Skip to main content
Log in

Acute Myelogenous Leukemia WithPIG-A Gene Mutation Evolved from Aplastic Anemia—Paroxysmal Nocturnal Hemoglobinuria Syndrome

  • Case Report
  • Published:
International Journal of Hematology Aims and scope Submit manuscript

Abstract

We report a patient with aplastic anemia (AA)—paroxysmal nocturnal hemoglobinuria (PNH) syndrome who developed acute myelogenous leukemia (AML). Flow cytometric analysis showed that the leukemic cells in the bone marrow lacked CD59 antigen on their surface and were positive for P-glycoprotein. Heteroduplex and single-strand conformation polymorphism analysis followed by sequencing of the leukemic cells in the bone marrow disclosed 1 frameshift-type mutation in exon 2 of the phosphatidylinositol glycan-class A (PIG-A) gene, which deductively produces truncated PIG-A protein. These findings provide direct evidence that the leukemic cells evolved from the affected PNH clone. Cytogenetic analysis in the bone marrow in each stage of AA-PNH, AML, and at relapse of AML showed normal, −7, and −7 plus −20, respectively, showing evidence of a clonal evolution. Because complete remission of AML was not achieved by intensive chemotherapies, allogeneic peripheral blood stem cell transplantation (PBSCT) from the patient’s HLA-matched sister was performed successfully with recovery of CD59 antigen on bone marrow hematopoietic cells; however, leukemia relapsed 4 months after PBSCT. Leukemia derived from PNH may be resistant to intensive chemotherapy, and a highly myeloablative regimen may be required for stem cell transplantation to eradicate the PNH-derived leukemia clone.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Takeda J, Miyata T, Kawagoe K, et al. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria.Cell. 1993;73:703–711.

    Article  PubMed  CAS  Google Scholar 

  2. Kinoshita T, Inoue N, Takeda J. Defective glycosyl phosphatidylinositol anchor synthesis and paroxysmal nocturnal hemoglobinuria.Adv Immunol. 1995;60:57–103.

    Article  PubMed  CAS  Google Scholar 

  3. Nishimura J, Murakami Y, Kinoshita T. Paroxysmal nocturnal hemoglobinuria: an acquired genetic disease.Am J Hematol. 1999;62:175–182.

    Article  PubMed  CAS  Google Scholar 

  4. Azenishi Y, Ueda E, Machii T, et al. CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia.Br J Haematol. 1999;104:523–529.

    Article  CAS  PubMed  Google Scholar 

  5. Harris JW, Koscick R, Lazarus HM, Eshleman JR, Medof ME. Leukemia arising out of paroxysmal nocturnal hemoglobinuria.Leuk Lymphoma. 1999;32:401–426.

    Article  PubMed  CAS  Google Scholar 

  6. Devine DV, Gluck WL, Rosse WF, Weinberg JB. Acute myeloblastic leukemia in paroxysmal nocturnal hemoglobinuria: evidence of evolution from the abnormal paroxysmal nocturnal hemoglobinuria clone.J Clin Invest. 1987;79:314–317.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  7. Nakahata J, Takahashi M, Fuse I, et al. Paroxysmal nocturnal hemoglobinuria with myelofibrosis: progression to acute myeloblastic leukemia.Leuk Lymphoma. 1993;12:137–142.

    Article  PubMed  CAS  Google Scholar 

  8. Shichishima T, Terasawa T, Hashimoto C, et al. Discordant and heterogeneous expression of GPI-anchored membrane proteins on leukemic cells in a patient with paroxysmal nocturnal hemoglobinuria.Blood. 1993;81:1855–1862.

    PubMed  CAS  Google Scholar 

  9. van Kamp H, Smit J, van den Berg E, Ruud Halie M, Vellenga E. Myelodysplasia following paroxysmal nocturnal hemoglobinuria: evidence for the emergence of a separate clone.Br J Haematol. 1994;87:399–400.

    Article  PubMed  Google Scholar 

  10. Jin JY, Tooze JA, Marsh JCW, Matthey F, Gordon-Smith EC. Myelodysplasia following aplastic anaemia-paroxysmal nocturnal haemoglobinuria syndrome after treatment with immunosuppression and G-CSF: evidence for the emergence of a separate clone.Br J Haematol. 1996;94:510–512.

