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原发性肺尤文肉瘤:年轻女孩大量血胸的罕见病因——病例报告。

Primary pulmonary Ewing's sarcoma: rare cause of massive hemothorax in a young girl-case report.

机构信息

Respiratory Medicine Department, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.

Pathology Department, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.

出版信息

BMC Pediatr. 2021 Apr 22;21(1):194. doi: 10.1186/s12887-021-02672-6.

Abstract

BACKGROUND

Ewing's sarcoma is a common malignant bone tumor in children and young adults. Rarely, extra-skeletal soft tissues and visceral organs can also be the site of origin of Ewing's sarcoma. Primary pulmonary Ewing's sarcoma is an extremely rare malignancy.

CASE PRESENTATION

We report an unusual case of primary pulmonary Ewing's sarcoma in a 15-year-old girl who initially presented with massive hemothorax. By histopathology evaluation of surgical biopsy specimens, the diagnosis of extraosseous Ewing's sarcoma was confirmed by both light microscopy and immunohistochemistry. Emergency, open surgery was performed by thoracic surgery at an early stage. After 3 cycles of chemotherapy, the patient was found to be stable at follow-up examination. No more hydrothorax or other symptoms.

CONCLUSIONS

We have described an extremely rare case of primary pulmonary Ewing's sarcoma with massive hemothorax. The patient underwent surgical resection and postoperative chemotherapy, no sign of recurrence to date as an outcome.

摘要

背景

尤因肉瘤是儿童和青少年常见的恶性骨肿瘤。罕见情况下,骨骼外的软组织和内脏器官也可能是尤因肉瘤的起源部位。原发性肺尤因肉瘤是一种极其罕见的恶性肿瘤。

病例介绍

我们报告了一例 15 岁女孩的原发性肺尤因肉瘤的不寻常病例,该患者最初表现为大量血胸。通过手术活检标本的组织病理学评估,光镜和免疫组织化学均证实为骨外尤因肉瘤的诊断。胸外科在早期进行了紧急开放性手术。3 个化疗周期后,在随访检查中发现患者病情稳定。无胸水或其他症状。

结论

我们描述了一例极为罕见的原发性肺尤因肉瘤伴大量血胸的病例。该患者接受了手术切除和术后化疗,目前尚无复发迹象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d337/8061173/23927963f5ad/12887_2021_2672_Fig1_HTML.jpg

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