Song Linfeng, Zhang Jiaren, Tian Binlin, Li Yongzhe, Gu Xiaoyu, Zhang Youlun, Jiang Lin
Department of Radiology, The Third Affiliated Hospital of Zunyi Medical University (The First People's Hospital of Zunyi), Zunyi, China.
Department of Pathology, The Third Affiliated Hospital of Zunyi Medical University (The First People's Hospital of Zunyi), Zunyi, China.
Front Oncol. 2024 Oct 16;14:1408456. doi: 10.3389/fonc.2024.1408456. eCollection 2024.
Ganglioneuroma (GN) is a rare benign neurogenic tumor that originates from the sympathetic nerves. It is extremely uncommon to find a lesion originating from the mediastinum that occupies the entire left hemithorax. In this report, we present the case of a 48-year-old female patient with a large mediastinal GN who presented with cough, sputum, and wheezing. Multislice spiral-enhanced CT and magnetic resonance imaging (MRI) revealed a large oval mass in the left thoracic cavity. The surgical operation completely resected the lesion, and the histopathological examination of the resected specimen confirmed the diagnosis of giant ganglion cell neuroma of the mediastinum. Due to the low incidence of GN and the lack of specific imaging manifestations, many radiologists may lack sufficient knowledge of GN and may be prone to misdiagnosis, resulting in delayed treatment. To enhance radiologists' awareness of giant ganglion cell neuroma of mediastinal origin occupying the thoracic cavity, we provided detailed CT/MRI imaging information for this case, along with a brief summary of similar previously reported cases, to highlight the specific clinical and radiological features of this condition.
神经节神经瘤(GN)是一种罕见的良性神经源性肿瘤,起源于交感神经。发现起源于纵隔并占据整个左半胸的病变极为罕见。在本报告中,我们介绍了一例48岁女性患者,患有巨大纵隔GN,表现为咳嗽、咳痰和喘息。多层螺旋增强CT和磁共振成像(MRI)显示左胸腔有一个巨大的椭圆形肿块。手术完整切除了病变,对切除标本的组织病理学检查确诊为纵隔巨大神经节细胞瘤。由于GN发病率低且缺乏特异性影像学表现,许多放射科医生可能对GN认识不足,容易误诊,导致治疗延误。为提高放射科医生对起源于纵隔并占据胸腔的巨大神经节细胞瘤的认识,我们提供了该病例详细的CT/MRI影像学信息,并简要总结了既往报道的类似病例,以突出该疾病的特定临床和影像学特征。