    Article  PubMed  CAS  Google Scholar 

  11. Mortazavi Y, Tooze J, Gordon-Smith E, Rutherford T. N-RAS gene mutation in patients with aplastic anemia/paroxysmal nocturnal hemoglobinuria during evolution to clonal disease.Blood. 1999;95:646–650.

    Google Scholar 

  12. Imamura N, Kusunoki Y, Kawa-Ha K, et al. Aggressive natural killer cell leukemia/lymphoma: report of four cases and review of the literature: possible existence of a new clinical entity originating from the third lineage of lymphoid cells.Br J Haematol. 1990;75:49–59.

    Article  PubMed  CAS  Google Scholar 

  13. Imamura N, Kimura A. Neutropenia among survivors of atomic bomb explosion.Lancet. 2000;355:117.

    Article  PubMed  CAS  Google Scholar 

  14. Imamura N, Tanaka R, Kajihara H, Kuramoto A. Analysis of peroxidase-negative acute unclassifiable leukemias by monoclonal antibodies, I: acute myelogenous leukemia and acute myelomonocytic leukemia.Eur J Haematol. 1988;41:420–428.

    Article  PubMed  CAS  Google Scholar 

  15. Nishimura J, Inoue N, Wada H, et al. A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones.Blood. 1997;89:3470–3476.

    PubMed  CAS  Google Scholar 

  16. Stafford HA, Nagarajan S, Weinberg JB, Medof ME. PIG-A, DAF and proto-oncogene expression in paroxysmal nocturnal haemoglobinuria-associated acute myelogenous leukaemia blasts.Br J Haematol. 1995;89:72–78.

    Article  PubMed  CAS  Google Scholar 

  17. Nafa K, Bessler M, Deeg H, Luzzatto L. New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuria.Blood. 1998;92:3422–3427.

    PubMed  CAS  Google Scholar 

  18. Imashuku S, Hibi S, Kataoka-Morimoto Y, et al. Myelodysplasia and acute myeloid leukaemia in case of aplastic anaemia and congenital neutropenia following G-CSF administration.Br J Haematol. 1995;89:188–190.

    Article  PubMed  CAS  Google Scholar 

  19. Szer J, Deeg H, Witherspoon R, et al. Long-term survival after transplantation for paroxysmal nocturnal hemoglobinuria with aplastic anemia.Ann Intern Med. 1984;101:193–195.

    Article  PubMed  CAS  Google Scholar 

  20. Antin J, Ginsberg D, Smith B, Nathan D, Orkin S, Rapperport J. Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria: eradication of the PNH clone and documentation of complete lymphohematopoietic engraftment.Blood. 1985;66:1247–1250.

    PubMed  CAS  Google Scholar 

  21. Kolb H, Holler E, Bender-Gotze C, Walther U. Myeloablative conditioning for marrow transplantation in myelodysplastic syndromes and paroxysmal nocturnal haemoglobinuria.Bone Marrow Transplant. 1989;4:29–34.

    PubMed  CAS  Google Scholar 

  22. Bemba M, Guardiola P, Garderet L, et al. Bone marrow transplantation for paroxysmal nocturnal haemoglobinuria.Br J Haematol. 1999;105:366–368.

    Article  PubMed  CAS  Google Scholar 

  23. Kawahara K, Witherspoon RP, Storb R. Marrow transplantation for paroxysmal nocturnal hemoglobinuria.Am J Hematol. 1992;39: 283–288.

    Article  PubMed  CAS  Google Scholar 

  24. Raiola A, Van Lint M, Lamparelli T, et al. Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria.Haematologica. 2000;85:59–62.

    PubMed  CAS  Google Scholar 

  25. Saso R, Marsh J, Cevreska L, et al. Bone marrow transplants for paroxysmal nocturnal haemoglobinuria.Br J Haematol. 1999;104: 392–396.

    Article  PubMed  CAS  Google Scholar 

  26. Cornelis F, Montfort L, Osselaer J, et al. Acute leukemia in paroxysmal nocturnal haemoglobinuria: case report and review of the literature.Hematol Cell Ther. 1996;1996:285–288.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hideo Tanaka.

About this article

Cite this article

Tanaka, H., Imamura, N., Oguma, N. et al. Acute Myelogenous Leukemia WithPIG-A Gene Mutation Evolved from Aplastic Anemia—Paroxysmal Nocturnal Hemoglobinuria Syndrome. Int J Hematol 73, 206–212 (2001). https://doi.org/10.1007/BF02981939

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02981939

Key words

Navigation