[Atypical leukemia accompanied by vitamin B12 deficiency].

Abstract

A 76 year old female with atypical leukemia complicated by vitamin B12 deficiency demonstrated marked fluctuation in blast percentage and hemopoiesis over 8 month period. She underwent surgical removal of pancreas head cancer 5.5 years ago. In January 1989 severe pancytopenia and mild increase of bone marrow blast were found. Blood transfusions and inadvertent administration of Vitamin B12 resulted in alleviation of pancytopenia and decrease in blast percentage. Several months later her bone marrow blast exceeded 30%, when serum B12 concentration was below 90 pg/ml. B12 injection and blood transfusion resulted in significant improvement in her hematological condition, but shortly thereafter she died of fulminant hepatitis. Her bone marrow cells showed a polyclonal constitution, as assessed by the RFLP-methylation technique using the PGK gene as a probe. The coexistence of leukemic- and normal clones under Vitamin B12 deficiency conditions and the differing behavior of such clones to B12 supplementation may explain the unusual clinical course observed in this patient.

• Authors: N Tsukamoto, K Inose, T Matsushima, T Uchiyama, Y Sugita, T Takeuchi, S Sato, M Omine, T Naruse
• Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology (Rinsho Ketsueki) Vol. 33 Issue 4 Pg. 461-6 (Apr 1992) ISSN: 0485-1439 [Print] Japan
• PMID: 1602609 (Publication Type: Case Reports, English Abstract, Journal Article, Research Support, Non-U.S. Gov't)

Topics

• Aged
• Bone Marrow (pathology)
• Female
• Hematopoiesis
• Humans
• Leukemia, Myeloid, Acute (blood, complications, pathology)
• Vitamin B 12 Deficiency (complications)