Liver mucinous cystic neoplasm: a challenging diagnosis case report.

IF 0.6 Q4 SURGERY
International Journal of Surgery Case Reports Pub Date : 2026-09-16 eCollection Date: 2026-10-01 DOI:10.1097/RC9.0000000000000858
Sana Landolsi, Aymen Saidi, Aziz Atallah, Maroua Yengui, Mohamed Nafaa Arfa, Faouzi Chebbi
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Abstract

Introduction and importance: Liver mucinous cystic neoplasm is a rare tumor with a challenging pre-operative diagnosis, as for our patient.

Presentation of case: A 43-year-old woman complained of dull, aching pain in the left hypochondrial region. Abdominal ultrasound demonstrated a solitary hypoechoic cyst within the left hepatic lobe. The initial suspected diagnosis was a hepatic hydatid cyst due to the country's endemicity. Magnetic resonance imaging (MRI) was consistent with a hepatic mucinous cystic neoplasm. A left hepatectomy was performed. Histopathological examination of the surgical specimen confirmed the diagnosis. No recurrence was observed during postoperative follow-up.

Clinical discussion: Our case illustrated a rare entity with a challenging diagnosis. Liver mucinous cystic neoplasm could easily be misdiagnosed, especially in endemic areas. Appropriate exploration, such as MRI, had to be performed.

Conclusion: Liver mucinous cystic neoplasms are rare tumors, with diagnosis delayed due to insufficient recognition; hence, radiological workup plays a crucial role. Complete surgical excision remains the treatment of choice.

肝脏粘液囊性肿瘤:一个具有挑战性的诊断病例报告。
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
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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