Eosinophilic Ascites: A Rare Presentation of a Hematoma

Idiopathic eosinophilic ascites (IEA) is a condition characterized by the eosinophilic infiltration of the peritoneal cavity without an identifiable underlying cause. We present the case of a 39-year-old female patient with no significant medical history who was referred for leukocytosis and abdominal discomfort. Imaging revealed a large, peripherally calcified intra-abdominal fluid collection, and subsequent paracentesis demonstrated eosinophilic ascites (EA). A thorough evaluation, including peripheral eosinophilia workup, malignancy screening (including imaging and cytology), infectious serologies (parasitic and fungal panels), autoimmune markers, and upper and lower endoscopy with biopsies, failed to identify a definitive etiology. Diagnostic laparoscopy confirmed a hematoma, and post-laparoscopy, the patient's symptoms and peripheral eosinophilia resolved. This case highlights the diagnostic challenges of EA, the importance of a systematic exclusionary approach, and the potential for an idiopathic, reactive eosinophilic process. Given the risk of recurrence or progression to an underlying disorder, long-term follow-up is warranted.

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Publication Details

Journal
Cureus
Published
2025-04-21
DOI
https://doi.org/10.7759/cureus.82712
Primary Topic
Eosinophilic Disorders and Syndromes
Type
article
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article

Eosinophilic Ascites: A Rare Presentation of a Hematoma

Vivek Ramarathnam, Mary Amar, Shovendra Gautam, Mufaddal M Jafferjee
Cureus
Eosinophilic Disorders and Syndromes
article

Eosinophilic Ascites: A Rare Presentation of a Hematoma

Vivek Ramarathnam, Mary Amar, Shovendra Gautam, Mufaddal M Jafferjee
article en

Abstract

Idiopathic eosinophilic ascites (IEA) is a condition characterized by the eosinophilic infiltration of the peritoneal cavity without an identifiable underlying cause. We present the case of a 39-year-old female patient with no significant medical history who was referred for leukocytosis and abdominal discomfort. Imaging revealed a large, peripherally calcified intra-abdominal fluid collection, and subsequent paracentesis demonstrated eosinophilic ascites (EA). A thorough evaluation, including peripheral eosinophilia workup, malignancy screening (including imaging and cytology), infectious serologies (parasitic and fungal panels), autoimmune markers, and upper and lower endoscopy with biopsies, failed to identify a definitive etiology. Diagnostic laparoscopy confirmed a hematoma, and post-laparoscopy, the patient's symptoms and peripheral eosinophilia resolved. This case highlights the diagnostic challenges of EA, the importance of a systematic exclusionary approach, and the potential for an idiopathic, reactive eosinophilic process. Given the risk of recurrence or progression to an underlying disorder, long-term follow-up is warranted.

CureusVol. 17(4)
Baylor Scott & White All Saints Medical Center (US)
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Openalex Percentile: Top 88%
Eosinophilic Disorders and Syndromes
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Eosinophilic Ascites: A Rare Presentation of a Hematoma — Vivek Ramarathnam, Mary Amar, et al. · Cureus (2025) | TGRS Research Map | TGRS