Spinal drop of atypical choroid plexus papilloma in an adult patient: A case report and literature review

Author:

Ochoa-Cacique Diego1,Córdoba-Mosqueda María1,Aguilar-Calderón José Ramón1,Sánchez-Silva Martha Cristina2,Vicuña-González Rosa María3,Torre Abraham Ibarra-de la1,Reyes-Rodríguez Victor Andrés4,Lomelí-Ramírez José de Jesús5,Medina-Carrillo Óscar1,Sánchez-Calderón Mauricio Daniel1,Castañeda-Ramírez Erick Alberto1,García-González Ulises1

Affiliation:

1. Department of Neurosurgery, Hospital Central Sur de Alta Especialidad PEMEX, Tlalpan, Ciudad de Mexico, Mexico,

2. Department of Imaging, Hospital Central Sur de Alta Especialidad PEMEX, Tlalpan, Ciudad de Mexico, Mexico,

3. Department of Anatomical Pathology, Hospital Central Sur de Alta Especialidad PEMEX, Tlalpan, Ciudad de Mexico, Mexico,

4. Department of Neurosurgery, Hospital Central Norte PEMEX, Azcapotzalco, Estado de Mexico, Mexico,

5. Department of Neurosurgery, Hospital Vossan, Campeche, Mexico.

Abstract

Background: Choroid plexus papillomas (CPPs) are benign extra-axial tumors that originate from the choroid plexus; these tumors rarely have metastases, being at the spinal level the location with few reported cases. Case Description: We report the case of a 48-year-old man with a history of atypical fourth ventricular CPP and gross total resection (GTR) in 2008. In 2015, he presented with radicular pain, decreased strength, and paresthesia in the left leg. Magnetic resonance imaging revealed a well-defined intradural ovoid lesion in the vertebral canal at the level of the L3-L4 intersomatic space. Subtotal resection of the tumor was performed. The patient recovered well, with relief of pain and no neurological deficit. A literature research few cases of CPP metastasis in adults. We describe here a fifth-decade male patient with a lumbar neoplasm, which according to the histopathologic characteristics and location is the first case of an atypical papilloma implant of the choroid plexus at this spinal level. Conclusion: GTR of primary lesions and associated implants remains the gold standard for surgical treatment of CPP. Radiotherapy, stereotactic radiosurgery, and chemotherapy are adjuvant therapies for CPP but there is no definitive protocol for the management of implants. Proper follow-up of these patients is essential since spinal drop can appear many years after the initial presentation of CPP.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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