Results 61 to 70 of about 1,080,266 (216)
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 +7 more
doaj +1 more source
Immune thrombocytopenic purpura in pregnancy
MGM Journal of Medical Sciences, 2020 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
Immunology, EarlyView.This systematic review establishes disease‐specific dysregulations of human innate lymphoid cells (ILCs), demonstrating that an ILC1/ILC3 imbalance compromises mucosal barriers in inflammatory bowel disease, while activated ILC2s drive allergic airway inflammation.
Luan F. Lückmann +7 more
wiley +1 more source
Haematologica, 2009 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
Transplant Infectious Disease, EarlyView.Among 135 cases of post‐liver transplant HHV8 disease (4 from NSW), presentations varied, and mortality was high (44%). Donor screening was rare, and donor‐derived infection was suspected in 33%. Survival improved with mTORi, reduced immunosuppression, chemotherapy, and, for non‐KS disease, donor screening. ABSTRACT Background Human herpesvirus 8 (HHV8)
Karen M. J. Waller +12 more
wiley +1 more source
NEONATAL THROMBOCYTOPENIC PURPURA: REPORT OF TWO CASES AND REVIEW OF LITERATURE [PDF]
Kanem Journal of Medical Sciences, 2018 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
Transfusion Medicine, EarlyView.Abstract Background Thrombocytopenia arises from heterogeneous inherited and acquired disorders, and identifying the underlying platelet clearance mechanisms remains challenging. Platelet desialylation, characterised by loss of sialic acid and consequent exposure of terminal β‐galactose residues recognised by the Ashwell–Morell receptor, represents an ...
Karen Nogueira Chinoca Ziza +14 more
wiley +1 more source
Indian Journal of Anaesthesia, 2007 Acute immune thrombocytopenic purpura in children, though a benign self limiting condition, at times complicated with life threatening haemorrhage. In spite of bleeding episode it is inevitable that surgical procedure will be performed on patients with ...
Minati Choudhury, Nirvik Pal, Usha Kiran
doaj
Evans Syndrome Associated with Pregnancy and COVID-19 Infection
Case Reports in Obstetrics and Gynecology, 2020 Background. Evans syndrome (ES) is a chronic autoimmune disease characterized by autoimmune hemolytic anemia along with immune thrombocytopenic purpura. Few case reports of ES in pregnancy have been published, and ES may be difficult to distinguish from ...
Gayathri Vadlamudi +2 more
doaj +1 more source
PATHOPHYSIOLOGY, INVESTIGATIONS, AND TREATMENT OF PATIENTS WITH IMMUNE THROMBOCYTOPENIC PURPURA [PDF]
, 2022 In otherwise healthy children or adults, immune thrombocytopenic purpura (ITP) has a low platelet count, usually less than 100,000, in the presence of common petechiae, bruises, or bleeding. It is explained that there is.
ADEL GAMIL, MOHAMED +5 more
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