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1.
Int J Immunopathol Pharmacol ; 24(2): 377-86, 2011.
Article in English | MEDLINE | ID: mdl-21658312

ABSTRACT

Patients with obstructive sleep apnea hypopnea syndrome (OSAHS) and thyroid function abnormalities, such as hypothyroidism and Hashimoto's thyroiditis, usually have closely resembling clinical features. Differentiation between these disorders is made more difficult because hypothyroid patients are also at risk for secondary sleep-disordered breathing. The aim of our study is to evaluate the prevalence of thyroid function abnormalities in children with OSAHS. Forty-four children (15 females: 29 males), 2.5-14.5 (7.43±2.98) years old were studied with overnight polysomnography. Biochemical screening of thyroid gland function was also carried out. Patients were judged to have OSAHS based mainly on the evaluation of Apnea Hypopnea index per hour of sleep (AHI). 15/44 (34.1%) children had mild OSAHS, 17/44 (38.6%) moderate and 12/44 (27.3%) severe OSAHS. Hypothyroidism was recorded only in 5/44 (11.4%) and Hashimoto's thyroiditis in 3/44 (6.8%) of OSAHS patients. Two patients with hypothyroidism showed mild and three severe OSAHS, while from the 3 children with Hashimoto's thyroiditis one presented mild, one moderate and one severe degree of OSAHS. Although the majority of studies in bibliography worldwide do not consider necessary the systemic evaluation of thyroid gland function in patients with breathing disorders during sleep, it seems that in children this type of screening is required for the differential diagnosis between primary sleep apnea and hypothyroid sleep-disordered breathing in order to differentiate these two conditions. Therefore, the laboratory investigation of thyroid gland function could be considered necessary.


Subject(s)
Hashimoto Disease/diagnosis , Hypothyroidism/diagnosis , Sleep Apnea, Obstructive/diagnosis , Thyroid Function Tests , Thyroid Gland/physiopathology , Adolescent , Analysis of Variance , Chi-Square Distribution , Child , Child, Preschool , Diagnosis, Differential , Female , Greece , Hashimoto Disease/epidemiology , Hashimoto Disease/physiopathology , Humans , Hypothyroidism/epidemiology , Hypothyroidism/physiopathology , Male , Polysomnography , Predictive Value of Tests , Prevalence , Severity of Illness Index , Sleep , Sleep Apnea, Obstructive/epidemiology , Sleep Apnea, Obstructive/physiopathology
3.
Hippokratia ; 13(4): 242-6, 2009 Oct.
Article in English | MEDLINE | ID: mdl-20011090

ABSTRACT

BACKGROUND: Acute exacerbations of respiratory diseases are a common cause of hospitalization among infants and children. AIM: To assess the epidemiological characteristics of asthma, bronchiolitis and croup among hospitalized children in Thessaloniki, from 1990 to 2003 included. METHODS: Data from the patient registry with discharge diagnosis "asthma", "bronchiolitis" and "croup" were analyzed retrospectively, in five Paediatric Departments of Thessaloniki. Age and sex of the patients, as well as the month of admission were taken into consideration. RESULTS: A total of 8762 admissions of children (aged 3 months-14 years) with the diagnosis of asthma, "bronchiolitis" and "croup", were identified. Sex distribution was 65.86% males (64.86% bronchiolitis, 65.26% asthma and 70.31% croup). Asthma admissions decreased by 53.65%, croup admissions decreased by 4.73%, while bronchiolitis admissions increased by 25.03%, during the study period. A clear seasonal variation was found in all the three diseases, with the lowest incidence during summer months. Moreover there were two peaks for asthma (one during spring and a second during autumn), one peak for bronchiolitis (during winter early spring) and one peak for croup (during autumn). CONCLUSIONS: Paediatric asthma and croup admissions have declined during the last 14 years, in contrast with bronchiolitis admissions, which showed an increased tendency. More frequent use of inhaled steroids and induction of asthma education programs may have contributed to decreasing asthma admission rates.

4.
Int J Oral Maxillofac Surg ; 24(4): 303-5, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7490496

ABSTRACT

Late recurrence or a delayed form of Caffey's disease is an exceedingly rare condition of unknown cause. A 3 1/2-year-old boy is presented with delayed Caffey's disease showing unilateral involvement of maxilla and zygoma.


Subject(s)
Hyperostosis, Cortical, Congenital/pathology , Maxillary Diseases/pathology , Zygoma/pathology , Child, Preschool , Edema/pathology , Fibrosis , Humans , Male , Palate/pathology , Periosteum/pathology , Periostitis/pathology , Recurrence
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