Odontogenic keratocyst in the mandible of a 7‐year‐old child: A case report and literature review

IF 0.6 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Tadashi Chida, Yoshihiro Morita, Satoko Kishimoto, Ken Wakabayashi, Narikazu Uzawa, Tomohiko Kanesaki
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引用次数: 0

Abstract

Abstract Odontogenic keratocysts (OKCs) are one of the most frequently encountered cystic diseases of the jaw in clinical practice. Although OKC has been reported as a manifestation of nevoid basal cell carcinoma syndrome (Gorlin syndrome) in many pediatric patients, there have been few reports of OKC occurring in isolation. Herein, we report the case of a relatively large OKC in the mandibular body of a 7‐year‐old girl who was treated conservatively using cystectomy and open wound surgery, and the permanent teeth were unaffected. Regular check‐ups, including radiographic examinations, starting in childhood may contribute to the early detection of lesions in the maxillofacial region.
7岁儿童下颌骨牙源性角化囊肿1例报告并文献复习
牙源性角化囊肿(Odontogenic keratocysts, OKCs)是临床上最常见的颌囊性疾病之一。虽然OKC已被报道为许多儿科患者的瘤状基底细胞癌综合征(Gorlin综合征)的表现,但很少有OKC单独发生的报道。在此,我们报告了一名7岁女孩在下颌骨体中出现相对较大的OKC的病例,她采用膀胱切除术和开放性伤口手术进行保守治疗,而恒牙未受影响。从儿童时期开始的定期检查,包括x线检查,可能有助于早期发现颌面部病变。
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来源期刊
Oral Science International
Oral Science International DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
1.00
自引率
20.00%
发文量
43
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