Naggar Amine, Andour Hajar, Bensaghir Hamza, Kabila Badr, Ben Driss Chaimae, El Aouni Soukaina, Ochan Monim, Kisra Mounir, Lamalmi Najat, El Haddad Siham, Allali Nazik, Chat Latifa
Ibn Sina University Hospitals Center, Mohammed V University, Rabat, Morocco.
Glob Pediatr Health. 2023 Aug 18;10:2333794X231193560. doi: 10.1177/2333794X231193560. eCollection 2023.
Mesenchymal hamartoma (MH) is a benign liver tumor accounting for 3% to 8% of all liver tumors in children, commonly manifesting before 3 years of life. Distinguishing MH from hepatoblastoma and other liver tumors relies on imaging and alpha-fetoprotein (which is usually within normal range in MH), before histologic examination. We report a case of a hepatic MH associated with elevated alpha-fetoprotein, leading to a misdiagnosis of hepatoblastoma and the administration of chemotherapy. We draw the attention to the diagnostic difficulty and pitfalls related to alpha-fetoprotein elevation in the setting of a liver tumor, and we highlight the importance of imaging and histology in establishing the diagnosis.
间叶性错构瘤(MH)是一种良性肝脏肿瘤,占儿童所有肝脏肿瘤的3%至8%,通常在3岁前出现。在组织学检查之前,将MH与肝母细胞瘤和其他肝脏肿瘤区分开来依赖于影像学检查和甲胎蛋白(在MH中通常在正常范围内)。我们报告一例肝MH伴有甲胎蛋白升高的病例,导致误诊为肝母细胞瘤并进行了化疗。我们提请注意在肝脏肿瘤情况下与甲胎蛋白升高相关的诊断困难和陷阱,并强调影像学和组织学在确立诊断中的重要性。