RESUMEN
AIMS: Few reports have assessed the relationship between Type 1 diabetes and sleep disorders. The purposes of our study were to determine the prevalence of obstructive sleep apnoea in Type 1 diabetes and to compare the clinical profile of people with Type 1 diabetes with or without obstructive sleep apnoea. METHODS: In this cross sectional study of 67 consecutive people with Type 1 diabetes, we performed polysomnography as part of their yearly check-ups. RESULTS: In our cohort, with a mean BMI of 25.8 ± 4.7 kg/m(2), the prevalence of obstructive sleep apnoea [apnoea-hypopnoea index (AHI) > 10/h] was 46%. Severe obstructive sleep apnoea (AHI ≥ 30/h) was present in 19% of the patients. We found no significant differences in age, sex, body mass index, HbA1c or Epworth sleepiness scale score between people with or without obstructive sleep apnoea. People with obstructive sleep apnoea had a longer course of diabetes mellitus (P < 0.01) and a higher prevalence of retinopathy (P < 0.01), neuropathy (P = 0.05), cardiovascular disease (P < 0.01) and hypertension (P < 0.01). The occurrence of macrovascular complications was independently associated with the presence of OSA [odds ratio (OR) 8.28; 95% confidence interval (CI), 1.56-43.97; P = 0.013] and the duration of diabetes (OR 1.08; 95% CI, 1.02-1.15; P = 0.01). Moreover, retinopathy was independently associated with OSA (OR 4.54; 95% CI, 1.09-18.82; P = 0.04) and the duration of diabetes (OR 1.09; 95% CI, 1.04-1.15; P = 0.001). CONCLUSIONS: The prevalence of obstructive sleep apnoea was high in people with Type 1 diabetes. Obstructive sleep apnoea was independently associated with macrovascular complications and retinopathy. Obesity and excessive daytime sleepiness were uncommon in this population.
Asunto(s)
Enfermedades Cardiovasculares/epidemiología , Diabetes Mellitus Tipo 1/complicaciones , Angiopatías Diabéticas/epidemiología , Neuropatías Diabéticas/epidemiología , Apnea Obstructiva del Sueño/epidemiología , Adulto , Índice de Masa Corporal , Enfermedades Cardiovasculares/etiología , Estudios Transversales , Diabetes Mellitus Tipo 1/epidemiología , Angiopatías Diabéticas/etiología , Neuropatías Diabéticas/etiología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Polisomnografía , Prevalencia , Factores de Riesgo , Apnea Obstructiva del Sueño/etiologíaRESUMEN
INTRODUCTION: Neuroborreliosis can be a difficult diagnosis which requires epidemiologic, clinical and biologic arguments. CASE REPORTS: We report two patients who presented with a recurrent laryngeal nerve palsy with positive Lyme serology and favorable outcome after antibiotic therapy. In one case, a lymphocytic meningitis with intrathecal production of specific antibodies was evidenced. CONCLUSION: Recurrent laryngeal nerve palsy is an uncommon manifestation of neuroborreliosis. Lyme serology is an important tool when neurologic disorder occurs because of an atypical course of Lyme disease.
Asunto(s)
Borrelia burgdorferi/aislamiento & purificación , Neuroborreliosis de Lyme/complicaciones , Neuroborreliosis de Lyme/diagnóstico , Parálisis de los Pliegues Vocales/diagnóstico , Parálisis de los Pliegues Vocales/microbiología , Anciano de 80 o más Años , Antibacterianos/uso terapéutico , Femenino , Humanos , Enfermedad de Lyme/complicaciones , Enfermedad de Lyme/diagnóstico , Neuroborreliosis de Lyme/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Sensibilidad y Especificidad , Pruebas Serológicas , Resultado del Tratamiento , Parálisis de los Pliegues Vocales/tratamiento farmacológicoRESUMEN
INTRODUCTION: The granulomatous mastitis is an inflammatory pseudotumor of the breast of which evolution benign but likely to generate important morphological after-effects among young women. This anatomoclinic entity of dubious etiology until these last years poses a problem of differential diagnosis with other etiologies of granulomatosis and especially with inflammatory carcinoma of the breast. The infectious theory is actually based on solid arguments and mainly explains the physiopathology of this affection. INTERPRETATION: A 26 years old young woman developed an inflammatory tumor of the left breast of which the catch of load by surgery and an antibiotherapy had shown trailing local continuations and of the esthetic after-effects. One year later, a very inflammatory repetition on the level of the right breast was dealt with in a different way: by steroids and immunomodulating drugs associated with iterative punctures with the purulent collections, the objective being to be less dilapidating that left side. The initial answer was rather favorable and encouraging but the purulent reappearance bulky granulomas with sinus way made reconsider the therapeutic attitude and antibiotics were undertaken after description of a lipophilic corynebactery in the material of puncture (Corynebacteria kroppenstedtii). The effectiveness of the amoxicilline introduced on the data of the antibiogram was undeniable. CONCLUSION: This observation illustrates the therapeutic and diagnostic difficulties of an exceptional affection. Potentially accessible to antibiotics it generally requires a joint surgical assumption of responsibility, at the same time to ensure the histological diagnosis but also with a therapeutic aim. The interest of steroids and the immunomodulation by methotrexate is debatable, these treatments cannot however be conceived without antibiotherapy and sometimes surgery.
