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1.
Neuroendocrinology ; 114(10): 950-957, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38972302

RESUMO

INTRODUCTION: In 2011, we reported the overall incidence of Cushing's disease (CD) in Iceland from 1955 through 2009 to be 1.5 cases per million per year with highest incidence in the last decade of the study, a higher incidence then earlier reported. We now present a follow-up study reporting the epidemiology of the disease in Iceland during the 10-year period from 2010 to 2019. METHODS: In this nationwide retrospective study, clinical information on patients diagnosed with CD was obtained from electronic medical records, reviewed by consulting endocrinologists. RESULTS: Seventeen patients were diagnosed with CD, 12 women (71%) and 5 men (29%) giving an overall incidence of 5.2 cases per million per year. The mean age at diagnosis was 46 years (range 13-85 years). Biochemical analysis was recorded for all patients and 12 patients (71%) had visible pituitary adenoma on imaging studies. Sixteen patients (94%) were treated with transsphenoidal surgery of which 4 patients (24%) had gamma knife radiosurgery and three (18%) bilateral adrenalectomy after pituitary surgery. Two patients died during the study period. CONCLUSION: The overall incidence of CD of 5.2 cases per million per year is higher than previously reported, indicating the importance of awareness of CD. As all patients with CD are diagnosed and/or treated at the only University Hospital in Iceland, housing the only department of endocrinology as well as neurosurgery, we are confident that all cases diagnosed during the study period were included in the study.


Assuntos
Hipersecreção Hipofisária de ACTH , Humanos , Islândia/epidemiologia , Pessoa de Meia-Idade , Hipersecreção Hipofisária de ACTH/epidemiologia , Hipersecreção Hipofisária de ACTH/diagnóstico , Hipersecreção Hipofisária de ACTH/terapia , Feminino , Masculino , Adulto , Incidência , Idoso , Adolescente , Idoso de 80 Anos ou mais , Adulto Jovem , Estudos Retrospectivos , Seguimentos
2.
Laeknabladid ; 106(10): 460-463, 2020 10.
Artigo em Islandês | MEDLINE | ID: mdl-32991308

RESUMO

Woman in her thirties presented to the emergency room with a two-week history of worsening headache and diplopia. For eight years she had suffered from progressive weight gain, diabetes and hypertension that didn't improve with lifestyle modification. A lumbar puncture demonstrated increased intracranial pressure and MRI a pituitary adenoma. Physical examination was consistent with Cushing's syndrome and endocrine workup confirmed Cushing's disease. Treatment was complex, including unsuccessful pituitary surgery and gamma knife radiosurgery, and eventually bilateral adrenalectomy with subsequent development of Nelsons syndrome. This case illustrates the diagnostic delay that many patients with CD suffer from.


Assuntos
Adenoma Hipofisário Secretor de ACT/complicações , Adenoma/complicações , Obesidade/etiologia , Hipersecreção Hipofisária de ACTH/etiologia , Adenoma Hipofisário Secretor de ACT/diagnóstico por imagem , Adenoma Hipofisário Secretor de ACT/cirurgia , Adenoma/diagnóstico por imagem , Adenoma/cirurgia , Adulto , Diagnóstico Tardio , Feminino , Humanos , Imageamento por Ressonância Magnética , Obesidade/diagnóstico , Hipersecreção Hipofisária de ACTH/diagnóstico , Fatores de Risco , Resultado do Tratamento
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