Results 81 to 90 of about 6,740 (215)
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Invasive aspergillosis, though typically seen in immunocompromised patients, can also affect immunocompetent individuals and mimic pulmonary malignancy. This case highlights the importance of considering fungal infections in the differential diagnosis of chronic respiratory symptoms, particularly in patients with risk factors such as heavy ...
Kumail Khandwala +4 more
wiley +1 more source
Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients
Biomedical PapersIntroduction. Congenital hypofibrinogenemia (CH) and congenital dysfibrinogenemia (CD) are rare coagulation disorders caused by quantitative or qualitative defects in the fibrinogen gene.
Dominika Jaraskova +11 more
doaj +1 more source
Haematologica, 2007 Fibrinogen is an essential component of the coagulation cascade and the acute phase response. The native 340 kDa molecule has a symmetrical trinodular structure composed of a central E-domain connected to outer D-domains by triple helical coiled-coils.1 ...
Ryan L. Davis +5 more
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A Case of Severe Pre‐Eclampsia Complicated by HELLP Syndrome and Extensive Hepatic Infarction
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Extensive hepatic infarction is a rare but potentially fatal complication of HELLP syndrome and is often difficult to recognize because of nonspecific clinical manifestations. A 34‐year‐old woman developed HELLP syndrome shortly after cesarean delivery for severe pre‐eclampsia, presenting with oliguria, marked thrombocytopenia (50 × 109/L ...
Tiange Xia +3 more
wiley +1 more source
Thrombosis Journal, 2019 Background The usefulness of the activated partial thromboplastin time (APTT) waveform has been reported in hemophilia, acquired hemophilia and monitoring for anticoagulants.
Kei Suzuki +8 more
doaj +1 more source
Alterações da coagulação associadas à leucemia promielocítica aguda [PDF]
, 2009 Acute promyelocytic leukemia is frequently accompanied by coagulation abnormalities usually described as laboratorial disseminated intravascular coagulation, which is the main cause of morbidity and early mortality. Aberrant activation of the coagulation
JACOMO, Rafael H., REGO, Eduardo M.
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A case of hypofibrinogenemia presenting with submental hamatoma
Bangabandhu Sheikh Mujib Medical University Journal, 2016 Hereditary hypofibrinogenemia is a rare disease and the usual presentation is difficult to stop bleeding or hamatoma in the muscle or intracranial space after injury. There may also be adverse pregnancy outcome, and increased tendency to thrombosis. The
Mujahida Rahman +2 more
doaj +1 more source
Percutaneously Inserted AngioVac Suction Thrombectomy for the Treatment of Filter-Related Iliocaval Thrombosis [PDF]
, 2015 In the setting of acute iliocaval thrombosis due to reversible causes, thrombus removal is preferred by many in the management of inferior vena cava (IVC) thrombosis as it is thought likely to minimize the long-term complications of chronic venous ...
Butty, Sabbah D. +2 more
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Treatment of adult-onset Still's disease: a review [PDF]
, 2014 Adult-onset Still's disease (AOSD) is a rare inflammatory disorder that has been recently classified as a polygenic autoinflammatory disorder. The former classification, based on the disease course, seems to be quite dated.
Gerfaud-Valentin, M. +3 more
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Frontiers in Cardiovascular MedicineThe most frequent haematological malignancy associated with acquired hypo/dysfibrinogenemia is multiple myeloma. We present an unusual case of severe haemorrhagic diathesis due to acquired hypofibrinogenemia in a patient with early T-cell precursor acute
Luca Spiezia +4 more
doaj +1 more source