alexa Congenital Acute Lymphoblastic Leukemia: A Rare Presentation in a One Month Old Boy
ISSN: 2161-0665

Pediatrics & Therapeutics
Open Access

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Case Report

Congenital Acute Lymphoblastic Leukemia: A Rare Presentation in a One Month Old Boy

Hafiz MG* and Khaleque MA

Department of Pediatric Hematology and Oncology, Bangabandhu Sheikh Mujib Medical University, Shahbag, Dhaka, Bangladesh

*Corresponding Author:
Hafiz MG
Associate Professor
Department of Pediatric Hematology and Oncology
Bangabandhu Sheikh Mujib Medical University
Shahbag, Dhaka, Bangladesh
Tel: +8801756216979
E-mail: [email protected]

Received Date: January 24, 2014; Accepted Date: April 04, 2014; Published Date: April 07, 2014

Citation: Hafiz MG, Khaleque MA (2014) Congenital Acute Lymphoblastic Leukemia: A Rare Presentation in a One Month Old Boy. Pediat Therapeut 4:204. doi:10.4172/2161-0665.1000204

Copyright: © 2014 Hafiz MG, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

A one month old boy of non-consanguineous parents was admitted with gradual distension of abdomen, yellow coloration of whole body, progressive pallor and respiratory distress since birth. Septic investigations were done and found negative. His complete blood count with peripheral blood film examination revealed hyperleukocytosis, thrombocytopenia and presence of significant number of blasts cell. Cerebrospinal fluid (CSF) examination showed central nervous system (CNS) status 3(≥5 WBC/cmm3 with blasts). Other causes of leukemoid reaction were ruled out. Karyotyping had done and found normal chromosomal pattern (46XY). Bone marrow aspiration findings were suggestive of ALL-L1.His myeloperoxidase (MPO) and Sudan black stain was negative but Periodic acid schiff (PAS) stain was positive. Immunophenotype showed blasts cells which were positive for CD5(1.10%), CD8(0.4%), CD10(0.74%), CD13(13.7%) and CD19(62.4%). Finally, the boy was diagnosed as congenital acute lymphoblastic leukemia (ALL-L1, B-lineage, CNS status 3). Following chemotherapy, the child suddenly deteriorated and on the second day of therapy suddenly he expired possibly due to leukostasis or coagulopathy or non responsive of drugs or MLL gene translocation.So, congenital acute lymphoblastic leukemia (CALL) should be kept in mind in a newborn child with clinical features of sepsis, leukocytosis, thrombocytopenia, huge hepatosplenomegaly.

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