ArticleCureus2025
Spontaneous Hepatic Subcapsular Haematoma Due to Hepatic Artery Pseudo-Aneurysm Rupture: A Rare Case in an Elderly Male.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
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Abstract
Hepatic artery pseudo-aneurysm (HAPA) is a rare vascular complication that is typically associated with trauma or hepatobiliary procedures. Spontaneous rupture usually occurs without preceding trauma or intervention and is exceptionally uncommon. This case highlights a rare presentation of HAPA leading to a hepatic subcapsular haematoma in an elderly male. An 80-year-old male was admitted with confusion and had an unwitnessed fall at home. Initial investigations demonstrated severe hyponatraemia, elevated C-reactive protein, and left-basal consolidation on chest X-ray, along with a subsequent diagnosis of syndrome of inappropriate ADH secretion (SIADH) due to pneumonia. During admission, the patient then developed hypotension and a significant drop in haemoglobin. Subsequent contrast-enhanced CT scan revealed a hepatic subcapsular haematoma caused by a ruptured HAPA. The patient was urgently referred to interventional radiology, where selective catheterisation and coil embolisation were performed to secure complete haemostasis. Post-procedure, the patient's haemoglobin was stabilised, and liver function improved. This case illustrates that spontaneous rupture of a HAPA should be considered in elderly or septic patients with unexplained anaemia and abnormal liver function. Early imaging with contrast-enhanced CT scan and timely interventional radiology are essential for successful management.
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