Acute Pulmonary Insufficiency 1985
DOI: 10.1515/9783110850123-007
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Distribution Patterns of Microthrombi in Disseminated Intravascular Coagulation (Dic)

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Cited by 31 publications
(39 citation statements)
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“…First, many organs show fibrin deposition at pathologic examination, and the presence of intravascular thrombi seems to be clearly related to the clinical dysfunction of the organs (19). Autopsy findings in patients with overt DIC include diffuse bleeding, hemorrhagic necrosis, microthrombi in small blood vessels, and thrombi in midsize and larger arteries and veins (20,21). Fibrin deposition in small and midsize vessels in patients with DIC in these studies was invariably associated with ischemia and necrosis and with clinical dysfunction of organs.…”
Section: Clinical Setting and Relevancementioning
confidence: 66%
“…First, many organs show fibrin deposition at pathologic examination, and the presence of intravascular thrombi seems to be clearly related to the clinical dysfunction of the organs (19). Autopsy findings in patients with overt DIC include diffuse bleeding, hemorrhagic necrosis, microthrombi in small blood vessels, and thrombi in midsize and larger arteries and veins (20,21). Fibrin deposition in small and midsize vessels in patients with DIC in these studies was invariably associated with ischemia and necrosis and with clinical dysfunction of organs.…”
Section: Clinical Setting and Relevancementioning
confidence: 66%
“…The extent of necrotic tissue injury was shown to be dependent on the quantity and duration of thrombosis, and a clear correlation was also demonstrated between thrombi and ischemic tissue damage (11,12). Shimamura et al (13) studied the distribution pattern of microthrombi in 37 autopsy cases of DIC. They reported that the incidence of microthrombi differed between organs: lung (100%), liver (94.6%), kidney (75.5%), heart (56.8%), pancreas (48.7%), adrenal gland (32.4%), and gastrointestinal tracts (18.9%).…”
Section: Microvascular Thrombosismentioning
confidence: 99%
“…The liver can be injured and its function altered by the activation of coagulation and inflammatory processes in sepsis (63). In patients with DIC associated with sepsis, hepatocellular necrosis and formation of fibrin thrombi in the sinusoids around the necrotic area are frequently demonstrated at autopsy (12,13,16). Using experimental models, Shibayama (64) confirmed that LPS administration induces fibrin deposition and infiltration of neutrophils in the hepatic sinusoid, leading to coagulative hepatocellular necrosis and liver injury.…”
Section: Microvascular Thrombosis and Organ Dysfunctionmentioning
confidence: 99%
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“…El incremento de la expresión de citoquinas y de procoagulantes contribuyen al desarrollo de la CID con un fenotipo trombótico 20 demostrándose en autopsias la existencia de microtrombosis diseminada 21 . Las endotoxinas bacterianas, como el lipopolisacárido, se unen a receptores endoteliales desencadenando una respuesta inflamatoria con incremento de la expresión de citoquinas (TNF-a, IL-1b, y IL-6) 22 , expresión de moléculas de adhesión (selectinas E y P), activación del complemento, expresión de factor tisular en la superficie endotelial, en monocitos y macrófagos y generación de micropartículas portadoras de factor tisular, que lleva a la activación de la coagulación 23 .…”
Section: Sepsis Coagulación Intravascular Diseminadaunclassified