Results 31 to 40 of about 1,112 (136)
Quadrigeminal cistern lipoma: A rare case report with review of literature
Two cases, one of a 6-old-year male and another of 18-year-old female with an intracranial lipoma of quadrigeminal region is reported. Intracranial lipomas usually occur in midline areas and are extremely uncommon with an incidence of 0.1% of all ...
Dhaval K Thakkar +5 more
doaj +1 more source
Background Tentorial hypoplasia is a rare congenital condition characterized by underdevelopment or absence of the tentorium cerebelli, a dural structure separating the cerebrum from the cerebellum. It is often detected incidentally on computed tomography (CT) or magnetic resonance imaging (MRI) and may be associated with conditions such as Dandy ...
Husam Hamshary +10 more
wiley +1 more source
MYB Alterations in Angiocentric Gliomas
ABSTRACT We performed a systematic review of the literature to better define the scope of MYB alterations in angiocentric glioma and their associated clinical characteristics, as well as to include a novel MYB mutation in an angiocentric glioma case. We also review MYB alterations in the context of oncologic disease.
Isabela Peña Pino +7 more
wiley +1 more source
Triple pathological findings in a surgically amenable patient with mesial temporal lobe epilepsy
Mesial temporal sclerosis (MTS) is a well-recognized cause of intractable epilepsy; however, coexistence with focal cortical dysplasia (FCD) is less common. Middle fossa epidermoid cysts are rare and may involve the temporal lobe.
Fumin Tong +4 more
doaj +1 more source
ABSTRACT We are reporting the case of a hypertensive middle‐aged adult with a triad of right cerebellar hematoma, acute obstructive tri‐ventricular hydrocephalus, and spontaneous subarachnoid hemorrhage. A 45‐year‐old male with a 3‐year history of uncontrolled hypertension presented with a severe thunderclap headache, left lower facial weakness, left ...
William Ntchompbopughu Tih +1 more
wiley +1 more source
ABSTRACT We report a patient with clinically confirmed Schimmelpenning–Feuerstein–Mims (SFM) syndrome but many overlapping features with oculoectodermal syndrome (OES) and encephalocraniocutaneous lipomatosis (ECCL). Whole exome sequencing revealed a mosaic KRAS c.436G>A, p.(Ala146Thr) mutation, previously identified in three OES and ECCL patients ...
Hyvönen Hanna +7 more
wiley +1 more source
Cerebral ischemia may be rarely associated with a hypoplastic vertebrobasilar system. Intracranial lipoma is also a very rare congenital malformation.
Kyu-On Jung +4 more
doaj +1 more source
Introduction PHACE syndrome is a neurocutaneous syndrome characterized by large facial segmental hemangiomas as the most typical manifestation. Its prevalence in East Asian is not well studied. Methods The retrospective study included 98 infants with facial segmental hemangiomas who underwent brain MRI/MRA, cardiac ultrasound, and ophthalmology ...
Jingjing Sun +8 more
wiley +1 more source
Late favorable results of duroplasty with biocellulose: clinical retrospective study of 20 cases
Objective: Considering the importance of dural replacement in neurosurgery, mainly in times of advanced endoscopic skull base approaches, the authors report the late results after implanting of pure biocellulose membrane in 20 patients harboring ...
Luis Renato Mello +3 more
doaj +1 more source
Abstract Objective To describe the approach for placement of a transcerebellar fourth ventriculoperitoneal shunt for management of presumed fourth ventricle arachnoid diverticulum and secondary obstructive hydrocephalus of a dog. To describe the outcome of this procedure. Study design Case report. Animals Male entire English springer spaniel, 3 years 9
Sophie Wyatt, Joe Fenn, Elsa Beltran
wiley +1 more source

