心脏单发纤维瘤--一种极其罕见但可能致命的诊断。

IF 0.6 Q4 SURGERY

Kardiochirurgia I Torakochirurgia Polska Pub Date : 2024-03-01 Epub Date: 2024-03-30 DOI:10.5114/kitp.2024.138574

Mateusz Szot, Aleksandra Zub, Paweł Kurzawa, Magdalena Janus, Ewa Goszczyńska, Marek Jemielity, Bartłomiej Perek

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引用次数: 0

摘要

这篇综述的背景是描述一名 28 岁男性的病例，他患有极其罕见的心脏单发纤维瘤（SFT）。虽然该肿瘤已被手术切除，且在 6 个月的随访检查中未发现复发，但 4 个月后的磁共振成像检查发现并证实该肿瘤复发。本文对 SFT 的发病率、症状和体征、治疗方案和预后进行了综述。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Cardiac solitary fibrous tumor - an extremely rare but potentially fatal diagnosis.

The background of this review is a description of the case of a 28-year-old man with an extremely rare cardiac solitary fibrous tumor (SFT). Although this tumor was removed surgically and in the 6-month follow-up examination no relapse was noted, recurrence was observed and confirmed in the magnetic resonance imaging 4 months later. SFT prevalence, symptoms and signs, treatment options and prognosis are reviewed.

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来源期刊

Kardiochirurgia I Torakochirurgia Polska 医学-外科

CiteScore

0.90

自引率

14.30%

发文量

审稿时长

6-12 weeks

期刊介绍： Polish Journal of Thoracic and Cardiovascular Surgery is a quarterly aimed at cardiologists, cardiosurgeons and thoracic surgeons. Includes the original works (experimental, research and development), illustrative and casuistical works about cardiology and cardiosurgery.