1887
Volume 6 (2025) Number 2
  • EISSN: 2708-0463

Abstract

هدفت الدراسة الحالية إلى تشخيص طفيلي المتبرعمة الكيسية من عينات المرضى المشتبه بإصابتهم بالملتوية البوابية، إذ جمعت خلال هذه الدراسة 200 عينة غائط من الذكور والإناث من مختلف الأعمار من مستشفيات مدينة الموصل للفترة من يناير 2024 لغاية مارس 2025، للتحري عن الإصابة المشتركة بالملتوية البوابية والمتبرعمة الكيسية بالطرق المجهرية والمناعية، كما استُخدمت الخزع النسجية المعزولة من نفس الأشخاص، بواقع 100 عينة من المعدة لتشخيص البكتيريا، و100 عينة من الإثنى عشر؛ لتشخيص الطفيلي. وأظهرت نتائج اختبار مستضد الجرثومة الملتوية البوابية السريع Ag Rapid خلال فحص 200 عينة غائط، أن 61 عينة موجبة للملوية البوابية، كما أظهرت نتائج الفحص الجزيئي أن 76% من الخزع النسجية للمعدة أعطت نتيجة موجبة للملوية البوابية، في حين سجلت نتائج فحص عينات الغائط (أعطت نتيجة موجبة باستخدام اختبار مستضد الجرثومة الملتوية البوابية) بواقع 60 عينة غائط، أن نسبة 30.3% من العينات أعطت نتيجة موجبة لطفيلي المتبرعمة الكيسية. وأعطت الخزع النسجية للإثنى عشر نسبة إصابة موجبة قدرها 31.6% بالمتبرعمة الكيسية من المرضى المصابين بالملتوية البوابية خلال فحصها بواسطة تفاعل البلمرة المتسلسل.

This study aimed to diagnose from samples of patients suspected of being infected with . During this study, 200 stool samples were collected from gastrointestinal disorders males and females patients of all ages, to investigate co-infection with H. pylori and using microscopic and immunological methods. In addition, tissue biopsies were taken from the same individuals—100 gastric samples for bacterial diagnosis and 100 duodenal samples for parasitic diagnosis.

The results of the Antigen Rapid Test on 200 stool samples showed that 61 samples were positive for Histological examination revealed that 76% of the gastric biopsies tested positive for . Meanwhile, stool sample analysis using the antigen test showed that 60 stool samples tested positive. Additionally, 30.3% of the samples tested positive for Duodenal biopsies showed a positive infection rate of 31.6% for in patients infected with , as determined by polymerase chain reaction (PCR) testing.

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2025-09-30
2025-12-13

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