Results 71 to 80 of about 22,958 (212)
eJHaem, Volume 7, Issue 4, August 2026.ABSTRACT Background Significant splenomegaly remains a major barrier to successful allogeneic hematopoietic cell transplantation (allo‐HCT) in myelofibrosis (MF), contributing to delayed engraftment and an increased risk of graft failure. Systemic JAK inhibition and splenic irradiation are commonly used as independent pretransplant strategies; however,
Peng Ke +8 more
wiley +1 more source
Distinct clinical characteristics of myeloproliferative neoplasms with calreticulin mutations
Haematologica, 2014 Somatic insertions/deletions in the calreticulin gene have recently been discovered to be causative alterations in myeloproliferative neoplasms. A combination of qualitative and quantitative allele-specific polymerase chain reaction, fragment-sizing ...
Hajnalka Andrikovics +13 more
doaj +1 more source
Essential thrombocythemia and acute myocardial infarction treated with rescue coronary angioplasty
Arquivos Brasileiros de Cardiologia, 1999 A 48-year-old man with essential thrombocythemia suffered an extensive anterior acute myocardial infarction; this is a rare association. A pharmacological thrombolysis was performed, without success.
Antonio Esteves Fº +4 more
doaj +1 more source
Annals of Gastroenterological Surgery, Volume 10, Issue 4, Page 1356-1364, July 2026.Unlike deceased‐donor liver transplantation, living‐donor liver transplantation (LDLT) for Budd‐Chiari Syndrome (BCS) presents distinctive challenges in hepatic venous (HV)‐outflow reconstruction because diseased HV–inferior vena cava (IVC) cannot be entirely replaced with healthy donor vessels.
Koichiro Hata +4 more
wiley +1 more source
Oman Medical Journal, 2014 The risk of thrombosis is high in patients with essential thrombocythemia. Special precaution needed for those patients who will undergo Coronary artery bypass grafting. We are reporting a 62 years old patient with ischemic heart disease who was found to
Edem Ziadinov +3 more
doaj +1 more source
American Journal of Hematology, Volume 101, Issue 9, Page 2463-2468, September 2026.
Rodrigo Ortega Perez +19 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Systemic mastocytosis (SM) is a rare clonal myeloproliferative neoplasm typically characterized by cutaneous lesions and mediator‐release symptoms. Presentations dominated by visceral organ involvement without skin findings are uncommon and pose a significant diagnostic challenge, often mimicking hematologic malignancies.
Muhammad Sadam Zeb +9 more
wiley +1 more source
A CASE OF IDIOPATHIC THROMBOCYTHEMIA
Nihon Naika Gakkai Zasshi, 1969 二次的栓球増多をきたす明らかな原因疾患がなく,著明な持続的栓球増多と血栓および出血傾向を示す疾患は, 1920年Diguglielmoがpiastrinemiaとして報告したのをはじめとして,いろいろな名称を冠した本症の報告が散見される.著者らは, 64才の男子で,本症と診断される1例を経験した.本症例は,両側足趾に次々と疼痛・壊死が出現し,時に,鼻出血・歯肉出血をみた.末梢血中の栓球数はほとんど常に100万/mm3を越え,最高238万/mm3に達し,軽度の貧血と白血球増多を伴つた.骨髄所見では,骨髄巨核球が237/mm3と増加し,また,栓球生成能の亢進が示唆された.しかし,赤・白血球系細胞には異常をみなかつた.止血機能検査はいずれも正常値を示したが,栓球の粘着能および第1, 2 ...
MIYAHARA, Mitsuo +4 more
openaire +3 more sources
Case Reports in Oncological Medicine, 2020 A few types of myeloproliferative neoplasms may be significant for Janus-associated kinase 2 mutation, JAK2 V617F, including polycythemia vera, essential thrombocythemia, and primary myelofibrosis.
Muhammed Atere +4 more
doaj +1 more source