Intramedullary and intratumoral hemorrhage in spinal hemangioblastoma: Case report and review of literature

Satoshi Kiyofuji, Christopher S. Graffeo, Munehiro Yokoyama, Shigeo Sora

Date of publication: 04-Dec-2018

Background:Intramedullary hemorrhages involving spinal hemangioblastomas are rare. They are frequently associated with devastating neurologic outcomes, despite with emergent surgical intervention. Here, we presented an example of an intramedullary hemorrhage occurring in a spinal hemangioblastoma, where the patient markedly improved with surgery. Additionally, the appropriate literature was reviewed (including intraoperative video).

Comprehensive review of neuromyelitis optica and clinical characteristics of neuromyelitis optica patients in Puerto Rico

Sara Zarei, James Eggert, Laura Franqui-Dominguez, Yonatan Carl, Fernando Boria, Marina Stukova, Alessandro Avila, Cristina Rubi, Angel Chinea

Date of publication: 03-Dec-2018

Abstract

Neuromyelitis optica (NMO) is an immune-mediated inflammatory disorder of the central nervous system. It is characterized by concurrent inflammation and demyelination of the optic nerve (optic neuritis [ON]) and the spinal cord (myelitis). Multiple studies show variations in prevalence, clinical, and demographic features of NMO among different populations. In addition, ethnicity and race are known as important factors on disease phenotype and clinical outcomes. There are little data on information about NMO patients in underserved groups, including Puerto Rico (PR). In this research, we will provide a comprehensive overview of all aspects of NMO, including epidemiology, environmental risk factors, genetic factors, molecular mechanism, symptoms, comorbidities and clinical differentiation, diagnosis, treatment, its management, and prognosis. We will also evaluate the demographic features and clinical phenotype of NMO patients in PR. This will provide a better understanding of NMO and establish a basis of knowledge that can be used to improve care. Furthermore, this type of population-based study can distinguish the clinical features variation among NMO patients and will provide insight into the potential mechanisms that cause these variations.

Cervicomedullary primitive neuroectodermal tumor of the spine: Case report

Breno Nery, Leandro César Tângari Pereira, Rodrigo Antônio Fernandes Costa, Rodolfo Mendes Queiroz, Lucas Giansante Abud, Eduardo Quaggio, Lígia Henriques Coronatto, Isadora Salviano Teixeira Prado, Cecília Hissae Miyake, Fred Bernardes Filho

Date of publication: 28-Nov-2018

Background:Intramedullary primitive neuroectodermal tumors (PNETs) are tumors found rarely in the cervical region, with only five such cases described in the literature. The available literature contains only one report regarding cervicomedullary junction PNET.

Odontoid fracture with missed diagnosis of Transverse Atlantal Ligament (TAL) injury resulting in late-onset instability

Mukesh Kumar Haritwal, Shankar Acharya, Kashmiri Lal Kalra, Rupinder Chahal, Nikhil Jain, Nitin Adsul

Date of publication: 28-Nov-2018

Background:Concurrent injuries to both the odontoid and transverse atlantal ligament are rare and can be easily missed. Failure to diagnose both lesions potentially leads to the late onset of sagittal plane instability and acute myelopathy. Here, we present a patient with an odontoid fracture whose transverse atlantal ligament (TAL) injury was originally missed on magnetic resonance imaging (MRI) and computed tomography (CT) scans. He later developed atlantoaxial instability requiring surgery.

Primary tuberculous psoas abscess as a postpartum complication: Case report and literature review

Ali Akhaddar, Walter Hall, Mohammed Ramraoui, Mehdi Nabil, Ahmed Elkhader

Date of publication: 28-Nov-2018

Background:Primary psoas abscess is an unusual clinical entity rarely encountered in the postpartum period. Only seven cases have been reported to date. Here, we present a woman with a primary psoas abscess caused by Mycobacterium tuberculosis and occurred 2 months following a normal vaginal birth. We highlight the difficulties in the management of this uncommon condition in light of the relevant literature.

Acute subdural hematomas in shunted normal-pressure hydrocephalus patients – Management options and literature review: A case-based series

Assaf Berger, Shlomi Constantini, Zvi Ram, Jonathan Roth

Date of publication: 28-Nov-2018

Background:Ventriculoperitoneal shunting (VPS) is considered a risk factor for developing subdural hematomas (SDH). Treating cases of acute SDH (aSDH) in shunted normal-pressure hydrocephalus (NPH) patients can be challenging, and data in this field are scarce. We report our experience treating shunted NPH patients presenting with aSDH.

Fourth ventricle meningioma with cervical extension: An unusual entity

Ankit S. Shah, Robin Gupta, Ghanshyam Singhal, Anita Jagetia, Daljit Singh

Date of publication: 28-Nov-2018

Clinical and radiological features of Forestier's disease presenting with dysphagia

Giuseppe Roberto Giammalva, Domenico Gerardo Iacopino, Francesca Graziano, Carlo Gulì, Maria Angela Pino, Rosario Maugeri

Date of publication: 28-Nov-2018

Background:Diffuse idiopathic skeletal hyperostosis (DISH), also known as Forestier's disease, is a rheumatologic condition characterized by ossification of the spinal ligaments and tendons. Large anterior osteophytes are typically present in the lower cervical levels, while upper cervical ossification resulting in dysphagia is very rare.

Unedited microneurosurgery of a posterior fossa pilocytic astrocytoma

Joham Choque-Velasquez, Juha Hernesniemi

Date of publication: 28-Nov-2018

Background:Pilocytic astrocytoma (PA) is a WHO grade I glioma and the most common pediatric brain tumor. PA is most commonly localized in the cerebellum with extremely rare disemination and progression to higher grade astrocytomas. Thus, overall survival rates are excellent after gross total resection. Herein, we present an unedited microneurosurgery of a histologically confirmed cerebellar PA. Our aim is to demonstrate the efficiency and safety of our microsurgical technique into deep brain territories. For this, a paramedian supracerebellar infratentorial approach and a proper praying sitting position are essential.

Unedited microneurosurgery of a large recurrent papillary tumor of the pineal region

Joham Choque-Velasquez, Juha Hernesniemi

Date of publication: 28-Nov-2018

Background:Papillary tumor of the pineal region (PTPR) is a new entity introduced in the 2007 World Health Organization (WHO) nomenclature to describe a rare grade II–III pineal lesion with epithelial-like papillary architecture and particular immunohistochemical features. PTPR is extremely rare in children. Herein, we present an unedited gross total microsurgical resection of a histologically confirmed WHO grade III PTPR. Our aim is to demonstrate the efficiency and safety of our microsurgical technique into deep brain territories under the principle “simple, clean, and preserving the normal anatomy.” For this, a posterior occipital interhemispheric approach and a proper praying sitting position were essential.