Cai Zi-Hui, Li Lin-Yi, Man Qi-Wen, Lv Jun-Zhou, Yu Zi-Li, Wang Fang, Zhang Wei
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, School & Hospital of Stomatology, Wuhan University, Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University.
Department of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, Wuhan University.
J Craniofac Surg. 2025 Apr 7. doi: 10.1097/SCS.0000000000011296.
The clinical imaging typically presents as a multicystic lesion in the jawbone, which is mostly diagnosed as ameloblastoma, myxoma, or odontogenic keratocyst. Preoperative biopsy is often challenging due to the intraosseous location of these lesions. Consequently, clinicians frequently rely on these characteristic multicystic imaging features to diagnose either ameloblastoma or odontogenic keratocyst, subsequently planning treatments ranging from marginal resection to mandibular segmental osteotomies with concurrent autogenous bone grafting. However, we encountered two cases of multicystic lesions in the jawbone with a pathological diagnosis of periapical cyst. The treatment for periapical cyst typically involves only curettage of the periapical lesion, eliminating the necessity for bone resection or grafting procedures. In most cases, tooth extraction is also unnecessary. Therefore, compared with the management of ameloblastomas and odontogenic keratocysts, periapical cyst treatment results in significantly less irreversible damage and patient discomfort. This study reports 2 rare cases of multicystic periapical cysts with detailed clinical, imaging, and pathological analyses. Through these cases, we aim to enhance clinicians' awareness of the possibility that multicystic jaw lesions with multilocular radiographic features could represent periapical cysts. When necessary, a biopsy should be performed to determine the pathological type before formulating a treatment plan.
临床影像学表现通常为颌骨内的多囊性病变,大多被诊断为成釉细胞瘤、黏液瘤或牙源性角化囊肿。由于这些病变位于骨内,术前活检往往具有挑战性。因此,临床医生常常依靠这些典型的多囊性影像学特征来诊断成釉细胞瘤或牙源性角化囊肿,随后制定从边缘切除到下颌节段性截骨并同期自体骨移植的治疗方案。然而,我们遇到了两例颌骨多囊性病变,病理诊断为根尖囊肿。根尖囊肿的治疗通常仅需刮除根尖病变,无需进行骨切除或植骨手术。在大多数情况下,也无需拔牙。因此,与成釉细胞瘤和牙源性角化囊肿的治疗相比,根尖囊肿治疗造成的不可逆损伤和患者不适明显更少。本研究报告了2例罕见的多囊性根尖囊肿病例,并进行了详细的临床、影像学和病理分析。通过这些病例,我们旨在提高临床医生对具有多房影像学特征的颌骨多囊性病变可能为根尖囊肿的认识。必要时,在制定治疗方案前应进行活检以确定病理类型。