Laboratory Aspects and Diagnostic Challenges in a Case of Hypereosinophilic Syndrome
Vanessa Rossi, Silvia Velocci, Sergio Bernardini, Maria Morello

TL;DR
A 35-year-old woman with hypereosinophilic syndrome experienced severe multi-organ complications, highlighting the importance of early diagnosis and laboratory monitoring.
Contribution
This case report emphasizes the diagnostic challenges and clinical importance of idiopathic hypereosinophilic syndrome in rapidly progressive cases.
Findings
The patient exhibited severe hypereosinophilia and systemic inflammation leading to multi-organ failure.
Exclusion of secondary causes confirmed idiopathic hypereosinophilic syndrome.
Early recognition and laboratory findings are critical for timely intervention in rapidly progressive cases.
Abstract
Hypereosinophilia is defined by a persistent increase in eosinophil levels and can lead to multi-organ damage with highly variable symptoms. The most common manifestations involve the skin, lungs, and gastrointestinal tract, while cardiac and neurological complications can be particularly severe and sometimes fatal. Within this context, we describe the case of a 35-year-old woman with hypereosinophilic syndrome (HES), whose symptoms began during pregnancy. Three months after giving birth, she contracted SARS-CoV-2, which resolved without complications. However, shortly thereafter, laboratory tests revealed marked leukocytosis accompanied by a rapid clinical deterioration. At admission, the patient displayed severe hypereosinophilia associated with systemic inflammation, liver injury, myocardial necrosis, and multi-organ involvement affecting the kidneys, brain, heart, and lungs. As her…
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Taxonomy
TopicsEosinophilic Disorders and Syndromes · Eosinophilic Esophagitis · Autoimmune and Inflammatory Disorders
