Steiner Michael A, Giles Henry W
Department of Diagnostic Radiology, University of Mississippi, Jackson, MS 39216, USA.
Pediatr Radiol. 2008 Nov;38(11):1232-4. doi: 10.1007/s00247-008-0942-6. Epub 2008 Jul 22.
Mesenchymal hamartoma of the liver is a rare benign hepatic tumor that typically presents in the first 2 years of life. Approximately 85% of affected children present before the age of 3 years and less than 5% present after the age of 5 years. Although spontaneous regression has been reported in this benign tumor, most mesenchymal hamartomas gradually increase in size and can reach enormous proportions. We present an atypical case of mesenchymal hamartoma in a 12-year-old boy. The boy's age and presence of calcifications on CT demonstrate a unique presentation of this rare entity.
肝脏间叶性错构瘤是一种罕见的肝脏良性肿瘤,通常在出生后的头两年出现。大约85%的患病儿童在3岁前发病,5岁后发病的不到5%。尽管已有报道称这种良性肿瘤可自发消退,但大多数间叶性错构瘤会逐渐增大,甚至可能长得非常大。我们报告一例12岁男孩的非典型间叶性错构瘤病例。该男孩的年龄以及CT上出现的钙化表现出了这种罕见病症的独特表现形式。