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Low-frequency inherited complement receptor variants are associated with purpura fulminans.
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Acute phase proteins as early non-specific biomarkers of human and veterinary diseases [PDF]
, 2011 Dubois, G. +4 more
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Annals of Plastic Surgery, 1988
The purpose of this article is to call attention to an unusual syndrome that may lead to a major loss of soft tissue, limb, and life. The application of principles learned from trauma and burn care may substantially reduce the morbidity and mortality, which in the past have been associated with purpura fulminans.
M B, Seagle, H G, Bingham
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The purpose of this article is to call attention to an unusual syndrome that may lead to a major loss of soft tissue, limb, and life. The application of principles learned from trauma and burn care may substantially reduce the morbidity and mortality, which in the past have been associated with purpura fulminans.
M B, Seagle, H G, Bingham
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The Journal of Hand Surgery, 1990
Purpura fulminans is a rare disease that typically begins as a benign infectious process and subsequently progresses to severe sepsis, hypotension, purpura ecchymosis, and disseminated intravascular coagulation. We present an unusual case of an adult who was seen initially with pneumococcal sepsis that subsequently developed into purpura fulminans with
R M, Singer, J E, Gorosh
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Purpura fulminans is a rare disease that typically begins as a benign infectious process and subsequently progresses to severe sepsis, hypotension, purpura ecchymosis, and disseminated intravascular coagulation. We present an unusual case of an adult who was seen initially with pneumococcal sepsis that subsequently developed into purpura fulminans with
R M, Singer, J E, Gorosh
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The American Journal of Medicine, 1976
Purpura fulminans is a rare disease characterized by cutaneous ecchymosis, hypotension and fever associated with disseminated intravascular coagulation. It usually follows a preparatory infectious illness. A case in a 55 year old woman challenges the concept that this disease is limited to childhood.
T E, Spicer, J M, Rau
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Purpura fulminans is a rare disease characterized by cutaneous ecchymosis, hypotension and fever associated with disseminated intravascular coagulation. It usually follows a preparatory infectious illness. A case in a 55 year old woman challenges the concept that this disease is limited to childhood.
T E, Spicer, J M, Rau
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The Indian Journal of Pediatrics, 1987
Seven children with purpura fulminans are reported. All were very sick and had extensive purpuric and ecchymotic skin lesions. Five of them had septicemia, one had meningitis and one had viral respiratory tract infection. The bacteria cultured were Staphylococcus aureus (1), Hemophilus influenzae (1), Pseudomonas aeroginosa (1), Klebsiella pneumoniae ...
L, Kumar +3 more
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Seven children with purpura fulminans are reported. All were very sick and had extensive purpuric and ecchymotic skin lesions. Five of them had septicemia, one had meningitis and one had viral respiratory tract infection. The bacteria cultured were Staphylococcus aureus (1), Hemophilus influenzae (1), Pseudomonas aeroginosa (1), Klebsiella pneumoniae ...
L, Kumar +3 more
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Postgraduate Medical Journal, 2019
A 48-year-old diabetic woman presented with 2-day history of fever and skin discolouration over hand. On admission, her vital parameters were stable and systemic examination unremarkable. Cutaneous examination revealed well-defined dusky ecchymotic patches with tender indurated margins, haemorrhagic bulla, focal gangrenous necrosis and ulceration ...
Abheek Sil +2 more
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A 48-year-old diabetic woman presented with 2-day history of fever and skin discolouration over hand. On admission, her vital parameters were stable and systemic examination unremarkable. Cutaneous examination revealed well-defined dusky ecchymotic patches with tender indurated margins, haemorrhagic bulla, focal gangrenous necrosis and ulceration ...
Abheek Sil +2 more
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Pediatrics, 1964
A case of purpura fulminans following varicella was shown to be a defibrinating syndrome and was treated successfully with fibrinogen alone. The similarities between the Shwartzman phenomenon and purpura fulminans are discussed and are shown to support the hypothesis that purpura fulminans is primarily an immunological disease, similar to the ...
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A case of purpura fulminans following varicella was shown to be a defibrinating syndrome and was treated successfully with fibrinogen alone. The similarities between the Shwartzman phenomenon and purpura fulminans are discussed and are shown to support the hypothesis that purpura fulminans is primarily an immunological disease, similar to the ...
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