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Abdominal surgery in patients with essential thrombocythemia: A case report and systematic review of literature.
Zhu Y, Jiang H, Chen Z, Lu B, Wu J. Zhu Y, et al. Medicine (Baltimore). 2017 Nov;96(47):e8856. doi: 10.1097/MD.0000000000008856. Medicine (Baltimore). 2017. PMID: 29381999 Free PMC article. Review.
Two patients had postoperative bleeding that occurred on the first postoperative day. There was one case of pseudohyperkalemia after surgery and one case of Budd-Chiari syndrome caused by hepatic vein thrombosis. ...
Two patients had postoperative bleeding that occurred on the first postoperative day. There was one case of pseudohyperkalemia after …
CSF3R-mutant chronic myelomonocytic leukemia is a distinct clinically subset with abysmal prognosis: a case report and systematic review of the literature.
Guastafierro V, Ubezio M, Manes N, Milanesi C, Della Porta M, Bonometti A. Guastafierro V, et al. Leuk Lymphoma. 2023 Sep;64(9):1566-1573. doi: 10.1080/10428194.2023.2227750. Epub 2023 Jul 3. Leuk Lymphoma. 2023. PMID: 37395413
Chronic myelomonocytic leukemia (CMML) is a myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) chacaterized by persistent peripheral blood monocytosis, hypercellular bone marrow and dysplasia at least in one myeloid lineage. ...
Chronic myelomonocytic leukemia (CMML) is a myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) chacaterized by per …
Clinical and hematological presentation of children and adolescents with polycythemia vera.
Cario H, McMullin MF, Pahl HL. Cario H, et al. Ann Hematol. 2009 Aug;88(8):713-9. doi: 10.1007/s00277-009-0758-y. Epub 2009 May 26. Ann Hematol. 2009. PMID: 19468728 Free PMC article. Review.
Budd-Chiari syndrome was diagnosed in seven patients indicating a particular risk of young patients of developing this disorder. One patient presented with ischemic stroke, one patient with gangrene, and three patients with severe hemorrhage. ...
Budd-Chiari syndrome was diagnosed in seven patients indicating a particular risk of young patients of developing this disorder. One …
Longitudinal sequencing of RUNX1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignancies.
Duarte BKL, Yamaguti-Hayakawa GG, Medina SS, Siqueira LH, Snetsinger B, Costa FF, Rauh MJ, Ozelo MC. Duarte BKL, et al. Br J Haematol. 2019 Sep;186(5):724-734. doi: 10.1111/bjh.15990. Epub 2019 May 24. Br J Haematol. 2019. PMID: 31124578 Free article.
DNA samples were collected from bone marrow, peripheral blood and buccal swabs at different time points. One patient had clonal haematopoiesis, represented by an SRSF2 p.P95R variant, prior to his AML diagnosis, when he developed an additional NRAS p.G12D variant. ...
DNA samples were collected from bone marrow, peripheral blood and buccal swabs at different time points. One patient had clonal haema …