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4.
SD, Rev. med. int. Síndr. Down (Ed. castell.) ; 15(3): 37-40, nov. 2011. ilus
Article in Spanish | IBECS | ID: ibc-93851

ABSTRACT

Discusión y revisión de la bibliografía a partir de un caso de un varón joven con síndrome de Down (SD) y trombosis venosa cerebral (TVC). Caso clínico. Varón de 27 años que comienza con cefalea, vómitos y hemiparesia izquierda. Tras encontrarse hallazgos en la neuroimagen compatibles con trombosis venosa cerebral, se inició tratamiento anticoagulante, con una evolución clínica favorable. Discusión. Los pacientes con SD están predispuestos a la aparición de ictus embólicos secundarios a cardiopatías congénitas; sin embargo, las causas de TVC en el SD son inciertas, teniendo probablemente un origen multifactorial. Hasta la fecha hay dos casos publicados de TVC en pacientes con SD (AU)


This review and discussion of the current literature is based on the case of a young man with Down’s syndrome (DS) and cerebral venous thrombosis (CVT). Clinical case. Twenty-seven-year-old male who presented with headache, vomiting and left hemiparesis. After finding signs consistent with cerebral venous thrombosis on neuroimaging, anticoagulant treatment was started, and eventuated in a favorable clinical outcome. Discussion. DS patients are predisposed to the occurrence of embolic stroke secondary to congenital heart disease. However, the causes of CVT in DS are uncertain, but probably have a multifactorial origin. There are to date two published cases of CVT in patients with DS (AU)


Subject(s)
Humans , Male , Adult , Down Syndrome/complications , Venous Thrombosis/complications , Venous Thrombosis/diagnosis , Intracranial Thrombosis/complications , Anticoagulants/therapeutic use , Heparin/therapeutic use , Sensitivity and Specificity , Down Syndrome/physiopathology , Vomiting/complications , Vomiting/etiology , Skull/pathology , Skull , Magnetic Resonance Imaging , /methods
8.
Rev. esp. patol. torac ; 22(3): 228-230, jul.-sept. 2010. ilus
Article in Spanish | IBECS | ID: ibc-97264

ABSTRACT

La linfagioleiomiomatosis (LAM) es una enfermedad rara, progresiva y sistemática de etiología desconocida, que afecta al parénquima pulmonar y sistema linfático. Indice principalmente en mujeres con edades reproductivas (..) (AU)


Lymphangioleiomyomatosis is a rare progressive disease of unknown atiology which affects the lungs (..) (AU)


Subject(s)
Humans , Female , Adult , Lymphangioleiomyomatosis/complications , Tuberous Sclerosis/complications , Dyspnea/etiology , Chest Pain/etiology , Radiography, Thoracic
10.
Rev. esp. patol. torac ; 22(2): 138-141, abr.-jun. 2010. ilus
Article in Spanish | IBECS | ID: ibc-97254

ABSTRACT

Presentamos una serie de tres pacientes con secuestros pulmonares intralobares del lóbulo inferior derecho, correlacionándolos con la clínica, los hallazgos histológicos de los pacientes sometidos a cirugía y los hallazgos radiológicos en pacientes tratados mediante embolización, una alternativa actual en el tratamiento de esta entidad (AU)


A series of three patients is presented with intralobar pulmonary sequestration of the right lower lobe, correlating with the clinical and histological findings of patients undergoing surgery and the radiological findings in patients treated by arterial embolization, the current alternative in the treatment of this problem (AU)


Subject(s)
Humans , Female , Young Adult , Adult , Middle Aged , Bronchopulmonary Sequestration/diagnosis , Hemoptysis/etiology , Bronchopulmonary Sequestration/surgery , Embolization, Therapeutic/methods , Bronchopulmonary Sequestration/drug therapy
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