Rare Brain Tumors with Infrequent Clinical Manifestations: Illustrative Cases

José Luis Navarro-Olvera, A. Armas-Salazar, José Damián Carrillo-Ruiz, Jesús Q. Beltrán, G. Parra-Romero, G. Aguado-Carrillo
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Abstract

This chapter describes the epidemiology, clinical and neuroimaging features, histological characteristics, surgical approach, outcomes, and prognostic factors of different cases of very rare intracranial tumors, associated with complex clinical syndromes. Highlighting the important aspects in the diagnosis and management that were considered relevant through the experience of our center. Here we included an intracranial Rosai-Dorfman disease manifested as an apparent multiple meningiomatosis, a choroid plexus papilloma clinically manifested as a hemifacial spasm originated by a compression of the facial colliculus, and a neuroenteric cyst associated with Klippel-Feil syndrome. This type of tumor presents a challenge to the neurosurgeon, originating various questions about its management. In this chapter, we present the experience we had with these pathologies to establish the most appropriate management decisions.
临床表现罕见的罕见脑肿瘤:具有说明意义的病例
本章描述了与复杂临床综合征相关的非常罕见的颅内肿瘤的不同病例的流行病学、临床和神经影像学特征、组织学特征、手术入路、结局和预后因素。通过本中心的经验,强调诊断和管理的重要方面。我们包括一例颅内Rosai-Dorfman病,表现为明显的多发性脑膜瘤病,一例脉膜丛乳头状瘤,临床表现为由面神经丘压迫引起的面肌痉挛,以及一例与Klippel-Feil综合征相关的神经肠囊肿。这种类型的肿瘤对神经外科医生提出了挑战,对其治疗提出了各种问题。在本章中,我们将介绍我们处理这些病态的经验,以建立最适当的管理决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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