Please use this identifier to cite or link to this item: https://doi.org/10.5114/pjp.2014.42664
Title: Review of small cell carcinoma of the kidney with focus on clinical and pathobiological aspects
Authors: Kuroda, N.
Imamura, Y.
Hamashima, T.
Ohe, C.
Mikami, S.
Nagashima, Y.
Inoue, K.
Perez-Montiel, D.
Petersson, F. 
Michal, M.
Hes, O.
Keywords: Dismal prognosis
Kidney
Small cell carcinoma
Issue Date: 2014
Citation: Kuroda, N., Imamura, Y., Hamashima, T., Ohe, C., Mikami, S., Nagashima, Y., Inoue, K., Perez-Montiel, D., Petersson, F., Michal, M., Hes, O. (2014). Review of small cell carcinoma of the kidney with focus on clinical and pathobiological aspects. Polish Journal of Pathology 65 (1) : 15-19. ScholarBank@NUS Repository. https://doi.org/10.5114/pjp.2014.42664
Abstract: Small cell carcinoma (SmCC) of the kidney is extremely rare. In this article, we present a review of SmCC of the kidney with the focus on clinical and pathobiological aspects. Macroscopically, this tumor often shows a bulky mass extensively replacing the renal parenchyma with vascular invasion and metastasis to lymph nodes. Histologically, the tumor is composed of small cells with scant cytoplasm, round to oval nuclei, finely granular chromatin and inconspicuous nucleoli. Rosette or tubular formation may be present. Immunohistochemically, neoplastic cells show variable positivity for neuron-specific enolase, chromogranin A, synaptophysin, CD57 (Leu7) and CD56. A dot-like staining pattern for cytokeratin may also be observed. An electron microscopic examination may identify electron-dense neurosecretory granules in the cytoplasm. As a therapeutic option, nephrectomy and systemic chemotherapy should be considered. However, despite multimodal therapy, most patients have a dismal outcome and die of widely metastatic disease within one to two years. As there are limited genetic data on SmCC of the kidney, a large series studying this will be needed in the future.
Source Title: Polish Journal of Pathology
URI: http://scholarbank.nus.edu.sg/handle/10635/125889
ISSN: 12339687
DOI: 10.5114/pjp.2014.42664
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