Acquired Cystic Disease Associated Renal Cell Carcinoma Clinically Manifested as a Retroperitoneal Hematoma – Brief Presentation and Review of the Literature

Abstract Acquired cystic disease associated renal cell carcinoma is an entity first described in 2006 and recognized in the WHO (World Health Organization) guidelines of 2016, also present in the current edition, which develops in the context of chronic kidney disease. We present the case of a 61 years old patient with significant comorbidities, on hemodialysis for 15 years, who was admitted to the hospital’s Emergency Department for a retroperitoneal hematoma. The histopathological examination of the left nephrectomy specimen revealed polycystic kidney disease, chronic pyelonephritis, and a malignant neoplastic proliferation. Immunohistochemical tests established the diagnosis of acquired cystic disease associated renal cell carcinoma. The particularity of this case consisted in its clinical presentation, the incidental finding of the malignant renal tumor in the context of polycystic kidney disease, and the variable immunoexpression of the CK7 marker within the tumor tissue.

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Publication Details

Journal
Ars medica tomitana
Published
2025-05-01
DOI
https://doi.org/10.2478/arsm-2025-0009
Primary Topic
Tuberous Sclerosis Complex Research
Type
article
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article

Acquired Cystic Disease Associated Renal Cell Carcinoma Clinically Manifested as a Retroperitoneal Hematoma – Brief Presentation and Review of the Literature

Ars medica tomitana
Tuberous Sclerosis Complex Research
article

Acquired Cystic Disease Associated Renal Cell Carcinoma Clinically Manifested as a Retroperitoneal Hematoma – Brief Presentation and Review of the Literature

article en

Abstract

Abstract Acquired cystic disease associated renal cell carcinoma is an entity first described in 2006 and recognized in the WHO (World Health Organization) guidelines of 2016, also present in the current edition, which develops in the context of chronic kidney disease. We present the case of a 61 years old patient with significant comorbidities, on hemodialysis for 15 years, who was admitted to the hospital’s Emergency Department for a retroperitoneal hematoma. The histopathological examination of the left nephrectomy specimen revealed polycystic kidney disease, chronic pyelonephritis, and a malignant neoplastic proliferation. Immunohistochemical tests established the diagnosis of acquired cystic disease associated renal cell carcinoma. The particularity of this case consisted in its clinical presentation, the incidental finding of the malignant renal tumor in the context of polycystic kidney disease, and the variable immunoexpression of the CK7 marker within the tumor tissue.

Ars medica tomitanaVol. 31(2)
Ovidius University (RO), County Hospital (GB)
Good health and well-being
Openalex Percentile: Top 41%
Tuberous Sclerosis Complex Research
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