Kronik Lösemi Paneli (KLL)
Sanal Hastane||1 dk okuma

Kronik lenfositik lösemi (KLL) tüm lösemilerin yaklaşık %30’unu
oluşturur. Yetişkinlerdeki en yaygın nedenidir. Tanısının konulduğu
ortalama yaş 64’dür. KLL, B-lenfositlerin klonal bozukluğudur.
KLL alt grupları ve diğer lösemi çeşitleri;
B-KLL (tipik) % 90-95
Diğerleri % 1-5
*Prolenfositik lösemi,
*Malign lenfoma, lösemi,
*Geniş granüler lenfositik lösemi,
*Yetişkin T hücreli lenfoması/lösemisi,
*Mycozis fungoides/ Sezary sendromu,
*Plazma hücreli lösemi,
*Hairy cell lösemi.
#Geniş granüler lenfositik lösemi#Hairy cell lösemi#KLL#Kronik lenfositik lösemi#Lösemi#Malign lenfoma#Mycozis fungoides/ Sezary sendromu#Plazma hücreli lösemi#Prolenfositik lösemi#Yetişkin T hücreli lenfoması/lösemisi
Kaynaklar ve Referanslar
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- [3]Hallek M, Cheson BD, Catovsky D, et al. “iwCLL guidelines for diagnosis, indications for treatment, response assessment, and supportive management of CLL.”. Blood. 2018. PMID: 29540348. PubMed →
- [4]Adrados A, Pérez-Fernández J, García-Vicente R, et al.. “Enhancing immunotherapy efficacy in multiple myeloma and chronic lymphocytic leukemia: from combinatorial therapeutic approaches to gut microbiota modulation.”. Front Immunol. 2026. PMID: 42389542. PubMed →
- [5]Parry EM, Leshchiner I, Guièze R, et al. “Evolutionary history of transformation from chronic lymphocytic leukemia to Richter syndrome.”. Nature medicine. 2023. PMID: 36624313. PubMed →
- [6]Medina A, Muntañola A, Crespo M, et al.. “Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia and small lymphocytic lymphoma from Chronic Lymphocytic Leukemia Spanish Group (GELLC)”. Medicina Clinica (Barc). 2025. PMID: 39799061. PubMed →

