serum alpha-fetoprotein, carcinoembryonic antigen, and carbohydrate antigen 19-9, were in the normal range. Repeated biopsies showed no malignancy. After exclusion of infectious diseases through an inflammation scan, she underwent S6/7 bisegmen-tectomy. The final report of pathology was undifferentiated embryonal sarcoma. No evidence of recurrence or metastases was noted dining follow-up visits. The rate of misdiagnosis before operation is high. The enhancing of radiological feature-reading skills and clinical awareness are considered to be necessary to reduce misdiagnosis. The prognosis was considered to be poor before. Multimodal treatment with complete surgical excision and chemotherapy provided the best chance of long-term disease-free survival. We concluded that undifferentiated embryonal sarcoma should be included in the differential diagnostic list of malignant liver tumors in adults.
机译:肝脏的未分化胚胎肉瘤通常存在于儿童时期。其成人的发生率极低。一名70岁的女性患有右上象限腹痛,发热,体重减轻10公斤半年。腹部超声和计算机断层扫描揭示了肝脏S6 / S7的囊性组分的一个9厘米肿瘤。肿瘤标志物,例如血清α-胎蛋白,癌胚抗原和碳水化合物抗原19-9位于正常范围内。反复的活组织检查显示没有恶性肿瘤。通过炎症扫描排除传染病后,她经历了S6 / 7 Bisegmen-Tectomy。病理学的最终报告是未分化的胚胎肉瘤。没有注意到在随访的后续访问中没有复发或转移的证据。操作前误诊率高。考虑提高放射性特征阅读技能和临床意识,以减少误诊。预后被认为是穷人。用完全手术切除和化疗的多式联算治疗提供了长期无病生存的最佳机会。我们得出结论,未分化的胚胎肉瘤应包括在成人中恶性肝肿瘤的差异诊断列表中。

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