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1.
Rinsho Shinkeigaku ; 59(8): 530-535, 2019 Aug 29.
Artigo em Japonês | MEDLINE | ID: mdl-31341129

RESUMO

A 41-year-old woman experienced back pain upon waking up. Immediately afterward, she experienced a continual orthostatic headache. Thereafter, right ear fullness and dizziness also occurred. One month later, she became aware of repeated numbness that started in the right hand and spread to the right half of the body and lower limbs and continued for repeated periods of approximately 20-30 min. Neurological examination revealed no abnormal findings except for orthostatic headache. Electroencephalography showed no epileptic discharge. Head MRI revealed left convexal subarachnoid hemorrhage (cSAH) restricted to the prefrontal sulcus, left frontal cerebral venous thrombosis, diffuse dural thickening with gadolinium enhancement, and subdural hematoma in the posterior cranial fossa. Spinal MRI revealed epidural fluid accumulation around the thoracic spine. CT myelography revealed cerebrospinal fluid leakages at the cervical, thoracic, and lumbar vertebrae levels. The patient was diagnosed with spontaneous intracranial hypotension (SIH), which was treated effectively with a blood patch. In this case, cSAH may have resulted from rupturing of the vessel wall as a result of cortical venous thrombosis induced by SIH. The repeated transient neurologic symptoms suggesting migraine aura may have originated from cSAH, which in turn led to cortical spreading depression. The diagnosis and management of SIH can be often difficult; therefore, repeated migraine-aura-like symptoms are a critical sign of complication with cSAH and cortical venous thrombosis.


Assuntos
Cefaleia/etiologia , Hipotensão Intracraniana/diagnóstico por imagem , Adulto , Placa de Sangue Epidural , Vazamento de Líquido Cefalorraquidiano/diagnóstico por imagem , Vazamento de Líquido Cefalorraquidiano/etiologia , Diagnóstico Diferencial , Feminino , Humanos , Hipotensão Intracraniana/complicações , Hipotensão Intracraniana/terapia , Trombose Intracraniana/diagnóstico por imagem , Trombose Intracraniana/etiologia , Imageamento por Ressonância Magnética , Mielografia , Recidiva , Hemorragia Subaracnóidea/etiologia , Síndrome , Tomografia Computadorizada por Raios X
2.
Clin Neurol Neurosurg ; 182: 58-62, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-31078957

RESUMO

OBJECTIVES: Small vessel disease (SVD) has been associated with motor and cognitive impairments in neurodegenerative diseases. We investigated SVD markers using brain magnetic resonance imaging (MRI) and the global SVD score in Parkinson's disease (PD). PATIENTS AND METHODS: Seventy-one patients with PD were assessed for vascular risk factors, motor severity, and motor phenotype. Global cognition was evaluated using the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA). Based on the MoCA score, we categorized cases into normal (>23) or cognitively impaired (≤23). We calculated the total SVD score (range, 0-4) based on white matter hyper intensities (WMHs), lacunae, cerebral microbleeds (MBs), and enlarged perivascular spaces (PVSs). In addition, we evaluated global brain atrophy. RESULTS: There were no significant associations with total SVD score and vascular risk factors, PD severity, and motor phenotype. Increasing age and reduced MMSE and MoCA scores were associated with increased SVD burden. Logistic regression analyses demonstrated that periventricular WMH (PVH), PVS in the basal ganglia (BG-PVS), and atrophy were predictors of cognitive impairment in PD. CONCLUSION: The contribution of SVD may be important in elderly patients with PD. Impaired cognition due to SVD-related brain changes was associated with BG-PVS and PVH. These measures suggest that PD with PVS can provide novel insights into SVD.


Assuntos
Doenças de Pequenos Vasos Cerebrais/complicações , Transtornos Cognitivos/etiologia , Cognição/fisiologia , Disfunção Cognitiva/etiologia , Doença de Parkinson/etiologia , Doenças de Pequenos Vasos Cerebrais/fisiopatologia , Disfunção Cognitiva/complicações , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Doença de Parkinson/complicações , Fatores de Risco , Substância Branca/fisiopatologia
3.
Intern Med ; 58(10): 1495-1499, 2019 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-30713304

RESUMO

A 64-year-old woman with no previous mental illness took a single 500 mg tablet of levofloxacin for cystitis. Two hours later, she developed psychosis with involuntary movement and severe hyperventilation with respiratory alkalosis. Cranial magnetic resonance imaging findings were unremarkable, and an electroencephalogram revealed no epileptiform discharge. Her symptoms improved on the third day after levofloxacin was discontinued. Levofloxacin-associated encephalopathy with psychotic features is a rare adverse event. Disturbance of gamma-aminobutyric acid-ergic (GABAergic) interneurons by levofloxacin may lead to hyperventilation via dysfunction of the brainstem respiratory network. Physicians should be aware of hyperventilation as an additional serious symptom of levofloxacin-associated encephalopathy in acute settings.


Assuntos
Anti-Infecciosos Urinários/efeitos adversos , Anti-Infecciosos Urinários/uso terapêutico , Encefalopatias/induzido quimicamente , Cistite/tratamento farmacológico , Hiperventilação/induzido quimicamente , Levofloxacino/efeitos adversos , Levofloxacino/uso terapêutico , Feminino , Humanos , Pessoa de Meia-Idade , Resultado do Tratamento
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