Mishael Tom, Philip Babu, George Arun, S Sandeep
Radiology, St. John's Medical College Hospital, Bangalore, IND.
Cureus. 2023 Jul 24;15(7):e42373. doi: 10.7759/cureus.42373. eCollection 2023 Jul.
Head and neck paragangliomas are rare neuroendocrine tumors arising from the autonomic nervous system. Imaging hallmarks of paragangliomas of the head and neck include an enhancing soft-tissue mass in the carotid space, jugular foramen, or tympanic cavity on computed tomography; a salt-and-pepper appearance on standard spin-echo magnetic resonance imaging; and an intense blush on angiography. Imaging studies depict the location and extent of tumor involvement, help determine the surgical approach, and predict operative morbidity and mortality. However, an atypical presentation of paragangliomas, especially when co-existing with other middle ear pathologies that have overlapping imaging findings, can often be misleading. Here, we report a case of simultaneous occurrence of paraganglioma, cholesteatoma, and otomastoiditis in a young adult female.
头颈部副神经节瘤是起源于自主神经系统的罕见神经内分泌肿瘤。头颈部副神经节瘤的影像学特征包括计算机断层扫描显示颈动脉间隙、颈静脉孔或鼓室内有强化的软组织肿块;标准自旋回波磁共振成像呈椒盐样表现;血管造影时有明显的造影剂外溢。影像学检查可描绘肿瘤累及的部位和范围,有助于确定手术入路,并预测手术的发病率和死亡率。然而,副神经节瘤的非典型表现,尤其是与其他具有重叠影像学表现的中耳病变同时存在时,常常会产生误导。在此,我们报告一例年轻成年女性同时发生副神经节瘤、胆脂瘤和耳乳突炎的病例。