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1.
Ann Endocrinol (Paris) ; 83(1): 46-53, 2022 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-34921812

RESUMEN

Throughout the world, millions of people suffer from fragilizing osteopathies such as osteomalacia and osteoporosis. Osteomalacia is a rare disorder, corresponding to mineralization abnormalities in adult bone, as opposed to rickets in children. Renal phosphate loss and hypophosphatasia are the main causes of vitamin-resistant osteomalacia. Diagnosis is based on clinical history, phosphocalcic metabolism assessment and, if necessary, molecular characterization, and must be rapid in order to initiate the most appropriate treatment and consider new treatments such as burosumab if necessary. Osteoporosis is characterized by reduced bone mass and strength, which increases the risk of fragility fracture. Fracture-related burden is expected to increase over the coming decades linked to the aging of population and a treatment gap. In order to reduce this treatment gap, it is important to develop two strategies: improvement of screening and of treatment. Systematic screening using the FRAX® fracture risk assessment tool could be useful to increase anti-osteoporosis medical treatment and reduce fracture rates. The question of treatment sequencing in osteoporosis is another challenge, notably after denosumab cessation, complicated by a decrease in bone mineral density and increased risk of fracture. New treatments are also available, including romosozumab, a humanized monoclonal antibody, which promotes bone formation and inhibits bone resorption by inhibiting sclerostin. Romosozumab is approved in several countries, including France, for treating severe osteoporosis in postmenopausal women at high risk of fracture and free of cardiovascular comorbidity. Endocrinologists need to be aware of these fragilizing osteopathies in order to improve both diagnosis and treatment.


Asunto(s)
Conservadores de la Densidad Ósea/uso terapéutico , Densidad Ósea/efectos de los fármacos , Calcificación Fisiológica/efectos de los fármacos , Osteomalacia/tratamiento farmacológico , Osteoporosis/tratamiento farmacológico , Anticuerpos Monoclonales/uso terapéutico , Anticuerpos Monoclonales Humanizados/uso terapéutico , Huesos/efectos de los fármacos , Femenino , Fracturas Óseas/tratamiento farmacológico , Francia , Humanos
2.
J Hosp Infect ; 126: 81-86, 2022 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-35623470

RESUMEN

BACKGROUND: With the increase in international travel and development of insecticide resistance, a re-emergence of the bed bug has been observed since the 2000s and it is becoming a worldwide public health problem. Hospitals and other medical settings have not been spared, while the cases reported remain limited. However, there are no specific recommendations for the healthcare settings in the literature. AIM: To report our experience of a bed bug infestation in a medical unit, in the French University Hospital Centre of Brest, caused by the admission of a patient carrier in October 2020. We described the practical methods used to control bed bugs infestation, evaluated the cost of this episode and created a specific procedure to take care of at-risk patients or known carriers of bed bugs. FINDINGS: The decision to close the unit for global treatment was taken after the investigations using a sniffer dog revealed that four rooms were infested. The closure lasted 24 days. We estimated the total cost of the infestation to be approximately US$400,000. No other wave of infestation occurred. We created a specific protocol of care for patients who were known carriers or at risk of carriage of bed bugs to graduate a strategy of control. CONCLUSION: Bed bug infestations in health facilities have a major impact on the care of patients and relevant economic consequences. Prevention and education policies are an essential starting point to respond to the scale of the phenomenon.


Asunto(s)
Chinches , Infestaciones Ectoparasitarias , Animales , Perros , Infestaciones Ectoparasitarias/epidemiología , Infestaciones Ectoparasitarias/prevención & control , Hospitales Universitarios , Humanos
3.
Ann Endocrinol (Paris) ; 78 Suppl 1: S11-S20, 2017 Oct.
Artículo en Francés | MEDLINE | ID: mdl-29157485

