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Renal medullary carcinoma: the Bronx experience.

Renal medullary carcinoma: the Bronx experience. Research Abstract Details 

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  • Renal medullary carcinoma: the Bronx experience. Abstract Text:

    a ari hakimiA Ari Hakimi,phillip t koiPhillip T Koi,paul m milhouaPaul M Milhoua,netta m blitmanNetta M Blitman,maomi liMaomi Li,vladimir hugecVladimir Hugec,janice p dutcherJanice P Dutcher,reza ghavamianReza Ghavamian,a ari hakimiA Ari Hakimi,phillip t koiPhillip T Koi,paul m milhouaPaul M Milhoua,netta m blitmanNetta M Blitman,maomi liMaomi Li,vladimir hugecVladimir Hugec,janice p dutcherJanice P Dutcher,reza ghavamianReza Ghavamian,

    OBJECTIVES: Renal medullary carcinoma (RMC) is a devastating and extremely rare malignancy primarily afflicting young men with sickle cell trait. We present our clinical experience with 9 cases of RMC during a 10-year period and briefly review the published data. METHODS: A retrospective chart review of 9 cases of RMC during a 10-year period at our institutions was performed. The clinical patient characteristics, presentations, treatments, and outcomes were recorded. The radiographic images and pathologic specimens were reviewed. Applicable studies were selected from a Medline search. RESULTS: All 9 patients had sickle cell trait, the male/female ratio was 6:3, and the age range was 13 to 31 years. All the patients presented with flank pain, two thirds had hematuria, and 3 of the 9 patients presented with a palpable mass. Eight of the nine tumors were right sided, ranging from 4 to 12 cm in the greatest diameter. Of the 9 patients, 7 underwent radical nephrectomy. One patient was deemed to have unresectable disease by the operating surgeon, and one was given initial chemotherapy after biopsy of a metastatic lesion. The neoadjuvant therapies varied. Overall survival ranged from 4 to 16 months, with 2 patients still living at the last follow-up visit. CONCLUSIONS: Our urban setting likely explains our relatively large experience with this rare and extremely aggressive tumor. An early diagnosis is critical, and a high index of suspicion should be given to any individual with sickle cell trait and new-onset hematuria, especially in the setting of a right-sided mass. Prospective trials are needed for chemotherapy/immunotherapy, because surgical intervention alone is inadequate.

    Renal medullary carcinoma: the Bronx experience. Publishing Authors By Initials

    aa hakimiAA Hakimi,pt koiPT Koi,pm milhouaPM Milhoua,nm blitmanNM Blitman,m liM Li,v hugecV Hugec,jp dutcherJP Dutcher,r ghavamianR Ghavamian,aa hakimiAA Hakimi,pt koiPT Koi,pm milhouaPM Milhoua,nm blitmanNM Blitman,m liM Li,v hugecV Hugec,jp dutcherJP Dutcher,r ghavamianR Ghavamian,

    For similar abstracts research abstracts see: abstracts research

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    Renal medullary carcinoma: the Bronx experience. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Urology

    VOLUME: 70

    Page Numbers: 878-82

    Journal Abbreviation: Urology

    ISSN: 1527-9995

    DAY: 10

    MONTH: Nov

    YEAR: 2007

    Renal medullary carcinoma: the Bronx experience. Information

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    LANGUAGE: eng

    NlmUniqueID: 366151

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    Grant and Affiliation Information for Renal medullary carcinoma: the Bronx experience.

    AFFILIATION: Department of Urology, Montefiore Medical Center, Bronx, New York 10467, USA. ahakimi@montefiore.org

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Urology

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