منابع مشابه
The Mystery of Multiple Masses: A Case of Anaplastic Astrocytoma
Though most primary brain gliomas present as a single mass lesion in the brain, this potential diagnosis must be considered in the differential diagnosis when faced with a case of multifocal brain mass lesions. Among the most common brain tumors in humans, glioblastomas can be classified into four classes, one of which consists of anaplastic astrocytomas (AA). Due to its significant malignant p...
متن کاملSynchronous osteoclastoma and anaplastic astrocytoma: A case report
Multiple primary neoplasms are defined as multiple occurrences of malignant neoplasms of differing histological origin in the same individual. The present study describes the case of a 46-year-old male who suffered from two synchronous primary malignant neoplasms, an osteoclastoma of the left femoral trochanter and an anaplastic astrocytoma of the the Sylvian fissure area in the brain. At the 6...
متن کاملX-Linked Lissencephaly with Absent Corpus Callosum and Ambiguous Genitalia: A Case Report
Background: X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder, in which patients present with lissencephaly, agenesis of the corpus callosum, refractory epilepsy of neonatal onset, acquired microcephaly, and male genotype with ambiguous genitalia. XLAG is responsible for a severe neurological disorder of neonatal onset in boys. A gyration defect con...
متن کاملmöebius syndrome and corpus callosum agenesis; a case report
moebius syndrome is a rare congenital disorder of the facial and abducens nerve. other cranial nerves may be involved, such as v, ix and xii. several central nervous system anomalies including hypoplastic or dysplastic brain stem, straightening of the fourth ventricle floor, focal necrosis and calcifications of cranial nerve nuclei have been reported in association with moebius syndrome, but we...
متن کاملNeurodevelopmental Outcome of Patients With Agenesis of Corpus Callosum
Background: Agenesis of Corpus Callosum (ACC) is a type of brain dysgenesis with various clinical manifestations. Objectives: This study aimed to investigate the clinical and neurodevelopmental outcomes of patients with ACC. Materials & Methods: In this cross-sectional study, the clinical and neurodevelopmental conditions of 62 patients with complete ACC referred to subspecialty clinics of pe...
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ژورنال
عنوان ژورنال: American Journal of Medical Case Reports
سال: 2021
ISSN: 2374-2151
DOI: 10.12691/ajmcr-9-4-3