RESUMEN

The 2017 Endocrine Society annual meeting included several communications and debates on the conservative adrenal surgery in bilateral hereditary pheochromocytomas (BHP), bilateral adrenal macronodular hyperplasia (BAMH) and primary hyperaldosteronism (PHA). The general principle is to preserve a part of the adrenal cortex to prevent the occurrence of a definitive adrenal insufficiency. In BHP, cortical sparing surgery allows more than 50% of patients to maintain normal corticotropic function at 10 years with a low recurrence rate (~ 10%). Since the adrenal medulla cannot be removed entirely, recurrence seems inevitable and long-term follow-up is essential. Individual risk of malignancy must be taken into account. In BAMH responsible for Cushing syndrome, unilateral adrenalectomy induces a normalization of urinary free cortisol in 92 to 100% of cases and even corticotropic insufficiency in 40 to 100% of cases. This is most often transient. Late recurrences of Cushing's syndrome may occur in 13 to 60% of cases. Prolonged patient monitoring is therefore essential. In PAH with lateralized aldosterone production, minimally invasive partial adrenal surgery, which consists of removing only the adrenal adenoma visualized at TDM, allows an improvement blood pressure in about 94% of patients. However, failure or recurrence may occur. Its place therefore remains marginal in the treatment of the lateralized PAHs.


Asunto(s)
Corteza Suprarrenal/cirugía , Neoplasias de las Glándulas Suprarrenales/cirugía , Médula Suprarrenal/cirugía , Hiperaldosteronismo/cirugía , Neoplasia Endocrina Múltiple Tipo 2a/cirugía , Tratamientos Conservadores del Órgano/métodos , Feocromocitoma/cirugía , Corteza Suprarrenal/metabolismo , Neoplasias de las Glándulas Suprarrenales/complicaciones , Neoplasias de las Glándulas Suprarrenales/metabolismo , Médula Suprarrenal/metabolismo , Procedimientos Quirúrgicos Endocrinos/métodos , Humanos , Hiperaldosteronismo/etiología , Neoplasia Endocrina Múltiple Tipo 2a/complicaciones , Neoplasia Endocrina Múltiple Tipo 2a/metabolismo , Feocromocitoma/complicaciones , Feocromocitoma/metabolismo
5.
J Clin Endocrinol Metab ; 101(5): 2099-104, 2016 05.
Artículo en Inglés | MEDLINE | ID: mdl-27003306

RESUMEN

CONTEXT: Premature ovarian insufficiency (POI) may be secondary to chemotherapy, radiotherapy, or environmental factors. Genetic causes are identified in 20-25% of cases, but most POI cases remain idiopathic. OBJECTIVE: This study aimed to identify new genes involved in POI and to characterize the implication of CPEB1 gene in POI. DESIGN AND SETTING: This was a case report and cohort study replicate conducted in academic medical centers. PATIENTS AND METHODS: A deletion including CPEB1 gene was first identified in a patient with primary amenorrhea. Secondly, 191 sporadic POI cases and 68 familial POI cases were included. For each patient, karyotype was normal and FMR1 premutation was excluded. Search for CPEB1 deletions was performed by quantitative multiplex PCR of short fluorescent fragments or DNA microarray analysis. Gene sequencing of CPEB1 was performed for 95 patients. RESULTS: We identified three patients carrying a microdeletion in band 15q25.2. The proximal breakpoint, for the three patients, falls within a low-copy repeat region disrupting the CPEB1 gene, which represents a strong candidate gene for POI as it is known to be implicated in oocyte meiosis. No mutation was identified by sequencing CPEB1 gene. Therefore, heterozygous deletion of CPEB1 gene leading to haploinsufficiency could be responsible for POI in humans. CONCLUSION: Microdeletions of CPEB1 were identified in 1.3% of patients with POI, whereas no mutation was identified. This microdeletion is rare but recurrent as it is mediated by nonallelic homologous recombination due to the existence of low-copy repeats in the region. This result demonstrates the importance of DNA microarray analysis in etiological evaluation and counseling of patients with POI.


