Pancytopenia with Hyperpigmentation – Fanconi Anaemia : A Case Report

Authors

  • MB Uddin Associate Professor, Department of Paediatrics, Pabna Medical College, Pabna
  • J Ferdous IMO, Department of Paediatrics, Rajshahi Paediatrics, Rajshahi Medical College, Rajshahi
  • KI Jahan MD (3rd Part) Student, Department of Biochemistry, Rajshahi Medical College Hospital, Rajshahi
  • MH Tarafder Assistant Registrar, Department of Paediatrics, Rajshahi Medical College Hospital, Rajshahi
  • F Zaman Assistant Registrar, Department of Paediatrics, Rajshahi Medical College Hospital, Rajshahi
  • A Hossain Associate Professor, Department of Paediatrics, Jessor Medical College, Jessor
  • S Yeasmin Assistant Professor, Department of Paediatrics, Rajshahi Medical College, Rajshahi
  • HS Das Indoor Medical Officer, Department of Paediatrics, Rajshahi Medical College Hospital, Rajshahi

DOI:

https://doi.org/10.3329/taj.v25i0.37565

Abstract

Fanconi Anemia (FA) is a rare autosomal recessive disorder associated with pancytopenia, spontaneous chromosomal instability and a variety of congenital anomalies. A variable phenotype and age of onset of anemia makes the diagnosis difficult in some cases. We report a case of Fanconi anemia who had triangular facies, hyperpigmentation, a few café-au-lait spots, microcephaly and short stature. Peripheral blood film showed pancytopenia, bone marrow study revealed aplasia and the patient had history of sibling (elder brother) death from same problem consistent with Fanconi anaemia.

TAJ 2012; 25: 84-86

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Published

2018-11-28

How to Cite

Uddin, M., Ferdous, J., Jahan, K., Tarafder, M., Zaman, F., Hossain, A., Yeasmin, S., & Das, H. (2018). Pancytopenia with Hyperpigmentation – Fanconi Anaemia : A Case Report. TAJ: Journal of Teachers Association, 25, 84–86. https://doi.org/10.3329/taj.v25i0.37565

Issue

Vol. 25 (2012)

Section

Case Reports