Results 231 to 240 of about 61,273 (263)

Thrombotic Thrombocytopenic Purpura

Pediatric Emergency Care, 2011
In 1924, Dr Eli Moschcowitz described a 16-year-old adolescent girl with abrupt onset of petechiae, hemolytic anemia, followed by paralysis, coma, and death. Autopsy showed widespread hyaline thrombi in the terminal arterioles and capillaries of various organs. The syndrome described by Moschowitz is now known as thrombotic thrombocytopenic purpura.
Alex, Koyfman, Elizabeth, Brém, Vincent W, Chiang   +2 more
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Congenital thrombocytopenic purpura

The Journal of Pediatrics, 1947
Summary Congenital thrombocytopenic purpura has occurred as a familial condition in three successive children of a mother previously splenectomized for thrombocytopenic purpura. In each of these children there has been a gradual spontaneous recovery to a normal blood picture during the first 2 months of life, and following recovery there has been no ...
J, TALMADGE, B, BERMAN
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NEONATAL THROMBOCYTOPENIC PURPURA

Pediatrics, 1956
A case of neonatal thrombocytopenic purpura in the newborn infant of a mother with idiopathic thrombocytopenic purpura is reported. The mother and the baby both had platelet autoagglutinins, and isoagglutinins were present for each other's platelets. The infant's agglutinins had disappeared by the age of 3 months.
E J, SCHOEN, A L, KING, R T, DUANE
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Idiopathic Thrombocytopenic Purpura

Postgraduate Medicine, 1962
The acute form of ITP may be drug-induced or may follow infection or exposure to chemicals. The chronic form represents a self-perpetuating immunologic (auto-immune) disorder, at times associated with chronic lymphatic leukemia and other disorders. In some cases, it may be a prodrome of systemic lupus, to which it seems to be closely related.
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Thrombotic thrombocytopenic purpura

Disease-a-Month, 2014
Moschowitz first described thrombotic thrombocytopenic purpura (TTP) in 1925 in a 16-yearold female who presented with fever, petechiae, and a microangiopathic hemolytic anemia. Autopsy examination at the time revealed hyaline thrombi in the vascular beds of many organs. By 1947, several more cases were described and Singer suggested the term TTP.
Albara, Said, Rami Y, Haddad, Robert, Stein, Edgar V, Lerma   +3 more
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Immune Thrombocytopenic Purpura

JCR: Journal of Clinical Rheumatology, 1997
Thrombocytopenia is seen commonly in patients with rheumatic disorders. In general, thrombocytopenia is due to one of three mechanisms: reduced production, sequestration, or increased platelet destruction. In outpatients, the most common cause of thrombocytopenia is immune thrombocytopenia. Immune thrombocytopenia encompasses a broad group of disorders
M A, Crowther, J G, Kelton
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Thrombotic thrombocytopenic purpura

Journal of Thrombosis and Haemostasis, 2005
This overview summarizes the history of thrombotic thrombocytopenic purpura (TTP) from its initial recognition in 1924 as a most often fatal disease to the discovery in 1997 of ADAMTS-13 deficiency as a major risk factor for acute disease manifestation.
B, Lämmle, J A, Kremer Hovinga, L, Alberio   +2 more
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Thrombotic thrombocytopenic purpura

The Journal of Maternal-Fetal & Neonatal Medicine, 2012
A 34-year old primipara was admitted to hospital with dichorionic-diamniotic twins in 26+3 weeks of gestation. In suspicion of HELLP-syndrome, caesarean section was performed at 27+4 weeks of gestation, because of platelet count was reduced to 44000/µl. A re-laparotomy had to be performed because of intra-abdominal bleedings.
Charlotte, Kaiser, Ulrich, Gembruch, Viktor, Janzen, Anne-Sybil, Gast   +3 more
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Thrombotic Thrombocytopenic Purpura

JAMA: The Journal of the American Medical Association, 1991
CASE PRESENTATION —Charles T. Bingham III, MD A 27-YEAR-OLD man was transferred to The Johns Hopkins Hospital for evaluation of delirium. Five days prior to admission he had presented to another hospital with hematemesis and syncope. Esophagogastroduodenoscopy revealed the presence of a 0.5-cm gastric ulcer.
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Thrombotic thrombocytopenic purpura

Blood Coagulation & Fibrinolysis, 1992
Thrombotic thrombocytopenic purpura is an uncommon disorder, but it continues to be of considerable interest. The disease mechanisms are unclear and the aetiology is unknown. Perhaps most enigmatic of all, the mode of action of plasma therapy, which successfully induces remission in about two-thirds of cases, is wholly inexplicable. There are currently
W G, Murphy, J C, Moore, T E, Warkentin, C P, Hayward, J G, Kelton   +4 more
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