Hsiao Kuang-Hung, Lin Lung-Huang, Chen Der-Fang, Huang Shih-Hung
Department of Pediatrics, Cathay General Hospital, Taipei, Taiwan.
J Formos Med Assoc. 2007 Mar;106(3 Suppl):S1-4. doi: 10.1016/s0929-6646(09)60357-0.
Hepatic mesenchymal hamartoma is a rare benign tumor in children, and infantile hepatic hemangioendothelioma is also a rare liver neoplasm. We report a female newborn with an abdominal mass noted by the regular maternal ultrasound at 32 weeks of gestation. After birth, a liver mass was detected by computed tomography and magnetic resonance cholangiopancreatography. Frequent postprandial vomiting and progressive abdominal distension occurred 4 months later. Three tumor masses were detected this time, and the serum alpha-fetoprotein (AFP) was 6700 ng/mL. Segmental resection was performed initially and complete resection of these tumors and left lobectomy were performed 21 days later. Pathologic examination of these liver masses revealed mesenchymal hamartoma combined with infantile hepatic hemangioendothelioma. After half a year of regular follow-up, the AFP level decreased gradually to 79.5 ng/mL, without evidence of tumor recurrence.
肝间叶性错构瘤是儿童罕见的良性肿瘤,婴儿肝血管内皮瘤也是一种罕见的肝脏肿瘤。我们报告一例女性新生儿,其母亲在妊娠32周常规超声检查时发现腹部有肿块。出生后,通过计算机断层扫描和磁共振胰胆管造影检测到肝脏肿块。4个月后出现频繁餐后呕吐和进行性腹胀。此次检测到三个肿瘤肿块,血清甲胎蛋白(AFP)为6700 ng/mL。最初进行了节段性切除,21天后对这些肿瘤进行了完整切除并实施了左叶切除术。对这些肝脏肿块的病理检查显示为间叶性错构瘤合并婴儿肝血管内皮瘤。经过半年的定期随访,AFP水平逐渐降至79.5 ng/mL,无肿瘤复发迹象。