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肺尤因肉瘤:1例罕见病例。

Ewing's sarcoma of the lung: A rare case.

作者信息

Ekin Selami, Çobanoğlu Ufuk, Göya Cemil, Erten Remzi, Yıldız Hanifi

机构信息

Department of Chest Diseases, Dursun Odabas Medical Center, Van Yuzuncu Yil University, Van Turkey.

Department of Thoracic Surgery, Health Research and Pratice Hospital, Van Yuzuncu Yil University, Van, Turkey.

出版信息

Tuberk Toraks. 2019 Jun;67(2):146-148. doi: 10.5578/tt.68241.

Abstract

The Ewing's sarcoma family of tumors (ESFT) incorporates both the wellrecognized primary bone and the extraskeletal soft tissue sarcomas. Primitive neuroectodermal tumors (PNET) and ESFT have a similar neural phenotype and can be considered in the same entity. Here, we will present 28 years old patient with Ewing Sarcoma. Patient was admited chest pain. Chest radiograph showed a suspicious lesion in the left paracardiac area. Computed tomography (CT) scan and positron emission tomography (PET)/CT result were compatible with malignant tumor. The patient was underwent surgical resection as the bronchoscopic result couldn't a malignant finding and pathological finding was detected as Ewing's sarcoma. Ewing's sarcoma should be considered in patients who are very fast growing in the lungs, are properly confined and suspected of malignancy in FDG-PET/CT.

摘要

尤因肉瘤家族性肿瘤(ESFT)包括公认的原发性骨肿瘤和骨外软组织肉瘤。原始神经外胚层肿瘤(PNET)和ESFT具有相似的神经表型,可被视为同一实体。在此,我们将介绍一名28岁的尤因肉瘤患者。患者因胸痛入院。胸部X线片显示左心旁区有可疑病变。计算机断层扫描(CT)和正电子发射断层扫描(PET)/CT结果与恶性肿瘤相符。由于支气管镜检查结果未发现恶性病变,且病理检查结果为尤因肉瘤,因此患者接受了手术切除。对于肺部生长迅速、病变局限且在FDG-PET/CT中怀疑为恶性的患者,应考虑尤因肉瘤。

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