Gorlin Goltz Syndrome, or Nevoid Basal Cell Carcinoma is an autosomal dominant genetic disease characterized especially by the manifestation of basal cell carcinomas in skin and keratocysts jaws. Additionally, patients may present with several other manifestations, such as bifid ribs, hypertelorism calcification falx cerebri. The diagnosis has physicians dentists protagonists investigation invo...

We report on the case of a 32-years old male patient who was previously diagnosed with Gorlin-Goltz syndrome. The patient presented with sudden-onset right-sided hemiparesis, supranuclear facioparesis, and motor aphasia. He was treated with thrombolytic therapy, which successfully alleviated the symptoms. Subsequent radiologic work-up revealed anomalies in the vertebral arteries, a bifid rib, a...

In a 33 years-old epileptic woman with a traumatic impact to the vertex, clinical and radiological studies (skull X-R, CT and MRI) disclosed an extensive callosal section under the topography of the falx, associated to fronto-basal contusions. There was a significant improvement in the epileptic syndrome. No interhemispheric disconnection syndrome could be determined, which is compatible with t...

This report describes the case of a 50-year-old woman with carcinomatous meningitis from squamous cell carcinoma of the uterine cervix. Ultrasound showed an irregular hypoechoic mass in the cervix. Contrast enhanced computed tomography imaging revealed intense linear enhancement along the falx cerebri suggestive of pachymeningeal metastasis with involvement of the optic nerve. To our knowledge ...

Membranous or membranous-haemorrhagic lesions of the dura mater were found in 46 out of 1,044 consecutive necropsies after excluding those cases where their presence could be interpreted in terms of blood dyscrasia, local neoplastic processes, previous surgery, or marked craniocerebral trauma. The extent of old and recent manifestations of haemorrhage in the membranes increased in a statistical...