Asunto(s)
Eliminación de Gen , Menopausia Prematura/genética , Insuficiencia Ovárica Primaria/genética , Factores de Transcripción/genética , Factores de Escisión y Poliadenilación de ARNm/genética , Adulto , Estudios de Cohortes , Femenino , Humanos , Mutación
6.
Ann Endocrinol (Paris) ; 76(6 Suppl 1): S39-50, 2015 Oct.
Artículo en Francés | MEDLINE | ID: mdl-26776288

RESUMEN

Pregnancy is an immunological paradox that implies that a semi-allogeneic fetus is not rejected by the maternal immune system, from implantation of the embryo to delivery. Progesterone (P4), estradiol (E2) and human chorionic gonadotropin (hCG), contribute to the transformation of immune cells in a transient tolerance state, necessary to the maintenance of pregnancy. The effects of pregnancy hormones depend probably of their maternal plasma level. hCG is dangerous at high concentrations because it can stimulate autoantibodies production, whereas in physiological concentrations, hCG, P4 and E2 upregulate immune response expanding regulatory T and B cells, allowing the fetus to grow within the maternal uterus in a protective environment. A second example of fetal-maternal relation found recently is the role of maternal nutrition on development of the fetal hypothalamic neurons. Experiments in mice fed on a high fat diet reveal a critical timing when altered maternal metabolism affect formation of hypothalamic neurocircuits of the offspring and predispose him to long-term metabolic disorders.


Asunto(s)
Gonadotropina Coriónica/fisiología , Estradiol/fisiología , Intercambio Materno-Fetal/fisiología , Progesterona/fisiología , Animales , Enfermedades Autoinmunes , Femenino , Humanos , Hipotálamo/embriología , Inmunidad , Ratones , Embarazo
7.
Eur J Endocrinol ; 173(6): 819-26, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26392472

RESUMEN

BACKGROUND: MEN1, which is secondary to the mutation of the MEN1 gene, is a rare autosomal-dominant disease that predisposes mutation carriers to endocrine tumors. Most studies demonstrated the absence of direct genotype-phenotype correlations. The existence of a higher risk of death in the Groupe d'étude des Tumeurs Endocrines-cohort associated with a mutation in the JunD interacting domain suggests heterogeneity across families in disease expressivity. This study aims to assess the existence of modifying genetic factors by estimating the intrafamilial correlations and heritability of the six main tumor types in MEN1. METHODS: The study included 797 patients from 265 kindred and studied seven phenotypic criteria: parathyroid and pancreatic neuroendocrine tumors (NETs) and pituitary, adrenal, bronchial, and thymic (thNET) tumors and the presence of metastasis. Intrafamilial correlations and heritability estimates were calculated from family tree data using specific validated statistical analysis software. RESULTS: Intrafamilial correlations were significant and decreased along parental degrees distance for pituitary, adrenal and thNETs. The heritability of these three tumor types was consistently strong and significant with 64% (s.e.m.=0.13; P<0.001) for pituitary tumor, 65% (s.e.m.=0.21; P<0.001) for adrenal tumors, and 97% (s.e.m.=0.41; P=0.006) for thNETs. CONCLUSION: The present study shows the existence of modifying genetic factors for thymus, adrenal, and pituitary MEN1 tumor types. The identification of at-risk subgroups of individuals within cohorts is the first step toward personalization of care. Next generation sequencing on this subset of tumors will help identify the molecular basis of MEN1 variable genetic expressivity.


Asunto(s)
Neoplasias de las Glándulas Suprarrenales/genética , Neoplasias de los Bronquios/genética , Neoplasia Endocrina Múltiple Tipo 1/genética , Tumores Neuroendocrinos/genética , Neoplasias Pancreáticas/genética , Neoplasias de las Paratiroides/genética , Neoplasias Hipofisarias/genética , Neoplasias del Timo/genética , Adolescente , Neoplasias de las Glándulas Suprarrenales/epidemiología , Adulto , Distribución por Edad , Neoplasias de los Bronquios/epidemiología , Niño , Preescolar , Estudios de Cohortes , Femenino , Predisposición Genética a la Enfermedad , Humanos , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Tumores Neuroendocrinos/epidemiología , Neoplasias Pancreáticas/epidemiología , Neoplasias de las Paratiroides/epidemiología , Linaje , Neoplasias Hipofisarias/epidemiología , Neoplasias del Timo/epidemiología , Adulto Joven
8.
J Clin Endocrinol Metab ; 61(5): 957-62, 1985 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-3930556

