Combined venous and arterial thrombosis revealing underlying myeloproliferative disorder in a young patient: a case report.


Journal

Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382

Informations de publication

Date de publication:
16 Feb 2021
Historique:
received: 13 07 2020
accepted: 18 11 2020
entrez: 17 2 2021
pubmed: 18 2 2021
medline: 25 2 2021
Statut: epublish

Résumé

Myeloproliferative neoplasms (MPNs) such as polycythemia Vera (PV) and Essential Thrombocythemia (ET) can be associated with a high risk of both venous and arterial thrombosis. However, the co-existence between these two complications is very rare and has never been described before, especially in young adults with no known history of MPNs. We report the case of a 39 year-old Caucasian Moroccan male patient without cardiovascular risk factors (CVRF), who presented with acute chest pain. He also suffered from a severe headache since 2 weeks. Electrocardiogram (ECG) showed ST segment elevation myocardial infarction in the posterolateral leads. Cerebral Computed Tomography (CT) scan revealed subarachnoid hemorrhage (SAH), and cerebral Magnetic Resonance Angiography (MRA) found a Superior Sagittal Sinus Thrombosis (SSST). Routine blood tests showed raised hemoglobin and hematocrit in addition to leukocytosis and thrombocythemia. His coronary angiography revealed a thrombus in the ostial left circumflex artery (LCX). Further testing revealed positive Janus kinase 2 (JAK2) V617F mutation and low erythropoietin level, confirming the diagnosis of PV according to the 2008 World Health Organization (WHO) criteria. Antithrombotic and anti-ischemic treatments, in addition to myelosuppressive therapy with hydroxyurea, were initiated with a good clinical and biological evolution. This case shows that MPNs are an important cause of thrombosis, especially in young patients with no other risk factors. Early diagnosis and appropriate management are fundamental before the occurrence of life-threatening complications that can sometimes present in unusual forms associating arterial and venous thrombotic events.

Sections du résumé

BACKGROUND BACKGROUND
Myeloproliferative neoplasms (MPNs) such as polycythemia Vera (PV) and Essential Thrombocythemia (ET) can be associated with a high risk of both venous and arterial thrombosis. However, the co-existence between these two complications is very rare and has never been described before, especially in young adults with no known history of MPNs.
CASE PRESENTATION METHODS
We report the case of a 39 year-old Caucasian Moroccan male patient without cardiovascular risk factors (CVRF), who presented with acute chest pain. He also suffered from a severe headache since 2 weeks. Electrocardiogram (ECG) showed ST segment elevation myocardial infarction in the posterolateral leads. Cerebral Computed Tomography (CT) scan revealed subarachnoid hemorrhage (SAH), and cerebral Magnetic Resonance Angiography (MRA) found a Superior Sagittal Sinus Thrombosis (SSST). Routine blood tests showed raised hemoglobin and hematocrit in addition to leukocytosis and thrombocythemia. His coronary angiography revealed a thrombus in the ostial left circumflex artery (LCX). Further testing revealed positive Janus kinase 2 (JAK2) V617F mutation and low erythropoietin level, confirming the diagnosis of PV according to the 2008 World Health Organization (WHO) criteria. Antithrombotic and anti-ischemic treatments, in addition to myelosuppressive therapy with hydroxyurea, were initiated with a good clinical and biological evolution.
CONCLUSION CONCLUSIONS
This case shows that MPNs are an important cause of thrombosis, especially in young patients with no other risk factors. Early diagnosis and appropriate management are fundamental before the occurrence of life-threatening complications that can sometimes present in unusual forms associating arterial and venous thrombotic events.

Identifiants

pubmed: 33593422
doi: 10.1186/s13256-020-02593-5
pii: 10.1186/s13256-020-02593-5
pmc: PMC7885597
doi:

Substances chimiques

Erythropoietin 11096-26-7
JAK2 protein, human EC 2.7.10.2
Janus Kinase 2 EC 2.7.10.2

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

76

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Auteurs

Rime Benmalek (R)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco. Rime.benmalek@gmail.com.

Hanane Mechal (H)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

Hatim Zahidi (H)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

Karim Mounaouir (K)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

Salim Arous (S)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

Mohamed El Ghali Benouna (MEG)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

Abdenasser Drighil (A)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

Rachida Habbal (R)

Cardiology department, Hospital University Center Ibn Rochd, Casablanca, Morocco.

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Classifications MeSH