| Literature DB >> 34377694 |
Chidinma Ejikeme1, Sherif Elkattawy1, Fisayo Kayode-Ajala1, Sarah Ayad1, Abraheim Al-Nasseri2, William Kessler3.
Abstract
Reactive thrombocytosis after splenectomy is a feared cause of thrombosis throughout the arterial and venous system. There are many causes of splenomegaly, ranging from cirrhosis to lymphoma to hereditary spherocytosis. In this report, we will discuss a case of reactive thrombocytosis after splenectomy in a patient with hereditary spherocytosis. Splenomegaly is a relatively common finding in HD patients, causing extravascular haemolysis and thus leading to haemolytic anaemia. Splenectomy is usually considered when patients start to manifest severe symptoms such as abdominal pain, jaundice or worsening liver function tests. Our patient was a good surgical candidate and successfully underwent splenectomy but afterwards developed arterial and venous thrombosis due to reactive thrombocytosis. An extensive hypercoagulable work-up was unremarkable. The patient was started on hydroxyurea and anticoagulation with eventual improvement of platelet levels. LEARNING POINTS: Reactive thrombocytosis can be a significant complication after splenectomy and can range from mild (500,000-700,000/mm3), to moderate (700,000-900,000/mm3), severe (>900,000/mm3) and very severe thrombocytosis (>1,000,000/mm3).The use of low-dose hydroxyurea in patients with very severe thrombocytosis can reduce the platelet count to safe levels, and thus, the risk of developing thrombosis. © EFIM 2021.Entities:
Keywords: Thrombocytosis; hereditary spherocytosis; hypercoagulable; splenomegaly; thrombosis
Year: 2021 PMID: 34377694 PMCID: PMC8336755 DOI: 10.12890/2021_002673
Source DB: PubMed Journal: Eur J Case Rep Intern Med ISSN: 2284-2594