RESUMEN

The recovery of exocrine and endocrine testicular function was studied in six patients orchidectomized for an estrogen-producing Leydig cell tumor. Gynecomastia disappeared in four patients. The contralateral testis, whose volume was reduced, returned to normal size after 30 days. Sperm density returned to normal in only one of the four patients in whom the preoperative sperm count was reduced. One day after unilateral orchidectomy, plasma estradiol decreased to normal and testosterone (T) fell about 50%. On the 10th postoperative day, plasma T [5.60 +/- 1.20 ng/ml (SD)] was normal. On day 120, T was higher than on day 10 (6.83 +/- 1.20 ng/ml). There was no significant increase of T after a single injection of hCG (5000 IU) on day 10, and the T response was similar to that of normal men on day 120. Plasma FSH and LH were increased on the 10th postoperative day; they then decreased between 60 and 120 days after the operation but were still above the normal values on day 120. The FSH/LH ratio, which was 0.43 +/- 0.17 preoperatively returned to normal (1.60 +/- 0.25) 10 days postoperatively. In conclusion, after hemicastration for an estrogen-secreting tumor, testicular hormonal secretion returns to normal within 120 days but spermatogenesis may still be impaired at this time.


Asunto(s)
Ginecomastia/sangre , Tumor de Células de Leydig/sangre , Orquiectomía , Neoplasias Testiculares/sangre , 17-alfa-Hidroxiprogesterona , Adulto , Gonadotropina Coriónica , Estradiol/sangre , Hormona Folículo Estimulante/sangre , Ginecomastia/etiología , Humanos , Hidroxiprogesteronas/sangre , Tumor de Células de Leydig/complicaciones , Tumor de Células de Leydig/cirugía , Hormona Luteinizante/sangre , Masculino , Persona de Mediana Edad , Neoplasias Testiculares/complicaciones , Neoplasias Testiculares/cirugía , Testosterona/sangre
9.
Biochem Pharmacol ; 44(9): 1745-56, 1992 Nov 03.
Artículo en Inglés | MEDLINE | ID: mdl-1449532

RESUMEN

Kinetics of the 2- and 4-hydroxylations of estradiol (E2) by human liver microsomal samples were studied to determine the major P450 isoform involved in these endogenous reactions. Thirty human liver microsomal samples were analysed. Metabolism of 25 microM [14C]E2 produced 2-hydroxy and 4-hydroxy derivatives with a ratio of 3.2 +/- 1.5 and a great inter-individual variation. Kinetic analysis of the 2- and 4-hydroxylations of E2 exhibited a curvilinear double reciprocal plot with an apparent Km of 15 microM. Further experiments demonstrated that alpha-naphthoflavone, testosterone and progesterone increased the 2-hydroxylation activity, suggesting the involvement of a substrate activation mechanism. These two hydroxylations of E2 were shown to be catalysed by cytochrome P450 with an apparent dissociation constant Ks of 0.8 microM. These 2- and 4-hydroxylations inter-correlated significantly (r = 0.93; N = 30). The 2-hydroxylation of E2 correlated with four monooxygenase activities known to be supported by P450 3A4/3A5, namely nifedipine oxidation (r = 0.78; N = 29); erythromycin N-demethylation (r = 0.69; N = 27), testosterone 6 beta-hydroxylation (r = 0.66; N = 25) and tamoxifen N-demethylation (r = 0.64; N = 29). On the other hand, E2-hydroxylations did not correlate with activities supported by P450 1A2 and P450 2E1. Furthermore, drugs as cyclosporin, diltiazem, triacetyl-oleandomycin and 17 alpha-ethynylestradiol inhibited more than 90% of the E2-hydroxylations at concentrations < 250 microM, while weak inhibition was shown with 500 microM cimetidine and no significant inhibition with caffeine, phenacetin and omeprazole. Finally, 2- and 4-hydroxylations of E2 correlated significantly with the content of P450 3A4/3A5 immunodetected by a monoclonal antibody anti-human P450-nifedipine (r = 0.84; N = 28). E2-hydroxylation activities were inhibited by more than 80% with polyclonal anti-human anti-P450-nifedipine. Preincubation of human liver microsomes with 100 microM gestodene (a suicide substrate of P450 3A4) inactivated this P450 isoform and accordingly allowed evaluation of the contribution of other P450 isoforms to the E2 metabolism to about 21% (+/- 17%, N = 29). All these results taken together suggest that P450 3A4/3A5 are the major forms involved in the formation of catecholestrogens in the human liver microsomes.