Asunto(s)
Infecciones por Corynebacterium/diagnóstico , Granuloma de Células Plasmáticas/microbiología , Mastitis/microbiología , Adulto , Amoxicilina/uso terapéutico , Antibacterianos/uso terapéutico , Corynebacterium/clasificación , Corynebacterium/aislamiento & purificación , Diagnóstico Diferencial , Femenino , Glucocorticoides/uso terapéutico , Granuloma de Células Plasmáticas/diagnóstico , Humanos , Inmunosupresores/uso terapéutico , Mastitis/diagnóstico , Metotrexato/uso terapéutico , Prednisona/uso terapéutico , Punciones , RecurrenciaAsunto(s)
Ácido Ascórbico/uso terapéutico , Escorbuto/tratamiento farmacológico , Escorbuto/fisiopatología , Anciano , Diagnóstico Diferencial , Hemodinámica/efectos de los fármacos , Humanos , Masculino , Insuficiencia Multiorgánica/diagnóstico , Insuficiencia Multiorgánica/tratamiento farmacológico , Escorbuto/diagnósticoRESUMEN
INTRODUCTION: Pancreatic somatostatinoma is a rare entity and its association with Von Recklinghausen's disease has only been described on two occasions. We report a new observation, with clinical and evolving status differing from those described in isolated cases of somatostatinoma. OBSERVATION: A 28 year-old man presenting with familial Von Recklinghausen's disease, had suffered for 10 years from paroxysmic abdominal pain. He was hospitalized for intense pain. Imaging revealed a retroperineal tumoral formation. Following duodenopancreatectomy, somatostatinoma was diagnosed. Diffuse metastatic miliary was revealed and multiple glandular metastases. DISCUSSION: Other than the rarity of the morbid association (pancreatic somatostatinoma and Von Recklinghausen's disease) described, this case is particular in that the patient was very young, symptomatology was unapparent and tumoral evolution was minimal.
Asunto(s)
Neurofibromatosis 1/complicaciones , Neoplasias Pancreáticas/complicaciones , Somatostatinoma/complicaciones , Adulto , Humanos , Masculino , Neurofibromatosis 1/diagnóstico , Páncreas/patología , Neoplasias Pancreáticas/diagnóstico , Neoplasias Pancreáticas/patología , Neoplasias Pancreáticas/cirugía , Somatostatina/sangre , Somatostatinoma/diagnóstico , Somatostatinoma/patología , Somatostatinoma/cirugíaRESUMEN
Disulfiram self poisoning is exceptional. The authors report on the case of such an intoxication related to the ingestion of a potentially lethal dose of this drug (30 g) and draw the attention on the following points: 1) The initial signs may be misleading because they include both psychiatrics and neurological signs such as phonation abnormalities, myoclonias and tetraparesia. 2) The evolution is unforseeable with the possible occurrence of severe psychological and motricity sequaelae, associated with bilateral and symetric injuries of the putamen, the palladium and the basal nuclei on CT-scan (or MRI). The pathophysiologic al mechanisms of theses signs are discussed, and the need for disulfiram in the care of alcoholic patients seeking for withdrawal as well.
Asunto(s)
Disuasivos de Alcohol/envenenamiento , Disulfiram/envenenamiento , Intoxicación/diagnóstico , Adulto , Encéfalo/diagnóstico por imagen , Encéfalo/patología , Diagnóstico Diferencial , Femenino , Humanos , Imagen por Resonancia Magnética , Intoxicación/fisiopatología , Intoxicación/psicología , Intento de Suicidio , Tomografía Computarizada por Rayos XRESUMEN
BACKGROUND: Stenosis of the inferior vena cava is a rare cause of Budd-Chiari's syndrome. We report on such a case related to a specific cause with a dramatic improvement after endovascular treatment. CASE REPORT: A 53-year old woman was admitted to hospital because she demonstrated circulatory collapse, inferior limbs edema and post-prandial epigastralgia. These signs were related to the occurrence of a stenosis of the sus-hepatic segment of the inferior vena cava related to the presence of the distal part of a catheter. An angioplasty with the insertion of a stent was followed by a total recovery with a one-year survey. CONCLUSION: Angioplasty with the insertion of a stent should be considered in a Budd-Chiari syndrome related to the stenosis of the inferior vena cava. This option should be evaluated with reference to classic surgical techniques.
