Results 71 to 80 of about 43,474 (218)
A Red Skin in the Setting of Chickenpox: A Rare Report of Eosin Toxicity
Clinical Case Reports, Volume 13, Issue 6, June 2025.ABSTRACT Eosin Yellowish (Eosin‐Y) is an effective treatment option for a range of dermatological conditions. It is crucial to carefully identify patients presenting systemic adverse reactions related to topical aqueous Eosin‐Y overuse and to monitor them closely during short‐term use to prevent severe complications.
Bahareh Abtahi‐Naeini +5 more
wiley +1 more source
Idiopathic Thrombocytopenic Purpura after Mastectomy and Axillary Lymph Node Dissection
Case Reports in Surgery, 2014 First described in 1916, idiopathic thrombocytopenic purpura (ITP) is an autoimmune disease resulting in the destruction of platelets. Here, we present a case of an 85-year-old patient diagnosed with invasive ductal carcinoma of the breast whose surgical
Wil L. Santivasi +2 more
doaj +1 more source
Idiopathic thrombocytopenic purpura as initial manifestation of juvenile systemic lupus erythematosus [PDF]
, 2003 Patients with Idiopathic Thrombocytopenic Purpura (ITP) present a high trend to develop Systemic Lupus Erythematosus (SLE), especially those with chronic presentation.
Braga, Josefina Aparecida Pellegrini +3 more
core +3 more sources
Clinical Case Reports, Volume 13, Issue 6, June 2025.ABSTRACT Hypertensive emergency is an acute, significant elevation of blood pressure accompanied by end‐organ damage. We present a case of a 27‐year‐old gentleman who acquired multiple complications of hypertensive emergency, including renal failure and microangiopathy.
Tatiana Gusan +4 more
wiley +1 more source
Journal of Medical Case Reports, 2018 Background Vitamin B12 deficiency-induced thrombotic microangiopathy, known as pseudothrombotic microangiopathy, is a rare condition which resembles the clinical features of thrombotic thrombocytopenic purpura but requires a markedly different treatment.
Jennifer Vanoli +4 more
doaj +1 more source
Subdural Hematoma in Grave’s Disease Induced Thrombocytopenia. [PDF]
, 2013 Subdural hematoma (SDH) usually occurs secondary to trauma, in bleeding disorders it may occur spontaneously. It is a rare complication of immune thrombocytopenia.
Chandek, S +4 more
core +1 more source
Graves disease-induced thrombotic thrombocytopenic purpura: a case report
Journal of Medical Case Reports, 2019 Background Thrombotic thrombocytopenic purpura is an autoimmune disease that carries a high mortality. Very few case reports in the literature have described a relationship between Graves disease and thrombotic thrombocytopenic purpura. We present a case
Saira Chaughtai +6 more
doaj +1 more source
SAGE Open Medical Case Reports, 2018 Wiskott–Aldrich syndrome is a rare X-linked recessive disease resulting from variations in the WAS gene. Wiskott–Aldrich syndrome is sometimes difficult to differentiate from immune thrombocytopenic purpura. A 2-month-old boy was admitted to our hospital
Ryota Kaneko +8 more
doaj +1 more source
A case of refractory thrombotic thrombocytopenic purpura treated with plasmapheresis and rituximab [PDF]
, 2016 Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disorder with no prevalence or incidence studies in sub-Saharan Africa. Acquired TTP has several causes, all of which lead to decreased activity of von Willebrand factor cleaving ...
Kirui, Nicholas, Sokwala, Ahmed
core +4 more sources
Long-term Kidney Outcomes in Patients With Acquired Thrombotic Thrombocytopenic Purpura
Kidney International Reports, 2017 Severe acute kidney injury (AKI) and chronic kidney disease (CKD) are considered to be uncommon in patients with acquired thrombotic thrombocytopenic purpura.
Dustin J. Little +5 more
doaj +1 more source