Suppr超能文献

一名患有原发性心脏内膜肉瘤的年轻患者的挑战性治疗方法:病例报告

The challenging approach of a young patient with a primary intimal sarcoma of the heart: a case report.

作者信息

Martinho Mariana, Machado Bárbara, Cruz Inês, Fernandes Isabel, Pereira Hélder

机构信息

Serviço de Cardiologia, Hospital Garcia de Orta, Avenida Torrado da Silva, Almada 2805-267, Portugal.

Serviço de Oncologia Médica, Centro Hospitalar Entre-Douro e Vouga, Santa Maria da Feira, Portugal.

出版信息

Eur Heart J Case Rep. 2024 Feb 5;8(2):ytae071. doi: 10.1093/ehjcr/ytae071. eCollection 2024 Feb.

Abstract

BACKGROUND

Primary intimal sarcomas of the heart are extremely rare and have a dismal prognosis. Their management represents a complex clinical challenge since complete surgical resection is the only reliable possibility of cure but is only possible in 50% of patients. In non-resectable disease, anthracycline-based therapy is the most effective treatment, but pazopanib may be used in patients unfit to receive anthracyclines.

CASE SUMMARY

A 38-year-old man presented with acute right heart failure symptoms due to a primary intimal sarcoma of the heart. A definite diagnosis was made after cardiac surgery. Multi-modality cardiac imaging showed early recurrence of disease with mitral valve and pulmonary veins' invasion, and the patient was deemed inoperable. Due to chronic kidney disease and previous heart failure symptoms, he was started on first-line pazopanib palliative treatment. After 11 months of chemotherapy, there was good clinical tolerance and no evidence of disease progression, which occurred after 13 months.

DISCUSSION

This case highlights the value of a multi-modality imaging approach for cardiac masses. Most importantly, it reports the successful treatment of a young patient with a primary intimal sarcoma of the heart who was started on palliative pazopanib, with a significantly higher progression-free survival than is reported in the literature. This finding may support pazopanib as a good alternative as first-line treatment when there is contraindication for anthracycline-based chemotherapy.

摘要

背景

原发性心脏内膜肉瘤极为罕见,预后不良。其治疗是一项复杂的临床挑战,因为完整手术切除是唯一可靠的治愈方法,但仅50%的患者可行。对于不可切除的疾病,基于蒽环类药物的治疗是最有效的治疗方法,但帕唑帕尼可用于不适于接受蒽环类药物治疗的患者。

病例摘要

一名38岁男性因原发性心脏内膜肉瘤出现急性右心衰竭症状。心脏手术后确诊。多模态心脏成像显示疾病早期复发并侵犯二尖瓣和肺静脉,该患者被认为无法手术。由于慢性肾病和既往心力衰竭症状,他开始接受一线帕唑帕尼姑息治疗。化疗11个月后,临床耐受性良好,无疾病进展证据,疾病进展发生在13个月后。

讨论

本病例突出了心脏肿物多模态成像方法的价值。最重要的是,它报道了一名原发性心脏内膜肉瘤年轻患者接受帕唑帕尼姑息治疗取得成功,其无进展生存期明显高于文献报道。这一发现可能支持帕唑帕尼作为基于蒽环类化疗有禁忌时一线治疗的良好替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c14/10875919/c04414ba556c/ytae071il2.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验