Pleuropulmonary blastoma (PPB) with central nervous system metastasis: case report, imaging findings, and review of literature.

IF 0.6 4区 医学 Q4 SURGERY
Acta Chirurgica Belgica Pub Date : 2024-12-01 Epub Date: 2024-06-18 DOI:10.1080/00015458.2024.2365503
Dusan J Petrovic, Polina Pavicevic
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引用次数: 0

Abstract

Pleuropulmonary blastoma (PPB) is a very rare tumor of the chest seen predominantly in young children with great heterogeneity and clinical, biochemical, and biological complexity and recognized, described, and classified as distinct from the pulmonary blastoma typically encountered in adults. Unfortunately, it has a poor and dismal prognosis and is mainly classified as cystic (type 1), mixed type (type 2), and solid (type 3). Herein, we present one case of PPB type 2 presenting clinically with a right pulmonary abscess, a rare clinical presentation of PPB, which was initially treated with surgery, and after approximately 1 year of follow-up, pulmonary rest-recurrence and central nervous system secondary deposits were detected. When a large pleural-based mass is identified in a young child, PPB should also be considered, especially in a patient with a positive oncological family history. Suggestive findings include the absence of chest wall invasion, presence of pleural fluid, right-sided location, and heterogeneous native (NECT) low attenuation with variable postcontrast enhancement. The authors believe that a modern therapeutic approach should consider these results for a better understanding of the genetic nature and complex mechanism and process of PPB disease development (both clinical and preclinical data concerning PPB pathophysiology are still lacking and are not completely understood) so that it would be possible to establish new possible therapeutic options (i.e. nuclear medicine theranostics in PPB treatment, developments and innovation in FLASH radiotherapy and proton therapy) and approaches, and so that, given the severity of the disease, it would be possible to indicate the importance of genetic testing and counseling of close relatives. In line with the previous, the rapid development of artificial intelligence could potentially bring the development of a novel fusion of radio mics and semantic features and MRI-based machine learning in distinguishing PPB from similar pathology.

伴有中枢神经系统转移的胸膜肺母细胞瘤(Ppb):病例报告、影像学发现和文献综述。
胸膜肺泡瘤(PPB)是一种非常罕见的胸部肿瘤,主要见于幼儿,具有很大的异质性和临床、生化及生物学复杂性,已被公认、描述和分类为有别于成人常见的肺泡瘤。不幸的是,它的预后很差,主要分为囊性(1 型)、混合型(2 型)和实性(3 型)。在此,我们介绍一例临床表现为右肺脓肿的 PPB 2 型患者,这是 PPB 的一种罕见临床表现,患者最初接受了手术治疗,经过约一年的随访,发现肺部复发和中枢神经系统继发性沉积。当发现幼儿胸膜有巨大肿块时,也应考虑 PPB,尤其是有阳性肿瘤家族史的患者。提示性结果包括:无胸壁侵犯、有胸腔积液、右侧位置、异质原发(NECT)低衰减且对比后增强不一。作者认为,现代治疗方法应考虑这些结果,以便更好地了解 PPB 疾病的遗传性质和复杂的发病机制和过程(目前仍缺乏有关 PPB 病理生理学的临床和临床前数据,对其也不完全了解),从而确定新的可能治疗方案(即 PPB 治疗中的核医学疗法、FLASH 放射疗法和质子疗法的发展和创新)和方法,并鉴于该疾病的严重性,指出对近亲进行基因检测和咨询的重要性。与前述观点相一致,人工智能的快速发展有可能带来一种新的无线电模拟和语义特征与基于核磁共振成像的机器学习的融合,以区分 PPB 和类似病症。
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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来源期刊
Acta Chirurgica Belgica
Acta Chirurgica Belgica 医学-外科
CiteScore
1.60
自引率
12.50%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Acta Chirurgica Belgica (ACB) is the official journal of the Royal Belgian Society for Surgery (RBSS) and its affiliated societies. It publishes Editorials, Review papers, Original Research, and Technique related manuscripts in the broad field of Clinical Surgery.
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