Evidence map›Paper›PMID 41733827›Full record

ArticleDigestive diseases and sciences2026

Perivascular Epithelioid Cell Tumor (PEComa): A Rare Type of Liver Cancer.

Konstantinos Papantoniou, Tatiana S Driva, Stratigoula Sakellariou, Nikolaos Machairas, Georgios Sotiropoulos, Christos Triantos

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Article in Digestive diseases and sciences, 2026. 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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5 · Who and what money

Authors and funding

6 authors.

Konstantinos PapantoniouDivision of Gastroenterology, Department of Internal Medicine, University of Patras, 26504, Patras, Greece.
Tatiana S Driva1st Department of Pathology, General Hospital of Athens "Laiko", Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Stratigoula Sakellariou1st Department of Pathology, General Hospital of Athens "Laiko", Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Nikolaos MachairasLiver Transplant Unit, "Laiko" University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Georgios SotiropoulosLiver Transplant Unit, "Laiko" University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Christos TriantosDivision of Gastroenterology, Department of Internal Medicine, University of Patras, 26504, Patras, Greece. chtriantos@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perivascular epithelioid cell tumor (PEComa) is a rare liver tumor, with few cases reported in the literature. Clinical decisions regarding patients diagnosed with PEComa are based on studies with small sample sizes. Differential diagnosis between PEComa and other types of liver lesions is challenging due to non-specific radiological findings associated with this type of liver mass. We report the case of a 51-year-old female patient followed at the outpatient hepatology clinic of Patras, General University Hospital, Greece, for chronic hepatitis B. The patient was asymptomatic, with positive hepatitis B surface antigen and normal liver function tests. An area with abnormal echogenicity and a diameter of 28 mm was observed in an abdominal ultrasound during routine follow up. Magnetic resonance imaging (MRI) was performed, and a mass with a diameter of 30.6 mm was found on surgical liver segment IV. A follow-up MRI 8 months later showed the lesion had increased to 36 mm and exhibited suspicious radiological characteristics. Surgical excision of liver segment IV was performed. Post-surgical pathological analysis of the tumor confirmed a diagnosis of PEComa, with no evidence of vascular or lymphatic invasion. The low mitotic index, the size of the tumor and the lack of nuclear atypia or diffuse pleomorphic morphology supported a favorable tumor behavior. In conclusion, PEComas are rare liver tumors without pathognomonic radiological features. Surgical excision of these masses is the safest treatment option, and post-surgical pathological analysis is essential for the diagnosis and prognosis of these patients.

Indexed as

Liver NeoplasmsPerivascular Epithelioid Cell NeoplasmsDiagnosis, DifferentialFemaleHumansMagnetic Resonance ImagingMiddle AgedTreatment OutcomeUltrasonographyImagingImmunohistochemistryLiver tumorPEComaSurgery

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.