Results 11 to 20 of about 1,710,432 (174)
Osteomalacia Following Iron Infusion Therapy in a Patient With Rendu‐Osler‐Weber Syndrome: F‐18‐FDG PET/CT Discrimination of a Stress Fracture in the Setting of a Musculoskeletal Tumor Mimic [PDF]
Clinical Case ReportsThis case report highlights a rare occurrence of osteomalacia induced by hypophosphatemia secondary to ferric carboxymaltose (FCM) therapy in a patient with hereditary hemorrhagic telangiectasia (HHT, or Rendu‐Osler‐Weber syndrome).
Ioannis S. Vasios +4 more
doaj +3 more sources
Open Medicine, 2020 Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present with a wide spectrum of clinical manifestations from epistaxis to clinically significant
Mikołajczyk-Solińska Melania +4 more
doaj +3 more sources
OSLER – WEBER – RENDU SYNDROME: A RARE CASE OF UPPER GASTROINTESTINAL BLEEDING [PDF]
Khyber Medical University Journal, 2022 BACKGROUND: Osler-Weber-Rendu syndrome (Hereditary hemorrhagic telengiectasia) cases present with recurrent epistaxis, gastrointestinal bleeding (hematemesis, melena), and arteriovenous malformations involving almost all organs of body.
Farrukh Sher +2 more
doaj +2 more sources
Journal of Medical Sciences, 2015 Osler-Weber-Rendu syndrome is a hereditary disease which is diagnosed by criterions of clinical symptoms and examinations. Here, we report a definite case of Osler-Weber-Rendu syndrome who had epistaxis, skin telangiectasia, and pulmonary arteriovenous ...
Kuan-Yu Wang, Jen-Chih Chen, Jane-Yi Hsu
doaj +2 more sources
From 78% oxygen saturation to 95% in 60 minutes: Osler-Weber-Rendu syndrome endovascular treatment [PDF]
Advances in Interventional Cardiology, 2020 Pulmonary arteriovenous malformations (PAVMs) are abnormal communications between the pulmonary artery and pulmonary vein without an intervening capillary system.
Maciej Szmygin +3 more
doaj +2 more sources
Rendu-Osler-Weber syndrome: A family investigation and review
Journal of Indian Academy of Oral Medicine and Radiology, 2009 Rendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency ...
V G Mahima +3 more
doaj +2 more sources
Osler-Weber-Rendu syndrome during pregnancy. [PDF]
BMJ Case Rep, 2013 Osler-Weber-Rendu syndrome is a very rare systemic fibrovascular dysplasia. Rupture of angiomas can cause haemorrhages, which sometimes can be severe with difficult bleeding control. The main manifestation is recurrent epistaxis. Treatment of this disorder is symptomatic. During pregnancy, there may be an increased risk of complications.
Inocêncio G +3 more
europepmc +4 more sources
Osler-Weber-Rendu syndrome: A case report with familial clustering [PDF]
Indian Journal of Dermatology, Venereology and Leprology, 2009 Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems. We present a case of Osler-Weber-Rendu syndrome with 11 affected members in her family.
Grover, Sanjiv +5 more
core +5 more sources
Osler-Weber-Rendu syndrome: an anaesthetic challenge? [PDF]
BMJ Case Rep, 2016 Osler-Weber-Rendu syndrome, or hereditary haemorrhagic telangiectasia (HHT), is an autosomal dominant vascular dysplasia characterised by mucocutaneous telangiectases and arteriovenous malformations (AVMs). Diagnosis is clinical and treatment is supportive. The authors demonstrate a safe anaesthetic approach for a patient with HHT.
Chieira D +3 more
europepmc +4 more sources