ABSTRACT
A clinical case study of a 50 year-old woman brought to the Rhematology Department is presented, who showed clinical dry syndrome with immune disorders (not currently defined) and developed tumors (benign at present) and analytical autoimmunity with positive antitopoisomerase type I (formerly Scl70) confirmed. The clinical case is commented and the metheorism causes are discussed, among it, a possible variation of abdominal epilepsy as ictal flatulence, secondary to a meningioma of the right brain convexity.
Subject(s)
Epilepsies, Partial/complications , Flatulence/etiology , Meningeal Neoplasms/complications , Meningioma/complications , Rheumatic Diseases/complications , Electroencephalography , Epilepsies, Partial/therapy , Female , Flatulence/therapy , Humans , Meningeal Neoplasms/pathology , Meningeal Neoplasms/therapy , Meningioma/pathology , Meningioma/therapy , Middle Aged , Rheumatic Diseases/pathology , Rheumatic Diseases/therapy , Tomography, X-Ray Computed , Treatment OutcomeABSTRACT
Se presenta el caso de una mujer de 50 años, remitida a la consulta de Reumatología para estudio de un síndrome seco clínico con una alteración inmunitaria (aún no definida), que desarrolla tumores (de momento benignos) y autoinmunidad analítica de tipo antitopoisomerasa 1 (anti Scl-70) confirmado. Se comenta el caso clínico y se discuten las causas de su meteorismo, entre ellas una posible variante de epilepsia abdominal como ventoseo comicial, secundario a un meningioma de la convexidad cerebral derecha (AU)
