Literature DB >> 22397045

A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis.

Müge Gökçe1, Sule Unal, Hayriye Gülşen, Ozge Başaran, Mualla Cetin, Fatma Gümrük, Nesrin Beşbaş, Aytemiz Gürgey.   

Abstract

A 13-year-old boy presented with nausea, fatigue, weight loss, and bone pain for two months. Complete blood count and serum renal and liver function tests were all normal. Blood gas analysis revealed severe metabolic acidosis with high anion gap. Lactate level was 61.2 mmol/L. Abdominal ultrasonography yielded bilateral nephromegaly and hepatomegaly with increased echogenicity. Peripheral blood smear revealed 2% blasts. Bone marrow aspiration showed 'Common ALL Antigen'-negative acute lymphoblastic leukemia by flow cytometric analysis. Metabolic acidosis dissolved as soon as chemotherapy was begun. Lactic acidosis at the presentation of acute lymphoblastic leukemia--especially with low tumor burden--is a very rare and almost always fatal complication. Our patient is still alive and in remission, which is a point of interest in this child.

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Year:  2012        PMID: 22397045

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  2 in total

Review 1.  Extramedullary manifestations in acute lymphoblastic leukemia in children: a systematic review and guideline-based approach of treatment.

Authors:  Mahdi Shahriari; Nader Shakibazad; Sezaneh Haghpanah; Khadijeh Ghasemi
Journal:  Am J Blood Res       Date:  2020-12-15

2.  Fanconi Syndrome: A Rare Initial Presentation of Acute Lymphoblastic Leukemia.

Authors:  Kamal Kant Sahu; Arjun Datt Law; Nidhi Jain; Alka Khadwal; Vikas Suri; Pankaj Malhotra; Subhash Chander Varma
Journal:  Indian J Hematol Blood Transfus       Date:  2014-12-27       Impact factor: 0.900

  2 in total

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