A Multicenter Case-Control Study on Predictive Factors Distinguishing Childhood Leukemia From Juvenile Rheumatoid Arthritis

Author:

Jones Olcay Y.1,Spencer Charles H.2,Bowyer Suzanne L.3,Dent Peter B.4,Gottlieb Beth S.5,Rabinovich C. Egla6

Affiliation:

1. Department of Pediatric Rheumatology, Children's National Medical Center and George Washington University, Washington, DC

2. Department of Pediatric Rheumatology, La Rabida Children's Hospital and University of Chicago, Chicago, Illinois

3. Department of Pediatric Rheumatology, James Whitcomb Riley Hospital, Indiana University, Indianapolis, Indiana

4. Division of Rheumatology, McMaster University, Hamilton, Ontario, Canada

5. Department of Pediatric Rheumatology, LIJ Schneider Children's Hospital, New Hyde Park, NY

6. Department of Pediatric Rheumatology, Duke University, Durham, North Carolina

Abstract

OBJECTIVE. Acute lymphocytic leukemia (ALL) often presents with musculoskeletal concerns such as pain or swelling, even before appearance of blasts in the peripheral blood. Such presentation may lead to misdiagnosis of a child with juvenile rheumatoid arthritis (JRA). This study was designed to identify the predictive factors for leukemia using basic clinical and laboratory information. METHODS. A retrospective chart review was performed using a simple questionnaire to compare the clinical and laboratory findings present during the initial visit to a pediatric rheumatology clinic for 277 children who were ultimately diagnosed with either JRA (n = 206) or ALL (n = 71). Sensitivity and specificity analysis of a variety of parameters, both singly and in combination, was performed to identify predictive value for ALL. RESULTS. The majority (75%) of children with ALL did not have blasts in the peripheral blood at the time of evaluation by pediatric rheumatologists. In children presenting with unexplained musculoskeletal complaints, the 3 most important factors that predicted a diagnosis of ALL were low white blood cell count (<4 × 109/L), low-normal platelet count (150–250 × 109/L), and history of nighttime pain. In the presence of all 3, the sensitivity and specificity for a diagnosis of ALL were 100% and 85%, respectively. Other findings, including antinuclear antibody, rash, and objective signs of arthritis, were not helpful in differentiating between these diagnoses because they occurred at similar rates in both groups. CONCLUSIONS. When a child develops new-onset bone-joint complaints, the presence of subtle complete blood count changes combined with nighttime pain should lead to consideration of leukemia as the underlying cause.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference26 articles.

1. Manners PJ, Bower C. Worldwide prevalence of juvenile arthritis why does it vary so much?J Rheumatol. 2002;29:1520–1530

2. Cassidy JT, Petty RE. Juvenile rheumatoid arthritis. In: Cassidy JT, Petty RE, eds. Textbook of Pediatric Rheumatology. Philadelphia, PA: WB Saunders; 2001:218–321

3. Cassidy JT, Levinson JE, Bass JC, et al. A study of classification criteria for a diagnosis of juvenile rheumatoid arthritis. Arthritis Rheum. 1986;29:274–281

4. Margolin JF, Poplack DG. Acute lymphoblastic leukemia. In: Pizzo PA, Poplack DG, eds. Principles and Practice of Pediatric Oncology. Philadelphia, PA: Lippincott-Raven Publishers; 1997:409–482

5. Cabral DA, Tucker JB. Malignancies in children who initially present with rheumatic complaints. J Pediatr. 1999;134:53–57

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