Asunto(s)
Sistema Enzimático del Citocromo P-450/metabolismo , Estradiol/metabolismo , Isoenzimas/metabolismo , Microsomas Hepáticos/enzimología , Adolescente , Adulto , Benzoflavonas/farmacología , Cafeína/farmacología , Preescolar , Citocromo P-450 CYP1A2 , Inhibidores Enzimáticos del Citocromo P-450 , Activación Enzimática , Femenino , Humanos , Hidroxilación , Lactante , Recién Nacido , Isoenzimas/antagonistas & inhibidores , Cinética , Masculino , Persona de Mediana Edad , Norpregnenos/farmacología , Oxidorreductasas/antagonistas & inhibidores , Oxidorreductasas/metabolismo , Fenacetina/farmacología , Congéneres de la Progesterona/farmacología , Tamoxifeno/farmacología , Testosterona/farmacología
10.
Diabetes Metab ; 29(6): 587-94, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14707887

RESUMEN

OBJECTIVE: Self monitoring of blood glucose (SMBG) in type 2 diabetes is a topic of current interest (imbalance between increased health-care costs and improvement in compliance with treatment and diet). An open label randomized prospective study was designed to compare changes in metabolic control over 6 months in patients managed with usual recommendations alone (conventional assessment group) or combined with SMBG. RESEARCH DESIGN AND METHODS: Patients not treated with insulin or previously self monitored, 40 to 75 years of age, with a diagnosis of type 2 diabetes > 1 year and standardized HbA(1c) level > =7.5 and< =11% were randomized to either a control group or SMBG group. They were followed up every 6 weeks over 24 weeks. Patients in the SMBG group were given the same device (Ascensia Esprit Discmeter, Bayer) and were required to perform at least 6 capillary assays a week (3 different days of the week, including weekend). Management of patients was standardized, including drugs, diet and physical activity. The primary efficacy criterion was change in HbA(1c) level in Intent To Treat (ITT) patients. Assays were performed at baseline, at 3 and 6 months using the calibrated DCA 2000(R) device (Bayer). RESULTS: Two hundred sixty five general practitioners randomized 988 patients (ITT Population), but 689 patients were evaluable for the primary criterion. At the endpoint, HbA(1c) was lower in the SMBG group (8.1 +/- 1.6%) than in the conventional treatment group (8.4 +/- 1.4%, P=0.012). The change in HbA(1c) levels between baseline and endpoint was classified into two classes: improvement if a change > 0.5% occurred, stability or worsening in case of a change< =0.5%; 57.1% of patients in the SMBG group vs 46.8% in the control group had an improvement in HbA(1c) level (P=0.007) after 3 months. A steady state was reached during the last 3 months. A multivariate logistic regression analysis was performed and identified factors predictive of improvement in HbA(1c) levels: HbA(1c) at baseline: odd ratio (OR)=1.749 (P<0.001), SMBG group (reference value: SMBG group): OR=0.665 (P=0.015), duration of diabetes: OR=0.953 (P=0.001) and BMI: OR=0.962 (P=0.039). CONCLUSIONS: This study is the first multicenter, controlled, prospective trial conducted on a large number of patients demonstrating that SMBG was statistically associated with a better quality of metabolic control than usual traditional recommendations alone in type 2 diabetes.


