Li Rong, Kelly David, Siegal Gene P
Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35233, USA.
Fetal Pediatr Pathol. 2012 Dec;31(6):415-22. doi: 10.3109/15513815.2012.659412. Epub 2012 Apr 16.
Mesenchymal chest wall hamartoma is an extremely rare tumor striking neonates and infants. Histologically, the tumor is composed of islands of hyaline cartilage intermixed with mesenchymal-like stroma and hemorrhagic cysts. We present a case of a congenital bilateral mesenchymal chest wall hamartoma (MCWH) in an infant boy. This extremely rare benign entity may be misdiagnosed as malignant tumor and shares features with another tumor of childhood-fibrocartilagenous mesenchymoma of bone.
间充质胸壁错构瘤是一种极其罕见的肿瘤,多见于新生儿和婴儿。从组织学上看,该肿瘤由透明软骨岛组成,其间夹杂着间充质样基质和出血性囊肿。我们报告一例男婴先天性双侧间充质胸壁错构瘤(MCWH)。这种极其罕见的良性病变可能被误诊为恶性肿瘤,并且与另一种儿童期肿瘤——骨纤维软骨间充质瘤有共同特征。