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Published on: January 6, 2023
An atypical pacemaker pocket hematoma containing chyliform fluid
Stefano Maffè1, Paola Paffoni1, Luca Bergamasco1
1Division of Cardiology, SS Trinita' Borgomanero Hospital, ASL NO, Novara, Italy.
Insights
Subcutaneous hematoma after cardiac device implantation can lead to rare pseudochyle fluid accumulation. This case highlights cholesterol-rich fluid formation in an implantable cardioverter-defibrillator pocket.
Area of Science:
- Cardiology
- Medical Complications
- Fluid Dynamics
Background:
- Subcutaneous hematoma is a known complication of cardiac device implantation.
- Accumulation of chyliform material in device pockets is exceptionally rare.
Observation:
- A 60-year-old male with antiphospholipid antibody syndrome and rheumatoid arthritis developed a subcutaneous hematoma post-ICD implantation.
- Seven months later, a large, asymptomatic swelling reappeared in the ICD pocket, yielding 100ml of gold-colored, odorless fluid upon drainage.
Findings:
- Chemical analysis revealed high cholesterol (704 mg/dl) and low triglycerides (80 mg/dl) in the drained fluid, consistent with pseudochyle fluid.
- Microscopic and cytologic examination showed macrophages laden with cholesterol, supporting degradation of a chronic hematoma.
Implications:
- This case presents extremely rare documentation of pseudochyle fluid formation within an implantable cardioverter-defibrillator pocket.
- It underscores the importance of considering chronic hematoma degradation as a cause of unusual fluid collections in implanted device sites.
Abstract:
Subcutaneous hematoma is a complication of cardiac device implantation. In most cases, it is drained or spontaneously reabsorbed. While cases of chylothorax are rare, and cases of pseudochylothorax even rarer, previous cases of accumulation of chyliform material in the subcutaneous pockets of cardiac devices are anecdotal. We present a case of a 60-year-old man with antiphospholipids antibody syndrome and rheumatoid arthritis, who underwent dual-chamber ICD implantation in December 2020; the procedure was complicated by a pocket hematoma, which required surgical drainage. After 7 months, the man returned owing to heart failure, with evidence of the reappearance of a large swelling in the ICD pocket; this was tolerated for months by the patient and was no longer controlled. We drained 100ml of gold-colored, odorless liquid, and found no evidence of blood material in the pocket. The liquid was not pus, as culture testing proved negative for bacterial growth. Chemical-physical examination revealed elevated cholesterol concentration (704 mg/dl) and low levels of triglycerides (80 mg/dl; plasma cholesterol values were 91mg/dl, and triglycerides 48 mg/dl). Microscopic examination revealed isolated leukocytes and rare erythrocytes immersed in mucoid material; cytological analysis showed a carpet of macrophages filled with cholesterol. This evidence supports the diagnosis of pseudochyle fluid, formed by the degradation of a hematoma left intact in a closed cavity for more than 6 months. This is an extremely rare case of chyliform fluid documented in an ICD pocket.
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