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一名男婴的双侧胸壁间叶性错构瘤

Bilateral mesenchymal hamartoma of the chest wall in an infant boy.

作者信息

Li Rong, Kelly David, Siegal Gene P

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35233, USA.

出版信息

Fetal Pediatr Pathol. 2012 Dec;31(6):415-22. doi: 10.3109/15513815.2012.659412. Epub 2012 Apr 16.

Abstract

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.

摘要

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。

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