Author, Subjects, Keywords

Cited Author

 

 
   » By Author or Editor
 » Browse Author by Alphabet
 » By Journal
 » By Subjects
 » Malaysian Journals
 » By Type
 » By Year
 » By Latest Additions
 
 
   » By Author
 » Top 20 Authors
 » Top 20 Article
 » Top Journal Cited
 » Top Article Cited
 » Journal Citation Statistics
 » Usage Since Sept 2007


 
 
 

Login | Create Account

Congenital Dyserythropoietic Anaemia Type II-like Dysplastic Anaemia Preceding the Development of Non-Hodgkin Lymphoma – A Case Report.

Leong, C.F. , and Zainina S., and Cheong, S.K. , (2005) Congenital Dyserythropoietic Anaemia Type II-like Dysplastic Anaemia Preceding the Development of Non-Hodgkin Lymphoma – A Case Report. Malaysian Journal of Pathology, 27 (1). pp. 39-43. ISSN 0126-8635

[img]
Preview
PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
527Kb

Official URL: http://www.mjpath.org.my/past_issue/MJP2005.1/08Congenital.pdf

Affiliations

MAKNA-HUKM Cancer Institute, Kuala Lumpur. Clinical Haematology and Stem Cell Transplantation Services
MAKNA-HUKM Cancer Institute, Kuala Lumpur. Clinical Haematology and Stem Cell Transplantation Services
MAKNA-HUKM Cancer Institute, Kuala Lumpur. Clinical Haematology and Stem Cell Transplantation Services

Abstract

Anaemia is a frequent complication in patients with haematological malignancies and is caused by a variety of mechanisms including neoplastic cell infiltration into the bone marrow, haemolysis, nutritional deficiencies and defect in erythropoiesis or dysplastic anaemia as a result of the disease itself. However, acquired dysplastic anaemia which mimic congenital dyserythropoietic anaemia (CDA) type II morphology in the bone marrow is very rare. A 41-year-old Chinese man presented with refractory symptomatic anaemia in September 2001. He was clinically pale with no other significant physical finding. His initial peripheral blood picture showed normochromic normocytic anaemia with haemoglobin level of 26g/L, with no evidence of haemolysis and a poor reticulocyte response of 0.6%. Bone marrow aspiration was done and showed congenital dyserythropoietic anaemia (CDA) type II-like morphology. He was treated symptomatically with regular blood transfusions approximately every 3 weeks, until August 2002 when he developed multiple cervical lymphadenopathy with loss of appetite, loss of weight and low grade fever. Biopsy of the lymph node confirmed the diagnosis of small lymphocytic lymphoma. Staging with computed tomography and bone marrow aspirate revealed the infiltration of lymphoma cells into the marrow cavity consistent with the staging of IVB. This case report illustrates that CDA type II-like dysplastic anaemia can preceed the development of lymphoma.

Item Type:Journal
Keywords:CDA type II-like morphology, non-Hodgkin’s lymphoma.
Subjects:R Medicine, Dentistry, Pharmacy, Nursing
ID Code:3822

1. Heimpel H, Wendt F. Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts. Helv Med Acta 1968 34: 103-15.

2. Sandstrom H, Wahlin A, Eriksson M, Bergstrom I, Wickramasinghe SN. Intravascular hemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III. Eur J Haematol 1994 52: 42-6.

3. Byrnes RK, Dhru R, Brady AM, Galen WP and Hopper B. Congenital dyserythropoietic anaemia in treated Hodgkin’s disease (letter). Hum Pathol. 1980; 11: 485-6.

4. McCluggage WG, Hull D, Mayne E, Bharucha H,Wickramasinghe SN. Malignant lymphoma in congenital dyserythropoietic anaemia type III. J Clin Pathol 1996; 49: 599-602.

5. Achille L, Jean D, Sunitha N et al. Natural history of congenital dyserythropoietic anemia type II. Blood 2001; 8: 1258-60.

6. Okamura A, Matsui T, Yamaguchi A et al. Elderly dyserythropoietic anemia first diagnosed after presentation of hemorrhagic gastric ulcer. (Japanese) Rinsho Ketsueki 1999; 40: 1074-80. (abstract).

7. Wickramasinghe SN. Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data. Blood Rev 1998; 12: 178-200.

Repository Staff Only: item control page