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Angiomyxoma coexisting with focal nodular hyperplasia: A case report
Xin Li1, Wanghong Li1, Chen Liu1
1Department of Hepatopancreatobiliary Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, Xinjiang Uygur Autonomous Region 830011, P.R. China.
This study reports a rare case of liver angiomyxoma (AM) coexisting with focal nodular hyperplasia (FNH). Surgical excision proved effective, highlighting the need for careful diagnosis and follow-up for this uncommon liver tumor presentation.
Area of Science:
- Hepatology
- Pathology
- Surgical Oncology
Background:
- Angiomyxoma (AM) is a rare soft tissue tumor typically found in the pelvic and perineal regions.
- Extrapelvic AM, particularly in the liver, is exceptionally uncommon and prone to misdiagnosis.
- Focal Nodular Hyperplasia (FNH) is a common benign liver lesion.
Observation:
- A 56-year-old woman presented with two asymptomatic liver space-occupying lesions.
- Preoperative imaging failed to definitively diagnose the intrahepatic lesions, leading to initial misdiagnosis as other hepatic tumors.
- The coexistence of liver AM and FNH presented a diagnostic challenge due to the rarity of AM in this location.
Findings:
- Histopathological examination confirmed the presence of both angiomyxoma and focal nodular hyperplasia.
- Surgical excision was performed, and the patient experienced no recurrence or metastasis during a 1-year follow-up.
- Microscopic features were consistent with AM and FNH.
Implications:
- Accurate diagnosis of liver AM requires high clinical suspicion, especially when coexisting with more common lesions like FNH.
- Surgical resection is an effective treatment for liver AM.
- Long-term follow-up is crucial to monitor for potential recurrence of AM.
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