Results 71 to 80 of about 19,877 (193)
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
A case of propylthiouracil induced antineutrophil cytoplasmic antibody associated vasculopathy
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Nikhil Dwivedi +2 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Systemic lupus erythematosus (SLE) can rarely present as concurrent acute pancreatitis (AP), splenic infarction, and renal failure. This case demonstrates that prompt diagnosis and immunosuppression are crucial for reversing organ damage—even in male patients, expanding the known clinical spectrum of this disease.
Jian‐mei Gong, Xu Jun
wiley +1 more source
Respiratory Medicine Case Reports, 2018 A 26 year old female presented for recurrent blood tinged sputum during the previous year with development of frank hemoptysis three days prior to admission. Diffuse alveolar hemorrhage (DAH) was confirmed with serial lavages.
Ryan Hyde +4 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.Brain MRI demonstrating left hemispheric watershed infarctions and CTA showing high‐grade left internal carotid artery dissection with complete radiological resolution on follow‐up imaging.
Mohammad Ahmad Al‐Jazi +2 more
wiley +1 more source
Antiphospholipid Antibody Induced by Nivolumab
Case Reports in Hematology, 2018 Nivolumab is a monoclonal antibody against the programmed death protein 1 and is used for patients with advanced melanoma. It is associated with potentially immune-related adverse events, including disorders of the skin, GI tract, and the thyroid; these ...
Ahmed Aburahma +3 more
doaj +1 more source
Complement Inhibition in the Clinic: Are We Doing Enough to Protect Patients From Infection?
European Journal of Immunology, Volume 56, Issue 7, July 2026.Excessive complement activation is implicated in a broad range of diseases. Therapeutic approaches targeting the complement cascade, from pathway‐selective inhibition to terminal blockade, can effectively control disease activity. However, increasing degrees of complement inhibition are associated with a heightened susceptibility to bacterial, viral ...
Serena Bettoni +4 more
wiley +1 more source
Antiphospholipid Syndrome in a Pregnant Female Presenting with Severe Thrombocytopenia and Bleeding
Case Reports in Medicine, 2015 The antiphospholipid antibody syndrome (APS) is defined by the persistent presence of antiphospholipid antibodies in patients with recurrent venous or arterial thromboembolism or pregnancy morbidity.
Kunal Mahajan +3 more
doaj +1 more source
Branch retinal artery occlusion due to patent foramen ovale in a teenager
Experimental Physiology, Volume 111, Issue 7, Page 3173-3178, 1 July 2026.Abstract This report demonstrates the diagnostic evaluation and clinical management of a 16‐year‐old girl who developed branch retinal artery occlusion secondary to patent foramen ovale. The goal is to increase awareness of this rare presentation in adolescents among clinicians, with a summary of the important clinical features, multimodal imaging ...
Jie Zu +4 more
wiley +1 more source
Primary Adrenal Failure due to Antiphospholipid Syndrome
Case Reports in Endocrinology, 2015 Background. Antiphospholipid syndrome (APS) characterized by thrombosis and abortus may rarely cause primary adrenal failure. Case Presentations. A 34-year-old male presented with hypotension, hypoglycemia, hyperpigmentation on his skin and oral mucosa ...
Murat Sahin +6 more
doaj +1 more source