ABSTRACT
Immune abnormalities have been found in many patients receiving anti-epileptic drugs. However, the effects of carbamazepine are still conflicting. We report the case of a 31-year-old woman who began carbamazepine treatment because of idiopathic epilepsy of adulthood. After three years of treatment she developed arthralgias and malaise. Complete immunologic evaluation showed a total absence of immunoglobulin M with decreased levels of immunoglobulin A, positive antinuclear antibodies and monoclonal paraproteinemia type IgG-kappa. The possibility of B cell lymphoma or myeloma was ruled out. Skin testing was negative. Bone marrow examination was normal. After carbamazepine discontinuation, levels of IgA and IgM increased until reaching normal values over 3 years. The monoclonal gammopathy of undetermined significance also disappeared over this period. During this period of immunodeficiency, the patient did not complain of any infectious complications.
Subject(s)
Agammaglobulinemia/chemically induced , Anticonvulsants/adverse effects , Carbamazepine/adverse effects , IgA Deficiency/chemically induced , Immunoglobulin M/deficiency , Immunologic Deficiency Syndromes/chemically induced , Monoclonal Gammopathy of Undetermined Significance/chemically induced , Adult , Bone Marrow/pathology , Diagnosis, Differential , Epilepsy/complications , Epilepsy/drug therapy , Female , Humans , Immunoglobulin kappa-Chains/blood , Lymphoma, B-Cell/diagnosis , Monoclonal Gammopathy of Undetermined Significance/diagnosis , Multiple Myeloma/diagnosisABSTRACT
BACKGROUND: A decrease in hemoglobin production is probably the main cause of anemia observed in patients poisoned by lead although hemolysis caused by the effects on membrane or by inhibition of other enzymes such as 5'-pyrimidine nucleotidase may also play a key role. The main lead exposure source comes from lead use in industry; however, outside occupational exposure, food and water consumption is the main cause of lead exposure. MATERIALS AND METHODS: Clinical and analytical characteristics are reported of twelve patients with lead poisoning of food and water source occurred in the last 14 years in two health areas in north Extremadura. RESULTS: The exposure source was wine, vinegar and olives in one case, hand-made brandy in five, water consumption in houses with lead piping, and in two cases the cause was not determined. The clinical picture was similar in all cases with the exception of one female patient who had encephalopathy and hepatic failure. Diagnosis was suggested by regenerative anemia with basophilic stippling of erythrocytes. All patients received oral calcium disodium EDTA. CONCLUSIONS: Lead poisoning in non-industrial areas is a rare entity. Nevertheless, owing to the use of artisanal procedures for wine elaboration and derivatives, its occurrence is increasing. In a patient with symptoms of lead poisoning and regenerative anemia, a peripheral blood smear should be reviewed.
Subject(s)
Anemia, Hemolytic/chemically induced , Lead Poisoning/complications , Aged , Aged, 80 and over , Female , Humans , Male , Middle AgedABSTRACT
Introducción. La disminución en la producción de hemo es probablemente la causa principal de la anemia observada en pacientes intoxicados por plomo, si bien la hemólisis provocada por los efectos sobre la membrana o por inhibición de otras enzimas tales como la 5'-pirimidin nucleotidasa también pueden tener una importancia capital. La mayor fuente de exposición al plomo proviene de su utilización en actividades industriales; sin embargo, fuera del ámbito laboral el origen alimentario es la principal causa de contacto con este tóxico. Material y métodos. Presentamos las características clínicas y analíticas de 12 casos de saturnismo de origen alimentario producidos en los últimos 14 años en 2 áreas sanitarias del norte de Extremadura. Resultados. La fuente de exposición fue vino, vinagre y aceitunas en un caso, aguardiente artesanal en 5, en 2 pacientes fue por el consumo de agua canalizada por tuberías de plomo y en 2 no se determinó la causa. El cuadro clínico fue superponible en todos, excepto en 1 paciente con encefalopatía y fallo hepático. La anemia regenerativa con punteado basófilo sugirió el diagnóstico. Todos recibieron tratamiento con ácido etilendiaminotetracético (EDTA) cálcico disódico oral. Conclusiones. La intoxicación por plomo en zonas no industriales constituye una rareza; sin embargo, debido al uso de procedimientos artesanales en la elaboración del vino y sus derivados nuevamente se está incrementando. En un paciente con síntomas de saturnismo y con anemia regrenerativa debe revisarse la extensión de sangre periférica (AU)
Subject(s)
Middle Aged , Aged, 80 and over , Aged , Male , Female , Humans , Anemia, Hemolytic , Lead PoisoningABSTRACT
No disponible
Subject(s)
Adolescent , Aged , Female , Humans , Vitamins , Drug Labeling , Pharmaceutical Preparations , Amphetamines , Splenic Rupture , Rupture, Spontaneous , Spain , Triazines , Purpura, Thrombocytopenic, Idiopathic , Peliosis Hepatis , Anticonvulsants , Danazol , Agranulocytosis , EpilepsyABSTRACT
