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Iranian Journal of Blood and Cancer، جلد ۱۶، شماره ۳، صفحات ۸-۱۳
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چکیده فارسی مقاله
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عنوان انگلیسی Management of Hypoxia in the Simultaneous Presentation of Sickle Cell Trait and Cystic Fibrosis. Exploring a Rare Case with a Comprehensive Review
چکیده انگلیسی مقاله
Background: Cystic fibrosis (CF) is an inheriting disorder that has a strong impact on the pulmonary systems of individuals, as a result, hypoxia might be presented among patients who have CF. In addition, hypoxia is a pathological condition that might be present among patients with sickle cell trait (SCT). However, the simultaneous presentation of both SCT and CF in a patient is rare.
Case presentation: A 7-year-old boy came to the hospital with a chief complaint of cyanosis and cough. In his physical examination, he has low SpO2. His fiber-optic bronchoscopy depicted purulent secretion in the main bronchus. As well, his sweet chloride test was above 80 mmol/L. Thus, by the impression of CF exacerbation, he got HARD treatment and antibiotics. Additionally, during hospitalization, SCT as another impression was diagnosed for him.
Conclusion: Although the co-existence of CF and SCT is rare among patients. The physicians must consider both CF and SCT when a child comes to the emergency room with hypoxia.
کلیدواژه‌های انگلیسی مقاله Cystic fibrosis, Sickle cell trait, Hypoxia
نویسندگان مقاله | Seyed Ahmad Tabatabaii
Department of Pediatric Pulmonology, Mofid Pediatrics Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran


| Neda Entezari Farahabadi
Department of Pediatric Pulmonology, Mofid Pediatrics Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
نشانی اینترنتی http://ijbc.ir/browse.php?a_code=A-10-1196-1&slc_lang=en&sid=1
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کد مقاله (doi)
زبان مقاله منتشر شده en
موضوعات مقاله منتشر شده Pediatric Hematology & Oncology
نوع مقاله منتشر شده گزارش مورد
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