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Erschienen in: Journal of Cancer Research and Clinical Oncology 2/2011

01.02.2011 | Original Paper

Improved outcomes after complete resection of underlying tumors for patients with paraneoplastic pemphigus: a single-center experience of 22 cases

verfasst von: Jun Zhang, Qi-lu Qiao, Xi-xue Chen, Ping Liu, Jian-xing Qiu, Hu Zhao, Jian-xun Zhao, Yu-cun Liu, Yuan-lian Wan

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 2/2011

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Abstract

Background

Paraneoplastic pemphigus (PNP) is an autoimmune-related acquired bullous disease. Delayed diagnosis and treatment of this clinically rare disease often result in poor prognosis.

Methods

Between January 1999 and December 2009, 22 patients with confirmed PNP who underwent surgical resection of underlying tumors were enrolled in this study. Clinicopathologic characteristics, treatment options, and perioperative and long-term results were analyzed.

Results

Among 22 patients, 2 patients died of severe infection several weeks after surgery. Postoperative major complications included pulmonary infections (n = 10) and septicemia (n = 4). Respiratory symptoms persisted in 13 patients. Tumors were completely resected in 20 patients. Two patients whose tumors were not completely resected died of relapse 2 and 32 months after surgery. Two patients with completely resected tumors died of respiratory failure 10 and 24 months after surgery, respectively. One patient whose pathological result was follicular dentritic cell sarcoma had a relapse recently. The remaining 15 patients have survived till now.

Conclusions

Early detection, prompt treatment, and complete resection of PNP can effectively decrease the mortality and speed up the recovery.
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Metadaten
Titel
Improved outcomes after complete resection of underlying tumors for patients with paraneoplastic pemphigus: a single-center experience of 22 cases
verfasst von
Jun Zhang
Qi-lu Qiao
Xi-xue Chen
Ping Liu
Jian-xing Qiu
Hu Zhao
Jian-xun Zhao
Yu-cun Liu
Yuan-lian Wan
Publikationsdatum
01.02.2011
Verlag
Springer-Verlag
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 2/2011
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-010-0874-z

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