Asunto(s)
Síndrome de Budd-Chiari/etiología , Vena Cava Inferior , Angioplastia de Balón , Síndrome de Budd-Chiari/diagnóstico , Síndrome de Budd-Chiari/terapia , Constricción Patológica/complicaciones , Constricción Patológica/diagnóstico , Constricción Patológica/terapia , Femenino , Humanos , Persona de Mediana Edad , StentsAsunto(s)
Síndromes de Malabsorción/complicaciones , Infarto del Miocardio/etiología , Trombosis de la Vena/etiología , Deficiencia de Vitamina B 12/complicaciones , Anciano , Enfermedades del Sistema Digestivo/complicaciones , Enfermedades del Sistema Digestivo/diagnóstico , Femenino , Humanos , Absorción Intestinal , Síndromes de Malabsorción/diagnóstico , Masculino , Persona de Mediana Edad , Flebitis/etiología , Deficiencia de Vitamina B 12/diagnósticoAsunto(s)
Amiodarona/efectos adversos , Enfermedades Pulmonares Intersticiales/inducido químicamente , Isquemia Miocárdica/tratamiento farmacológico , Síndrome de Abstinencia a Sustancias/diagnóstico , Vasodilatadores/efectos adversos , Anciano , Amiodarona/uso terapéutico , Humanos , Cuidados a Largo Plazo , Enfermedades Pulmonares Intersticiales/diagnóstico , Masculino , Vasodilatadores/uso terapéuticoRESUMEN
Campylobacter fetus is an uncommon cause of meningitis in the adult. We report a case observed in an 84-year-old man with alcoholic cirrhosis. The patient presented fever, jaundice and a state of mental confusion. Blood and cerebrospinal fluid cultures identified Campylobacter fetus sensitive to several antibiotics. Ciprofloxacine-ceftriaxone combination replaced the antibiotics prescribed empirically prior to identification and led to regression of the fever and normal mental status within 4 days. Spinal tap on day 7 showed 20 white cells, 85% lymphocytes and normal protein level. Unfortunately, the patient later developed edema and ascitis with major jaundice. Oligo-anuria could not be controlled and the patient died two weeks after admission. Campylobacter fetus meningitis is predominantly seen in men, mean age of onset 50 years. Clinical signs are not specific and diagnosis can only be obtained on the basis of cerebrospinal fluid results. Adapted antibiotics are required.
Asunto(s)
Infecciones por Campylobacter , Campylobacter fetus , Meningitis Bacterianas , Anciano , Anciano de 80 o más Años , Antibacterianos , Infecciones por Campylobacter/líquido cefalorraquídeo , Infecciones por Campylobacter/tratamiento farmacológico , Quimioterapia Combinada/uso terapéutico , Humanos , Masculino , Meningitis Bacterianas/líquido cefalorraquídeo , Meningitis Bacterianas/tratamiento farmacológicoRESUMEN
Amiodarone, an iodine-rich benzofuranic derivative, may often induce hyperthyroidism and hypothyroidism. We report two cases of complex dysthyroidism, in which hypothyroidism and then hyperthyroidism alternated: we recall five former observations found in the literature. Their nosologic position and pathophysiologic mechanisms are discussed.
Asunto(s)
Amiodarona/efectos adversos , Antiarrítmicos/efectos adversos , Hipertiroidismo/inducido químicamente , Hipotiroidismo/inducido químicamente , Anciano , Femenino , Humanos , Hipertiroidismo/fisiopatología , Hipotiroidismo/fisiopatología , Masculino , Persona de Mediana EdadRESUMEN
The yellow nail syndrome is a clinical syndrome without specific biological parameters. It is characterized by the following threesome of symptoms: nail abnormalities, primary lymphedema, and pleuropulmonary manifestations. In most cases lymphography shows abnormalities of the lymphatic vessels and spirometry shows a restrictive defect and rarely obstructive disorders. Pathogenesis of this syndrome is still unknown. It is, however, remarkable that the yellow nail syndrome may occur in association with other diseases, the most frequent of which are cancer affections and immune disorders. We report two cases of the yellow nail syndrome which were associated with cancer (neoplasm of the larynx and breast).
