Results 31 to 40 of about 30,665 (264)

Hemangioblastoma: An Uncommon Cause of Polycythemia in a Child

open access: yesJournal of Nepal Health Research Council
Polycythemia is a rare condition in children. Myeloproliferative neoplasms, including polycythemia vera although rare, is an important cause of childhood primary polycythemia.
Surabhi Aryal, Arun Kumar Sharma
doaj   +1 more source

Co-occurrence of Dermatomyositis and Polycythemia Unveiling Rare de Novo Neuroendocrine Prostate Tumor

open access: yesFrontiers in Oncology, 2018
We present a case of dermatomyositis together with polycythemia as initial manifestations of a particularly rare type of prostate cancer. A 69-year-old man was hospitalized for facial erythema and symptoms of fatigue.
Charalampos Papagoras   +5 more
doaj   +1 more source

Perinatal outcomes following single intrauterine death in monochorionic twin pregnancies complicated by twin anemia polycythemia sequence: Systematic review and meta-analysis. [PDF]

open access: yesActa Obstet Gynecol Scand
The aim of this systematic review was to report perinatal outcomes in monochorionic diamniotic (MCDA) twin pregnancies complicated by twin anemia polycythemia sequence (TAPS) after single intrauterine fetal death (IUFD). Abstract Introduction Most of the studies reporting the outcome of the surviving twin after single intra‐uterine fetal death (sIUFD ...
Piergianni M   +8 more
europepmc   +2 more sources

Undiagnosed polycythemia, an uncommon cause of Wallenberg syndrome: A case report

open access: yesClinical Case Reports, 2022
A 26‐year‐old man presented with difficulty swallowing, dizziness, hiccups, and Horner's syndrome. Clinical and neuroimaging collaboration confirmed lateral medullary syndrome. Polycythemia was identified as the only attributable risk factor.
Aadesh Rayamajhi   +3 more
doaj   +1 more source

Clinical and Laboratory Characterization of Acquired Von Willebrand Syndrome

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Acquired von Willebrand Syndrome (AVWS) is a rare bleeding disorder characterized by quantitative or qualitative defects of von Willebrand factor (VWF) in patients without a personal or family history of bleeding. It is frequently associated with systemic diseases, particularly lymphoproliferative disorders (LPDs) and myeloproliferative ...
Alessandro Ciavarella   +10 more
wiley   +1 more source

Relation of giant right atrial mass and thrombocytopenia; Recovery with surgery [PDF]

open access: yesJournal of Cardiovascular and Thoracic Research
As we know, cardiac myxoma is one of the most primary cardiac masses but laboratory findings in this type of tumor is non-specific and the diagnosis is by imaging.
Roghayeh Pourkia   +3 more
doaj   +1 more source

Ruxolitinib Pharmacokinetics and Exposure–Toxicity Relationship in Hematologic Malignancies and Immune‐Mediated Diseases: A Prospective Observational Study

open access: yesClinical Pharmacology &Therapeutics, EarlyView.
Ruxolitinib pharmacokinetics (PK) has been characterized in clinical trials but remains poorly documented in real‐world practice. This project aimed to investigate ruxolitinib PK in routine clinical practice, identify factors driving its variability, and explore exposure–response relationships to assess the potential role of therapeutic drug monitoring.
Jérémie Tachet   +11 more
wiley   +1 more source

Pheochromocytoma, polycythemia and venous thrombosis [PDF]

open access: yes, 1987
Polycythemia is rarely associated with pheochromocytoma. A patient with a 22-year history of malignant pheochromocytoma is presented in whom major complications developed as a result of long-standing polycythemia, apparently due to secretion of ...
Shulkin, Barry L.   +2 more
core   +1 more source

Prevalence of Obstructive Sleep Apnea Among Patients with Secondary Polycythemia: A Retrospective Cross-sectional Study

open access: yesOman Medical Journal
Objectives: Obstructive sleep apnea (OSA) and secondary polycythemia occasionally occur together, but their relationship remains unclear. This study aimed to explore the prevalence of OSA among patients with secondary polycythemia in our local population.
Ahmed Al-Siyabi   +3 more
doaj   +1 more source

Interstitial lung disease with congenital erythrocytosis

open access: yesJournal of Clinical and Scientific Research, 2022
A 45-year-old male weaver, smoker, known case of interstitial lung disease with cor pulmonale on long-term oxygen therapy diagnosed 6 months ago who is on tapering doses of oral steroids presented to our tertiary care teaching hospital with complaints of
D T Katyarmal   +5 more
doaj   +1 more source

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