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Primitive Neuroectodermal Tumor of the Proximal Phalanx of the First Toe. Case Report Yoshikazu Tanzawa 1 , Hiroyuki Tsuchiya 1 , Toshiharu Shirai 1 , Kensuke Yamauchi 1 , Akihiko Takeuchi 1 , Hiroaki Kimura 1 , Katsuro Tomita 1 , Yoh Zen 2 1Department of Orthopaedic Surgery, School of Medicine, Kanazawa University 2Department of Pathology, School of Medicine, Kanazawa University Keyword: 原始神経外爬胚葉腫瘍 , primitive neuroectodermal tumor , 足趾 , toe , 基節骨 , proximal phalanx pp.183-187
Published Date 2008/2/25
DOI https://doi.org/10.11477/mf.1408101232
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 We report a rare case of primitive neuroectodermal tumor (PNET) arising from the proximal phalanx of the first toe. A 21-year-old man presented with pain in the right first toe after minor trauma. A roentgenogram showed a radiolucent expansive lesion and thinning in the proximal phalanx of the right first toe. A benign tumor was suspected, and curettage followed by bone grafting was performed. The histological diagnosis, however, was PNET with a low mitotic index, and radiotherapy and chemotherapy were performed immediately. Additional wide excision was not performed. The patient has had no evidence of recurrence or metastasis during the 15 years since surgery. The prognosis of PNET is generally poor, but our patient is a long-term survivor. We think that the small tumor volume, low-grade malignancy, and good response to chemotherapy were factors that led to his long-term survival.


Copyright © 2008, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1286 印刷版ISSN 0557-0433 医学書院

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