S5715 A Rare Hepatic Mass Revealed as Intrahepatic Endometriosis

Introduction: Endometriosis is a chronic inflammatory disorder characterized by the presence of functional endometrial tissue outside the uterine cavity. Hepatic endometriosis is exceedingly rare and often mimics hepatic neoplasms on imaging. We present a unique case of intrahepatic endometriosis, incidentally discovered after a motor vehicle collision. Case Description/Methods: A 54-year-old woman with a history of laparoscopic resection of an ovarian endometrioma in 2017, class I obesity, and prior bariatric surgery was evaluated for a hepatic lesion incidentally discovered after a motor vehicle collision in 2022. Initial computed tomography (CT) imaging revealed a heterogeneous solid and cystic mass in the right hepatic lobe measuring 8.2 × 4.5 cm, along with a peritoneal nodule in the left anterior abdominal wall measuring up to 1.2 cm—both initially presumed to be traumatic hematomas. A follow-up MRI noted a 4 cm right hepatic lesion consistent with an intraparenchymal hematoma. After the patient obtained insurance coverage, a repeat MRI in March 2025 showed a complex right hepatic lesion measuring 8.9 × 8.0 cm with internal blood products and peripheral enhancement, as well as an enlarging anterior peritoneal nodule measuring 2.2 × 1.2 cm. Due to concern for malignancy, the patient underwent an ultrasound-guided liver biopsy. Histopathological analysis demonstrated hepatic parenchyma with smooth muscle hyperplasia, hemorrhage, and focal epithelial proliferation. Immunohistochemical staining was positive for PAX8, cytokeratin 7 (CK7), and estrogen receptor (ER), consistent with intrahepatic endometriosis. Discussion: Intrahepatic endometriosis is an exceptionally rare condition, with fewer than 30 cases reported worldwide. Its imaging appearance can mimic primary or metastatic hepatic tumors, making diagnosis challenging. This case highlights the importance of maintaining a broad differential in patients with atypical hepatic lesions, particularly those with a history of endometriosis, and underscores the critical role of histopathology and immunohistochemistry in establishing a definitive diagnosis.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001150320.55309.f3
Primary Topic
Endometriosis Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

S5715 A Rare Hepatic Mass Revealed as Intrahepatic Endometriosis

The American Journal of Gastroenterology
Endometriosis Research and Treatment
article

S5715 A Rare Hepatic Mass Revealed as Intrahepatic Endometriosis

article en

Abstract

Introduction: Endometriosis is a chronic inflammatory disorder characterized by the presence of functional endometrial tissue outside the uterine cavity. Hepatic endometriosis is exceedingly rare and often mimics hepatic neoplasms on imaging. We present a unique case of intrahepatic endometriosis, incidentally discovered after a motor vehicle collision. Case Description/Methods: A 54-year-old woman with a history of laparoscopic resection of an ovarian endometrioma in 2017, class I obesity, and prior bariatric surgery was evaluated for a hepatic lesion incidentally discovered after a motor vehicle collision in 2022. Initial computed tomography (CT) imaging revealed a heterogeneous solid and cystic mass in the right hepatic lobe measuring 8.2 × 4.5 cm, along with a peritoneal nodule in the left anterior abdominal wall measuring up to 1.2 cm—both initially presumed to be traumatic hematomas. A follow-up MRI noted a 4 cm right hepatic lesion consistent with an intraparenchymal hematoma. After the patient obtained insurance coverage, a repeat MRI in March 2025 showed a complex right hepatic lesion measuring 8.9 × 8.0 cm with internal blood products and peripheral enhancement, as well as an enlarging anterior peritoneal nodule measuring 2.2 × 1.2 cm. Due to concern for malignancy, the patient underwent an ultrasound-guided liver biopsy. Histopathological analysis demonstrated hepatic parenchyma with smooth muscle hyperplasia, hemorrhage, and focal epithelial proliferation. Immunohistochemical staining was positive for PAX8, cytokeratin 7 (CK7), and estrogen receptor (ER), consistent with intrahepatic endometriosis. Discussion: Intrahepatic endometriosis is an exceptionally rare condition, with fewer than 30 cases reported worldwide. Its imaging appearance can mimic primary or metastatic hepatic tumors, making diagnosis challenging. This case highlights the importance of maintaining a broad differential in patients with atypical hepatic lesions, particularly those with a history of endometriosis, and underscores the critical role of histopathology and immunohistochemistry in establishing a definitive diagnosis.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 30%
Endometriosis Research and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

S5715 A Rare Hepatic Mass Revealed as Intrahepatic Endometriosis · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS