RESUMEN
O objetivo é relatar um caso de acidente vascular encefálico isquêmico provocado por dissecção não traumática da artéria carótida interna em uma paciente jovem. Dissecções espontâneas de carótida interna e de artéria vertebral ocasionam aproximadamente 25% dos acidentes vasculares encefálicos isquêmicos em indivíduos com idade inferior a 45 anos. Confirmou-se o diagnóstico dessa entidade com imagens de ressonância magnética e angiotomografia cerebral. Seu tratamento incluiu anticoagulantes, fonoterapia e fisioterapia. Com melhora clínica, recebeu alta para controle ambulatorial, orientada sobre os riscos de anticoncepcionais orais. Relatos de caso podem aumentar o índice desuspeita dessa condição pouco diagnosticada.
The objective of this work is to report a case of ischemic brain stroke due to non-traumatic dissection of the internal carotid artery in a young patient.Spontaneous dissections of the internal carotid and of the vertebral artery cause nearly 25% of all ischemic strokes in individuals younger than 45 years of age. Imaging studies obtained from magnetic resonance and angiotomography of the brain confirmed the diagnosis. Treatment involved anticoagulation drugs, phonotherapy and physiotherapy. Based on herclinical improvement, she was discharged from the hospital and is now receiving outpatient care and has been advised about the risks of oral contraceptives. Case reports may raise the suspicion index about thisunderdiagnosed condition.
RESUMEN
O objetivo é descrever dados clínicos e de imagem em mulher de 24 anos com arterite de Takayasu, que apresentou extensa ulceração de difícil controle no couro cabeludo. Houve acometimento da pele, do tecido subcutâneo, de músculos e ossos parietais subjacentes. A paciente relatou fraqueza nos membros superiores, mais intensa à esquerda, e isquemia intermitente nas quatro extremidades. Ao exame, havia ausência bilateral de pulsos braquiais, radiais e ulnares. Os pulsos tibiais posteriores e pediosos tinham suas amplitudes diminuídas. Constatou-se pressão arterial de 86 por 54 mmHg no braço esquerdo e 100 por 62 mmHg no direito. A associação de arterite de Takayasu com ulceração cutânea é incomum, em especial no couro cabeludo, e deve ser considerada a dermatose pustulosa erosiva como diagnóstico diferencial dessa condição.
The aim is to describe clinical and imaging data of a 24-year-old woman with Takayasu?s arteritis and presenting an extensive ulceration of difficult control in the scalp. There was involvement of the skin and subcutaneouslayer, in addition to the subjacent muscles and parietal bones. The patient claimed of weakness on the upper limbs more intense at the left, and intermitent ischemia in all the extremities. Physical examination showed bilateral absence of brachial, radial, and ulnar pulses, and posterior tibial and dorsalis pedis pulses had reduced amplitudes. Blood pressure levels were 86/54 mmHg on the left arm and 100/62 mmHg on the right arm. Association between Takayasu?s arteritis and skin ulcers is uncommon, in special on the scalp, and erosive pustular dermatosis must be considered as a differential diagnosis of this condition.
RESUMEN
A 21-year-old mole was admitted because of fever, fatigue, headache, pharyngitis, abdominal pain, loss of appetite, vomiting and dark urine for three days. The patient denied recent use of medicines or any other drug. His physical examination disclosed jaundice, hepato-splenomegaly, whitish-yellow covered tonsils, bilateral anterior and posterior cervical lymph node enlargement associated with edema on the face and neck. Routine blood tests detected abnormalities in serum bilirubins and liver enzymes (total bilirubin: 14.5 mg/dl, direct-reacting bilirubin: 12.9 mg/dl, AST: 697 U/l, ALT: 619 U/l, alkaline phosphatases: 260 U/l, and GGT: 413 U/l). Serological tests showed negative results for viral hepatitis, cytomegalovirus, HIV-1 and HIV-2, and toxoplasmosis markers, while serology for recent infection by EBV was positive (IgM: 70 and 29 U/ml; EBV IgG: 25 and 156 U/ml). Although infrequently, EBV infection can cause acute hepatitis with accentuated cholestatic jaundice (5% of cases), which may constitute an additional diagnostic challenge for primary care physicians. The patient improved with supportive management and was discharged after 12 days. This case study might contribute to increase the suspicion index about acute hepatitis related to EBV.
Un paciente varón de 21 años, fue hospitalizado por fiebre, astenia, cefalea, faringitis, dolor abdominal, pérdida del apetito, vómitos y orina oscura desde tres días antes. El paciente negó uso reciente de medicamentos y cualquier otra droga. Su examen físico reveló ictericia, hepato-esplenomegalia, amigdalitis, adenopatías cervicales anteriores y posteriores, asociadas con edema facial y cervical. Los exámenes de laboratorio mostraron elevación sérica de bilirrubina y enzimas hepáticas (bilirrubina total: 14,5 mg/dl, bilirrubina directa: 12,9 mg/dl, AST: 697 U/l, ALT: 619 U/l, fosfatasas alcalinas: 260 U/l, y gama-GT: 413 U/l). Los tests serológicos resultaron negativos para hepatitis viral A, B o C, citomegalovirus, VIH-1 y VIH-2, y toxoplasmosis; pero la serología de infección reciente por VEB fue positiva (IgM: 70 y 29 U/ml; IgG: 25 y 156 U/ml). Aunque raramente, las infecciones por VEB pueden causar una hepatitis aguda con acentuada ictericia colestásica (5% de los casos), que suele constituir un desafío diagnóstico adicional para los médicos en atención primaria. El paciente mejoró durante un tratamiento de apoyo y recibió alta hospitalaria después de 12 días. Este caso estimula a aumentar el índice de sospecha de hepatitis aguda relacionada con VEB.