| Title: | Spontaneous remission of solitary-type infantile myofibromatosis |
| Authors: | Kikuchi, Kazuhiro Browse this author |
| Abe, Riichiro Browse this author →KAKEN DB |
| Shinkuma, Satoru Browse this author →KAKEN DB |
| Hamasaka, Erika Browse this author |
| Natsuga, Ken Browse this author →KAKEN DB |
| Hata, Hiroo Browse this author →KAKEN DB |
| Tateishi, Yasuki Browse this author |
| Shibata, Masahiko Browse this author |
| Tomita, Yuki Browse this author |
| Abe, Yukiko Browse this author |
| Aoyagi, Satoru Browse this author |
| Mukai, Makio Browse this author |
| Shimizu, Hiroshi Browse this author →KAKEN DB |
| Keywords: | Infantile myofibromatosis |
| Leiomyosarcoma |
| Solitary type |
| Issue Date: | Aug-2011 |
| Publisher: | Karger |
| Journal Title: | Case reports in dermatology |
| Volume: | 3 |
| Issue: | 2 |
| Start Page: | 181 |
| End Page: | 185 |
| Publisher DOI: | 10.1159/000331325 |
| PMID: | 21941483 |
| Abstract: | Infantile myofibromatosis is a rare fibrous tumor of infancy. The cutaneous solitary type has typically an excellent prognosis. However, histologically, it is important to rule out leiomyosarcoma, which has a poor prognosis. The low frequency of mitosis was definitive for a diagnosis of infantile myofibromatosis. We present a cutaneous solitary-type case of infantile myofibromatosis. Following incisional biopsy, the tumor remitted spontaneously. |
| Rights: | The final, published version of this article is available at http://www.karger.com/?doi=10.1159/000331325 |
| http://creativecommons.org/licenses/by-nc/3.0/ |
| Type: | article |
| URI: | http://hdl.handle.net/2115/67608 |
| Appears in Collections: | 医学院・医学研究院 (Graduate School of Medicine / Faculty of Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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