Dergiler / Cukurova Medical Journal / 2019 / Cilt: 44 - Sayı: 1

Fever of unknown origin: evaluation of 30 pediatric patients

Sayfa
215–220
Yayın Tarihi
2022-10-12
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

In our opinion, detailed patient history, carefullyphysical examination and close clinical follow-up mayreduce the number of the invasive procedures and noninvasive tests.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Purpose: The aim of this retrospective study is toevaluate the etiology clinical and laboratory features offever of unknown origin (FUO) diagnosed in 30 pediatricpatients.Materials and Methods: The clinical data including theetiology, diagnostic approaches and clinical characteristicswere retrospectively analysed in 30 pediatric patients withFUO who presented to our clinic in oneyear period.Results: The median age of the patients was 63 (6-192)months.
📊
Temel Bulgular & Veri:Among the patients, 12 were male (40%), while18 were female (60%).
💡
Sonuç & Katkı:In our opinion, detailed patient history, carefullyphysical examination and close clinical follow-up mayreduce the number of the invasive procedures and noninvasive tests.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Purpose: The aim of this retrospective study is toevaluate the etiology clinical and laboratory features offever of unknown origin (FUO) diagnosed in 30 pediatricpatients.Materials and Methods: The clinical data including theetiology, diagnostic approaches and clinical characteristicswere retrospectively analysed in 30 pediatric patients withFUO who presented to our clinic in oneyear period.Results: The median age of the patients was 63 (6-192)months. Among the patients, 12 were male (40%), while18 were female (60%). The median duration of the feverwas 22.5 (3-60) days during hospital admission. The mostcommon physical findings were hepatomegaly andsplenomegaly, which were observed in 53. 3 and 40patients, respectively. The cause of the FUO was detectedto be infection in 14 patients (46.6%), connective tissuevascular diseases in 8 patients (26.7%), malignancies in 5patients (16.7%), and miscellaneous diseases in 1 patient(3.3%). In two patients (6.6%) the etiology could not beidentified. Leishmaniasis, tuberculosis and Brucellosis werethe most commonly identified infections, whereas juvenilerheumatoid arthritis and acute lymphoblastic leukemiawere the most common non-infectious causes.Conclusion: The most common cause of FUO in ourstudy was infection diseases. Connective-vascular tissuediseases and malignancies are also important causes ofFUO. In our opinion, detailed patient history, carefullyphysical examination and close clinical follow-up mayreduce the number of the invasive procedures and noninvasive tests.

🔖

Bu Makaleye Atıf Yap

Aksaray, N., Alhan, E., Alabaz, D., Gündeşlioğlu, Ö. Ö., Kocabaş, E., Karagün, B. Ş. (2022). Fever of unknown origin: evaluation of 30 pediatric patients. Cukurova Medical Journal, Cilt: 44 - Sayı: 1, 215–220. https://ajindex.com/articles/476805

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (8)

  1. Özbolat G, Tuli A. Talasemi ve ilgili hemoglobinopatilerin moleküler tanı yöntemleri: günümüz ve gelecek. Adıyaman Üniversitesi Sağlık Bilimleri Dergisi, 2017;3:599-616
  2. Paglietti ME, Satta S, Sollaino MC, Barella S, Ventrella A, Desogus MF et al. The problem of borderline hemoglobin a2 levels in the screening for β-thalassemia carriers in Sardinia. Acta Haematol. 2016;135:193-9
  3. Özbolat G, Tuli A. Hematologic features of betaglobin gene mutation type (βo) with homozygous beta thalassemia. Ukr Biochem J. 2018;90:115-20
  4. Paglietti ME, Satta S, Sollaino MC, Barella S, Ventrella A, Desogus MF et al. the problem of borderline hemoglobin A2 levels in the screening for β-thalassemia carriers in Sardinia. Acta Haematol. 2016;135:193-9
  5. Menzel S, Garner C, Rooks H, Spector TD, Thein SL. HbA2 levels in normal adults are influenced by two distinct genetic mechanisms. Br J Haematol. 2013;160:101-5. 6. Șeicaru D, Constantinescu D, Corina F, Bulucea D. Heterozygous beta-thalassemia, a genetic haemolytic anaemia in continuous expansion. Acta Medica Marisiensis. 2013;59:154-7
  6. Kneifati-Hayek J. Fleischman W, Bernstein LH, Riccioli A, Bellevue R. A model for automated screening of thalassemia in hematology (math study). Lab Hematol. 2007;13:119-23
  7. Giambona A, Passarello C, Renda D, Maggio A. The significance of the hemoglobin A(2) value in screening for hemoglobinopathies. Clin Biochem. 2009;42:1786-96
  8. Özbolat G. Yılmaz N. Döğüş Y. Tuli A. The pregnancy variable in women with heterozygous beta thalassemia. Eur J Pharm Med Res. 2018;5:98-100.