2011
DOI: 10.4103/0973-6247.83265
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Idiopathic thrombocytopenic purpura coexisting with polycythemia vera

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Cited by 4 publications
(5 citation statements)
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“…Indeed the benefits provided by venetoclax were transitory (just over two months) and were followed shortly by a progression of her AML up to the irreversible evolution of the disease until the patient's death (May 2018). PV and other Ph-MPNs concomitantly associated with other blood-related disorders have been sporadically described [4][5][6], but the simultaneous occurrence of a secondary (AML), diagnosed at the failure of a long-term hypomethylating treatment of a high-risk MDS transformed from a long-lasting Ph-MPN, with a concomitant CLL is extremely rare. Our case posed the traditional therapeutic challenges that daily the practical hematologist encounters in the setting of transformed Ph-MPNs.…”
Section: Letter To the Editormentioning
confidence: 99%
“…Indeed the benefits provided by venetoclax were transitory (just over two months) and were followed shortly by a progression of her AML up to the irreversible evolution of the disease until the patient's death (May 2018). PV and other Ph-MPNs concomitantly associated with other blood-related disorders have been sporadically described [4][5][6], but the simultaneous occurrence of a secondary (AML), diagnosed at the failure of a long-term hypomethylating treatment of a high-risk MDS transformed from a long-lasting Ph-MPN, with a concomitant CLL is extremely rare. Our case posed the traditional therapeutic challenges that daily the practical hematologist encounters in the setting of transformed Ph-MPNs.…”
Section: Letter To the Editormentioning
confidence: 99%
“…Of note is that they did not exhibit a significant splenomegaly on physical examination, and ITP diagnosis was established by exclusion of other causes of thrombocytopenia. Moreover, low PLT count increased after steroids introduction [2]. Our PV patient presented with severe thrombocytopenia which was related to two independent mechanisms (1) the presence of autoimmunity and (2) hypersplenism.…”
mentioning
confidence: 95%
“…Thrombocytopenia in MF may be due to ineffective megakaryocytopoiesis as a result of bone marrow fibrosis or results from platelet sequestration and destruction in enlarged spleen [1]. Immune dysregulation with the production of immune complexes or antiplatelet antibodies may account for low platelet count in single cases [2]. It is noteworthy that thrombocytopenia remains an exceptional finding in polycythemia vera (PV).…”
mentioning
confidence: 99%
“…There is one source in literature relating to coexistence and treatment of these two diseases [5]. In our article, we have discussed two cases with coexisting PV and ITP and their treatment methods.…”
mentioning
confidence: 99%