scholarly journals Advanced Epithelioid Malignant Peripheral Nerve Sheath Tumor Showing Complete Response to Combined Surgery and Chemotherapy: A Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Tomohiro Minagawa ◽  
Ryuta Shioya ◽  
Chigusa Sato ◽  
Ryuji Shichinohe ◽  
Go Yasui ◽  
...  

Malignant peripheral nerve sheath tumor (MPNST) is a rare high-grade soft tissue sarcoma. The epithelioid variant accounts for 5% or less of MPNSTs; the clinical behavior of this variant is unclear. Reports of approximately 40 cases are available in the English literature; however, most reports addressed clinicopathological features rather than therapeutic procedures or clinical courses. We describe a case of a 62-year-old male with an epithelioid MPNST of the left foot. Multiple lung metastases developed after radical surgery on the primary lesion. The response to adjuvant chemotherapy including doxorubicin and ifosfamide was favorable, and thoracoscopic resection was subsequently performed on the remaining three metastases. No evidence of recurrence or metastasis was observed at the 12-month followup after the first operation. Further followup and chemotherapy may be required.

2018 ◽  
Vol 119 ◽  
pp. 335-339 ◽  
Author(s):  
Yuhui Ding ◽  
Hongtao Rong ◽  
Tong Liu ◽  
Yi Wang ◽  
Jinhao Zhang ◽  
...  

1999 ◽  
Vol 3 (5) ◽  
pp. 304-308 ◽  
Author(s):  
Isam A. Eltoum ◽  
R. Jemison Moore ◽  
William Cook ◽  
D. Ralph Crowe ◽  
William H. Rodgers ◽  
...  

2022 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Kristian Larson ◽  
Atlantis Russ ◽  
Hina Arif-Tiwari ◽  
Daruka Mahadevan ◽  
Alex Elliott ◽  
...  

2004 ◽  
Vol 33 (4) ◽  
pp. 223-225 ◽  
Author(s):  
Tuba Karag�lle Kendi ◽  
Aziz Erakar ◽  
H. Yusuf Yildiz ◽  
Yener Saglik ◽  
Selim Erekul

2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Maryam Tahmasbi ◽  
Johnny Nguyen ◽  
Masoumeh Ghayouri ◽  
Yuan Shan ◽  
Ardeshir Hakam

Schwannoma (neurilemmoma) is a benign peripheral nerve sheath tumor that occurs in a wide variety of locations; however, its finding in the uterine cervix is extremely rare. We report a case of an incidental primary benign cervical schwannoma in a 48-year-old woman. In the English literature, a few cases of primary schwannoma of the cervix have been reported, which include seven cases of primary malignant cervical schwannoma and only two that are benign. These cases are reviewed in the following discussion.


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