POLYPHENOTYPIC ANAPLASTIC SARCOMA OF THE KIDNEY: A RARE CASE REPORT AND REVIEW OF THE LITERATURE

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GERAMIZADEH BITA; BAHADOR ALI; KHALAFI NADIA

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

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Journal: Nephro-Urology Monthly Year:2017 | Volume:9 | Issue:4 Page(s): 0-0

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Title

POLYPHENOTYPIC ANAPLASTIC SARCOMA OF THE KIDNEY: A RARE CASE REPORT AND REVIEW OF THE LITERATURE

Author(s)

GERAMIZADEH BITA | BAHADOR ALI | KHALAFI NADIA | Issue Writer Certificate

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Abstract

Anaplastic sarcoma of the kidney is an extremely rare tumor, mostly observed in pediatric age group. This tumor is the counterpart of embryonal or undifferentiated sarcoma of the liver and pleuropulmonary blastoma of lung. To the best of the authors’ knowledge, only 26 cases were reported in the English literature and the current case, a 3-year-old male, was the 27th reported case with this tumor. It is very important to differentiate this tumor from the Wilm tumor as well as renal cell carcinoma, as they were preoperative diagnosed in all of the reported cases.

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References

Metachronous anaplastic sarcoma of the kidney and thyroid follicular carcinoma as manifestations of DICER1 abnormalities

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APA: Copy

GERAMIZADEH, BITA, BAHADOR, ALI, & KHALAFI, NADIA. (2017). POLYPHENOTYPIC ANAPLASTIC SARCOMA OF THE KIDNEY: A RARE CASE REPORT AND REVIEW OF THE LITERATURE. THE JOURNAL OF NEPHRO-UROLOGY MONTHLY, 9(4), 0-0. SID. https://sid.ir/paper/323811/en

Vancouver: Copy

GERAMIZADEH BITA, BAHADOR ALI, KHALAFI NADIA. POLYPHENOTYPIC ANAPLASTIC SARCOMA OF THE KIDNEY: A RARE CASE REPORT AND REVIEW OF THE LITERATURE. THE JOURNAL OF NEPHRO-UROLOGY MONTHLY[Internet]. 2017;9(4):0-0. Available from: https://sid.ir/paper/323811/en

IEEE: Copy

BITA GERAMIZADEH, ALI BAHADOR, and NADIA KHALAFI, “POLYPHENOTYPIC ANAPLASTIC SARCOMA OF THE KIDNEY: A RARE CASE REPORT AND REVIEW OF THE LITERATURE,” THE JOURNAL OF NEPHRO-UROLOGY MONTHLY, vol. 9, no. 4, pp. 0–0, 2017, [Online]. Available: https://sid.ir/paper/323811/en

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