Ubiquitous lytic osseous lesions in acute lymphoblastic leukemia: A rare case report

2015 ◽  
Vol 52 (2) ◽  
pp. 228
Author(s):  
V Annam ◽  
P Raghuram ◽  
DS Vasudeva ◽  
HT Narayana
2019 ◽  
Vol 61 (1) ◽  
pp. 97 ◽  
Author(s):  
Shilpa Khanna Arora ◽  
Swarnim Swarnim ◽  
Alok Hemal ◽  
Neha Bidhuri

2019 ◽  
Vol 67 (5) ◽  
pp. 1386
Author(s):  
SultanAydin Koker ◽  
Filiz Hazan ◽  
Yeşim Oymak ◽  
Ekin Soydan ◽  
TubaHilkay Karapınar ◽  
...  

2019 ◽  
Vol 8 (7) ◽  
pp. 469-471
Author(s):  
Priyanka Yadav ◽  
Rajendra Kumar Nigam ◽  
Varsha Rampuri ◽  
Abhinav Junwal ◽  
Nihan Khan

2021 ◽  
pp. 1040-1050
Author(s):  
Samah Kohla ◽  
Sarah EL Kourashy ◽  
Zafar Nawaz ◽  
Reda Youssef ◽  
Ahmad Al-Sabbagh ◽  
...  

T-acute lymphoblastic leukemia/lymphoblastic lymphoma (T-ALL/LBL) is rare and aggressive leukemia. Philadelphia chromosome positive (Ph+) is the most common cytogenetic abnormality in chronic myeloid leukemia (CML) and B-acute lymphoblastic leukemia (B-ALL). Ph+ T-ALL is exceeding rare and has a therapeutic and prognostic significance. The incidence and outcome of Ph+ T-ALL are unknown. Differentiation between Ph+ T-ALL/LBL and T-cell lymphoblastic crises of CML may be difficult. We report a rare case of adult de novo T-ALL with significant monocytosis, having Ph+ with (P190 <i>BCR-ABL1</i>) as a cytogenetic abnormality. He was treated with ALL induction chemotherapy and imatinib and achieved complete remission, then relapsed twice and expired shortly after the last CNS relapse.


Sign in / Sign up

Export Citation Format

Share Document