Disseminated Intravascular Coagulation With Excessive Fibrinolysis Following Diagnostic Prostatic Biopsy for Prostate Cancer.

disseminated intravascular coagulation (dic) epsilon aminocaproic acid excessive fibrinolysis hyperfibrinolysis patent foramen oval primary fibrinolysis prostate cancer secondary fibrinolysis

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Oct 2022
Historique:
accepted: 19 10 2022
entrez: 23 11 2022
pubmed: 24 11 2022
medline: 24 11 2022
Statut: epublish

Résumé

The most common hematological disorder associated with prostate cancer is disseminated intravascular coagulation (DIC). In most cases, cancer patients with DIC have compensated fibrinolysis with a low incidence of bleeding. However, DIC with excessive fibrinolysis is a rare albeit life-threatening variant that can present with massive bleeding and is thought to occur due to the unique properties of neoplastic cells of prostate cancer that activate both procoagulant and anticoagulant pathways simultaneously. Depending on the shift of the intricate balance between the two forces, the net result can be either systemic micro- (DIC) or macro-thrombi, deep venous thrombosis (DVT) or pulmonary embolism, or a bleeding syndrome from excessive vicious activation of fibrinolysis. Here, we present a unique case of suspected prostate cancer who underwent a diagnostic prostatic biopsy. Subsequently, he developed massive hematuria requiring intensive care unit admission with multiple supportive blood products. Additionally, he was administered epsilon-aminocaproic acid with a prophylactic dose of heparin, with prompt resolution of bleeding. After stabilization, he was discharged with planned outpatient chemotherapy. However, he subsequently presented with lower extremity DVT within a week, which led to a stroke in the setting of a patent foramen ovale. This unique case report highlights how a change in the intricate balance of the coagulation cascade causes a polar shift in clinical presentation and complications.

Identifiants

pubmed: 36415381
doi: 10.7759/cureus.30502
pmc: PMC9675043
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e30502

Informations de copyright

Copyright © 2022, Ghallab et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Muhammad Ghallab (M)

Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Internal Medicine, Queens Hospital Center, New York, USA.

Usman Ilyas (U)

Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Internal Medicine, Queens Hospital Center, New York, USA.

Lilian Tran (L)

Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Internal Medicine, Queens Hospital Center, New York, USA.

Toka Amin (T)

Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, USA.
Internal Medicine, Queens Hospital Center, New York, USA.

Salma Abdelmoteleb (S)

Internal Medicine, Cairo University School of Medicine, Cairo, EGY.

Classifications MeSH