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1.
Headache ; 37(3): 137-41, 1997 Mar.
Article de Anglais | MEDLINE | ID: mdl-9100397

RÉSUMÉ

Visual auras (VAs) of 100 patients with migraine with aura were studied by questionnaire. Visual auras accompanied the patients' first headache (HA) in 39% of patients. Only 19% had VAs with every attack. Patients with VAs over the entire HA history had a high frequency (greater than 50%) of attacks with VA; patients with VA during only part of the HA history had a low frequency (less than 50%) of attacks with VA. The auras occurred exclusively prior to the HA in 57%. The free interval between the end of the VA and the start of the HA was usually (75%) shorter than 30 minutes. Most (59%) patients had VAs that lasted from 1 to 30 minutes. They started in the periphery of the visual fields in 56%. The most common phenomena described were: small bright dots (42%), flashes of light (39%), "blind spots" (32%), and "foggy vision" (27%). Fortification spectra was reported by only 20%. Although most (65%) patients had a combination of phenomena, the majority (72%) had only one uniform constellation of manifestations. There was no clear-cut relationship between side of VA and side of HA. Migraine VA is a pleomorphic and complex symptom. Many patients not qualifying for the diagnostic criteria of migraine with aura, as proposed by the International Headache Society (IHS), unequivocally present with visual phenomena that strongly suggest this diagnosis.


Sujet(s)
Migraines/complications , Migraines/physiopathologie , Troubles de la vision/étiologie , Adolescent , Adulte , Âge de début , Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Migraines/classification , Facteurs temps , Troubles de la vision/physiopathologie , Perception visuelle
2.
Headache ; 36(5): 291-4, 1996 May.
Article de Anglais | MEDLINE | ID: mdl-8682669

RÉSUMÉ

Side effects associated with administration of repetitive intravenous dihydroergotamine (DHE) were prospectively studied in 72 patients with chronic daily headache who were hospitalized in a dedicated inpatient headache treatment program. All patients received 11 consecutive doses of DHE, starting with 0.25 mg and increasing by 0.25 mg up to a maximum dose of 1.25 mg, depending on side effects and/or headache relief. The adverse events were recorded after each dose administered. The great majority of patients (91.6%) reported at least one side effect. The most common were: nausea (72.2%), increase in previous headache (47.2%), lightheadedness (33.3%), "new" headache (27.8%), and leg cramps (23.6%). The overall number of side effect complaints did not increase proportionally with the strength of the dose of DHE administered. These complaints declined from the earlier to the later doses of DHE, except for leg cramps, which were more common with the later doses. Side effects determined the strength of subsequent doses of DHE in only 18.1% of patients. Only four patients had to have a decrease in dosage and none required termination of DHE due to side effects. Although repetitive intravenous DHE causes frequent side effects, they are usually mild and transient and decrease with subsequent doses, even at higher doses.


Sujet(s)
Dihydroergotamine/effets indésirables , Céphalée/étiologie , Adolescent , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Enfant , Maladie chronique , Dihydroergotamine/administration et posologie , Femelle , Céphalée/induit chimiquement , Humains , Perfusions veineuses , Mâle , Adulte d'âge moyen , Nausée/induit chimiquement , Études prospectives
3.
J Pediatr ; 105(4): 564-8, 1984 Oct.
Article de Anglais | MEDLINE | ID: mdl-6481532

RÉSUMÉ

Seven children ages 1 1/2 to 12 years with congenital pernicious anemia were detected in an extended Mexican family. All affected children had megaloblastic anemia accompanied by low serum B12 and normal serum folate levels. Gastric fluid analysis in six patients revealed normal gastric acidity and absent intrinsic factor. Serum antibodies to intrinsic factor or parietal cells were also absent. Schilling tests performed in six of the seven patients yielded abnormal results. Of the three patients in whom gastric biopsy was done, two had normal histologic findings (including examination by electron microscopy) and one had mild atrophy. All patients responded rapidly to parenterally administered vitamin B12 therapy. In addition, 170 family members were screened for the defect with complete blood counts and serum B12 levels. Such screening detected pernicious anemia in two of the children, but no other abnormalities that could be attributed to pernicious anemia were found in other family members. Based on the family pedigree, autosomal recessive inheritance is likely. The variability of age of presentation in this family is noteworthy and suggests that expression may be modified by still undefined factors.


