Hill D Ashley
Department of Pathology, Washington University Medical Center, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Pediatr Dev Pathol. 2005 Jan-Feb;8(1):77-84. doi: 10.1007/s10024-004-6069-3. Epub 2005 Feb 23.
Pleuropulmonary blastoma (PPB) was defined in 1988 by Manivel et al. in a series describing 11 intrathoracic pulmonary neoplasms in young children. The PPB is a unique peripheral pulmonary or pleural-based tumor of childhood that is characterized in its earliest form as a bland-appearing multiloculated cyst with small foci of tumor cells and in later forms as mixed and predominantly primitive, overtly malignant neoplasms. Prior to the introduction of the PPB as a distinct entity, this tumor had been reported in the literature as pulmonary blastoma, sarcoma arising in mesenchymal cystic hamartoma, embryonal sarcoma, malignant mesenchymoma, primary pulmonary rhabdomyosarcoma and rhabdomyosarcoma arising in congenital adenomatoid malformation or bronchogenic cyst. Over the past 15 years, PPB has come to be recognized in centers around the world. With the establishment of the Pleuropulmonary Blastoma Registry by Jack Priest, MD, and colleagues, there has been improved understanding of this rare pediatric neoplasm.
1988年,马尼韦尔等人在一篇描述11例幼儿胸腔内肺肿瘤的系列报道中对肺胚细胞瘤(PPB)进行了定义。PPB是一种独特的儿童期外周肺或起源于胸膜的肿瘤,其早期形态表现为外观平淡的多房性囊肿,伴有小灶肿瘤细胞,后期形态则为混合性且主要是原始的、明显恶性的肿瘤。在将PPB作为一种独立的疾病实体引入之前,该肿瘤在文献中曾被报道为肺母细胞瘤、间质性囊性错构瘤中发生的肉瘤、胚胎性肉瘤、恶性间叶瘤、原发性肺横纹肌肉瘤以及先天性腺瘤样畸形或支气管源性囊肿中发生的横纹肌肉瘤。在过去15年里,PPB已在世界各地的医疗中心得到认可。随着医学博士杰克·普里斯特及其同事建立肺胚细胞瘤登记处,人们对这种罕见的儿科肿瘤有了更深入的了解。