Results 61 to 70 of about 26,471 (221)
Diffuse petechiae and non‐palpable purpura (lower extremities below knee, admission photo). ABSTRACT Immune thrombocytopenia (ITP) is a rare but recognized hematologic complication of tuberculosis (TB), particularly miliary TB. We present a case of a 50‐year‐old female with severe thrombocytopenia and hemorrhagic manifestations secondary to miliary TB.
Hayatu Awel Abdela +3 more
wiley +1 more source
Immune thrombocytopenic purpura in pregnancy
We present a case of a 27-year-old primigravida, a known case of immune thrombocytopenic purpura (ITP), who is presented in our outpatient department in latent labor at 36 weeks of gestation with platelet count 36,000/µL.
Narayani Kalnawat, Archana Chatterji
doaj +1 more source
Clinical progress note: Rubella
Visual Abstract Abstract Rates of rubella infection and congenital rubella syndrome decreased significantly since the introduction of the rubella vaccine in 1969. Endemic rubella was declared eliminated in the United States in 2004, and since 2012, all rubella cases in the United States have been associated with infections acquired abroad. With vaccine
Adam E. Gailani +2 more
wiley +1 more source
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 +7 more
doaj +1 more source
Eradication of H. pylori improves thrombocytopenia in some patients with immune thrombocytopenic purpura by mechanisms that remain obscure. Platelet count responses may occur independently of H.
Donald M. Arnold +7 more
doaj +1 more source
IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic Purpura
ABSTRACT Pathogenic variants in IKZF1 (IKAROS) are linked to immunodeficiency, malignancy, and immune dysregulation. We describe a family with a rare IKZF1 variant presenting with humoral immunodeficiency and thrombotic thrombocytopenic purpura (TTP). A non‐consanguineous family was clinically monitored; clinical, immunological, and genetic data (exome
Ilia Spivak +7 more
wiley +1 more source
Acquired amegakaryocytic thrombocytopenic purpura with literature review
Acquired amegakaryocytic thrombocytopenic purpura (AATP) is an uncommon disorder with thrombocytopenia and selectively suppressed megakaryopoiesis, often mistaken as immune thrombocytopenic purpura (ITP). It usually does not respond to steroids, and bone
Mohammed Shafi Abdulsalam +4 more
doaj +1 more source
With its low morbidity and high mortality rates, thrombotic thrombocytopenic purpura (TTP) has imposed a critical physical and economic burden on both society and individuals.
Yingwei Ou +8 more
doaj +1 more source
Associated Autoimmunity in Myasthenia Gravis in Denmark: A Nationwide Case–Control Study
Myasthenia gravis (MG) often co‐occurs with other autoimmune diseases (ADs), but the temporal relationship is unclear. In this study, patients were twice as likely to have another AD, particularly females aged ≤ 50 years, suggesting a shared autoimmunity and a call for clinical awareness.
Josefine Jul Jarbæk Nielsen +2 more
wiley +1 more source
NEONATAL THROMBOCYTOPENIC PURPURA: REPORT OF TWO CASES AND REVIEW OF LITERATURE [PDF]
Introduction: Severe neonatal thrombocytopenia is a hematological emergency that can be due to increased platelet destruction (such as immune-mediated and peripheral platelet consumption) or congenital failure of platelet production.
Abiodun MT, Badejoko B, Oluwafemi RO
doaj

