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[Severe hypercalcemia complicated in acute lymphoblastic leukemia (ALL) with E2A-HLF fusion gene: report of two cases and literature review].

AbstractOBJECTIVE:
To improve the understanding of severe hypercalcemia complicated in acute lymphoblastic leukemia (ALL) with E2A-HLF fusion gene, and to explore the mechanism of pathogenesis and the relationship between the special gene translocation and severe hypercalcemia.
METHODS:
Two patients with severe hypercalcemia complicated in ALL were reported.
RESULTS:
Two patients with E2A-HLF fusion gene, which is generated by t(17;19) (q22, p13) translocation, suffered relapse of leukemia three months after chemotherapy, and developed severe hypercalcemia. After further chemotherapy, the hypercalcemia symptoms were corrected or alleviated.
CONCLUSION:
Severe hypercalcemia is one of rare complications of ALL. In B cell lymphoblastic leukemia with E2A-HLF fusion gene, the fusion gene showed be closely monitored for evaluating the disease situation.
AuthorsJun Yang, Xuan Zhou, Bin Wang, Chao Gao, Rui-dong Zhang, Bin Li
JournalZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi (Zhonghua Xue Ye Xue Za Zhi) Vol. 30 Issue 9 Pg. 615-8 (Sep 2009) ISSN: 0253-2727 [Print] China
PMID19954622 (Publication Type: Case Reports, English Abstract, Journal Article, Review)
Chemical References
  • DNA-Binding Proteins
  • E2a-Hlf fusion protein, human
  • Oncogene Proteins, Fusion
  • Transcription Factors
Topics
  • Child
  • DNA-Binding Proteins (genetics)
  • Female
  • Humans
  • Hypercalcemia (etiology, genetics)
  • Infant
  • Male
  • Oncogene Proteins, Fusion (genetics)
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma (complications, genetics)
  • Prognosis
  • Transcription Factors (genetics)

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