Results 11 to 20 of about 7,152 (164)
Congenital familial erythrocytosis: A case report with literature review
Saudi Journal of Medicine and Medical Sciences, 2015 Familial erythrocytosis is a heterogeneous group of hereditary conditions with an increased total red blood cell volume. The disease occurs in a familial pattern and follows a relatively benign course.
Ishrat H Dar +5 more
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ERYTHROCYTOSIS IN CHILDREN: CASE REPORT
Slovenska pediatrijaErythrocytosis is a condition characterized by an increased mass of red blood cells, which manifests as an elevated concentration of hemoglobin, increased count of red blood cells, and increased hematocrit levels.
Teja Leban, Janez Jazbec
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Congenital Familial Erythrocytosis: A case report with a review
Mediterranean Journal of Hematology and Infectious Diseases, 2014 Familial erythrocytosis is a heterogeneous group of hereditary conditions with an increased total RBC volume. The disease occurs in a familial pattern and follows a relatively benign course.
Muqtasid Ahmad Kamili +5 more
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A Case of Erythrocytosis in a Patient Treated with an Aromatase Inhibitor for Breast Cancer [PDF]
Case Reports in Hematology, 2013 A previously healthy 79-year-old female was referred to hematology for further evaluation of erythrocytosis. Two years earlier she had been diagnosed with ER/PR-positive ductal carcinoma of the breast and was receiving hormonal therapy with exemestane ...
Abhinav Iyengar, Dawn Sheppard
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Renal-Adenocarcinoma-Associated Erythrocytosis in a Cat [PDF]
Pakistan Veterinary Journal, 2013 A 9-year-old spayed female domestic shorthair cat was referred for erythrocytosis. Even after the correction of dehydration, blood analyses showed that there had been no improvement.
Sungjun Noh, Ji-Houn Kang*, Gonhyung Kim, Dongwoo Chang, Byeongwoo Ahn, Ki-Jeong Na and Mhan-Pyo Yang
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Cancer Medicine, 2023 Background Acquired erythrocytosis can be classified into polycythemia vera (PV) and non‐neoplastic erythrocytosis (NNE). The vast majority of PV patients harbor JAK2 mutations, but differentiating JAK2 mutation‐negative PV from NNE is challenging due to
Yosuke Mori +12 more
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"The long journey of unexplained erythrocytosis". Erythrocytosis due to high oxygen affinity hemoglobinopathy - hemoglobin variant Little Rock (HBB: c.432C>A) - A report of a Swiss Family and review of the literature. [PDF]
, 2023 The differential diagnosis of erythrocytosis is complex, involving a tailored algorithm. Congenital causes are rare and such patients commonly face a long journey looking for diagnosis.
Rovó, Alicia +5 more
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Surprising erythrocytosis resolution after myomectomy: myomatous erythrocytosis syndrome
, 2023 Myomatous erythrocytosis syndrome (MES) is a rare gynaecological condition associated with the presence of a uterine fibroid and isolated polycythaemia.
Adriano Salaroli +3 more
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Cardiovascular Diabetology, 2022 Background Sodium-glucose cotransporter-2 inhibitors (SGLT2i) have proven cardiovascular benefits in patients with type 2 diabetes (T2D). This self-controlled case series study aims to evaluate whether metformin use and SGLT2i-associated erythrocytosis ...
Carlos King Ho Wong +8 more
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Myomatous erythrocytosis syndrome: A case series
Case Reports in Women's Health, 2019 Uterine leiomyomas are tumor-associated causes of secondary erythrocytosis. Ectopic erythropoietin production by fibroid smooth muscles has been proposed and demonstrated in the literature.
Glaiza S. de Guzman, Eileen M. Manalo
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