Dergiler / Turkish Journal of Hematology / 2018 / Cilt: 35 - Sayı: 4

Diagnostic Problems in Chronic Basophilic Leukemia

Kronik Bazofilik Lösemide Tanısal Sorunlar

Sayfa
283–289
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The literature review failed to reveal specificcytogenetic findings in patients with primary and secondary types ofCBL.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Chronic basophilic leukemia (CBL) is an extremely rare type ofleukemia.
📊
Temel Bulgular & Veri:Dysplasticchanges in peripheral blood and bone marrow were described anddemonstrated in cases of primary and secondary CBL.
💡
Sonuç & Katkı:The literature review failed to reveal specificcytogenetic findings in patients with primary and secondary types ofCBL.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Chronic basophilic leukemia (CBL) is an extremely rare type ofleukemia. A literature review revealed six cases reported as primaryCBL and five patients with secondary CBL. Patients with primaryCBL may present with symptoms not related to leukemia. Dysplasticchanges in peripheral blood and bone marrow were described anddemonstrated in cases of primary and secondary CBL. The literaturereview also revealed that differential counts made by automatedblood cell counters may not characterize cells as basophils in patientswith primary and secondary CBL and may mislead physicians inmaking a differential diagnosis. For these reasons, laboratory studiesfor the diagnosis of CBL are required, including metachromaticstaining by toluidine blue and antigen expressions by flow cytometricanalysis, to detect the nature of the neoplastic cells as basophils for areliable diagnosis of CBL. The literature review failed to reveal specificcytogenetic findings in patients with primary and secondary types ofCBL.

Abstract

Kronik bazofilik lösemi (KBL) son derece nadir bir lösemi tipidir. Literatürün gözden geçirilmesi ile primer KBL olarak altı olgu ve sekonder KBL olarak beş olgu rapor edildiği görüldü. Primer KBL’li hastalar, lösemi ile ilgili olmayan yakınmalar ile başvurabilirler. Primer ve sekonder KBL hastalarının periferal kan ve kemik iliği yaymalarında anormal değişiklikler tanımlandı ve gösterildi. Literatür taraması, primer ve sekonder KBL hastalarında otomatik kan hücre sayıcıları tarafından yapılan ayırıcı sayımların hücreleri bazofil olarak karakterize edemeyeceğini ve doktorları ayırıcı tanıda yanıltabileceğini ortaya koymuştur. Bu nedenle güvenilir bir KBL tanısı için neoplastik hücre türünün bazofil olarak saptanması, toluidine mavisi ile metakromatik boyanmayı ve membranlarındaki antijen ekspresyonlarını akım sitometrik analizi ile yapan kanıtlayıcı laboratuvar incelemelerini gerektirir. Literatürün gözden geçirilmesi primer ve sekonder KBL hastalarında özel sitogenetik bulgular olmadığını göstermiştir.

🔖

Bu Makaleye Atıf Yap

ÇEHRELİ, C. (2018). Diagnostic Problems in Chronic Basophilic Leukemia. Turkish Journal of Hematology, Cilt: 35 - Sayı: 4, 283–289. https://ajindex.com/articles/412409

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (15)

  1. Beafus AD, Denburg JA. Basophilic leukocytosis: mast cells and basophils. In: Greer JP (ed). Wintrobe’s Clinical Hematology, Twelfth Edition,
  2. Volume One. Philadelphia, Wolters Kluwer/Lippincott Williams & Wilkins, 2009.
  3. Pardanani AD, Morice WG, Hoyer JD, Tefferi A. Chronic basophilic leukemia: a distinct clinico-pathologic entity. Eur J Haematol 2003;71:18-22.
  4. Tang G, Woods LJ, Wang SA, Brettler D, Andersen M, Miron PM, Pechet L, Woda BA, Hao S. Chronic basophilic leukemia: a rare form of chronic myeloproliferative neoplasm. Hum Pathol 2009;40:1194-1199.
  5. Cehreli C, Ates H, Cehreli R, Sercan Z, Demirkan F. New paraneoplastic syndrome in chronic basophilic leukemia. Int J Hematol 2013;97:498-504.
  6. Cehreli C, Alacacioglu I, Piskin O, Ates A, Cehreli R, Calibasi G, Yüksel E, Ozkal S, Ozsan GH. Mast cell leukemia associated with undefined morphology and chronic basophilic leukemia. BMC Hematol 2014;14:17. Kyle RA, Pease GL. Basophilic leukemia. Arch Intern Med 1966;118:205-210.
  7. Xue Y, Guo Y, Lu D, Gu J, Lu D, Gong J, Wang M, Zhu W, Lin B. A case of basophilic leukemia bearing simultaneous translocation t(8;21) and t(9;22). Cancer Genet Cytogenet 1991;51:215-221.
  8. Cunningham MT, Ganguly S. Chronic myeloid leukemia in accelerated phase with basophilic transformation of the bone marrow. Am J Hematol 2006;81:380-381.
  9. Vaidya S, Madkaikar M, Ghosh K, Vundinti BR. Deletion of ABL/BCR on der (9) associated with severe basophilia. Indian J Hum Genet 2011;17:100- 103. Guzmán C, Hallal-Calleros C, López-Griego L, Morales-Montor J. Interleukin-6: a cytokine with a pleiotropic role in the neuroimmunoendocrine network. Open Neuroendocrinology 2010;3:152-160.
  10. Kantarjian HM, Dixon D, Keating MJ, Talpaz M, Walters RS, McCredie KB, Freireich EJ. Characteristics of accelerated disease in chronic myelogenous leukemia. Cancer 1988;61:1441-1446.
  11. Hoyle CF, Sherrington PD, Fischer P, Hayhoe FG. Basophils in acute leukemia. J Clin Pathol 1989;42:785-792.
  12. Payne V, Kamp PC. Mast cell tryptase: a review of its physiology and clinical significance. Anesthesia 2004;59:695-703. Perkins SL. Examination of the blood and bone marrow. In: Greer JP (ed). Wintrobe’s Clinical Hematology, Twelfth Edition,
  13. Volume One. Philadelphia, Wolters Kumer/Lippincott Williams & Wilkins, 2009.
  14. Daniel MT, Flandrin G, Bernard J. Leucémie aiguë a mastocytes: etude cytochimique et ultrastructurale, à propos d’une observation. Nouv Rew Fr Hematol 1975;15:319-332.
  15. Pinkus GS, Pinkus JL. Myeloperoxidase: a specific marker