Life-threatening hypophosphatemia and/or phosphate depletion in a patient with acute lymphoblastic leukemia: a rare case report

2014 ◽  
Vol 32 (11) ◽  
pp. 1437.e3-1437.e5 ◽  
Author(s):  
Yasemin Soyoral ◽  
Mehmet Aslan ◽  
Senar Ebinc ◽  
Yaren Dirik ◽  
Cengiz Demir
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.


2016 ◽  
Vol 7 (2) ◽  
pp. 377-383 ◽  
Author(s):  
Christoph Palme ◽  
Nikolaos E. Bechrakis ◽  
Martin Stattin ◽  
Gertrud Haas ◽  
Claus Zehetner

This case illustrates that hematologic disorders must be considered as a potentially life-threatening cause for vision loss. Proper laboratory workup and timely interdisciplinary approach are essential to ensure the best possible care for ophthalmic patients. Historically, before the use of bone marrow biopsy, the ophthalmologist was often asked to assist in the diagnosis of leukemia. Since ophthalmological symptoms may be the initial presenting signs of leukemia as highlighted in this case, the ophthalmogist is still of crucial importance.


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