Journal of Laboratory Physicians (Oct 2019)

A case of myelodysplastic syndrome with t(10;18)(q26;q21)

  • Yusuke Ohba,
  • Minami Yamada-Fujiwara,
  • Tadanori Minagawa,
  • Suguru Watanabe,
  • Yoko Okitsu,
  • Yoshihiko Izumi,
  • Junichi Kameoka,
  • Shinichiro Takahashi

DOI
https://doi.org/10.4103/JLP.JLP_61_19
Journal volume & issue
Vol. 11, no. 04
pp. 382 – 384

Abstract

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An 82-year-old male was admitted. Pancytopenia, a slightly low white blood cell count (3400/μL), and low levels of red blood cells (2.65 × 106/μL), hemoglobin (10.4 g/dL), and platelets (118,000/μL) were observed. Bone marrow aspiration was performed, revealing hypocellular bone marrow and normal blast levels (0.6%) with no dysplasia. G-banding chromosome analysis revealed the karyotype 45,X,-Y[3]/45, idem, t(10;18)(q26;q21)[13]/46,XY[4]. The patient was diagnosed with myelodysplastic syndrome, unclassified (MDS–U). This is the first case report demonstrating a patient with the chromosomal translocation, t(14;18)(q32;q21), which is extremely rare. This chromosomal aberration was critical for the diagnosis of MDS in this patient.

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