Discrimination of acute lymphoblastic leukemia from systemic-onset juvenile idiopathic arthritis at disease onset

Authors

  • Mirian S. Tamashiro Universidade de São Paulo; Faculdade de Medicina; Instituto da Criança; Pediatric Rheumatology Unit
  • Nadia Emi Aikawa Universidade de São Paulo; Faculdade de Medicina; Division of Rheumatology
  • Lucia Maria A. Campos Universidade de São Paulo; Faculdade de Medicina; Instituto da Criança; Pediatric Rheumatology Unit
  • Lilian Maria Cristofani Universidade de São Paulo; Faculdade de Medicina; Instituto da Criança; Pediatric Oncology Unit
  • Vicente Odone-Filho Universidade de São Paulo; Faculdade de Medicina; Instituto da Criança; Pediatric Oncology Unit
  • Clovis A. Silva Universidade de São Paulo; Faculdade de Medicina; Division of Rheumatology

DOI:

https://doi.org/10.1590/S1807-59322011001000001

Keywords:

Acute lymphoblastic leukemia, Juvenile idiopathic arthritis, Children, Limb pain, Thrombocytopenia

Abstract

OBJECTIVE: To assess clinical and laboratory features that differentiate acute lymphoblastic leukemia from systemic juvenile idiopathic arthritis at disease onset. METHODS: Fifty-seven leukemia patients with musculoskeletal involvement, without blasts on peripheral blood and without glucocorticoid therapy at disease onset and 102 systemic juvenile idiopathic arthritis patients (International League of Associations for Rheumatology criteria) were retrospectively evaluated. The following features were examined: fever, rheumatoid rash, arthritis, limb pain, hepatomegaly, splenomegaly, pericarditis, myocarditis, pleuritis, weight loss, bleeding, anemia, leukopenia, neutropenia, thrombocytopenia, erythrocyte sedimentation rate, and lactic dehydrogenase levels. RESULTS: The median age at disease onset was significantly higher in leukemia patients than in those with systemic-onset juvenile idiopathic arthritis (5.8 vs. 3.8 years). In addition, the frequencies of limb pain, hepatomegaly, weight loss and hemorrhagic manifestations were significantly higher in leukemia patients than in systemic-onset juvenile idiopathic arthritis patients (70% vs. 1%, 54% vs. 32%, 30% vs. 8%, and 9% vs. 0%, respectively). Likewise, the frequencies of anemia, leukopenia, neutropenia, thrombocytopenia and high lactic dehydrogenase levels were statistically higher in leukemia patients than in patients with systemic-onset juvenile idiopathic arthritis (88% vs. 57%, 39% vs. 1%, 60% vs. 1%, 77% vs. 1%, and 56% vs. 14%, respectively). Remarkably, multivariate analysis revealed that limb pain (OR = 553; 95% CI =46.48-6580.42) and thrombocytopenia (OR = 754.13; 95% CI =64.57-8806.72) were significant independent variables that differentiated leukemia from systemic-onset juvenile idiopathic arthritis. The R2 of the Nagelkerke test was 0.91, and the Kaplan-Meier survival curves were similar for acute lymphoblastic leukemia patients with and without limb pain. CONCLUSION: Our study emphasizes the importance of investigating leukemia in patients presenting with musculoskeletal manifestations and, in particular, limb pain associated with thrombocytopenia.

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Published

2011-01-01

Issue

Section

Clinical Sciences

How to Cite

Discrimination of acute lymphoblastic leukemia from systemic-onset juvenile idiopathic arthritis at disease onset . (2011). Clinics, 66(10), 1665-1669. https://doi.org/10.1590/S1807-59322011001000001