Results 231 to 240 of about 85,301 (285)

Beyond Hepatitis: A Rare Case of Multisystem Langerhans Cell Histiocytosis in a Child

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Langerhans cell histiocytosis (LCH) is a rare neoplastic disorder involving abnormal proliferation of dendritic cells, with clinical presentations ranging from isolated lesions to life‐threatening multisystem involvement. This case report describes a 26‐month‐old girl who presented with progressive jaundice, fever, hepatomegaly, pruritic scalp
Dilip Neupane, Rishi Ram Banjade, Dhiraj Joshi, Pusp Raj Awasthi, Santosh Mishra   +4 more
wiley   +1 more source

Intersecting Anemias: PARP Inhibitor-Induced Toxicity and Autoimmune Hemolysis-A Case Report. [PDF]

EJHaem
Dereme J, Asonitis K, Grandoni F, Liapi A, Sarivalasis A, Tsilimidos G.   +5 more
europepmc   +1 more source

Budd–Chiari Syndrome in the Background of Chronic Kidney Disease: A Hypercoagulability‐Driven Association or Coincidence? A Case Report

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Budd–Chiari syndrome (BCS) is a rare condition characterized by hepatic venous outflow obstruction and is often associated with thrombosis or fibrous membranes (webs). To our knowledge, this is the first reported case of BCS occurring secondary to chronic kidney disease (CKD).
Anish Paudyal, Sanjay Dhungana, Sachin Bhatta, Sphurna Karki, Sapana Koirala, Parbatraj Regmi, Sagar Mani Regmi, Subhash Paudel   +7 more
wiley   +1 more source

Severe Warm Autoimmune Hemolytic Anemia With Anti-PO Antibody Positivity: A Diagnostic Dilemma in a Resource-Limited Setting. [PDF]

Cureus
Kataveni S, Gottimukkala SP, Bodla VTS.
europepmc   +1 more source

A Case of Myeloproliferative Neoplasm‐Associated Glomerulopathy in a Patient With Myelofibrosis

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Myeloproliferative neoplasm (MPN)‐related glomerulopathy is a rare, late complication of MPN. Mesangial matrix expansion seems to be the histopathological hallmark. Proteinuria may not always be present. Further exploration is warranted to determine whether risk factors—including disease entity, mutation status and treatment regimens ...
Saskia Leibowitz, Michelle Spanevello, Leo Francis, Prianka Puri, Kirsten Hepburn   +4 more
wiley   +1 more source

Uncovering Glucose-6-Phosphate Isomerase (GPI) Deficiency in a Five-Year-Old With Hemolytic Anemia in Bahrain. [PDF]

Cureus
Busehail M, Qasim FN, Alasheeri FJ, Aloraibi A.   +3 more
europepmc   +1 more source

Not All Hereditary Iron Overload Is Hemochromatosis: A Case of Hereditary Xerocytosis Unmasked by Blood Smear Morphology

American Journal of Hematology, Volume 100, Issue 11, Page 2091-2092, November 2025.
María‐Angustias Molina‐Arrebola, Barbara J. Bain   +1 more
wiley   +1 more source

A Case Report of Infective Endocarditis With Icterus

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Infective endocarditis, a severe condition with high morbidity and mortality, requires timely diagnosis and treatment. We present a case of a 49‐year‐old male with a 3‐day history of icterus, abdominal pain, loose stool, and high‐grade fever. He was unwell for 3 days prior to presenting.
Ramtin Rezaie Kalantari, AmirAbas Sadrian, Torkan Banaee Rezaeie, Masoud Mortezazadeh, Dalip Kumar, Michael Acidri, Abbas Mofidi   +6 more
wiley   +1 more source

Mixed Warm and Cold Autoimmune Hemolysis in an Elderly Patient With Sickle Cell Disease and End-Stage Renal Disease on Hemodialysis: A Diagnostic and Therapeutic Challenge. [PDF]

Cureus
Lorenz N, Brown-Gnarra J, Graham M, Bray K.   +3 more
europepmc   +1 more source

Autoimmune Hemolytic Anemia as an Initial Manifestation of Splenic Marginal Zone Lymphoma. [PDF]

Cureus
Nachammai K M N, K V, Lakshmanan S, Anwar S.   +3 more
europepmc   +1 more source