Results 131 to 140 of about 33,158 (281)

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

Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report

Caspian Journal of Pediatrics, 2018
Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or ...
Sayed Yousef Mojtahedi, Mohammad Kaji Yazdi   +1 more
doaj  

Case Report: Acute hepatitis A virus infection presenting with direct antiglobulin test-negative autoimmune hemolytic anemia and α-thalassemia trait [version 2; peer review: 2 approved, 1 approved with reservations]

F1000Research
Reports from the literature have discussed patients presenting Hepatitis A virus infection with hemolytic anemia, specifically with glucose-6-phosphate dehydrogenase deficiency. However, autoimmune hemolytic anemia (AIHA) has been rarely reported.
Habiba Debbabi, Eya Chakroun, Haythem Yacoub, Nadia Maamouri, Hela Kchir, Hajer Hassine, Dhouha Cherif   +6 more
doaj   +1 more source

Canine autoimmune hemolytic anemia: management challenges. [PDF]

, 2016
Immune-mediated hemolytic anemia is one of the most common manifestations of canine immune-mediated disease, yet treatment regimens remain nonstandardized and, in some cases, controversial.
Skelly, Barbara J, Swann, James W
core   +2 more sources

Cyclic autoimmune hemolytic anemia as a presenting manifestation of splenic Hodgkin's disease [PDF]

, 1982
Magnus Björkholm, Göran Holm, K. Merk
openalex   +1 more source

Autoimmune Hemolytic Anemia and Classical Hodgkin Lymphoma: An Often-Overlooked Alliance

, 2023
Richmond Ronald Gomes
openalex   +1 more source

Abatacept as salvage therapy for life-threatening refractory autoimmune hemolytic anemia: a case report [PDF]

, 2023
Joerg Hoffmann, Georg Schliesser, Andreas Neubauer   +2 more
openalex   +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

False-positive fourth-generation HIV test associated with autoimmune hemolytic anemia. Case report

Case Reports, 2019
Introduction: The fourth-generation ELISA human immunodeficiency virus (HIV) screening test has a high sensitivity and specificity >99% to detect both antigens and antibodies. Estimates are that only 0.5% yield false positive results. Case description:
Santiago Sánchez-Pardo, Jaime Andrés Osorio-Ramírez, Isabela Choi-Park, Daniel Felipe Rojas-Holguín, Adrián Bolívar-Mejía   +4 more
doaj   +1 more source

Beyond the Pulselessness: A Multifaceted Case of Takayasu Arteritis With Aneurysmal Complications and Extensive Upper Limb Vascular Occlusion in a 40‐Year‐Old Female

Clinical Case Reports, Volume 13, Issue 11, November 2025.
Central illustration summarizing the comprehensive case management of Takayasu arteritis in a 40‐year‐old female. The figure integrates key aspects: vascular pathology (left subclavian occlusion, right subclavian narrowing, 4.0 cm infrarenal aneurysm), clinical presentation (right arm pain, neck stiffness), inflammatory markers (CRP 18.4 mg/L, ESR 45 ...
Sakib Abrar, Ibrahim Khalil, Shah Tanvir Ahmed, Fabiha Rahman Spriha, Md. Imran Hossain, Md Abu Sayed   +5 more
wiley   +1 more source