Esfahani Hossein, Olad Elham, Dehghan Arash, Bazmamoun Hassan, Ghorbanpoor Manoochehr
Departments of *Pediatric Hematology/Oncology †Pediatrics ‡Pathology §Pediatric Gastroenterology, Hamadan University of Medical Science, Hamadan, Islamic Republic of Iran.
J Pediatr Hematol Oncol. 2014 Apr;36(3):241-5. doi: 10.1097/MPH.0b013e3182a0627f.
Pancreatoblastoma is an extremely rare tumor in children, especially under 3 months of age. This tumor may arise from any portion of the pancreas, but in more rare cases the ectopic pancreas is the origin. We are reporting a 3-month-old boy who was presented with an abdominal mass. Computed tomography images revealed a huge lobulated mass anterior to the kidneys, with internal calcification and enhancement after intravenous contrast media injection. He underwent a complete surgical resection of the mass that was located in the transverse mesocolon without any connection with the pancreas. Pathologic studies specified that the disease was pancreatoblastoma. His parents refused any chemotherapeutic regimen but continued postsurgical follow-ups.
胰腺母细胞瘤是儿童中极其罕见的肿瘤,尤其是3个月以下的婴儿。这种肿瘤可能起源于胰腺的任何部位,但在更罕见的情况下,异位胰腺是其起源。我们报告一例3个月大的男孩,他因腹部肿块就诊。计算机断层扫描图像显示,双侧肾脏前方有一个巨大的分叶状肿块,内部有钙化,静脉注射造影剂后有强化。他接受了位于横结肠系膜内、与胰腺无任何连接的肿块的完整手术切除。病理研究确定该疾病为胰腺母细胞瘤。他的父母拒绝任何化疗方案,但继续进行术后随访。