揭示未知:心脏未分化多形性肉瘤1例报告。

IF 2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Clinical Medicine Insights. Cardiology Pub Date : 2026-09-07 eCollection Date: 2026-01-01 DOI:10.1177/11795468251408695
Dina Fa Alwaheidi, Mohd Lateef Wani, Ashfaq Patel
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引用次数: 0

摘要

心脏未分化多形性肉瘤是一种非常罕见且侵袭性很强的肿瘤。我们提出的情况下,66岁的男性与历史的I期前列腺腺泡腺癌谁是偶然发现有左心房肿块在癌症检查。多模态影像(超声心动图、CMR、PET-CT)初步提示为良性病变。患者行手术切除肿块,经组织病理学和免疫组织化学证实为UPS。术后,患者出现右侧心力衰竭,复发性皮肤溃疡需要移植,心房心律失常。尽管有并发症,他的病情稳定下来,并开始化疗和肿瘤随访。本病例强调了心脏UPS的诊断缺陷,组织确认的必要性,以及协调多学科护理的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling the Unknown: A Case Report of Undifferentiated Pleomorphic Sarcoma in the Heart.

Undifferentiated pleomorphic sarcoma (UPS) of the heart is an exceedingly rare and highly aggressive tumor. We present the case of a 66-year-old male with a history of stage I prostatic acinar adenocarcinoma who was incidentally found to have a left atrial mass during cancer workup. Multimodal imaging (echocardiography, CMR, PET-CT) initially suggested a benign lesion. The patient underwent surgical excision of the mass, which revealed UPS confirmed by histopathology and immunohistochemistry. Postoperatively, the patient experienced right-sided heart failure, recurrent skin ulcers requiring grafting, and atrial arrhythmia. Despite complications, he stabilized and started chemotherapy and oncologic follow-up. This case highlights the diagnostic pitfalls of cardiac UPS, the necessity for tissue confirmation, and the role of coordinated multidisciplinary care.

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来源期刊
Clinical Medicine Insights. Cardiology
Clinical Medicine Insights. Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
5.20
自引率
3.30%
发文量
16
审稿时长
8 weeks
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