Baretton G, Stehr M, Nerlich A, Löhrs U
Pathologisches Institut der Universität, München, Germany.
Pediatr Pathol. 1994 Jan-Feb;14(1):3-9. doi: 10.3109/15513819409022020.
We present one case of a chest wall hamartoma diagnosed in a 4-week-old boy. This entity is an extremely rare but characteristic congenital malformation of the ribs in infancy. To avoid maltreatment, it has to be distinguished from benign and malignant neoplasms on the basis of distinct histological features presented here. The immunohistochemical localization of various collagen types supports the notion of the hamartomatous nature of this lesion.
我们报告一例4周龄男婴被诊断为胸壁错构瘤的病例。该实体是婴儿期肋骨极为罕见但具有特征性的先天性畸形。为避免误诊,必须根据此处呈现的独特组织学特征将其与良性和恶性肿瘤区分开来。多种胶原类型的免疫组化定位支持了该病变错构瘤性质的观点。