Middle Ear Neuroendocrine Tumor: Case Report of a Tympanic Adenoma.

Ilinko Vrebac, Filip Pavlic, Andro Košec
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Abstract

Middle ear neuroendocrine tumors (MeNETs) are an exceptionally rare occurrence. These benign tumors stem from the tympanic mucosa and can easily be misinterpreted by the clinician and the pathologist. Clinical characteristics, otoscopic findings and medical imaging in these cases are non-specific. We present a case of a 60-year-old male patient with bilateral hearing loss following recent coronavirus disease 2019 disease. Diagnostic work-up revealed a soft tissue neoplasm of the left middle ear. Surgical resection of the tumor mass with implantation of a partial ossicular replacement prosthesis (PORP) was the main modality of treatment. Middle ear neuroendocrine tumors was confirmed through positive immunohistochemistry for neuroendocrine tumor markers. Follow-up magnetic resonance imaging 12 months after the surgery reported no tumor recurrence or significant residual disease with a stable PORP. Our report highlights challenges in diagnosing and treating these rare tumors, while emphasizing surgical resection pitfalls and resulting improvement of quality of life of the patient. We recommend a through followup of patients with unclear soft tissue masses in the middle ear to obtain a definitive diagnosis.

中耳神经内分泌瘤:鼓室腺瘤病例报告
中耳神经内分泌瘤(MeNETs)异常罕见。这些良性肿瘤源自鼓室粘膜,很容易被临床医生和病理学家误诊。这些病例的临床特征、耳镜检查结果和医学影像均无特异性。我们介绍了一例 60 岁男性患者的病例,该患者近期患 2019 年冠状病毒病后出现双侧听力损失。诊断检查发现左中耳软组织肿瘤。手术切除肿瘤肿块并植入部分听骨替代假体(PORP)是主要的治疗方式。中耳神经内分泌肿瘤标记物免疫组化阳性,证实为中耳神经内分泌肿瘤。术后 12 个月的磁共振随访显示,肿瘤没有复发,也没有明显的残留病灶,PORP 保持稳定。我们的报告强调了诊断和治疗这类罕见肿瘤的挑战,同时也强调了手术切除的误区,以及由此带来的患者生活质量的改善。我们建议对中耳软组织肿块不明确的患者进行全程随访,以获得明确诊断。
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