A rare renal neoplasm: Case report of mucinous tubular and spindle cell carcinoma
Salma El Aouadi, Soukaina Allioui, Soukaina Bahha, Ouiam Taibi, Fatima Zahra Laamrani, Youssef Omor, Rachida Latib, Sanae Amalik
TL;DR
This paper presents a case of a rare kidney tumor with a good outcome, highlighting its diagnosis and favorable prognosis.
Contribution
The paper adds a new clinical case of MTSRCC, emphasizing its imaging and histological diagnostic features.
Findings
Imaging showed a well-defined solid renal mass with mild enhancement.
Histology confirmed the diagnosis of MTSRCC with a favorable postoperative outcome.
Abstract
Mucinous tubular and spindle cell renal cell carcinoma (MTSRCC) is a rare subtype of renal cell carcinoma with distinctive histological features and generally favorable prognosis. We report the case of a 52-year-old woman who presented with right lumbar pain. CT and MRI revealed a well-defined solid renal mass with mild, homogeneous enhancement. The patient underwent tumorectomy, and histological examination confirmed mucinous tubular and spindle cell renal cell carcinoma. The favorable postoperative outcome in this case illustrates both the diagnostic value of imaging and histology and the good prognosis associated with MTSRCC.
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Taxonomy
TopicsRenal cell carcinoma treatment · Urinary and Genital Oncology Studies · Bladder and Urothelial Cancer Treatments