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原发性未分化心脏肉瘤的罕见病例的处理方法。

Maneuvering the Management of a Rare Case of Primary Undifferentiated Cardiac Sarcoma.

机构信息

Division of Cancer Medicine, Hematology-Oncology Fellowship Program, University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Diagnostic Radiology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Am J Case Rep. 2020 Mar 21;21:e918878. doi: 10.12659/AJCR.918878.

Abstract

BACKGROUND Primary cardiac tumors are rare and mostly benign. Cardiac sarcomas are the most common malignant neoplasms of the heart and harbor a dismal prognosis of 6 to 12 months. The diagnosis of cardiac sarcomas may be challenging. Treatment entails surgical resection despite the high rate of recurrence, as well as adjuvant chemotherapy. CASE REPORT In this report, we discuss a case of a 58-year-old male with undifferentiated pleomorphic primary cardiac sarcomas who received multiple lines of treatment that included surgery, chemotherapy, and targeted therapy and was alive more than 4 years after his diagnosis. Herein, we discuss the different treatment regimens utilized and we present detailed imaging of his case findings at different treatment stages. CONCLUSIONS Treatment of undifferentiated pleomorphic cardiac sarcoma requires a multidisciplinary approach. Surgery and adjuvant treatment are commonly utilized, while neoadjuvant treatment is under investigation.

摘要

背景

原发性心脏肿瘤较为罕见,且多为良性。心脏肉瘤是心脏最常见的恶性肿瘤,预后极差,6 至 12 个月内死亡率为 100%。心脏肉瘤的诊断具有挑战性。尽管复发率很高,但仍需进行手术切除,以及辅助化疗。

病例报告

本报告讨论了一例 58 岁男性患有未分化多形性原发性心脏肉瘤,他接受了多种治疗方法,包括手术、化疗和靶向治疗,在诊断后 4 年多仍存活。在此,我们讨论了所使用的不同治疗方案,并展示了他在不同治疗阶段的详细影像学检查结果。

结论

未分化多形性心脏肉瘤的治疗需要多学科方法。手术和辅助治疗是常用的方法,而新辅助治疗正在研究中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8014/7117855/e5cee1a66518/amjcaserep-21-e918878-g001.jpg

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