TY - JOUR T1 - Assessment of tumor lysis syndrome cases TT - Tümör lizis sendromlu olguların değerlendirilmesi AU - Hüzmeli, Can PY - 2019 DA - March Y2 - 2019 DO - 10.7197/223.vi.460369 JF - Cumhuriyet Medical Journal JO - CMJ PB - Sivas Cumhuriyet University WT - DergiPark SN - 1305-0028 SP - 28 EP - 33 VL - 41 IS - 1 LA - en AB - Objective: Tumor lysissyndrome (TLS) is a clinical picture that occurs with the rapid destruction oftumor cells and with life-threatening metabolic disorders. The aim of our studyis to evaluate the etiologic causes, diagnosis and treatment of TLS cases. Method: The study wasconducted between January 2015 and December 2017 in KahramanmarasNecip Fazıl city Hospital.[HT1]Atotal of 32 patients diagnosed with TLS were included in the study. Laboratoryvalues of patients were scanned (blood urea nitrogen, creatinine, potassium,phosphorus, calcium, serum uric acid, lactate dehydrogenase) and diagnoses,chemotherapy and treatments were noted.Results: Of the 32 patientswho were included in the study, 17 were male and 15 were female. The averageage of the patients was found as 62,06 ± 12,10 (35-86) years. Hematologicmalignancy was detected in the etiology of11 of the TLS cases and solid tumor was detected in 21 of the TLS cases. Atotal of 12 (37.5%) patients had spontaneous TLS (5 in haematologicalmalignancy and 7 in solid tumor). Hyperpotassaemia 50%, hypocalcaemia 46.9%,hyperphosphatemia, hyperuricemia and acute kidney damage was present in allpatients. Mortality rate was found as 40.6%.Conclusions: Inour study, spontaneous TLS was detected at a high rate. In addition, themortality rate was also high. Early diagnosis and urgent treatment should beplanned to avoid mortalities. KW - Tumor lysis syndrome KW - malignancy KW - hyperuricemia KW - acute renal damage N2 - Amaç:Tümör lizis sendromu (TLS), tümörhücrelerinin hızlı bir şekilde yıkılmasıyla ortaya çıkan ve yaşamı tehditedebilen metabolik bozukluklarla seyreden klinik bir tablodur.Çalışmamızdaki amaç TLS olguların etyolojik nedenleri, tanı ve tedavilerini değerlendirmektir.Yöntem:Çalışma Ocak 2015 ile Aralık 2017tarihleri arasındaKahramanmaras Necip Fazıl Şehir[HT1]hastanesindeyapıldı. Çalışmaya, TLS tanısı konan toplam 32 hasta alındı. Hastalarındosyaları taranarak laboratuvar değerleri (kan üre azotu, kreatinin, potasyum,fosfor, kalsiyum, serum ürik asit, laktat dehidrogenaz), tanıları, aldıklarıkemoterapi ve tedavileri not edildi.Bulgular:Çalışmaya alınan toplam 32 hastanın17’si erkek, 15’i bayandı. Hastaların ortalama yaşları 62,06±12,10 (35-86) olaraksaptandı. TLS olgularının 11’nin etiyolojisinde hematolojik malignensi, 21’indeise solid tümör saptandı. Toplam 12 (37,5%) hastada spontan TLS (5’ihematolojik malignensi ve 7’si solid tümör) tespit edildi. Hiperpotasemi 50%oranında, hipokalsemi 46,9% oranında, hiperfosfatemi, hiperürisemi ve akutböbrek hasarı ise hastaların tümünde mevcuttu. Mortalite oranı 40,6% olaraksaptandı.Sonuç:Çalışmamızda spontan TLS yüksek orandasaptandı. Ayrıca mortalite oranıda yüksekti. Mortaliteden kaçınmak için erkentanı ve acil tedavi planlanmalıdır. CR - 1. Cairo MS, Bishop M. Tumour lysis syndrome: new therapeutic strategies and classification. Br J Haematol 2004; 127: 3-11. CR - 2. Annemans L, Moeremans K, Lamotte M, Garcia Conde J, van den Berg H, Myint H, et al. Incidence, medical resource utilisation and costs of hyperuricemia and tumour lysis syndrome in patients with acute leukaemia and non-Hodgkin's lymphoma in four European countries. Leukemia& lymphoma 2003;44:77-83. CR - 3. Darmon M, Vincent F, Camous L, Canet E, Bonmati C, Braun T, et al. 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