Results 131 to 140 of about 37,831 (254)
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant bleeding disorder. The incidence of venous thromboembolisms among HHT patients is significantly greater than the general population. However, providing therapeutic anticoagulation in patients with an increased propensity for bleeding creates a clinical dilemma.
Christina Carfagnini, Manasa Kandula
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Ectopic Olfactory Neuroblastoma of the Maxillary Sinus: A Case Report
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Olfactory neuroblastoma is a rare neuroendocrine tumor typically arising from the superior nasal cavity, and primary occurrence in the maxillary sinus is exceptionally uncommon, often leading to diagnostic confusion with other sinonasal malignancies. A 34‐year‐old man presented with bilateral nasal obstruction, recurrent epistaxis, and frontal
Hesam Jahandideh +2 more
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Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Hemolacria is a rare condition characterized by bloody tears. Its etiology is often multifactorial, but functional/psychosomatic mechanisms have been proposed when organic causes are excluded. A 48‐year‐old woman with a history of multiple traumatic brain injuries (coma in 2008, car accident in 2017) presented with refractory generalized ...
Roghayeh Mohammadi, Ahmad Alipour
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Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Persistent facial lesions with benign superficial histopathology should prompt suspicion of deeper vascular anomalies. Clinicopathological discordance warrants early vascular imaging, as superficial biopsy may fail to detect underlying arteriovenous malformations, leading to delayed diagnosis and inappropriate management.
Qazi Syed Irfanullah Shah +3 more
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Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Massive transfusion protocols are essential in trauma resuscitation but may inadvertently increase the risk of acute hemolytic transfusion reactions (AHTRs), which are typically caused by ABO incompatibility. Recognition is difficult because signs of hemolysis can mimic trauma‐related hemorrhage or coagulopathy.
Mohammad Javad Entezari Meybodi +3 more
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Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Progressive familial intrahepatic cholestasis type 3 (PFIC‐3), caused by pathogenic variants in the ABCB4 gene, is a rare inherited cholestatic liver disorder that often presents later in childhood. In some patients, hematologic manifestations may dominate the clinical picture and delay recognition of the underlying liver disease.
Njood Alwadei
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Exploring Floristic Diversity and Medicinal Plant Uses in Venda, Limpopo, South Africa
Feddes Repertorium, Volume 137, Issue 2, June 2026.ABSTRACT Plants have been an important source of medicine for thousands of years. To better understand the current diversity and usage of medicinal plants, floristic studies are essential. This report documents an expedition conducted in the Venda region of Limpopo, South Africa. The study was carried out in Shanzha and surrounding villages, as well as
Gurusamy Manikandan +2 more
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Food Science &Nutrition, Volume 14, Issue 6, June 2026.Achillea millefolium Linn., commonly known as yarrow, is an extraordinary medicinal plant. A. millefolium has broad therapeutic potential due to its phytochemistry and essential oil composition. It possesses pharmacological properties, including antidiabetic, antioxidant, anti‐inflammatory, liver‐protective, antimicrobial, and gastroprotective effects,
Tooba Majeed +14 more
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eJHaem, Volume 7, Issue 3, June 2026.ABSTRACT Background Multiple myeloma (MM) carries a high venous thromboembolism (VTE) risk; aspirin shows limited efficacy, while factor‐Xa inhibitors show promise. Objectives Evaluate apixaban for primary thromboprophylaxis in newly diagnosed MM (NDMM).
K. Alexandra Sanchez +5 more
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