Ameloblastic fibrosarcoma of the maxilla arising in an old woman, a rare case report and literature review

Author:

Liu Shiyue,Li Hong,Dong Youhong,Zhang Dongdong

Abstract

Abstract Background Ameloblastic fibrosarcoma (AFS) is a rare malignant odontogenic tumor, commonly occurring in young adults and typically affecting the mandibular region. We report an exceptionally rare and highly atypical case of AFS in an elderly female patient originating from the maxillary bone. Case presentation A 66-year-old woman was admitted with a two-week history of a lump in her left upper molar. CT scans suggested a cyst in the maxillary bone. An incisional biopsy revealed a spindle cell neoplasm. MRI showed abnormalities in the left maxilla, indicating a possible tumorous lesion. The patient underwent a subtotal maxillectomy, wide tumor excision, intraoral epithelial flap transplantation, and dental extraction. Histology identified atypical tumor cells with visible mitotic figures. Immunohistochemistry showed negative for PCK and CD34 expression, but positive for Vimentin and SMA expression. The Ki-67 proliferation index ranged from 30 to 50%. These findings suggested a potentially malignant soft tissue tumor in the left maxilla, leaning towards a diagnosis of AFS. The patient received postoperative radiotherapy. There was no recurrence during the six-month follow-up. Conclusion Based on repeated pathological evidence, we report a rare case of an elderly female with AFS originating from the maxillary bone. Surgery and postoperative radiotherapy resulted in a favorable outcome.

Funder

Hubei Xiangyang No. 1 People’s Hospital of Youth programs

Key Research and Development Project of Hubei

Hubei Natural Science Foundation

National Natural Science Foundation of China

Young and middle-aged talent program of Hubei Education Bureau

Platform Special Fund for Scientific Research of Xiangyang No.1 People’s Hospital

Instructional projects of Hubei Provincial Health and Health Commission

Publisher

Springer Science and Business Media LLC

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