Results 11 to 20 of about 56,061 (148)

Coexistence of thrombotic thrombocytopenic purpura and immune thrombocytopenic purpura in an Asian woman: a case report

open access: yesJournal of International Medical Research, 2022
A 33-year-old Chinese woman with a history of immune thrombocytopenic purpura presented with heavy menstrual bleeding. She was found to have thrombocytopenia, plasma ADAMTS13 activity of 0%, and positivity for the plasma ADAMTS13 inhibitor.
Hangping Ge   +7 more
doaj   +1 more source

PÚRPURA TROMBOCITOPENIA ALOIMUNE NEONATAL

open access: yesHematology, Transfusion and Cell Therapy, 2021
Introdução: A púrpura trombocitopênica aloimune neonatal (TNA) é uma patologia grave, em que a mãe produz anticorpos contra antígenos plaquetários do feto herdados do pai. Na gravidez, a mãe forma anticorpos antiplaquetários da classe de imunoglobulina G
CSR Araújo   +9 more
doaj   +1 more source

Acute Epstein-Barr Virus Hepatitis in a 32 Month Old Female Manifesting as Henoch-Schönlein Purpura [PDF]

open access: yesChildhood Kidney Diseases, 2015
Henoch-Schönlein purpura can result from exposure to an antigen after infection with several types of organisms. However, Henoch-Schönlein purpura caused by a primary Epstein-Barr virus infection has been rarely reported. Here, we report the case of a 32-
Hee Jin Kim, Su Jin Jung, Jun Ho Lee
doaj   +1 more source

Dermatosis purpúrica pigmentada. A propósito de un caso con localización atípica

open access: yesMedisur, 2019
Se presenta el caso de una paciente femenina de 29 años de edad, con antecedentes de salud referida que acude a consulta por la presencia de máculas hiperpigmentadas asintomáticas de 21 días de evolución, distribuidas de forma lineal en el miembro ...
Daymí Martínez Rodríguez
doaj   +2 more sources

Pneumococcal purpura fulminans in asplenic or hyposplenic patients: a French multicenter exposed-unexposed retrospective cohort study

open access: yesCritical Care, 2020
Background Pneumococcal infections remain the main cause of overwhelming post-splenectomy infections, and purpura fulminans may develop in almost 20% of patients with overwhelming post-splenectomy infection.
Damien Contou   +8 more
doaj   +1 more source

VASCULITE POR IgA SOB FORMA DE APRESENTAÇÃO CUTÂNEA EM MULHER DE 45 ANOS TRATADA COM CORTICOSTEROIDE: RELATO DE CASO

open access: yesRevista Uningá, 2021
A Vasculite por imunoglobulina A (IgAV) é conhecida por ser uma vasculite sistêmica de pequenos vasos. Apesar desta condição ser capaz de se estabelecer em qualquer faixa etária, o perfil epidemiológico desta doença afeta, majoritariamente, a população ...
Daniella Mendes de Souza Sobrinho   +9 more
doaj  

Fresh approach to Henoch–Schönlein purpura. Comparison of its course and complications inchildren and adults inthelight of the latest reports

open access: yesPediatria i Medycyna Rodzinna, 2014
Henoch–Schönlein purpura is a disease that belongs to the group of vasculitides. The disease in children is usually mild, but if it occurs in adulthood it can bring many adverse consequences. In mild forms, the major manifestation is skin lesions.
Dorota Mehrholz   +3 more
doaj   +1 more source

Henoch-Schönlein purpura with acute pancreatitis: analysis of 13 cases

open access: yesBMC Pediatrics, 2018
Background Henoch-Schönlein purpura is a common small vessel vasculitis in children. Acute pancreatitis rarely presents as a complication of Henoch-Schönlein purpura and has not been well characterized.
Qin Zhang   +6 more
doaj   +1 more source

Purpura with regular shape in an adolescent: Beware of dermatitis artefacta

open access: yesFrontiers in Pediatrics, 2022
BackgroundPurpura is common in pediatric patients, mostly diagnosed as IgA-related vasculitis (Henoch–Schönlein purpura), idiopathic thrombocytopenic purpura (ITP), and thrombotic thrombocytopenic purpura (TTP). However, in some cases, for example, cases
Yuhao Chen   +4 more
doaj   +1 more source

Novel Mutation of Upshaw-Schulman Syndrome Associated with Coarctation of Aorta in Palestinian Child [PDF]

open access: yesĶazaķstannyṇ Klinikalyķ Medicinasy, 2020
Upshaw-Schulman syndrome is a rare inherited form of thrombotic thrombocytopenic purpura disease caused by deficiency of ADAMTS13 and reversible by fresh frozen plasma infusions.
Mahdi Zaid   +5 more
doaj   +1 more source

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