Journals / Turkish Journal of Pediatrics / 2000 / Cilt: 42 - Sayı: 2

Juvenile rheumatoid arthritis presented with thrombocytopenia

Pages
162–164
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

After treatment with acetylsalicylic acid, leukocyte and platelet counts returned to normal levels, and after two months chronic arthritis developed.

📌 3 Key Takeaways

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Objective & Hypothesis:Leukopenia and thrombocytopenia are rare findings in systemic onset juvenile rheumatoid arthritis (S-JRA), and if present, bone marrow (BM) examination is necessary to exclude malignant diseases.
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Key Findings & Data:We report here a 13.5-year-old boy with S-JRA who had severe thrombocytopenia and mild leukopenia, without arthritis, at the onset of the disease.
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Conclusion & Impact:After treatment with acetylsalicylic acid, leukocyte and platelet counts returned to normal levels, and after two months chronic arthritis developed.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Leukopenia and thrombocytopenia are rare findings in systemic onset juvenile rheumatoid arthritis (S-JRA), and if present, bone marrow (BM) examination is necessary to exclude malignant diseases. We report here a 13.5-year-old boy with S-JRA who had severe thrombocytopenia and mild leukopenia, without arthritis, at the onset of the disease. BM was hypercellular with increased numbers of myeloid precursors and megakaryocytes. After treatment with acetylsalicylic acid, leukocyte and platelet counts returned to normal levels, and after two months chronic arthritis developed.

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Cite This Article

KOÇ, A., TATLI, M. M., EMİROĞLU, H. H., KÖSECİK, M., ATAŞ, A. (2022). Juvenile rheumatoid arthritis presented with thrombocytopenia. Turkish Journal of Pediatrics, Cilt: 42 - Sayı: 2, 162–164. https://ajindex.com/articles/613383

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