Asunto(s)
Automonitorización de la Glucosa Sanguínea , Diabetes Mellitus Tipo 2/sangre , Diabetes Mellitus Tipo 2/terapia , Adulto , Anciano , Automonitorización de la Glucosa Sanguínea/estadística & datos numéricos , Diabetes Mellitus Tipo 2/complicaciones , Dieta , Ejercicio Físico , Hemoglobina Glucada/análisis , Humanos , Hipoglucemia/epidemiología , Hipoglucemiantes/administración & dosificación , Persona de Mediana Edad , Oportunidad Relativa , Cooperación del Paciente , Estudios Prospectivos
11.
Neurophysiol Clin ; 19(5): 367-72, 1989 Nov.
Artículo en Francés | MEDLINE | ID: mdl-2615748

RESUMEN

A 60-year-old woman with acromegaly associated with sleep apnea was treated with the somatostatin analogue SMS 201-995 (Sandoz) for several months. Growth hormone levels were normalized and a rapid improvement in sleep apnea was controlled with polygraphic nocturnal monitoring. Hypophysectomy seems to have variable effects on sleep apnea in acromegaly. The origin of obstructive apnea in acromegaly is therefore unclear.


Asunto(s)
Acromegalia/complicaciones , Octreótido/uso terapéutico , Síndromes de la Apnea del Sueño/tratamiento farmacológico , Femenino , Humanos , Persona de Mediana Edad , Síndromes de la Apnea del Sueño/complicaciones , Factores de Tiempo
12.
Neurophysiol Clin ; 19(4): 311-25, 1989 Aug.
Artículo en Francés | MEDLINE | ID: mdl-2796927

RESUMEN

Ten subjects from 2 families with adrenoleukodystrophy (ALD) and adrenomyeloneuropathy (AMN), hereditary X-linked diseases, were systematically explored. We performed endocrinological, biochemical assays and neurophysiological tests; the latter consisted of nerve conductions (CNV), Hoffmann's reflex and multimodal evoked potentials: visual (flash and pattern, VEP), brainstem auditory (BAEP) and somesthetic (SEP) using median nerve stimulation at the wrist. We only considered values above 2 SD. The purpose of our study was to determine the correlation between neurophysiological and endocrinological perturbations and the presence of pathological traits. Our results suggest that the correlation is high in diseased male patients, lower for the ALD carriers (BAEP, SEP and CNV were more frequently abnormal) and very low for the AMN carriers. Only the biochemical assays appeared to have any value for the characterization of female carriers of ALD and AMN.


Asunto(s)
Enfermedades de las Glándulas Suprarrenales/genética , Adrenoleucodistrofia/genética , Esclerosis Cerebral Difusa de Schilder/genética , Enfermedades de la Médula Espinal/genética , Adolescente , Enfermedades de las Glándulas Suprarrenales/fisiopatología , Adrenoleucodistrofia/fisiopatología , Adulto , Niño , Preescolar , Potenciales Evocados Auditivos , Potenciales Evocados Somatosensoriales , Potenciales Evocados Visuales , Femenino , Humanos , Masculino , Nervio Mediano/fisiopatología , Persona de Mediana Edad , Conducción Nerviosa , Linaje , Enfermedades de la Médula Espinal/fisiopatología
13.
Ann Endocrinol (Paris) ; 55(5): 181-4, 1994.
Artículo en Francés | MEDLINE | ID: mdl-7857084

RESUMEN

A study has been realized in six patients with estrogen secreting Leydig cell tumors from 18 to 120 months after hemicastration. Testicular contralateral volume is normalized, gynecomastia can be completely reduced, sex steroids are normalized while gonadotropins can be temporary increased. Spermogram which is abnormal can be normalized. These results confirm the heterogeneity of these tumors.


