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1.
Tunis Med ; 87(2): 123-6, 2009 Feb.
Article in French | MEDLINE | ID: mdl-19522445

ABSTRACT

BACKGROUND: Hydatidosis is a parasitic endemic disease in Tunisia. The liver and lung are the most common sites of involvement; however, it can develop anywhere in the body. AIM: The aim of the present study was to analyse the epidemiological features of extrapulmonary hydatid cysts and compare our results with those reported in literature. METHODS: A retrospective study of 265 extrapulmonary hydatid cysts collected over the 18-year period from 1990 to 2007 was undertaken. RESULTS: There were 101 male and 164 female patients (sex ratio M/F = 0.61) ranging in age from 2 to 84 years (mean age = 38.7). In our series, hydatid cysts involved mainly the kidney (24.1%), the central nervous system (22.6%), the liver (19.6%) and the spleen (11.3%). The other less frequent sites included the peritoneum (n = 9), heart (n = 9), bone (n = 6), adrenal gland (n = 4), epiploon (n = 4), orbit (n = 4), ovary (n = 3), prostate (n = 2), bladder (n = 2), breast (n = 2), Douglas' cul-de-sac (n = 2), diaphragm (n = 1), testis (n = 1), broad ligament (n = 1), mediastinum (n = 1), nasal cavity (n = 1), soft tissue (n = 1), abdominal wall (n = 1), parotid gland (n = 1), psoas muscle (n = 1), synovia (n = 1), thymus (n = 1) et le pancreas (n = 1). CONCLUSION: In contrast to literature, our results show that hydatid cysts of the kidney and of the central nervous system are more frequent than hepatic location which occupies the 3rd rank.


Subject(s)
Echinococcosis/epidemiology , Echinococcosis/parasitology , Adolescent , Adult , Aged , Aged, 80 and over , Central Nervous System Parasitic Infections/epidemiology , Child , Child, Preschool , Digestive System Diseases/epidemiology , Digestive System Diseases/parasitology , Echinococcosis/pathology , Endocrine System Diseases/epidemiology , Endocrine System Diseases/parasitology , Female , Female Urogenital Diseases/epidemiology , Female Urogenital Diseases/parasitology , Heart Diseases/epidemiology , Heart Diseases/parasitology , Humans , Incidence , Male , Male Urogenital Diseases/epidemiology , Male Urogenital Diseases/parasitology , Mediastinal Diseases/epidemiology , Mediastinal Diseases/parasitology , Middle Aged , Musculoskeletal Diseases/epidemiology , Musculoskeletal Diseases/parasitology , Retrospective Studies , Tunisia/epidemiology
2.
Acta Trop ; 104(1): 16-24, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17767911

ABSTRACT

Symptoms consistent with hypothyroidism or adrenal insufficiency, such as lethargy, anorexia, cold intolerance, weakness, hypotension or paraesthesia, are frequently reported in the literature in patients with Human African Trypanosomiasis (HAT), but an endocrine origin for these symptoms has not yet been demonstrated. Thyroid and adrenocortical function were assessed in 60 patients with late-stage HAT and compared to those in 60 age- and gender-matched healthy controls. Clinical assessment and endocrine laboratory examinations were performed on admission, within 2 days after the end of treatment and at follow-up 3 months later. Signs and symptoms of hypothyroidism, such as fatigue, cold sensation, constipation, paraesthesia, peripheral oedema and dry skin, were significantly more frequent in HAT patients than in the controls. However, these signs and symptoms could not be attributed to hypothyroidism due to the lack of supporting laboratory data, and thus empirical replacement therapy for the clinically suspected hypothyroidism was not warranted. Signs and symptoms consistent with adrenal insufficiency, such as weakness, anorexia, weight loss or hypotension, were significantly more frequent in HAT patients than in controls, but they could not be associated with an insufficiency of the adrenocortical axis. Higher basal levels of cortisol were found in HAT patients than in controls, which can be viewed as a stress response to the infection. However, a transitory adrenal insufficiency was suspected in 8% of HAT patients at admission and in 9% at discharge. All values were normal at follow-up 3 months later.


Subject(s)
Endocrine System Diseases/metabolism , Trypanosoma brucei gambiense/isolation & purification , Trypanosomiasis, African/metabolism , Adolescent , Adrenal Insufficiency/metabolism , Adrenal Insufficiency/parasitology , Adult , Animals , Endocrine System Diseases/parasitology , Female , Humans , Hypothyroidism/metabolism , Hypothyroidism/parasitology , Male , Middle Aged , Trypanosomiasis, African/parasitology
3.
J Helminthol ; 79(1): 91-4, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15831119

ABSTRACT

European chub Leuciscus cephalus collected from five localities in the lowland and subalpine regions of Austria were analysed for oestrogenic effects of endocrine-disrupting chemicals and the presence of the plerocercoid of the tapeworm Ligula intestinalis. Of 1494 chub analysed, only seven (six males, one female) were found to be infected with single, but large plerocercoids up to 15 cm in length. Ligula-infected fish showed comparatively immature gonads, as demonstrated by the gonadosomatic index and gamete developmental stages. Plasma levels of the egg precursor protein vitellogenin also showed concentrations ranging below the detection limit. The present results indicate that chub infected with L. intestinalis and exposed to exogenous oestrogenic compounds can result in reduced gonadal maturation and produce false oestrogen-positive diagnoses in male fish. For plasma vitellogenin levels, L. intestinalis infections can result in false oestrogen-negative diagnoses in male and female fish.


