We experienced a case of nephrotic syndrome (membranous nephropathy) complicated by extensive small cell carcinoma of unknown primary etiology that was diagnosed based on the findings of bilateral cervical and mediastinal lymphadenopathy. A complete cancer response and proteinuria remission following radical chemoradiation therapy were documented. The status of a complete response and nephrosis remission persisted for more than three years. This is the first report to demonstrate the long-term survival of a patient with extensive small cell carcinoma of unknown primary etiology complicated by paraneoplastic nephrotic syndrome. © 2014 The Japanese Society of Internal Medicine.
CITATION STYLE
Ishikawa, G., Nishimura, N., Mochizuki, S., Yamano, Y., Kitamura, A., Tomishima, Y., … Chohnabayashi, N. (2014). Long-term survival of a patient with extensive small cell carcinoma of unknown primary etiology complicated by nephrotic syndrome. Internal Medicine, 53(2), 159–162. https://doi.org/10.2169/internalmedicine.53.1323
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