首页> 外文期刊>Pediatric and developmental pathology: the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society >Benign Cystic Mesothelioma Associated with Ipsilateral Renal Agenesis: A Case Report and Review of Literature
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Benign Cystic Mesothelioma Associated with Ipsilateral Renal Agenesis: A Case Report and Review of Literature

机译:良性囊性间皮瘤与同侧肾脏发育不全:一例病例报告并文献复习

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摘要

Benign Cystic Mesothelioma (BCM) is an uncommon peritoneal lesion that usually occurs in reproductive age females with a history of abdominal surgery. Occasional expression of estrogen and progesterone receptor in these cells may explain female predilection. Reports of BCM in males are rare. We describe a case of BCM associated with ipsilateral renal agenesis in a young male without any surgical history. The cyst lining stained positive for cytokeratin, Wilms Tumor-1, epithelial membrane antigen, CD10, estrogen receptor, and progesterone receptor, and negative for PAX-8. Only three cases of BCM associated with congenital renal anomalies have been reported. To the best of our knowledge, this is the first case of BCM associated with ipsilateral renal agenesis in an adult male and the first male case of BCM displaying estrogen and progesterone receptor positivity. Such a case reveals the presence of congenital anomalies should be considered in patients with BCM.
机译:良性囊性间皮瘤(BCM)是一种罕见的腹膜病变,通常发生在有腹部手术史的育龄女性中。这些细胞中雌激素和孕激素受体的偶尔表达可能解释了女性的好发。男性中BCM的报道很少。我们描述了一名年轻男性无手术史的伴有同侧肾不育的BCM病例。囊肿衬里细胞角蛋白,Wilms Tumor-1,上皮膜抗原,CD10,雌激素受体和孕激素受体染色阳性,而PAX-8染色阴性。仅报道了三例伴有先天性肾脏异常的BCM病例。据我们所知,这是在成年男性中首例伴有同侧肾脏发育不全的BCM病例,也是首例显示雌激素和孕激素受体阳性的BCM男性病例。这种情况表明,BCM患者应考虑先天性异常的存在。

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