Subject(s)
Cestoda/physiology , Cestode Infections/blood , Cestode Infections/veterinary , Endocrine System Diseases/parasitology , Fish Diseases/parasitology , Fishes/physiology , Animals , Austria , Biomarkers/blood , Endocrine System Diseases/blood , Estrogens/physiology , Female , Fish Diseases/blood , Fishes/blood , Fishes/parasitology , Fresh Water , Gonads/growth & development , Male , Reproduction/physiology , Vitellogenins/blood
4.
J Clin Endocrinol Metab ; 89(5): 2228-36, 2004 May.
Article in English | MEDLINE | ID: mdl-15126546

ABSTRACT

Carriers of congenital adrenal hyperplasia due to 21-hydroxylase (21-OH) deficiency demonstrate increased secretion of cortisol precursors after ACTH stimulation, suggestive of impaired cortisol production and compensatory increases in hypothalamic CRH secretion. Because both cortisol and CRH have behavioral effects, and hypothalamic CRH hypersecretion has been associated with chronic states of anxiety and depression, we performed endocrine and psychologic studies in consecutively admitted parents of patients with classic congenital adrenal hyperplasia due to 21-OH deficiency and parents of children with other chronic endocrine disorders. The number of excluded carriers because of pathologic reasons was higher than that of controls (P = 0.05). Carriers of 21-OH deficiency had a lower mean 24-h urinary free cortisol excretion (26.4 +/- 3.4 vs. 42.7 +/- 6.4 microg/d, P = 0.03) and higher peak ACTH (75.7 +/- 8.1 vs. 54.2 +/- 5.9 pg/ml, P = 0.04) and 17-hydroxyprogesterone (224.2 +/- 28.1 vs. 107.1 +/- 12.5 ng/dl, P < 0.001) concentrations post CRH stimulation than control subjects. Cortisol and androstenedione responses were similar in the two groups. Psychometric assessment performed by administering the State-Anxiety Inventory, Beck Depression Inventory, Profile of Mood States, Symptom Checklist-90R, and Temperament and Character Inventory revealed no differences between the two subject groups. Interestingly, a stepwise multiple linear regression model analysis in each population sample revealed that in carriers of 21-OH deficiency but not in the control subjects, a lower mean 24-h urinary free cortisol excretion and a higher ACTH response to ovine CRH stimulation predicted predisposition to obsessive-compulsive behavior, novelty seeking, reward dependence, and harm avoidance. We conclude that carriers of 21-OH deficiency appear to have mild hypocortisolism and compensatory changes of CRH secretion secondary to lower cortisol concentrations. These changes might predict mild predisposition of these subjects to physical and psychologic pathology, suggesting that larger studies are necessary.


Subject(s)
Adrenal Hyperplasia, Congenital/physiopathology , Adrenal Hyperplasia, Congenital/psychology , Endocrine Glands/physiopathology , Heterozygote , Psychological Tests , Stress, Physiological/etiology , Adrenal Hyperplasia, Congenital/complications , Adrenal Hyperplasia, Congenital/genetics , Adult , Case-Control Studies , Chronic Disease , Disease Susceptibility , Endocrine System Diseases/complications , Endocrine System Diseases/genetics , Endocrine System Diseases/parasitology , Endocrine System Diseases/physiopathology , Female , Humans , Linear Models , Male , Middle Aged , Psychometrics
5.
Exp Clin Endocrinol ; 101(3): 166-72, 1993.
Article in English | MEDLINE | ID: mdl-8223986

ABSTRACT

The disorders of the gonadotropic axis have been studied during the course of a "chronic" african trypanosomiasis induced experimentally in rats inoculated by the variant Trypanosoma brucei brucei AnTat 1.1.E. The levels of serum and pituitary LH as well as serum testosterone and corticosterone have been determined, during the infestation, at a particular period of the circadian cycle, in regard to the parasitemia variations. In addition, the inoculation of trypanosomal component fractions [obtained by concanavalin-A sepharose chromatography (conA-components)], has been performed in an attempt to define more exactly the nature of factor(s) producing the hypotestosteronemia in rats. This work evidenced that the hormonal parameter levels were predominantly decreased at the trypanolytic phase during the evolution of the disease. The action towards the hypothalamo-pituitary gonadal axis was attributed not only to peculiar trypanosomal enzyme(s) [a serine, thiol-dependent, cation sensitive endoprotease with a post-proline cleaving activity (purified from unretained conA fraction)], but also to protein and/or glycoprotein factor(s) released by the trypanosomes (components with affinity to the lectin).


Subject(s)
Endocrine System Diseases/physiopathology , Endocrine System Diseases/parasitology , Trypanosoma brucei brucei/growth & development , Trypanosomiasis, African/physiopathology , Trypanosomiasis, African/parasitology , Animals , Chronic Disease , Circadian Rhythm/physiology , Corticosterone/blood , Endocrine System Diseases/blood , Iodine Radioisotopes , Luteinizing Hormone/blood , Male , Rats , Rats, Sprague-Dawley , Testosterone/blood , Trypanosomiasis, African/blood
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