B. Ammari, M. Muheilan, Hassan A Khatatbeh, Malik Ayyad, Tareq Qsus, F. Obeidat
{"title":"Mixed Epithelial Stromal Tumor of the Kidney (MESTK): A Case Report","authors":"B. Ammari, M. Muheilan, Hassan A Khatatbeh, Malik Ayyad, Tareq Qsus, F. Obeidat","doi":"10.12816/0039755","DOIUrl":null,"url":null,"abstract":"Mixed epithelial stromal tumor of the kidney (MESTK) is a newly introduced and rare kidney tumor subtype; approximately 100 cases have been reported. \nWe report a case of MESTK with detailed clinicopathological findings, presented to emergency department with gross hematuria and clot retention managed by radical nephrectomy. \nAlthough MESTK are benign tumors, they cannot be distinguished from other malignant neoplasms until after nephrectomy due to lack of typical radiological features. They can cause serious sequelae; including gross hematuria and serious drop in hemoglobin as the case we present here shows. This is why it is important to early diagnose and treat this condition. \nThis case highlights the importance of early introduction of imaging in patients presenting with gross hematuria. Failure to diagnose this lesion as the underlying cause of hematuria may lead to recurrence and malignant transformation.","PeriodicalId":39681,"journal":{"name":"Jordan Medical Journal","volume":"51 1","pages":"39-46"},"PeriodicalIF":0.0000,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jordan Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12816/0039755","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1
Abstract
Mixed epithelial stromal tumor of the kidney (MESTK) is a newly introduced and rare kidney tumor subtype; approximately 100 cases have been reported.
We report a case of MESTK with detailed clinicopathological findings, presented to emergency department with gross hematuria and clot retention managed by radical nephrectomy.
Although MESTK are benign tumors, they cannot be distinguished from other malignant neoplasms until after nephrectomy due to lack of typical radiological features. They can cause serious sequelae; including gross hematuria and serious drop in hemoglobin as the case we present here shows. This is why it is important to early diagnose and treat this condition.
This case highlights the importance of early introduction of imaging in patients presenting with gross hematuria. Failure to diagnose this lesion as the underlying cause of hematuria may lead to recurrence and malignant transformation.