EN
A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy
Abstract
Cystic neoplasms of the kidney are quite rare. Because they contain various differential diagnoses and their radiological features are not specific, their diagnosis is very difficult except for histopathological data. Usually, they can be confused radiologically with benign cysts of the kidney or angiomyolipoma. Radical or partial nephrectomy is the most commonly preferred curative treatment method when it shows features like rapidly growing or malignancy. Histopathological examination is required for definitive diagnosis. In this article, we aimed to present a rare case of tubulocystic renal cell carcinoma after partial nephrectomy in our clinic, who was followed up in another center for years with the pre-diagnosis of angiomyolipoma, in the light of the literature.
Keywords
References
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Details
Primary Language
English
Subjects
Clinical Sciences (Other)
Journal Section
Case Report
Publication Date
December 30, 2023
Submission Date
December 19, 2022
Acceptance Date
October 26, 2023
Published in Issue
Year 2023 Volume: 14 Number: 50
APA
Ördek, E., Albayrak, İ. H., Karadeniz, M. N., & Katı, B. (2023). A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy. Interdisciplinary Medical Journal, 14(50), 209-213. https://doi.org/10.17944/interdiscip.1410378
AMA
1.Ördek E, Albayrak İH, Karadeniz MN, Katı B. A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy. Interdiscip Med J. 2023;14(50):209-213. doi:10.17944/interdiscip.1410378
Chicago
Ördek, Eser, İbrahim Halil Albayrak, Muhammed Nur Karadeniz, and Bülent Katı. 2023. “A Rare Malignity Observed in the Appearance of Angiomyolipoma; Tubulocystic Renal Cell Carcinoma After Partial Nephrectomy”. Interdisciplinary Medical Journal 14 (50): 209-13. https://doi.org/10.17944/interdiscip.1410378.
EndNote
Ördek E, Albayrak İH, Karadeniz MN, Katı B (December 1, 2023) A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy. Interdisciplinary Medical Journal 14 50 209–213.
IEEE
[1]E. Ördek, İ. H. Albayrak, M. N. Karadeniz, and B. Katı, “A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy”, Interdiscip Med J, vol. 14, no. 50, pp. 209–213, Dec. 2023, doi: 10.17944/interdiscip.1410378.
ISNAD
Ördek, Eser - Albayrak, İbrahim Halil - Karadeniz, Muhammed Nur - Katı, Bülent. “A Rare Malignity Observed in the Appearance of Angiomyolipoma; Tubulocystic Renal Cell Carcinoma After Partial Nephrectomy”. Interdisciplinary Medical Journal 14/50 (December 1, 2023): 209-213. https://doi.org/10.17944/interdiscip.1410378.
JAMA
1.Ördek E, Albayrak İH, Karadeniz MN, Katı B. A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy. Interdiscip Med J. 2023;14:209–213.
MLA
Ördek, Eser, et al. “A Rare Malignity Observed in the Appearance of Angiomyolipoma; Tubulocystic Renal Cell Carcinoma After Partial Nephrectomy”. Interdisciplinary Medical Journal, vol. 14, no. 50, Dec. 2023, pp. 209-13, doi:10.17944/interdiscip.1410378.
Vancouver
1.Eser Ördek, İbrahim Halil Albayrak, Muhammed Nur Karadeniz, Bülent Katı. A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy. Interdiscip Med J. 2023 Dec. 1;14(50):209-13. doi:10.17944/interdiscip.1410378