Asunto(s)
Estrógenos/metabolismo , Tumor de Células de Leydig/metabolismo , Neoplasias Testiculares/metabolismo , Adulto , Estudios de Seguimiento , Humanos , Tumor de Células de Leydig/cirugía , Masculino , Orquiectomía , Neoplasias Testiculares/cirugía
14.
Ann Endocrinol (Paris) ; 64(5 Pt 1): 370-5, 2003 Nov.
Artículo en Francés | MEDLINE | ID: mdl-15067748

RESUMEN

The purpose of our study was to evaluate the incidence and risk factors of SIADH (syndrome of inappropriate antidiuretic hormone) and diabetes insipidus after pituitary adenoma surgery in patients and report follow-up data collected in our department of endocrinology. This retrospective study included 78 patients seen in the last 5 years. Possible risk factors of SIADH and diabetes insipidus were studies: patient age and gender, type of secretion, tumor volume, surgical approach, presence of postoperative pituitary failure. The incidence of SIADH and diabetes insipidus were similar: 12.8%. We did not find any risk factor for SIADH associated with postoperative anterior pituitary failure. This study illustrates the importance of postoperative follow-up after pituitary adenoma surgery.


Asunto(s)
Adenoma/cirugía , Diabetes Insípida/epidemiología , Síndrome de Secreción Inadecuada de ADH/epidemiología , Neoplasias Hipofisarias/cirugía , Complicaciones Posoperatorias , Adolescente , Adulto , Anciano , Niño , Diabetes Insípida/etiología , Femenino , Humanos , Síndrome de Secreción Inadecuada de ADH/etiología , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores de Riesgo
15.
Ann Endocrinol (Paris) ; 65(5): 459-65, 2004 Oct.
Artículo en Francés | MEDLINE | ID: mdl-15550888

RESUMEN

Oral manifestations of endocrine dysfunction often may be observed initially by the dentist. Objective manifestations, such as ophtalmos in hyperthyroidism, signs of hypersecretion of GH in acromegaly, are easily recognized. Dentists should have some knowledge of many other diseases in this category that occasionally come in our attention. The present article will discuss the effects of over and under-secretion of each endocrine gland separately, showing its influence on the development and maintenance of the health of the teeth and supporting structures. Diabetes mellitus is the most common endocrinological disease, with an incidence of 3%. Periodontitis risk is three time greater in diabetic patients than in general population and it may worsen the diabetes evolution. Periodontitis in diabetic patients needs an rapid diagnosis and treatment. We also presents the oral aspects of thyroid, parathyroid, suprarenalian, growth hormone and female hormones pathology. The incidence of these troubles is less important, but oral manifestations may reveal an endocrine disfunction.


Asunto(s)
Enfermedades del Sistema Endocrino/fisiopatología , Salud Bucal , Anorexia Nerviosa , Diabetes Mellitus , Enfermedades del Sistema Endocrino/patología , Femenino , Humanos , Enfermedades de las Paratiroides , Periodontitis , Enfermedades de la Hipófisis , Embarazo , Enfermedades de la Tiroides , Enfermedades Dentales , Síndrome de Turner
16.
Ann Endocrinol (Paris) ; 59(1): 20-2, 1998 Apr.
Artículo en Francés | MEDLINE | ID: mdl-9752394

RESUMEN

The aim of the study was to evaluate dexamethazone test in a patient with primary aldosteronism caused by an adrenocortical adenoma. We observed a 50% decrease of plasma aldosterone as in glucocorticoid suppressible aldosteronism (GSA) but absolute value of aldosterone remained higher than 40 pg/ml. Basal plasma and urinary values of 18 OXO and 18 OH cortisol were not significantly elevated as in GSA. Inversely, the evaluation of 11 beta-hydroxylase activity of mineralocorticoids was in favor of a benign adrenal tumor.


Asunto(s)
Adenoma/complicaciones , Neoplasias de la Corteza Suprarrenal/complicaciones , Aldosterona/sangre , Dexametasona/uso terapéutico , Hormonas/uso terapéutico , Hiperaldosteronismo/tratamiento farmacológico , Hiperaldosteronismo/etiología , Aldosterona/orina , Cortisona/análogos & derivados , Cortisona/sangre , Humanos , Hiperaldosteronismo/sangre , Masculino , Persona de Mediana Edad , Mineralocorticoides/sangre
17.
Ann Endocrinol (Paris) ; 54(6): 421-4, 1993.
Artículo en Francés | MEDLINE | ID: mdl-7944285

RESUMEN

Intracardiac ectopic thyroid tissue was removed in a 51 years old woman, after echography has discovered a tumor in the right ventricle. There was a normal thyroid gland in the neck and thyroid function tests were normal. Intra-cardiac ectopic thyroid tissue is very rare; it is due to an abnormality of embryological development, when thyroid anlage is in close contact with the embryonic heart.


