A case report of rare congenital disease of encephalo-trigeminal angiomatosis (Sturge-Weber Syndrome) (SWS), is presented to alert the anesthesiologist of its potential risk. The case was anesthetized for emergency orthopedic surgery. Anesthesia management is directed towards observing the clinical manifestations of localized superficial skin lesions, extensive systemic involvement, evaluating ...

Encephalotrigeminal angiomatosis or SturgeWeber's disease is an uncommon congenital disorder which can vary greatly in the extent of its manifestations, but which in severe cases can lead to infantile hemiplegia associated with fits, behavioural disorders and mental backwardness. Until comparatively recently specific therapy was largely limited to anticonvulsant drugs. Only a few isolated repor...

FINCA (Fibrosis, Neurodegeneration, Cerebral Angiomatosis) syndrome is a new genetic multiorgan disease caused by mutation in NHLRC2 (NHL repeat-containing protein 2). Disease manifests at an early age interstitial lung disease, neurodegenerative disorders, hemolytic anemia, gastrointestinal liver dysfunction and other changes. The was first described 2018 three children who died before the of ...

1Diagnostic Imaging Department, SARAH Hospital-Brasilia Center, SARAH Network of Rehabilitation Hospitals, Brasília DF, Brazil; 2Surgical Pathology Laboratory, SARAH Hospital-Brasilia Center, SARAH Network of Rehabilitation Hospitals, Brasília DF, Brazil. Correspondence: Paulo Cesar Rocha Oliveira; Diagnostic Imaging Department, Hospital SARAH-Brasília, SARAH Network of Rehabilitation Hospitals...