Literature DB >> 32968992

Hyperfibrinolysis in Patients with Solid Malignant Neoplasms: A Systematic Review.

Anne Winther-Larsen1,2, Birgitte Sandfeld-Paulsen1, Anne-Mette Hvas1,3.   

Abstract

Solid malignant neoplasms have the capability of disturbing the fibrinolytic system, leading to primary hyperfibrinolysis, a paraneoplastic syndrome that potentially results in severe bleeding. Yet, the full extent of primary hyperfibrinolysis in solid malignant neoplasms is unknown. Thus, the purpose of this study was to systematically review the current literature regarding clinical manifestations, biochemical diagnosis, and treatment of primary hyperfibrinolysis in patients with solid malignant neoplasms. The review was performed in agreement with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The databases PubMed, Embase, Scopus, and Web of Science were searched on December 5, 2019, without time limits. Studies were included if they comprised at least one biochemical marker of fibrinolysis in addition to fibrinogen degradation products such as D-dimer, and furthermore included a correlation between biochemical marker and clinical outcome. In total, 12 studies were included. All studies were case reports including a total of 21 patients. Prostate cancer was the most frequently represented cancer type (76%), and the majority of cancer patients had metastatic disease (81%). Spontaneous bleeding was the clinical presentation in the majority of patients (76%), and the most frequently localization for the bleedings was subcutaneous. Antifibrinolytic agents were the most commonly used treatment and ceased bleedings in 80% of patients. Three patients died of uncontrolled bleedings. In conclusion, primary hyperfibrinolysis induced by solid malignant neoplasms is a rare but potentially life-threatening condition that should be considered, especially in patients with metastatic disease presenting with serious, spontaneous subcutaneous bleedings. A standardized diagnostic strategy is strongly needed. Thieme. All rights reserved.

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Year:  2020        PMID: 32968992     DOI: 10.1055/s-0040-1715795

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  2 in total

1.  [Diagnostics and treatment of clinically relevant paraneoplastic syndromes].

Authors:  Katharina Schütte; Karolin Trautmann-Grill
Journal:  Schmerz       Date:  2022-10-19       Impact factor: 1.629

2.  Paraneoplastic Evans Syndrome in a Patient With Prostate Cancer With Small Cell Transformation.

Authors:  Adarsh Sidda; Gurusidda Manu; Mahmoud Abdallah; Doreen Griswold; Mohamed Alsharedi; Toni Pacioles
Journal:  Cureus       Date:  2022-04-26
  2 in total

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