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Dergiler / Turkish Journal of Hematology / 2001 / Cilt: 18 - Sayı: 3

A case with micromegakaryocytes

Tiraje CELKAN
Hilmi APAK
Alp ÖZKAN
Hilal AKI
Mustafa TAŞYÜREKLİ
Lebriz YÜKSEL
İnci YILDIZ
Sayfa
203–206
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Micromegakaryocytes must always be treated with suspicion, as they may provide an important clue for dyshematopoesis.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:A boy with no previous history of bleeding presented with ecchymoses and splenomegaly.
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Temel Bulgular & Veri:He was followed up for thrombocytopenia and micromegakaryocytes for 20 months till clinically malignancy was diagnosed.
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Sonuç & Katkı:Micromegakaryocytes must always be treated with suspicion, as they may provide an important clue for dyshematopoesis.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Lösemi · Megakaryositler · Kemik iliği

Özet

A boy with no previous history of bleeding presented with ecchymoses and splenomegaly. He was followed up for thrombocytopenia and micromegakaryocytes for 20 months till clinically malignancy was diagnosed. Micromegakaryocytes must always be treated with suspicion, as they may provide an important clue for dyshematopoesis.

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Bu Makaleye Atıf Yap

CELKAN, T., APAK, H., ÖZKAN, A., AKI, H., TAŞYÜREKLİ, M., YÜKSEL, L., YILDIZ, İ. (2001). A case with micromegakaryocytes. Turkish Journal of Hematology, Cilt: 18 - Sayı: 3, 203–206. https://ajindex.com/articles/412980

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Kaynakça (10)

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  9. Wong KF, Chan JK. Are “dysplastic” and hypogranular megakaryocytes specific markers for myelodysplastic syndrome? Br J Haematol 1991;77: 509-14
  10. Olson TA, Levine RF, Kelleher J. Familial Thrombocytopenia with Micromegakaryocytes. Am J Pediatr Hematol Oncol 1992;14:248-54.