Results 91 to 100 of about 55,777 (181)
Deficiência congênita da proteína C: Relato de caso [PDF]
, 2017 Congenital protein C deficiency is a rare thrombotic disease manifested in the neonatal or early childhood period leading to the development of fulminant purpura, massive venous thrombosis with tissue necrosis, bilateral blindness from vitreous vein ...
Errante, Paolo Ruggero +1 more
core +1 more source
Fatal case of meningococcal meningitis in a child from rural Bhutan: A case report
Clinical Case Reports, Volume 12, Issue 9, September 2024.Key Clinical Message N meningiditis remains an important cause of central nervous system infection. A high index of suspicion is required especially in infants. While empirical antibiotics may be initiated, diagnostic measures must be adopted for guided therapy.
Purushotam Bhandari +3 more
wiley +1 more source
Thrombosis 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
Acute hemorrhagic edema of infancy: 20‐year experience from an Italian tertiary referral center
Pediatric Dermatology, Volume 41, Issue 5, Page 825-830, September/October 2024.Abstract Purpose Data on acute hemorrhagic edema of infancy (AHEI) are derived from small case series or case reports. We report a 20‐year experience at a national referral center. Methods We performed a single‐center retrospective study including patients who were diagnosed with AHEI from January 1, 2004, to June 30, 2023.
Adele Fiordelisi +6 more
wiley +1 more source
Estudio sobre las características clínicas y la influencia genética en la susceptibilidad a la enfermedad meningocócica en la edad pediátrica [PDF]
, 2012 Antecedentes: La enfermedad meningocócica es la principal causa de muerte por infección en la infancia en los países industrializados. A pesar de los avances preventivos y terapéuticos, en el mundo se producen aproximadamente, 500.000 casos de ...
Marcos Alonso, Sonia
core +1 more source
International Journal of Laboratory Hematology, Volume 46, Issue S1, Page 12-26, May 2024.Abstract Hematology is a clinical specialty with strong roots in the laboratory; accordingly, the lab can help solve perplexing clinical problems. This review highlights clinical‐pathological conundrums addressed during my 35‐year hematology career at McMaster University.
Theodore E. Warkentin
wiley +1 more source
Purpura fulminans as the presenting manifestation in a patient with juvenile SLE
The 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
Clinical Case Reports, Volume 12, Issue 4, April 2024.Key clinical message In a rare occurrence, primary varicella infection led to rhabdomyolysis in a 24‐year‐old with no medical history. Presenting with rash, fever, and weakness, he developed diffuse myalgia at 72 h. Elevated muscle enzymes confirmed rhabdomyolysis secondary to varicella zoster virus (VZV) infection.
Yannick Laurent Tchenadoyo Bayala +7 more
wiley +1 more source
Gangrena simétrica periférica asociada a norepinefrina en una paciente con urosepsis por Escherichia coli [PDF]
, 2018 Background: symmetrical peripheral gangrene is a devastating complication associated with norepinephrine use in critically ill patients, characterized for ischemia of acral distribution in absence of large vessel obstruction. Objective: to underscore the
Alzate Piedrahita, John Alexander +3 more
core +1 more source
The Turkish Journal of Pediatrics, 2002 Purpura fulminans is a rare but dramatic disease which occurs most commonly during or after an infection. It is characterized by extensive involvement of the skin and extremities and involvement of visceral organs.
Cengiz Canpolat, Mustafa Bakir
doaj