2015
DOI: 10.4103/1742-6413.171135
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Mucinous tubular and spindle cell carcinoma of the kidney: Diagnosis by fine needle aspiration and review of the literature

Abstract: Renal mucinous tubular and spindle cell carcinoma (MTSCC) was recently described as a distinct subtype of renal cell carcinoma (RCC) in the 2004 World Health Organization classification of kidney tumors. MTSCC is a rare low grade malignancy with < 100 cases reported in the literature. To the best of our knowledge, there are 5 case reports with a total of 6 patients describing its diagnosis by fine needle aspiration (FNA). All of these cases were diagnosed as conventional RCC on FNA. Subsequent excisions proved… Show more

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Cited by 10 publications
(3 citation statements)
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“…Mucinous and spindle cell tumors can have papillary areas, but these are uncommon. The presence of mucin is perhaps the best clue on cytology to this tumor . Finally, metastatic lesions can be papillary, but should have a history of tumor elsewhere; the staining profile will depend on the site of origin.…”
Section: Pattern 7 Renal Aspirate With Papillaementioning
confidence: 99%
“…Mucinous and spindle cell tumors can have papillary areas, but these are uncommon. The presence of mucin is perhaps the best clue on cytology to this tumor . Finally, metastatic lesions can be papillary, but should have a history of tumor elsewhere; the staining profile will depend on the site of origin.…”
Section: Pattern 7 Renal Aspirate With Papillaementioning
confidence: 99%
“…Insulin amyloidoma marked by extracellular fibrils at the injection site is a medical condition complicating insulin therapy. 1 The instability of monomeric insulin and its fibrillation also interfere with its manufacture, long-term storage, and pharmaceutical use. 2 Overcoming this problem through inclusion of a chemical chaperone such as small molecule, peptide or macrocycle may abrogate fibrilization in insulin formulations.…”
mentioning
confidence: 99%
“…Müsinöz tübüler ve iğsi hücreli karsinoma olgularında 1, 4q, 6, 8p, 11q, 13, 14, 15 kromozomlarında kayıp ve 11q, 17 ve 20q kromozomlarında kazanımlar bildirilmiştir. Genomik hibridizasyon verileri ortaya koymaktadır ki bu tümörlerde papiller renal hücreli karsinomada saptanan 7 ve 17 trizomi saptanmaz1,14,17 .Müsinöz tübüler ve iğsi hücreli karsinoma nadir görülen bir renal epitelyal karsinoma tipidir. Papiller karsinoma ile histopatolojik ve immünohistokimyasal bulgular açısından benzer özelliklere sahip olmasına rağmen prognozlarının farklı olması tümöre doğru tanı konulmasını daha da önemli hale getirmektedir.…”
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