Rhabdomyosarcoma in the maxillary gingiva of a child patient

Author:

Komatsu Yuko1,Kawai Tadashi1,Miura Shoko2,Takeda Yasunori3,Yamada Hiroyuki1

Affiliation:

1. Division of Oral and Maxillofacial Surgery, Department of Oral and Maxillofacial Reconstructive Surgery, School of Dentistry, Iwate Medical University, Morioka, Iwate, Japan

2. Department of Pediatrics, School of Medicine, Iwate Medical University, Yahaba-cho, Shiwa-gun, Iwate, Japan

3. Division of Clinical Pathology, Department of Oral and Maxillofacial Reconstructive Surgery, School of Dentistry, Iwate Medical University, Yahaba-cho, Shiwa-gun, Iwate, Japan

Abstract

Abstract Rhabdomyosarcoma (RMS) is a rare, rapidly growing and aggressive malignant neoplasm mainly affecting children. However, mean age at the diagnosis of patients with gingival RMS is 26.9 years. A 12-year-old girl presented to our clinic with a chief complaint of trismus. The examination findings indicated a malignant tumor in the left maxillary gingiva. We performed a biopsy of the tumor, and the histopathological diagnosis was RMS. We report a rare case of primary RMS of the maxillary gingiva in a child patient.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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