Results 191 to 200 of about 56,829 (249)
Relapsed Immune Thrombocytopenic Purpura Following COVID-19 Vaccination in a Patient With Autoimmune Cytopenias. [PDF]
J Med CasesLahart E +3 more
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Thrombotic thrombocytopenic purpura: a Trojan horse of acute leukemia?: a case report. [PDF]
J Med Case RepNassani BM +4 more
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Is congenital thrombotic thrombocytopenic purpura a risk factor for ischemic osteonecrosis of the hip joint (Legg-Calvé-Perthes disease)? [PDF]
Thromb JLaemmle A, Lämmle B.
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British Journal of Tuberculosis and Diseases of the Chest, 1952
Summary A case of tuberculosis and thrombocytopenic purpura is described, and the literature relating to the association of the two diseases is reviewed. The subject is discussed in relation to the forms of tuberculosis which may cause purpura, the ways in which it may do so and the prognosis in such cases; certain conclusions are reached.
P, ELLMAN, J H P, JOHNSON
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Summary A case of tuberculosis and thrombocytopenic purpura is described, and the literature relating to the association of the two diseases is reviewed. The subject is discussed in relation to the forms of tuberculosis which may cause purpura, the ways in which it may do so and the prognosis in such cases; certain conclusions are reached.
P, ELLMAN, J H P, JOHNSON
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Dermatologic Clinics, 1989
Purpura is a cutaneous manifestation of a wide variety of diseases. These include such diverse entities as platelet defects, vasculitides, and disorders of connective tissue. Uncovering the underlying disorder in a patient with purpura is a stimulating challenge to the clinician's diagnostic abilities.
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Purpura is a cutaneous manifestation of a wide variety of diseases. These include such diverse entities as platelet defects, vasculitides, and disorders of connective tissue. Uncovering the underlying disorder in a patient with purpura is a stimulating challenge to the clinician's diagnostic abilities.
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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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International Journal of Dermatology, 1992
Factitious purpura may present as a perplexing problem for the dermatologist and can mimic serious disease. This form of mechanical purpura, often caused by suction may be deliberately or unknowingly induced by the patient. Some cases may go unrecognized for a considerable length of time and undergo unnecessary investigation before the diagnosis is ...
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Factitious purpura may present as a perplexing problem for the dermatologist and can mimic serious disease. This form of mechanical purpura, often caused by suction may be deliberately or unknowingly induced by the patient. Some cases may go unrecognized for a considerable length of time and undergo unnecessary investigation before the diagnosis is ...
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The American Journal of Surgery, 1982
Purpura fulminans presents as a catastrophic illness with gangrene of the distal extremities and necrosis of skin. The clinical picture consists of septicemia, shock, and disseminated intravascular coagulation. The Shwartzman and Arthus reactions are thought to be responsible for the pathogenesis of purpura fulminans.
D Z, Chu, F W, Blaisdell
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Purpura fulminans presents as a catastrophic illness with gangrene of the distal extremities and necrosis of skin. The clinical picture consists of septicemia, shock, and disseminated intravascular coagulation. The Shwartzman and Arthus reactions are thought to be responsible for the pathogenesis of purpura fulminans.
D Z, Chu, F W, Blaisdell
openaire +2 more sources