Primary squamous cell carcinoma of the kidney: a case report and review of the literature
Autor: | Reubina Wadee, Seipati Bulane, Nicholas F. Brits |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Urology medicine.medical_treatment 030232 urology & nephrology Disease Nephrolithiasis lcsh:RC870-923 Sepsis 03 medical and health sciences 0302 clinical medicine medicine Hydronephrosis Primary renal squamous cell carcinoma Kidney business.industry Standard treatment medicine.disease lcsh:Diseases of the genitourinary system. Urology Nephrectomy medicine.anatomical_structure 030220 oncology & carcinogenesis Radiological weapon Radiology Renal pelvis business |
Zdroj: | African Journal of Urology, Vol 26, Iss 1, Pp 1-7 (2020) |
ISSN: | 1961-9987 1110-5704 |
Popis: | Background Primary squamous cell carcinoma (SCC) of the kidney is a rare entity which tends to be associated with nephrolithiasis, chronic irritation, and infection. Due to its rarity and the non-specific clinical signs and symptoms as well as radiological findings, it is often not suspected preoperatively. Patients with SCC of the renal pelvis typically present with advanced stage disease and have a poor outcome. Most of our current knowledge of SCC of the renal pelvis has been derived from case reports or limited case series, and there are no standard treatment guidelines. The clinical, radiological, and histopathological findings of this unusual neoplasm are described herein. Case presentation A 61-year-old female presented with left flank pain and sepsis. A computerized tomography (CT) scan showed renal calculi and hydronephrosis, and a mercapto-acetyl triglycine (MAG-3) scan showed a left-sided non-functioning kidney. She underwent a nephrectomy for an infected, non-functioning kidney. Histopathological examination revealed an invasive, moderately differentiated squamous cell carcinoma. Conclusion The significance of this case is highlighted by the unusual location of such a tumour, and while rare, it is an important consideration in the differential diagnoses of renal tumours. The present case report may assist patient management of this rare tumour by highlighting and documenting treatment and clinical outcome of our patient. |
Databáze: | OpenAIRE |
Externí odkaz: |