TY - JOUR
T1 - Renal cell carcinoma in autosomal dominant polycystic kidney disease
T2 - A case report
AU - Rooseno, Gullyawan
AU - Yatindra, Ida Bagus Gde Tirta Yoga
AU - Djatisoesanto, Wahjoe
AU - Djojodimedjo, Tarmono
N1 - Funding Information:
Ethical approval for this study (2224/129/4/VI/2023) was provided by the Ethical Committee Dr. Soetomo Hospital, Surabaya, Indonesia on 13 June 2023. Acknowledgments: This research received no specific grant from funding agencies in the public, commercial, or not-for-profit sectors. Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Publisher Copyright:
© 2023
PY - 2023/12
Y1 - 2023/12
N2 - Autosomal dominant polycystic kidney disease (ADPKD) is one of the congenital cystic renal diseases with the highest incidence. ADPKD was suspected of being a risk factor for the emergence of RCC. A 65-year-old male complained of numbness in both knees for a week. The patient came to a neurosurgeon and was advised to perform a lumbosacral MRI. The patient had no complaints. The patient had a history of hypertension but was never treated. Computed tomography intravenous pyelogram (CT-IVP) revealed a heterogeneous lobulated mass in the upper to the middle of the right kidney to the right renal hilus. It also revealed multiple cysts, in both kidneys. The patient underwent an open radical nephrectomy in the right kidney with minimal bleeding. Three years revealed no pain at the surgery site or hematuria. Abdominal MRI revealed no recidive mass. This case report comprehensively described an autosomal dominant polycystic kidney disease that coexists with RCC. malignant lesions were found in ADPKD cases without any clinical symptoms of malignancy. M malignant lesions could be discovered by chance in nephrectomy specimens. Autosomal dominant polycystic kidney disease with renal cell carcinoma is a unique presentation. Despite the rarity of the situation, the patient was successfully treated.
AB - Autosomal dominant polycystic kidney disease (ADPKD) is one of the congenital cystic renal diseases with the highest incidence. ADPKD was suspected of being a risk factor for the emergence of RCC. A 65-year-old male complained of numbness in both knees for a week. The patient came to a neurosurgeon and was advised to perform a lumbosacral MRI. The patient had no complaints. The patient had a history of hypertension but was never treated. Computed tomography intravenous pyelogram (CT-IVP) revealed a heterogeneous lobulated mass in the upper to the middle of the right kidney to the right renal hilus. It also revealed multiple cysts, in both kidneys. The patient underwent an open radical nephrectomy in the right kidney with minimal bleeding. Three years revealed no pain at the surgery site or hematuria. Abdominal MRI revealed no recidive mass. This case report comprehensively described an autosomal dominant polycystic kidney disease that coexists with RCC. malignant lesions were found in ADPKD cases without any clinical symptoms of malignancy. M malignant lesions could be discovered by chance in nephrectomy specimens. Autosomal dominant polycystic kidney disease with renal cell carcinoma is a unique presentation. Despite the rarity of the situation, the patient was successfully treated.
KW - Case report
KW - Incidental findings
KW - Multi cystic kidney
KW - Renal cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85173180398&partnerID=8YFLogxK
U2 - 10.1016/j.radcr.2023.09.011
DO - 10.1016/j.radcr.2023.09.011
M3 - Article
AN - SCOPUS:85173180398
SN - 1930-0433
VL - 18
SP - 4370
EP - 4373
JO - Radiology Case Reports
JF - Radiology Case Reports
IS - 12
ER -