Multiple biliary micro-hamartomas diagnosed in an unsuspecting elderly patient

Marina Balbino, Manuela Montatore, Giacomo Fascia, Ruggiero Tupputi, Federica Masino, Gianmichele Muscatella, Domenico Mannatrizio, Giuseppe Guglielmi
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Abstract

BACKGROUND AND AIM: Multiple biliary hamartomas are a benign incidental finding in the hepatic context. Recognizing them is not easy if one has never seen them and does not have access to the right imagery. The aim of the study is to expand the radiologist's digital image library, enabling a quick and precise differential diagnosis. Indeed, multiple biliary hamartomas can be challenging to differentiate from other liver lesions based on imaging alone. This case highlights the importance of thorough radiological assessment and the need for a multidisciplinary approach, involving radiologists, hepatologists, and pathologists, to ensure a precise diagnosis. METHODS: The patient in the study presented at the hospital for a CT scan and after an abdominal MRI recommended by his general practitioner to assess the biliary tree (Magnetic Resonance Cholangiopancreatography, MRCP) due to persistent abdominal pain. They had never undergone an abdominal MRI before in their life. The discovery of hepatic lesions was incidental and unexpected RESULTS: The MRI investigation revealed multiple benign lesions in both hepatic lobes compatible with the von Meyenburg complex. These lesions are multiple hamartomas and behave differently in all MRI sequences. CONCLUSIONS: The images acquired with the different MRI sequences were carefully examined. Despite being multiple and scattered throughout the liver, the lesions appeared immediately benign and consistent with the incidental diagnosis of multiple biliary hamartomas. Medical practitioners should be aware of the existence of multiple biliary hamartomas and consider them in the differential diagnosis when patients present with hepatic abnormalities. This knowledge can prevent unnecessary interventions and guide appropriate patient management.
一名毫无防备的老年患者被诊断出患有多发性胆道微小瘤
背景和目的:多发性胆道火腿肠瘤是肝脏的良性偶然发现。如果从未见过它们,又没有合适的图像,识别它们并不容易。这项研究的目的是扩大放射科医生的数字图像库,以便快速准确地进行鉴别诊断。事实上,仅凭影像学检查很难将多发性胆道火腿肠瘤与其他肝脏病变区分开来。本病例强调了全面放射学评估的重要性,以及放射科医生、肝病专家和病理学家共同参与的多学科方法的必要性,以确保准确诊断。方法:研究中的患者因持续腹痛到医院进行 CT 扫描,之后在全科医生的建议下进行了腹部核磁共振成像,以评估胆道树(磁共振胆胰造影,MRCP)。在此之前,他们从未做过腹部核磁共振检查。结果:核磁共振成像检查发现,两个肝叶都有多发良性病变,符合冯-梅恩伯格综合征。这些病变为多发性仓瘤,在所有磁共振成像序列中表现不同。结论:对不同磁共振成像序列获得的图像进行了仔细检查。尽管病变是多发性的,且散布在肝脏各处,但病变看起来是良性的,符合多发性胆道火腿肠瘤的偶然诊断。医务工作者应了解多发性胆道火腿肠瘤的存在,并在患者出现肝功能异常时将其纳入鉴别诊断。这些知识可以避免不必要的干预,并指导对患者进行适当的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
44
审稿时长
5 weeks
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