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An Atypical Case of Atypical Hemolytic Uremic Syndrome
Journal of Pediatric Hematology/Oncology, 2019We present the case of a 2-month-old infant presenting with pallor and laboratory results showing: hemoglobin 5.1 (10 to 1.5) g/dL, MCV 94.7 (75 to 105) fL, leukocytes 17.4 (7 to 15) ×103/μL, platelets 259 (150 to 450) ×103/μL, hyperbilirubinemia and renal dysfunction.
Tine, Francois +3 more
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Atypical hemolytic uraemic syndrome
Medicina Clínica (English Edition), 2015The hemolytic uremic syndrome (HUS) is a clinical entity characterized by thrombocytopenia, non-immune hemolytic anemia and renal impairment. Kidney pathology shows thrombotic microangiopathy (TMA) with endothelial cell injury leading to thrombotic occlusion of arterioles and capillaries.
Miquel, Blasco Pelicano +2 more
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Eculizumab for Atypical Hemolytic Uremic Syndrome in Pregnancy
Obstetrics & Gynecology, 2013Atypical hemolytic uremic syndrome (HUS) is a thrombotic microangiopathy often caused by mutations in complement genes. During pregnancy, disease outcome is poor both for mother and fetus. Since 2009, the humanized monoclonal antibody eculizumab has been successfully used in the treatment of atypical HUS in nonpregnant patients.A 26-year-old woman with
G. Ardissino +4 more
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Skin Involvement in Atypical Hemolytic Uremic Syndrome
American Journal of Kidney Diseases, 2014Skin involvement in atypical hemolytic uremic syndrome (aHUS) is very uncommon and therefore often unrecognized as a specific symptom of aHUS. We describe 3 cases of patients with aHUS who developed skin lesions that completely recovered when disease-specific treatment was established.
ARDISSINO, GIAN LUIGI +6 more
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Atypical hemolytic uremic syndrome in the Tunisian population
International Urology and Nephrology, 2010Hemolytic uremic syndrome consists of a triad of acquired hemolytic anemia, thrombocytopenia and renal failure.Our objectives were to determine epidemiology, clinical and laboratory characteristics of patients with atypical hemolytic uremic syndrome (aHUS) to determine the relationship between the complement protein deficit and aHUS in the Tunisian ...
Nadia, Leban +11 more
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Posttransplant recurrence of atypical hemolytic uremic syndrome
Journal of Nephrology, 2012Hemolytic uremic syndrome (HUS) is a rare disease characterized by microangiopathic hemolytic anemia, thrombocytopenia and acute renal failure. It is usually secondary to infections by strains of Escherichia coli (STEC) that produce Shiga-like toxin. In about 10% of patients, no STEC infections are reported.
Elisabetta, Valoti +2 more
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Hypertensive choroidopathy in atypical hemolytic-uremic syndrome
European Journal of Ophthalmology, 2019Purpose: We present the case of a 22-year-old woman, diagnosed as having atypical hemolytic uremic syndrome with a hypertensive crisis, who presented a bilateral serous retinal detachment. Case Description: A 22-year-old woman ...
Maria Sole Polito +3 more
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Atypical hemolytic uremic syndrome: a clinical conundrum
Pediatric Nephrology, 2016Patients negative for Shiga toxin-producing E. coli (STEC) are categorized as having atypical hemolytic uremic syndrome (HUS) and are associated with an increased risk for complement mutations and poorer prognosis compared with typical HUS. However, STEC identification is limited by the natural history of HUS.The current study is aimed at identifying ...
Prabesh, Bajracharya +4 more
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On the relevance of thrombomodulin variants in atypical hemolytic uremic syndrome
Kidney International, 2023JOSÉ María Portolés Perez +2 more
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