Cerebellopontine angle metastasis of a neuroendocrine tumor mimicking vestibular schwannoma: A case report

Author:

Yamada Shuhei1,Kijima Noriyuki1,Kinoshita Manabu1,Shinzaki Shinichiro2,Sato Kazuaki3,Kido Kansuke3,Hirayama Ryuichi1,Kagawa Naoki1,Takehara Tetsuo2,Morii Eiichi3,Kishima Haruhiko1

Affiliation:

1. Department of Neurosurgery, Graduate School of Medicine, Suita, Osaka, Japan,

2. Department of Gastroenterology and Hepatology, Graduate School of Medicine, Suita, Osaka, Japan,

3. Department of Pathology, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.

Abstract

Background: Neuroendocrine tumors (NETs) are uncommon neoplasms arising from neuroendocrine cells and are rarely associated with intracranial metastases. Case Description: We discuss the case of a 74-year-old woman with a right CPA tumor. She had a history of retroperitoneal NET, but was diagnosed with vestibular schwannoma due to a right-sided hearing loss and a right CPA tumor along the VII and VIII nerves. After a 3-year follow-up, she presented with repetitive vomiting, a 1-month history of gait instability, and a 3-month history of general fatigue. Brain imaging revealed tumor growth and edematous changes in the right cerebellum. She underwent retrosigmoid craniotomy and partial resection. Histopathological examination revealed metastatic NET. She underwent stereotactic radiosurgery for residual lesion and, at 11 months of follow-up, the lesion was confirmed to have shrunk on magnetic resonance imaging (MRI). Conclusion: This is the first case to report the natural course of cerebellopontine metastasis of a NET. The differential diagnosis of CPA tumors is diverse, and, in our case, we suspected a vestibular schwannoma because of the typical symptoms and imaging features. However, the tumor grew relatively faster than expected and showed intratumoral hemorrhage during the 3-year follow-up. Therefore, in patients with a history of a NET, a careful follow-up is advisable even for lesions highly suspected to be another benign tumor on MRI. Careful follow-up imaging and appropriate treatment strategies were useful to manage the brain metastasis. Although NETs metastasizing to the CPA are extremely rare, this possibility should be considered when patients with NETs have intracranial lesions.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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