Subject(s)
Antiretroviral Therapy, Highly Active/adverse effects , HIV Infections/complications , Myasthenia Gravis/complications , Cholinesterase Inhibitors/therapeutic use , Electrodiagnosis , Female , HIV Infections/drug therapy , Humans , Mediastinum/diagnostic imaging , Middle Aged , Myasthenia Gravis/diagnosis , Myasthenia Gravis/drug therapy , Pyridostigmine Bromide/therapeutic use , Thymus Hyperplasia/diagnostic imaging , Thymus Hyperplasia/etiology , Tomography, X-Ray ComputedABSTRACT
Occipital lobe seizures caused by nonketotic hyperglycemia (NKH) have been reported in only a few cases and are not fully characterized. We report two cases of NKH-related occipital lobe seizures with high hemoglobin A1C (HbA1C), epileptiform electroencephalograph (EEG) and MRI abnormalities. Both patients had moderate hyperglycemia (310-372 mg/dl) and mildly elevated serum osmolarity (295-304 mOsm/kg) but markedly elevated HbA1C (13.8-14.4%). One patient had a clinico-EEG seizure originating from the right occipital region during sleep. The other patient had an interictal epileptiform discharge consisting of unilateral occipital beta activity in sleep. None of the previously reported cases fulfilled the criteria of a nonketotic hyperglycemic hyperosmolar (NKHH) state, or showed any interictal beta paroxysms, spikes, sharp waves, or spike/sharp-slow wave complexes. We suggest that prolonged exposure to uncontrolled hyperglycemia, as indicated by HbA1C, rather than an acute NKHH state is crucial in the development of this peculiar seizure. We also suggest clinicians look for the presence of interictal focal beta paroxysms in addition to the usual epileptiform discharges while reading the EEG of these patients.
Subject(s)
Glycated Hemoglobin/metabolism , Occipital Lobe , Seizures/blood , Seizures/physiopathology , Acidosis/complications , Adult , Anticonvulsants/therapeutic use , Brain/pathology , Electroencephalography , Female , Humans , Hyperglycemia/complications , Hyperglycemic Hyperosmolar Nonketotic Coma/blood , Hyperglycemic Hyperosmolar Nonketotic Coma/complications , Hyperglycemic Hyperosmolar Nonketotic Coma/physiopathology , Hypoglycemic Agents/therapeutic use , Magnetic Resonance Imaging , Male , Middle Aged , Phenytoin/therapeutic useABSTRACT
BACKGROUND: Asian Americans suffer from liver and cervical cancers, both vaccine preventable, yet vaccine awareness has not been described. METHODS: Cross-sectional survey (6 languages, 380 adult women). RESULTS: Those with limited English proficiency (LEP) were less likely to have accurate knowledge of cervical cancer vaccine (44% vs. 76%, among the 34% aware of any cancer-preventive vaccines) and were more likely to believe vaccines existed for non-vaccine-preventable cancers. Awareness of anti-liver cancer vaccine was low for both LEP and non-LEP women. CONCLUSION: There is a great need to educate Asian Americans about vaccine-preventable cancers, especially among LEP women.
Subject(s)
Asian/education , Cancer Vaccines/therapeutic use , Communication Barriers , Health Knowledge, Attitudes, Practice , Language , Neoplasms/prevention & control , Adult , Female , Health Education , Humans , Middle Aged , Patient Education as Topic , Public Health , Surveys and QuestionnairesABSTRACT
Parkinsonian variant of multiple system atrophy (MSA-P) clinically presents as autonomic dysfunction with parkinsonian features. Parkinsonian features include bradykinesia, rigidity, tremor, postural instability and poor levo-dopa response. Neuropathologically, MSA-P is characterized by selective neuronal loss and gliosis mainly affecting the putamen and caudate nucleus, substantia nigra, olivopontocerebellar pathway and intermediolateral cell column of the spinal cord. Therefore, the target of magnetic resonance imaging (MRI) is focused on signal changes or volume reduction on putamen, including putaminal slit, gliosis by diffusion studies and reduction of putaminal volume. There have been no reports describing clinical manifestations of MSA-P with imaging abnormalities over globus pallidus. Here, we describe three patients with typical presentations of MSA-P with autonomic dysfunction and disturbances of axial motor function with minimal appendicular symptoms, including postural instability and gait difficulties. MRI showed symmetrical hyperintensity over the center of globus pallidus surrounded by a mild low-signal rims at T2-weighted image that is similar to that of eye of the tiger sign except for the marked hypointense rims. Dopamine transporter scans showed symmetric reduction of uptake over bilateral basal ganglia. This is the first report concerning these unusual imaging findings in MSA-P patients and we believe there is a subgroup of MSA-P with clinical presentation of axial impairment and symmetrically abnormal signal changes of globus pallidus in MRI.