Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Apr 11:12:865263.
doi: 10.3389/fonc.2022.865263. eCollection 2022.

Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Study of Clinical, Imaging Features and Treatment Outcomes

Affiliations

Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Study of Clinical, Imaging Features and Treatment Outcomes

Xiaofeng Xu et al. Front Oncol. .

Abstract

Purpose: To describe the clinical, imaging, pathological features and oncologic outcomes of mucinous tubular and spindle cell carcinoma (MTSCC) of the kidney.

Patients and methods: Twenty-two cases of MTSCC were pathologically identified between January 2004 and April 2021 at our institution. The clinical and imaging findings, pathological features, treatment methods and outcomes of the patients were reviewed.

Results: These cases included 17 women and 5 men, with a median age at diagnosis of 52.5 years. On contrast-enhanced CT, MTSCC was less enhanced than the adjacent renal parenchyma. Tumor attenuation values were 33.3 ± 6.8HU, 44.0 ± 9.1HU, 54.4 ± 13.9HU and 67.1 ± 11.8HU in the non-contrast, corticomedullary, nephrographic and excretory phases of CT, respectively. Contrast-enhanced ultrasonography and MRI also showed hypovascular features of the masses. On MRI, the tumors were isointense on T1-weighted images and slightly hypo- or hyperintense on T2-weighted images. Diffusion-weighted imaging revealed a low apparent diffusion coefficient of the tumor. The patients were managed with laparoscopic partial nephrectomy (n=5), radical nephrectomy (n=16), or robotic-assisted laparoscopic partial nephrectomy (n=1). The median follow-up time was 59.5 months. All the patients were free of local recurrence or distant metastasis.

Conclusions: MTSCC is generally indolent and has favorable outcomes. The imaging features of MTSCC are generally hypovascular, which is significantly different from clear cell renal cell carcinoma. However, it is still difficult to distinguish MTSCC from other hypovascular renal tumors preoperatively because their imaging features overlap. Further studies are essential to fully characterize the features of this rare RCC variant.

Keywords: imaging features; kidney; mucinous tubular and spindle cell carcinoma; prognosis; renal cell carcinoma.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

    1. Lopez-Beltran A, Scarpelli M, Montironi R, Kirkali Z. WHO Classification of the Renal Tumors of the Adults. Eur Urol (2006) 49:798–805. doi: 10.1016/j.eururo.2005.11.035 - DOI - PubMed
    1. Amin MB, Edge S, Greene F, Byrd DR, Brookland RK, Washington MK, et al. AJCC Cancer Staging Manual. 8th edition. New York: Springer; (2017).
    1. Shen SS, Ro JY, Tamboli P, Truong LD, Zhai QH, Jung SJ, et al. Mucinous Tubular and Spindle Cell Carcinoma of Kidney is Probably a Variant of Papillary Renal Cell Carcinoma With Spindle Cell Features. Ann Diagn Pathol (2007) 11:13–21. doi: 10.1016/j.anndiagpath.2006.09.005 - DOI - PubMed
    1. Wu XR, Chen YH, Sha JJ, Zhao L, Huang JW, Bo JJ, et al. Renal Mucinous Tubular and Spindle Cell Carcinoma: A Report of 8 Cases and Review of the Literature. Diagn Pathol (2013) 8:206. doi: 10.1186/1746-1596-8-206 - DOI - PMC - PubMed
    1. Ferlicot S, Allory Y, Compérat E, Mege-Lechevalier F, Dimet S, Sibony M, et al. Mucinous Tubular and Spindle Cell Carcinoma: A Report of 15 Cases and a Review of the Literature. Virchows Arch (2005) 447:978–83. doi: 10.1007/s00428-005-0036-x - DOI - PubMed