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钙化性无定形肿瘤与显微镜下多血管炎——病例报告及文献系统综述

Calcified Amorphous Tumor and Granulomatosis with Polyangiitis-Case Report and Systematic Review of the Literature.

作者信息

Suleiman Mathieu N, Agaimy Abbas, Dewald Oliver, Kaemmerer-Suleiman Ann-Sophie, Mellert Fritz, Weyand Michael, Harig Frank

机构信息

Department of Cardiac Surgery, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg, 91054 Erlangen, Germany.

Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg, 91054 Erlangen, Germany.

出版信息

J Clin Med. 2024 Dec 27;14(1):84. doi: 10.3390/jcm14010084.

Abstract

Calcified amorphous tumor (CAT) is a rare, mostly incidental tumor-like cardiac lesion of unknown histogenesis. Current imaging modalities do not differentiate between CAT and other masses. As it can be a source for embolization, surgical excision of CAT is mandatory. CAT in patients with Granulomatosis with polyangiitis (GPA) is exceedingly rare. This systematic literature review was prompted by the case of a CAT in a patient with GPA. The search of all types of studies in two databases (PubMed and Scopus) was conducted through November 2024 to identify the relevant studies. Nine studies were included describing cases of patients being diagnosed with GPA and a cardiac mass. All included patients had a histopathological examination of the either biopsied or surgically resected mass. Only one case reported a CAT. In our case, the patient was diagnosed with GPA through a kidney biopsy, whereas a cardiac mass in the right atrium was diagnosed by echocardiography during evaluation for possible kidney transplantation. One year later a progression was observed, and the mass was resected. The histopathological examination revealed a CAT. The patient could be successfully discharged in a good clinical condition. This systematic literature search and case report highlight the importance of regular echocardiographic examination in patients with GPA. Moreover, surgical excision is crucial for the diagnosis and for further therapy planning, regardless of whether the mass is neoplastic or not.

摘要

钙化性无定形肿瘤(CAT)是一种罕见的、大多为偶然发现的肿瘤样心脏病变,其组织发生不明。目前的影像学检查方法无法区分CAT与其他肿块。由于它可能是栓塞的来源,因此必须对CAT进行手术切除。肉芽肿性多血管炎(GPA)患者中出现CAT极为罕见。本系统文献综述是由一名GPA患者出现CAT的病例引发的。截至2024年11月,在两个数据库(PubMed和Scopus)中检索了所有类型的研究,以确定相关研究。纳入了9项描述诊断为GPA并伴有心脏肿块的患者病例的研究。所有纳入患者均对活检或手术切除的肿块进行了组织病理学检查。只有1例报告为CAT。在我们的病例中,患者通过肾脏活检被诊断为GPA,而在评估可能的肾脏移植时,经超声心动图诊断右心房有一个心脏肿块。1年后观察到病情进展,遂将肿块切除。组织病理学检查显示为CAT。患者最终得以成功出院,临床状况良好。本系统文献检索和病例报告强调了对GPA患者进行定期超声心动图检查的重要性。此外,无论肿块是否为肿瘤性,手术切除对于诊断和进一步的治疗规划都至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32c4/11722031/fe6cc2c94bfd/jcm-14-00084-g001.jpg

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