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1.
Front Endocrinol (Lausanne) ; 15: 1314752, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38327564

RESUMO

Precocious puberty is diagnosed when pubertal characteristics appear before the age of 8 years in females. The most common form is gonadotropin-dependent, called axial. The primary method of treatment is administration of gonadotrophin-releasing hormone analogues (GnRHa). The aim of the study was to verify hypothesis that GnRHa therapy in the childhood may be of additive risk factor for polycystic ovary syndrome (PCOS) in adulthood. Material and Methods: The study group consists of 24 women (median age 22 88 years, median BMI 23.5) treated with GnRHa for central precocious puberty in childhood. The control group includes 40 women (median age 23 years, median BMI 25.6) diagnosed with isolated premature thelarche and not using GnRHa in the childhood. Anthropometric measurements, ultrasound examination of minor pelvis and hormonal profile were performed. PCOS diagnosis was based on Rotterdam criteria. Results: The study confirmed a higher prevalence of PCOS in the study group (50%) than in the control group (10%); p=0.0006. Significant, linear correlation between free testosterone levels and ovarian size was found in the study group (R=0.45 p= 0.03). Conclusions: GnRHa therapy during childhood may have a potential influence on incidence of PCOS in the adulthood. Therefore, in this group of patients long-term follow-up focused on screening for PCOS would seem beneficial.


Assuntos
Síndrome do Ovário Policístico , Puberdade Precoce , Feminino , Humanos , Adulto Jovem , Adulto , Criança , Hormônio Liberador de Gonadotropina , Puberdade Precoce/tratamento farmacológico , Puberdade Precoce/epidemiologia , Puberdade Precoce/etiologia , Síndrome do Ovário Policístico/complicações , Síndrome do Ovário Policístico/tratamento farmacológico , Síndrome do Ovário Policístico/epidemiologia , Prevalência
2.
Ginekol Pol ; 93(10): 793-798, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36748173

RESUMO

OBJECTIVES: Vulvar lichen sclerosus (VLS) is a chronic inflammatory disease of unclear etiology. Recent studies show that 15-34% of cases in adult women and 14% in girls coexist with allergies or autoimmune diseases, among others - celiac disease (CD). Most of the research on the coexistence of VLS and autoimmune diseases has been carried out on a group of adult women. Literature data on this issue are very scarce. MATERIAL AND METHODS: The presented work is a pioneering project in which we tried to elucidate a possible relationship between celiac disease and lichen sclerosus in girls. The aim of the research was to study the antibodies characteristic of celiac disease in girls with VLS. The control group consisted of 35 heathy adolescent girls and the study group consisted of 20 girls aged 2-18 years old diagnosed with vulvar lichen sclerosus recruited at the Gynecological Clinic for Girls at the Women's Health Center in Katowice. RESULTS: There were no significant differences in the concentrations of antibodies characteristic for CD in the blood serum between the studied groups. CONCLUSIONS: The main limitation of our study was the small size of the study group. It is therefore legitimate to conduct further research on a larger study group to find themutual correlations between the analyzed antibodies and the onset and the course of VLS in girls. The finding of a positive correlation between the coexistence of VLS and CD may prevent potentially serious, long-term complications.


Assuntos
Doenças Autoimunes , Doença Celíaca , Hipersensibilidade , Líquen Escleroso e Atrófico , Líquen Escleroso Vulvar , Adulto , Adolescente , Feminino , Humanos , Pré-Escolar , Criança , Líquen Escleroso Vulvar/complicações , Líquen Escleroso Vulvar/diagnóstico , Doença Celíaca/complicações , Doença Celíaca/epidemiologia , Líquen Escleroso e Atrófico/complicações , Hipersensibilidade/complicações , Doenças Autoimunes/complicações
3.
Artigo em Inglês | MEDLINE | ID: mdl-34281089

RESUMO

Vulvar lichen sclerosus (VLS) is a chronic inflammatory condition affecting the anogenital region, which may present in a prepubertal or adolescent patient. The most popular theories are its autoimmune and genetic conditioning, although theories concerning hormonal and infectious etiology have also been raised. The most common presenting symptoms of VLS is vulva pruritus, discomfort, dysuria and constipation. In physical examination, a classic "Figure 8" pattern is described, involving the labia minora, clitoral hood, and perianal region. The lesions initially are white, flat-topped papules, thin plaques, or commonly atrophic patches. Purpura is a hallmark feature of VLS. The treatment includes topical anti-inflammatory agents and long-term follow-up, as there is a high risk of recurrence and an increased risk of vulvar cancer in adult women with a history of lichen sclerosus. This article reviews vulvar lichen sclerosus in children and provides evidence-based medicine principles for treatment in the pediatric population. A systematic search of the literature shows recurrence of VLS in children. Maintenance regimens deserve further consideration.


Assuntos
Líquen Escleroso e Atrófico , Doenças da Vulva , Líquen Escleroso Vulvar , Adolescente , Adulto , Anti-Inflamatórios/uso terapêutico , Criança , Feminino , Humanos , Líquen Escleroso e Atrófico/tratamento farmacológico , Líquen Escleroso Vulvar/tratamento farmacológico , Líquen Escleroso Vulvar/epidemiologia
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