Publications by authors named "H Latrech"

Introduction: Rathke cleft cyst apoplexy is exceedingly rare, particularly in infants. The most prevalent clinical manifestations include headaches, visual field defects, and endocrine dysfunction. Treatment options range from surgery to conservative methods, taking into consideration the balance of benefits and risks, especially during critical life stages such as childhood.

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Non-functioning pituitary adenomas (NFPAs) are hormonally inactive benign tumors, usually diagnosed as macro-adenoma. The aim of our research was to analyze the clinical and hormonal characteristics of NFPAs using Knosp and revised Knosp classifications. Furthermore, we aimed to assess the possibility of predicting surgical remission after surgery.

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Background: Managing type 1 diabetes in school is a real challenge for teachers, parents, and students themselves. Involving school educators in providing care and support is becoming more of a necessity than a luxury to facilitate access to healthcare services in schools for children with type 1 diabetes.

Objectives: Our work aimed to assess the background knowledge of teachers on type 1 diabetes and evaluate the impact of an educational intervention in improving this knowledge.

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Article Synopsis
  • Polycystic ovary syndrome (PCOS) is a widespread hormonal disorder in women of reproductive age, and this study focused on evaluating vitamin D levels in women with PCOS compared to healthy controls.
  • The study analyzed 176 women, finding that 40.2% of those with PCOS had vitamin D deficiency, significantly higher than the 24% observed in healthy controls, and those with both PCOS and obesity or insulin resistance had even lower vitamin D levels.
  • The research suggests that vitamin D deficiency may play a role in the development of PCOS, particularly in women with obesity or insulin resistance, indicating that vitamin D supplementation could be helpful in managing the condition.
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Article Synopsis
  • Paraganglioma is a rare neuroendocrine tumor that occurs outside the adrenal gland, and its pediatric form is particularly uncommon.
  • A 15-year-old boy experienced a hypertensive crisis caused by a left lateral-aortic paraganglioma, which was successfully managed with alpha-1 blockers before the complete surgical removal of the tumor.
  • Early intervention is crucial to prevent complications from high blood pressure, and preoperative care is necessary to minimize risks during and after surgery.
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