Basit öğe kaydını göster

dc.contributor.authorHaberal, Hakan Bahadir
dc.contributor.authorTonyali, Senol
dc.contributor.authorBaydar, Dilek Ertoy
dc.contributor.authorBilen, Cenk Yucel
dc.date.accessioned2019-12-12T06:43:54Z
dc.date.available2019-12-12T06:43:54Z
dc.date.issued2017
dc.identifier.issn1792-1074
dc.identifier.urihttps://doi.org/10.3892/ol.2017.6948
dc.identifier.urihttp://hdl.handle.net/11655/16841
dc.description.abstractThe majority of small cell carcinoma (SCC) cases originate from the lungs. SCC of the kidneys is rare. Among genitourinary tumors, renal cell carcinoma is the most common type of tumor to be associated with paraneoplastic syndromes. The majority of paraneoplastic syndromes disappear following nephrectomy in renal cell carcinoma cases. The present case involved the assessment of a female patient with SCC of the left kidney. The patient was diagnosed with acute renal failure and underwent a laparoscopic left radical nephrectomy. Surgical intervention removed the need for dialysis; the patient was under follow-up observation every week without any requirement for dialysis for 8 months and received adjuvant carboplatin-etoposide chemotherapy. Surgery is an option for dialysis-dependent patients with a renal tumor. The removal of the tumor burden may restore renal function and eliminate paraneoplastic syndromes.
dc.language.isoen
dc.publisherSpandidos Publ Ltd
dc.relation.isversionof10.3892/ol.2017.6948
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectOncology
dc.titleAcute Renal Failure Due To Small Cell Neuroendocrine Carcinoma Of The Left Kidney: A Case Report
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalOncology Letters
dc.contributor.departmentÜroloji
dc.identifier.volume14
dc.identifier.issue5
dc.identifier.startpage6117
dc.identifier.endpage6120
dc.description.indexWoS


Bu öğenin dosyaları:

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster