Ana Brusic1, June Oo2, Damien L Stella1,3, Paul M Simkin1,3, Benjamin Pt Loveday2,4,5. 1. Department of Radiology, Royal Melbourne Hospital, Parkville, Australia. 2. Surgical Oncology, Peter MacCallum Cancer Centre, Parkville, Australia. 3. Department of Radiology, University of Melbourne, Parkville, Australia. 4. Department of Surgery, Royal Melbourne Hospital, Parkville, Australia. 5. Department of Surgery, University of Auckland, Auckland, New Zealand.
Abstract
INTRODUCTION: Intracystic haemorrhage is a rare complication of hepatic cysts, and is often mistaken for a malignant lesion. CASE REPORT: A 55-year-old female with a history of polycystic kidney and liver disease presented with a six-month history of abdominal distension, abdominal pain, early satiety, shortness of breath and 5 kg of weight loss. Imaging revealed a 20 cm mixed solid-cystic hepatic lesion containing peripheral avascular mobile echogenic material with a flame-like morphology. After experiencing symptomatic relief from ultrasound-guided aspiration, the patient underwent cyst fenestration for more definitive treatment. DISCUSSION: Haemorrhagic hepatic cysts are uncommon and may present on imaging as having lace-like retractile clot, internal layering or shading of separating blood products or avascular mobile flame-like excrescences. The presence of avascular mobile flame-like excrescences appears to be a unique feature of haemorrhagic hepatic cysts. CONCLUSION: While haemorrhagic hepatic cysts are rare and commonly mistaken for biliary cystadenomas or adenocarcinomas, the identification of particular features on high-resolution magnetic resonance imaging and contrast-enhanced ultrasound can lead to the correct diagnosis.
INTRODUCTION: Intracystic haemorrhage is a rare complication of hepatic cysts, and is often mistaken for a malignant lesion. CASE REPORT: A 55-year-old female with a history of polycystic kidney and liver disease presented with a six-month history of abdominal distension, abdominal pain, early satiety, shortness of breath and 5 kg of weight loss. Imaging revealed a 20 cm mixed solid-cystic hepatic lesion containing peripheral avascular mobile echogenic material with a flame-like morphology. After experiencing symptomatic relief from ultrasound-guided aspiration, the patient underwent cyst fenestration for more definitive treatment. DISCUSSION: Haemorrhagic hepatic cysts are uncommon and may present on imaging as having lace-like retractile clot, internal layering or shading of separating blood products or avascular mobile flame-like excrescences. The presence of avascular mobile flame-like excrescences appears to be a unique feature of haemorrhagic hepatic cysts. CONCLUSION: While haemorrhagic hepatic cysts are rare and commonly mistaken for biliary cystadenomas or adenocarcinomas, the identification of particular features on high-resolution magnetic resonance imaging and contrast-enhanced ultrasound can lead to the correct diagnosis.
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