Tortoledo Maria, Galindo A, Ibarrola C
Department of Pathology, 12 de Octubre University Hospital, Universidad Complutense, Avenida de Cordoba s/n, Madrid, Spain.
Fetal Pediatr Pathol. 2010;29(4):261-70. doi: 10.3109/15513811003782474.
This report describes a 31-week stillborn female infant with placental mesenchymal dysplasia (PMD) in association with hepatic mesenchymal hamartoma (HMH) and pulmonary hamartoma. Placental mesenchymal dysplasia was initially misdiagnosed as a partial mole. However, histologically, no trophoblastic proliferation or inclusions were observed. Differential diagnosis of the hepatic mass with similar tumors is discussed. To our knowledge, this is the first case of lung hamartoma reported in a fetus and the first case related to PMD and HMH. A common anomalous development of the mesoderm, a reparative post-injury process and a genetic mechanism, have been proposed to explain their pathogenesis.
本报告描述了一名31周死产女婴,患有胎盘间质性发育异常(PMD),并伴有肝脏间叶性错构瘤(HMH)和肺错构瘤。胎盘间质性发育异常最初被误诊为部分性葡萄胎。然而,组织学检查未观察到滋养层细胞增生或包涵体。文中讨论了肝脏肿物与相似肿瘤的鉴别诊断。据我们所知,这是首例报道的胎儿肺错构瘤病例,也是首例与胎盘间质性发育异常和肝脏间叶性错构瘤相关的病例。已经提出中胚层的共同异常发育、损伤后的修复过程和遗传机制来解释它们的发病机制。