Asunto(s)
Cardiomiopatías/diagnóstico , Coristoma/diagnóstico , Neoplasias Cardíacas/diagnóstico , Glándula Tiroides , Femenino , Ventrículos Cardíacos , Humanos , Persona de Mediana Edad
18.
Artículo en Francés | MEDLINE | ID: mdl-6520357

RESUMEN

TwO cases of megaloblastic anaemia, of which one was very severe, occurring in women who had been taking oestrogen-progestogen oral contraception over a long period of time, are reported. The authors take the opportunity, after having reviewed the literature, of pointing out the role of oestro-progestogen products in bringing about vitamin deficiencies. They discuss how and where oestrogen-progestogen products work on folic metabolism and emphasize that there is an associated factor which starts off the deficiencies.


Asunto(s)
Anemia Macrocítica/inducido químicamente , Anemia Megaloblástica/inducido químicamente , Anticonceptivos Orales Combinados/efectos adversos , Anticonceptivos Orales/efectos adversos , Adulto , Etinilestradiol/efectos adversos , Femenino , Humanos , Norgestrel/efectos adversos , Norgestrienona/efectos adversos
19.
Presse Med ; 24(15): 711-4, 1995.
Artículo en Francés | MEDLINE | ID: mdl-7784402

RESUMEN

OBJECTIVE: Determine the frequency and changes in thyroid hormones in Cushing's disease. METHODS: Free thyroxin and thyrotropin levels were measured in 11 patients (age range 17 to 60 years) with Cushing's disease both before and after resection of the pituitary adenoma. RESULTS: Free thyroxin levels were low (8.3 to 11.7 pmol/l) in 7 patients. These patients had no clinical manifestations of hypothyroidism. In 4 patients, cure of the pituitary adenoma led to normalization of the thyroid hormones 10 days after operation (13 to 55 pmol/l); in the other cases surgical cure was unsuccessful and thyroxin levels remained low. Cortisol levels were finally normalized in these patients after irradiation of the pituitary, a second pituitary operation, or bilateral resection of the adrenal glands in 2 patients. Normal thyroxin levels were thus achieved. There was no correlation between serum cortisol and free thyroxin. CONCLUSION: Thyroid hormones should be assayed regularly in patients with Cushing's disease as a supplementary control of treatment effectiveness.


Asunto(s)
Síndrome de Cushing/sangre , Tirotropina/sangre , Tiroxina/sangre , Adolescente , Adulto , Terapia Combinada , Síndrome de Cushing/radioterapia , Síndrome de Cushing/cirugía , Femenino , Humanos , Hidrocortisona/sangre , Masculino , Persona de Mediana Edad , Cuidados Posoperatorios , Cuidados Preoperatorios , Reoperación , Estudios Retrospectivos
20.
Presse Med ; 17(40): 2117-9, 1988 Nov 12.
Artículo en Francés | MEDLINE | ID: mdl-2974140

RESUMEN

Fifteen patients with prolactin-secreting pituitary adenoma completed a total of 18 pregnancies. Changes in blood prolactin levels and computerized tomographic images of the pituitary gland were studied. No increase in size of the adenoma was observed, and in 2 cases the tumour was found to be necrotic in the post-partum period. In all patients the prolactinaemia significantly decreased immediately after delivery. Thus, by inducing partial necrosis of the adenoma pregnancy may result in post-partum reduction of blood prolactin levels.


Asunto(s)
Neoplasias Hipofisarias/sangre , Embarazo/sangre , Prolactina/sangre , Prolactinoma/sangre , Adulto , Femenino , Humanos , Necrosis , Neoplasias Hipofisarias/diagnóstico por imagen , Neoplasias Hipofisarias/patología , Periodo Posparto/sangre , Prolactinoma/diagnóstico por imagen , Prolactinoma/patología , Radiografía
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