Hb Lepore is one of the most common abnormal haemoglobins in Caucasians in Central Portugal and in the Spanish Alta Extremadura (0.28% in a survey of school children). A group of 19 Portuguese and 14 Spanish Hb Lepore carriers (all unrelated) was characterised at the molecular level by the polymerase chain reaction, sequencing and restriction enzyme analysis. The Portuguese and one Spanish carrier were heterozygous for Hb Lepore-Baltimore, whereas all other Spanish subjects were Hb Lepore-Washington-Boston carriers. Sequencing of the Hb Lepore-Baltimore gene further established the crossover at delta 68-beta 84, a region two codons (CDs) shorter than that previously described and easily confirmed by digestion with MaeI and BanI. Data from haplotype analysis suggest that this crossover occurred as an independent event on the Iberian Peninsula. The haematological data were similar in both groups except for the levels of Hb F and the G gamma chain, which were significantly higher in the Hb Lepore-Baltimore heterozygotes. Quantification of the globin chains and the mRNA transcripts showed that the delta beta gene is transcribed at a higher level than the delta gene with levels of translation giving rise to 10%-15% of Hb Lepore. The different levels of Hb F observed in the two groups are the results of the higher transcription rate of the gamma genes in Hb Lepore-Baltimore heterozygotes and an apparently less efficient translation of G gamma genes in Hb Lepore-Washington-Boston heterozygotes.
Subject(s)
Hemoglobins, Abnormal/genetics , Base Sequence , DNA Primers , Genetic Carrier Screening , Hemoglobins, Abnormal/biosynthesis , Humans , Polymerase Chain Reaction , Portugal , RNA, Messenger/biosynthesis , Regression Analysis , Restriction Mapping , Spain , Transcription, GeneticABSTRACT
PURPOSE: To detect carriers of thalassaemia and haemoglobin variants among the northern Extremadura school population. MATERIAL AND METHODS: The study was carried out in the Plasencia health service area, comprising about 120,000 people. All children between 4 and 15 years of age were offered to take part in the programme. The first-stage screen was mean corpuscular volule (MCV) measured in a Coulter STKS automatic counter. When low VCM was detected, ferritin estimation was carried out; if ferritin was normal, hemoglobin A2 was quantified. Haemoglobin electrophoresis at pH 8.4 was performed in all samples whatever the MCV, and patients were classified into the following groups: iron deficiency, beta-thalassaemia, Hb Lepore, structural haemoglobin variant, or atypical microcytosis. RESULTS: Out of 22 schools from 20 towns, 2,818 children were studied, the participation reaching 75.48%. Lower than normal MCV was found in 162 children (5.74%), who were grouped as follows: thalassaemia, 15 cases (0.53%), Hb Lepore, 8 cases (0.28%), iron deficiency, 77 cases (2.73%), atypical microcytosis, 55 cases (1.95%), and structural variants 7 cases (0.24%). These variants were further identified as HbS (3), Hb Hofu (1), in natives, and HbC (3) in children from Morocco. Higher prevalence of anomalies was seen in some places: Riolobos, 1.5%, Galisteo, 2.5%, Jaraiz de la Vera, 3.02%; a significant group of Hb Lepore carriers was detected in this last town. CONCLUSIONS: The prevalence of abnormalities seen in some small towns or villages grants this type of programmes as such places, which could be considered as isolated communities, might provide a number of high-risk couples.
Subject(s)
Hemoglobinopathies/epidemiology , Mass Screening , Thalassemia/epidemiology , Adolescent , Blood Protein Electrophoresis , Child , Child, Preschool , Erythrocyte Indices , Female , Ferritins/analysis , Genetic Carrier Screening , Globins/genetics , Hemoglobin A2/analysis , Hemoglobinopathies/prevention & control , Hemoglobins, Abnormal/analysis , Hemoglobins, Abnormal/genetics , Humans , Male , Prevalence , Spain/epidemiology , Thalassemia/prevention & controlABSTRACT
Leprosy is an infrequent disease in Spain. 4,714 cases of leprosy was registered in the last national census (1979). The disease is still common in certain regions, such as Levant, Andalusia, Extremadura, Canary Island and Galicia. Lepromatous type is more frequent, a typical hallmark of endemies with low activity or characterized by regression. We report a patient affected of borderline lepromatous leprosy with the following characteristics: 1) the only known case in his locality, 2) lack of reaction after the treatment, and 3) due to its clinic, histological, and bacteriological characteristics was quite difficult to determine the leprosy's type. Even though the leprosy is an infrequent disease, it can be seen in everyday's practice, so that the internist and specialist. Have to know the disease in order to make an early diagnosis and to treat the patient effectively.
