Solitary Neurofibroma of Mandible in a 2-Year-Old Child: A Rare Case Report and Review of Literature

被引：2

作者：

Sarkar, Dibya Falgoon ^{[1
]}

Mishra, Niranjan ^{[1
]}

Pati, Debashish ^{[1
]}

Samal, Sandeep Kumar ^{[2
]}

机构：

[1] SCB Dent Coll & Hosp, Dept Oral & Maxillofacial Surg, Cuttack 753007, Odisha, India

[2] Hitech Dent Coll & Hosp, Dept Oral & Maxillofacial Surg, Bhubaneswar 751025, Odisha, India

来源：

JOURNAL OF MAXILLOFACIAL & ORAL SURGERY | 2022年 / 21卷 / 04期

关键词：

Solitary intraosseous neurofibroma; Mandible; Nerve sheath tumour; Case report; INFERIOR ALVEOLAR NERVE; INTRAOSSEOUS-NEUROFIBROMA; INFRATEMPORAL FOSSA;

D O I：

10.1007/s12663-021-01670-6

中图分类号：

R78 [口腔科学];

学科分类号：

1003 ;

摘要：

Solitary intraosseous neurofibromas of mandible are very rare and only 40 cases are documented. This case report presents one of the youngest documented case of solitary neurofibroma of mandible, in a 2-years old male child. The tumour was symptomatic and presented as a swelling over right posterior region of mandible. The patient underwent conservative excision under general anaesthesia. The inferior alveolar nerve was preserved. Histopathology was suggestive of benign nerve sheath tumour. Immunohistochemistry showed moderate S-100 and strong CD34 positivity. Postoperative healing was uneventful. This report also reviews forty previously reported cases of solitary intraosseous neurofibromas of the mandible.

引用

页码：1320 / 1325

页数：6

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