Caro-Osorio Enrique, Perez-Ruano Luis A, Martinez Hector R, Rodriguez-Armendariz Ana G, Lopez-Sotomayor Dulce M
Neurosurgery, Tecnologico de Monterrey, Monterrey, MEX.
Neurological Surgery, Tecnologico de Monterrey, Monterrey, MEX.
Cureus. 2022 Aug 1;14(8):e27564. doi: 10.7759/cureus.27564. eCollection 2022 Aug.
Primary intracranial neuroendocrine tumors are extremely rare malignancies with very few cases reported in the world literature. We describe a primary neuroendocrine carcinoma arising from the right cerebellopontine angle, the second case that has been described in this location. The possible origin in this place and treatment are described. A 29-year-old male patient, diagnosed with schwannoma of the right cerebellopontine angle, and treated with radiosurgery at another institution, came to our hospital six months later, The patient presented with a history of rapid progression of numbness on the right side of the face, diplopia, dizziness, vomiting, and facial palsy. On examination, the right cranial nerves V, VI, VII, VIII, and IX were affected. The MRI showed tumor growth occupying the right cerebellopontine angle, with compression of the brain stem and cerebellum. A right retromastoid craniectomy removed the tumor partially and the histopathological examination revealed a high-grade neuroendocrine carcinoma. We describe a primary neuroendocrine tumor of the brain that, despite its rarity, must be considered in the differential diagnosis. There are currently no guidelines for the management of these tumors. According to previously reported cases, surgery is the first line of treatment, followed by radiotherapy or chemotherapy. We consider that such a rare case is needed to be reported for a better understanding of the disease and its neurobiology.
原发性颅内神经内分泌肿瘤是极为罕见的恶性肿瘤,世界文献中报道的病例极少。我们描述了一例起源于右侧桥小脑角的原发性神经内分泌癌,这是该部位报道的第二例。本文描述了该肿瘤可能的起源及治疗方法。一名29岁男性患者,在另一机构被诊断为右侧桥小脑角神经鞘瘤,并接受了放射外科治疗,6个月后前来我院就诊。患者有右侧面部麻木迅速进展、复视、头晕、呕吐及面神经麻痹的病史。检查发现右侧第Ⅴ、Ⅵ、Ⅶ、Ⅷ及Ⅸ颅神经受累。磁共振成像(MRI)显示肿瘤生长占据右侧桥小脑角,压迫脑干和小脑。经右侧乳突后颅骨切除术部分切除肿瘤,组织病理学检查显示为高级别神经内分泌癌。我们描述了一种原发性脑内神经内分泌肿瘤,尽管其罕见,但在鉴别诊断中必须予以考虑。目前尚无针对这些肿瘤的管理指南。根据既往报道的病例,手术是一线治疗方法,其次是放疗或化疗。我们认为需要报道这样罕见的病例,以便更好地了解该疾病及其神经生物学特性。