Publications by authors named "L Kaynar"

Early T-precursor acute lymphoblastic leukemia/lymphoma (ETP-ALL/LBL) is a rare and aggressive subtype of T-cell leukemia with poor prognosis and resistance to standard treatments. We report a 21-year-old male with ETP-ALL/LBL who, after an initial complete remission with the HOELZER protocol, experienced early relapse and was refractory to subsequent FLEND and BFM protocols. Following disease progression and complications, he was treated with a combination of daratumumab, venetoclax, azacitidine, and dexamethasone.

View Article and Find Full Text PDF

Homeobox (HOX) transcript antisense RNA (HOTAIR) and HOX genes are reported to be more expressed in various cancers in humans in recent studies. The role of HOTAIR and HOXD genes in acute myeloid leukemia (AML) and chronic myeloid leukemia (CML) is not well known. In this study, expression levels of HOXD8, HOXD9 and HOXD11 from HOXD gene family and HOTAIR were determined from peripheral blood samples of 30 AML and 30 CML patients and 20 healthy volunteers by quantitative Real Time PCR.

View Article and Find Full Text PDF
Article Synopsis
  • Pneumocystis jirovecii pneumonia (PJP) is an opportunistic infection that primarily affects immunocompromised individuals, presenting with symptoms like cough, fever, and especially aggressive courses in patients who have undergone allogeneic stem cell transplants.
  • A case study details a 56-year-old male who, after an allogeneic stem cell transplant for acute myeloid leukemia, developed hypercalcemia and renal failure along with fatigue, leading to a confirmed diagnosis of PJP.
  • Treatment included hydration, furosemide, and denosumab, and ultimately resolved both the hypercalcemia and the PJP infection with the patients’ follow-up showing improvement in symptoms.*
View Article and Find Full Text PDF

Background: Hairy cell leukemia (HCL) is a rare mature B-cell malignancy that is primarily treated with purine analogues. However, relapse remains a significant challenge, prompting the search for alternative therapies. The BRAF V600E mutation prevalent in HCL patients provides a target for treatment with vemurafenib.

View Article and Find Full Text PDF