Results 61 to 70 of about 6,242 (170)

Purpura fulminas: Informe de tres casos y revisión de la literatura [PDF]

open access: yes, 1995
El púrpura fulminans es una enfermedad que se pre­senta principalmente en la infancia y se acompaña de una alta tasa de mortalidad. Los tres principales hallaz­gos clínicos son: 1. Grandes áreas purpúricas y equi­ móticas de la piel, 2.
Gómez Molina, María Clemencia   +4 more
core  

Uso de Terapia VAC® en paciente pediátrico con exposición ósea postamputación tras púrpura fulminans

open access: yes, 2011
La sepsis meningocóccica se asocia con un alto índice de mortalidad. Los pacientes afectados pueden mostrar signos de coagulación intravascular diseminada (CID) y necrosis de partes blandas debidas a baja perfusión tisular. Los procedimientos quirúrgicos
León Llerena,C.   +2 more
core   +1 more source

Severe Nasofacial Necrosis From Capnocytophaga canimorsus: A Case Report of Disease and Reconstruction

open access: yes
Eye &ENT Research, Volume 3, Issue 1, Page 33-36, March 2026.
Armon Hadian   +2 more
wiley   +1 more source

Rosacea fulminans in pregnancy

open access: yes, 2004
Rosacea fulminans is a rare condition with a female preponderance and unknown aetiology, characterized by the abrupt onset of papules, pustules and erythema affecting the face.
Lewis, Victoria J.   +3 more
core   +1 more source

Purpura fulminans as the presenting manifestation in a patient with juvenile SLE

open access: yesThe Turkish Journal of Pediatrics, 2009
We present a 12-year-old girl with systemic lupus erythematosus and associated antiphospholipid syndrome who developed an unusual manifestation of purpura fulminans in an accelerated fashion.
Erkan Demirkaya   +5 more
doaj  

Genotypic and phenotypic character of Chinese neonates with congenital protein C deficiency: a case report and literature review

open access: yesThrombosis Journal, 2019
Background Our objective was to study the phenotype of and molecular genetic mechanisms underlying congenital protein C (PC) deficiency in Chinese neonates.
Xiaoying Li   +5 more
doaj   +1 more source

Thrombosis in Brothers With Protein S Deficiency: Case Series

open access: yesClinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Hereditary protein S deficiency is a rare thrombophilia that increases the risk of venous thromboembolism (VTE), including thrombosis in unusual sites. Early diagnosis, familial screening, and long‐term anticoagulation are essential for preventing complications and improving outcomes.
Abate Bane Shewaye   +5 more
wiley   +1 more source

Meningococcal purpura fulminans in children: I. Initial orthopedic management

open access: yesJournal of Children's Orthopaedics, 2010
Background Purpura fulminans is a rare and extremely severe infection, mostly due to Neisseria meningitidis frequently causing early orthopedic lesions. Few studies have reported on the initial surgical management of acute purpura fulminans.
E. Nectoux   +5 more
doaj   +1 more source

Púrpura de Schönlein-Henoch asociada a infección por Helicobacter pylori [PDF]

open access: yes, 2023
La púrpura de Schönlein-Henoch una vasculitis causada por mecanismo inmunológico frecuente en niños varones de 3 a 15 años. Se caracteriza por una púrpura palpable, artritis o artralgias, dolor cólico abdominal o hemorragia gastrointestinal y nefritis ...
Belaunde Clausell, Antonio   +3 more
core  

Acral Purpura Fulminans With Erythrocyte-Associated Streptococcus pneumoniae: A Case Report

open access: yesAnnals of Internal Medicine: Clinical Cases
A patient presented with acral purpura fulminans caused by Streptococcus pneumoniae septicemia. With antibiotics and intensive care, he survived but required amputations of both hands and feet due to ischemic necrosis.
Donald L. Granger   +2 more
doaj   +1 more source

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