Multicystic nephroma is a rare renal pathology, which is characterized usually by a unilateral renal mass with multiple thin-walled cysts divided by septa. We report the case of a boy aged 2 years, who was diagnosed in utero with an abdominal cystic lesion during routine antenatal ultrasonography examination. The patient underwent a nephrectomy, and diagnosis of cystic nephroma was confirmed by histology.
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Int J Surg Case Rep
December 2024
Department of Urology A, Ibn Sina Hospital, University of Rabat, Morocco. Electronic address:
Introduction: Multilocular cystic nephroma is an uncommon condition with only few cases described in the literature, although its benign nature is well-recognized.
Case Presentation: We present a case of a 28-year-old male patient who presented with a right flank pain, imaging suspected a multicystic renal cell carcinoma. A radical nephrectomy was performed view the size of the cyst and the high tumor complexity, which histology confirmed the diagnosis of multilocular cystic nephroma.
Indian J Pathol Microbiol
April 2024
Department of Pathology, Maulana Azad Medical College and Lok Nayak Hospital, New Delhi, India.
Objectives: Multicystic dysplastic kidney (MCDK) is defined as the presence of multiple noncommunicating cysts of various sizes, detected sonographically, without evidence of functioning renal parenchyma on dimercaptosuccinic acid renal scan. It has an incidence of 1:4000 live births. They are more commonly diagnosed in boys, usually on the left side, but may also be bilateral.
View Article and Find Full Text PDFCancer Diagn Progn
January 2024
Urology Department, Korgialenio-Benakio Hellenic Red Cross Hospital, Athens, Greece.
Background/aim: Cystic nephroma (CN) is a very rare, benign, renal cystic lesion, which is characterized by a usually unilateral, multicystic kidney mass. In adults it is seen more frequently in females (1:8 male-to-female ratio). The peak incidence of CN is between 50 and 60 years of age.
View Article and Find Full Text PDFJ Kidney Cancer VHL
December 2023
Department of Urology, Faculty of Medicine, Bezmialem Vakif University, Fatih, Istanbul, Türkiye.
The incidence of renal cell cancer (RCC) is low in individuals aged less than 40 years; however several studies have shown this increasing trend over the years. Hereditary syndromes are associated with RCC and are more frequently observed in early-onset cases. In this study, we investigated the characteristics of the patients, aged less than 40 years, who were operated for a renal mass with the suspicion of RCC.
View Article and Find Full Text PDFJ Cancer Res Ther
April 2023
Department of Pediatric Surgery, Lady Hardinge Medical College, New Delhi, India.
Wilms' tumor (or nephroblastoma) is the most common renal malignancy in the pediatric population which consists of blastemal, epithelial, and stromal elements in variable proportions. The occurrence of renal cysts in children and infants is a rare phenomenon and is possibly an outcome of developmental aberrations in mesonephric blastema. The coincidental association of nephroblastoma with renal cysts is a very rare finding.
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