Asunto(s)
Neoplasias de la Mama/complicaciones , Neoplasias Laríngeas/complicaciones , Linfedema/complicaciones , Enfermedades de la Uña/etiología , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , SíndromeRESUMEN
The Lyme disease, which was first found in Lyme, USA, in 1975 is an infectious multi-system disorder whose agent, the Borrelia Burgdorferi, was identified in 1983. Various disease manifestations have been reported since them. We report a case of Lyme disease manifestation in the muscle revealed by serious amyotrophy in the scapular muscles, in the neck and in the trunk with scapula alata accompanied by noctural lumbago which is resistant to non steroïd anti-inflammatory drugs. Electromyography showed patterns of the myogenic type in the serrate anterior and infraspinous muscles on both sides and patterns of the neurogenic peripheral type in the lower extremities. The histological, immunohistochemical and electron-microscopal studies of the muscle biopsy have been without any pathological result. Creatine kinase and aldolase proved normal. Serological antibodies were not significantly increased. A positive diagnosis was obtained by lumbar puncture which showed lymphocytic meningitis, by demonstrating specific antibodies in the cerebrospinal fluid and by Western Blot antibodies analysis. Efficacy of the antibiotic therapy has resulted in a rapid regression of the symptoms, which is a further confirmation of the previous diagnosis.
Asunto(s)
Enfermedad de Lyme/complicaciones , Distrofias Musculares/etiología , Anciano , Antibacterianos/uso terapéutico , Humanos , Inmunohistoquímica , Enfermedad de Lyme/diagnóstico , Enfermedad de Lyme/tratamiento farmacológico , Enfermedad de Lyme/inmunología , Masculino , Distrofias Musculares/tratamiento farmacológico , Distrofias Musculares/inmunología , Dolor/etiologíaRESUMEN
The five suppressors SUP35, SUP43, SUP44, SUP45 and SUP46, each mapping at a different chromosomal locus in the yeast Saccharomyces cerevisiae, suppress a wide range of mutations, including representatives of all three types of nonsense mutations, UAA, UAG and UGA. We have demonstrated that ribosomes from the four suppressors SUP35, SUP44, SUP45 and SUP46 translate polyuridylate templates in vitro with higher errors than ribosomes from the normal stain, and that this misreading is substantially enhanced by the antibiotic paromomycin. Furthermore, ribosomal subunit mixing experiments established that the 40 S ribosomal subunit, and this subunit only, is responsible for the higher levels of misreading. Thus, the gene products of SUP35, SUP44, SUP45 and SUP46 are components of the 40 S subunit or are enzymes that modify the subunit. In addition, a protein from the 40 S subunit of the SUP35 suppressor has an altered electrophoretic mobility; this protein is distinct from the altered protein previously uncovered in the 40 S subunit of the SUP46 suppressor. In contrast to the ribosomes from the four suppressors SUP35, SUP44, SUP45 and SUP46, the ribosomes from the SUP43 suppressor do not significantly misread polyuridylate templates in vitro, suggesting that this locus may not encode a ribosomal component or that the misreading is highly specific.
Asunto(s)
Proteínas Ribosómicas/genética , Saccharomyces cerevisiae/genética , Supresión Genética , Centrifugación por Gradiente de Densidad , Electroforesis , Código Genético/efectos de los fármacos , Sustancias Macromoleculares , Paromomicina/farmacología , Biosíntesis de Proteínas , Supresión Genética/efectos de los fármacosRESUMEN
Tetrahymena thermophila is a eucaryotic organism that is highly susceptible to growth inhibition by aminoglycoside antibiotics. Concentrations of paromomycin, gentamicin G418, and hygromycin B at 22, 10, and 17 microM, respectively, inhibited growth by 50%. A combination of in vitro and in vivo methods was used to determine the mechanisms of action of these aminoglycoside antibiotics on protein synthesis in T. thermophila. Analysis of polysome profiles from paromomycin- and gentamicin G418-treated cells showed clear, progressive depletions of polysomes concomitant with an inhibition of in vivo [14C] lysine incorporation. In vitro, paromomycin and gentamicin G418, which are disubstituted 2-deoxystreptamine-containing molecules, were not very effective inhibitors of either the translocation of peptidyl-tRNA or the elongation of nascent polypeptide chains on polysomes. In contrast, we found that the translocation of phe-tRNA on polyuridylate programmed ribosomes was susceptible to inhibition by paromomycin. We conclude that the primary inhibitory action of paromomycin and gentamicin G418 was at (i) an early stage of elongation after initiation, (ii) the initiation stage of translation, or (iii) a stage of translation before initiation. Hygromycin B, which is a monosubstituted 2-deoxystreptamine-containing aminoglycoside, potently inhibited the elongation of nascent chains during the translation of polysomes. In addition, the in vitro translation of polysomes from two hygromycin B-resistant mutants was resistant to the inhibition of elongation caused by hygromycin B.