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Abstract
Myelodysplasia syndromes (MDS) are a heterogenous group of clonal stem cell disorders which generally occur in adults. MDS are rare seen in patients with end-stage renal disease (ESRD). In this study, we presents a 38-year-old woman with ESRD who had regularly received hemodialysis therapy for two years. In this patient, we observed pancytopenia and the patient who survived for nine months by supportive therapy. In conclusion, supportive therapy should be prefered in MDS' patients with ESRD.
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Article Info
Published In
Journal
Turkish Journal of Nephrology
Volume / Issue
Volume 12 · Issue 2
Pages
112-115
History
Published Online
February 25, 2019
Copyright
Copyright (c) 2003 Turkish Journal of Nephrology
Affiliations
İdris ŞAHİN
Yüzüncü Yıl Üniv. Tıp Fak. İç Hastalıklan AD Nefroloji BD, Van
Mustafa KÖSEM
Yüzüncü Yıl Üniv. Tıp Fak. Patoloji AD, Van
Rıdvan MERCAN
Yüzüncü Yıl Üniv. Tıp Fak. İç Hastalıklan AD, Van
Doğan KOCA
Yüzüncü Yıl Üniv. Tıp Fak. İç Hastalıklan AD, Van
Lokman EMİNOV
Yüzüncü Yıl Üniv. Tıp Fak. İç Hastalıklan AD, Van
Reha ERKOÇ
Yüzüncü Yıl Üniv. Tıp Fak. İç Hastalıklan AD Nefroloji BD, Van
Cite this Article
ŞAHİN, İdris, KÖSEM, M., MERCAN, R., KOCA, D., EMİNOV, L., & ERKOÇ, R. (2019). A RARE CAUSE OF PANCYTOPENIA IN A PATIENT WITH END-STAGE RENAL DISEASE : MYELODYSPLASTIC SYNDROME (A CASE REPORT). Turkish Journal of Nephrology, 12(2), 112–115. Retrieved from https://www.turkjnephrol.org/index.php/pub/article/view/345
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