Results 31 to 40 of about 14,442 (233)

Acute Kidney Injury, Immune Thrombocytopenic Purpura, and the Infection That Binds Them Together: Disseminated Histoplasmosis

Journal of Investigative Medicine High Impact Case Reports, 2017
Untreated human immunodeficiency virus (HIV) can be complicated by opportunistic infections, including disseminated histoplasmosis (DH). Although endemic to portions of the United States and usually benign, DH can rarely act as an opportunistic infection
Pooja Sethi MD, Jennifer Treece MD, MBA, Chidinma Onweni MD, Vandana Pai MD, Sowminya Arikapudi MD, Lakshmi Kallur MD, Varun Kohli MD, Jonathan Moorman MD, PhD, FACP   +7 more
doaj   +1 more source

Síndrome de Evans - presentación atípica de un linfoma raro

Galicia Clínica, 2022
Evans Syndrome is a rare autoimmune condition characterized by two or more cytopenias, usually autoimmune haemolytic anaemia and immune thrombocytopenic purpura. It can be primary/idiopathic or secondary to other diseases.
Catarina Teles Neto, Marta Valentim, Filipa Pedro, Pedro Luís, Ana Gameiro, Luís Siopa   +5 more
doaj   +1 more source

Canine Idiopathic Thrombocytopenic Purpura [PDF]

Journal of Veterinary Internal Medicine, 1996
Canine idiopathic thrombocytopenic purpura (ITP) is a disease in which antibodies bound to the surface of platelets mediate premature platelet destruction by macrophages. ITP in dogs and chronic ITP in humans are analogous diseases. This article draws on information from the literature on ITP in dogs and in humans, and reviews the pathogenesis ...
David C. Lewis, Kenneth M. Meyers
openaire   +3 more sources

Avatrombopag for the Treatment of Immune Thrombocytopenia

European Journal of Haematology, Volume 114, Issue 5, Page 733-746, May 2025.
ABSTRACT Avatrombopag, a second‐generation thrombopoietin receptor agonist (TPO‐RA), represents a significant advancement in the treatment of chronic immune thrombocytopenic purpura (cITP) and a potential therapeutic option for other thrombocytopenic disorders.
Caterina Labanca, Ernesto Vigna, Enrica Antonia Martino, Antonella Bruzzese, Francesco Mendicino, Giulio Caridà, Eugenio Lucia, Virginia Olivito, Noemi Puccio, Antonino Neri, Fortunato Morabito, Massimo Gentile   +11 more
wiley   +1 more source

Prognostic factors and long‐term outcome in dogs diagnosed with primary and secondary immune thrombocytopenia in Ireland

Journal of Small Animal Practice, Volume 66, Issue 5, Page 305-313, May 2025.
Objectives The objectives of this study were to describe the outcome and prognostic factors in dogs diagnosed with primary and secondary immune thrombocytopenia (ITP). Materials and Methods Medical records of dogs diagnosed with primary and secondary ITP in a referral hospital in Ireland were retrospectively evaluated.
E. López‐Bailén, A. Duclos, D. Mullany, K. Le Boedec, B. Cuq   +4 more
wiley   +1 more source

Platelet count response to Helicobacter pylori eradication for idiopathic thrombocytopenic purpura in northeastern Brazil

Hematology, Transfusion and Cell Therapy, 2018
Background: Several studies have demonstrated that platelet counts in Helicobacter pylori-positive patients with chronic idiopathic thrombocytopenic purpura improved significantly after successful eradication of the infection.
Alzira Maria de Castro Barbosa, Rosangela Albuquerque Ribeiro, Cícero Ígor Simões Moura Silva, Francisco Will Saraiva Cruz, Orleancio Gomes Ripardo de Azevedo, Maria Helena da Silva Pitombeira, Lucia Libanez Campelo Braga   +6 more
doaj  

Rumpel-Leede phenomenon following radial artery catheterisation

European Journal of Case Reports in Internal Medicine, 2023
Rumpel-Leede phenomenon is a rarely diagnosed entity that can be seen in patients following the application of tourniquet-like forces to the extremities. This phenomenon describes petechiae and purpura secondary to venous compression and congestion, with
Floyd A. Pirtle, Dylan Maldonado, Pitchaporn Yingchoncharoen, Jerapas Thongpiya, Natnicha Leelaviwat, Annia Cavazos, Cloyce L. Stetson   +6 more
doaj   +1 more source

Immune Dysregulation in a Child With SOD1‐Related Neurological Disease

American Journal of Medical Genetics Part A, Volume 197, Issue 4, April 2025.
ABSTRACT Spastic tetraplegia and axial hypotonia (STAHP) associated with biallelic SOD1 deficiency is a recently described neurological disorder affecting children. Five studies have described a total of nine cases thus far, all characterized by the onset of progressive spastic tetraplegia beginning before 2 years of age. All but two of these cases are
Rozlyn Claire Thomas Boutin, Farzaneh Shobeirian, Shelin Adam, Anna Lehman, Ramona Salvarinova, Jan M Friedman   +5 more
wiley   +1 more source

IDIOPATHIC THROMBOCYTOPENIC PURPURA (i.T.P.) [PDF]

Acta Medica Iranica, 1987
The course of t he disorder is acute and chronic.The acute form o f the disease occurs most c ommonly in children , but is seen i n adults as well . The chronic recurrent f orm occurs most o f t e n in women between t wenty and forty years of age.
Sh. MOHAMEDI M ZAMANIANPOUR ML GHASEMI
doaj   +1 more source

Thrombocytopenia and hyperthyroidism: A case report and literature review

Clinical Case Reports, 2023
Key Clinical Message Immune thrombocytopenic purpura (ITP) is very challenging to diagnose with concurrent comorbidities affecting platelet count including PAH and autoimmune thyroid disease.
Pitchaporn Yingchoncharoen, Mahmoud Abdelnabi, Jerapas Thongpiya, Alexandra Hoffman, Hira Tariq, Neha Mittal   +5 more
doaj   +1 more source