Sujet(s)
Anémie pernicieuse/génétique , Anémie pernicieuse/congénital , Anémie pernicieuse/diagnostic , Enfant , Enfant d'âge préscolaire , Femelle , Hispanique ou Latino , Humains , Nourrisson , Mâle , Pedigree
5.
J Pediatr ; 90(4): 548-54, 1977 Apr.
Article de Anglais | MEDLINE | ID: mdl-320298

RÉSUMÉ

Children with localized and metastatic neuroblastoma were studies to determine their immune status at the time of diagnosis and while they were receiving intensive intermittent chemotherapy; Investigations included leukocyte and differential counts, delayed hypersensitivity response, quantitative serum immunoglobulins, percentages of T and Fc receptor lymphocytes, PHA-induced mitogenesis, and antibody-and PHA-dependent cellular cytoxicity. Abnormalities related to the neoplasm at diagnosis were limited to depressed leukocyte and lymphocyte counts and increased concentrations of serum IgM in patients with metastases to bone marrow and other sites. No abnormalities were observed in those with localized tumors. Intermittent chemotherapy of metastatic neuroblastoma caused immunosuppression. Effects were most marked during five-day courses of chemotherapy; they included abrogation of DH and decreased leukocyte and lymphocyte counts and percentages of Fc receptor lymphocytes. Recovery of DH with partial recovery of leukocyte and lymphocyte counts was observed three weeks, later, prior to the next course, We conclude that both metastatic tumor and chemotherapy cause abnormalities of the immune system in children with neuroblastoma.


Sujet(s)
Antinéoplasiques/usage thérapeutique , Immunité cellulaire , Immunité , Neuroblastome/immunologie , Anticorps antitumoraux , Antinéoplasiques/pharmacologie , Enfant , Enfant d'âge préscolaire , Cyclophosphamide/pharmacologie , Cyclophosphamide/usage thérapeutique , Tests de cytotoxicité immunologique , Humains , Hypersensibilité retardée/immunologie , Immunité/effets des médicaments et des substances chimiques , Immunité cellulaire/effets des médicaments et des substances chimiques , Immunoglobulines/métabolisme , Techniques immunologiques , Nourrisson , Lectines/pharmacologie , Numération des leucocytes , Activation des lymphocytes , Lymphocytes/immunologie , Métastase tumorale , Neuroblastome/traitement médicamenteux , Facteurs temps
7.
J Pediatr ; 88(4 Pt 1): 553-6, 1976 Apr.
Article de Anglais | MEDLINE | ID: mdl-943492

RÉSUMÉ

The limulus lysate assay was utilized to detect and quantitate endotoxin in cerebrospinal fluid from 232 patients with suspected meningitis. The assay was positive in initial specimens of CSF from all 86 patients with gram-negative bacterial meningitis and was uniformly negative in the remaining 146 patients with a variety of infectious and noninfectious processes. Endotoxin concentrations in initial specimens of CSF from patients with gram-negative meningitis ranged from 4 to 2,000 ng/ml. No correlation between initial CSF levels of endotoxin and initial clinical or laboratory variables of infection was noted. With antibiotic therapy, CSF concentrations of endotoxin fall rapidly to undetectable levels after five days.


Sujet(s)
Endotoxines/liquide cérébrospinal , Méningite à hémophilus/liquide cérébrospinal , Méningite à méningocoques/liquide cérébrospinal , Méningite à pneumocoques/liquide cérébrospinal , Adulte , Enfant , Humains , Méningite à hémophilus/traitement médicamenteux , Méningite à méningocoques/traitement médicamenteux , Méningite à pneumocoques/traitement médicamenteux , Méthodes
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