• 한국치위생학회지
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• 제15권6호
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• pp.941-946
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• 2015

Objectives: Since World Health Organization reclassified the odontogenic keratocyst as a keratocystic odontogenic tumor(KCOT) in 2005, management of KCOT remains controversial. The purpose of the this study is to present a current concept of the treatment of the KCOT. Methods: Recent articles were focused on the method of the surgical therapy and the recurrence rate of KCOT. Results: The treatment modality is divided into conservative treatment-such as simple enucleation with or without curettage or marsupialization-and aggressive treatment including peripheral ostectomy, chemical curettage with Carnoy's solution, and resection. Conclusions: Keratocystic odontogenic tumors have higher recurrence rates than other odontogenic lesions; thus, the selected type of treatment is very important.

• Imaging Science in Dentistry
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• 제32권4호
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• pp.227-230
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• 2002

The central odontogenic fibroma is a rare benign neoplasm, and considered to be derived from the mesenchymal tissue of dental origin. It is a poorly defined tumor of the jawbones which has only been infrequently reported in the literature. We report a histologically proven case of simple-type central odontogenic fibroma, which affected the left canine-premolar region of the maxilla in a 52-year-old woman.

• 대한소아치과학회지
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• 제36권3호
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• pp.489-497
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• 2009

악골에서 다수로 발생하는 낭은, 단독으로 발생하는 낭에 비해 매우 드물게 나타난다. 증후군을 동반하지는 않고, 악골 내에 다수의 낭이 발생한 경우를 다발성 악골낭 이라고 하는데, 소아에서 발생하는 다발성 악골 낭의 대부분은 각화낭성 치성종양(Keratocystic odontogenic tumor, KCOT)이다. 소아에서 나타나는 악골의 다발성 각화낭성 치성종양은, 기저세포모반증후군의 한 증상으로 발생할 수 있으므로, 악골의 방사선 사진에서 다발성 낭이 발견되면, 증후군을 의심해보고 임상 및 병리 검사를 하게 된다. 본 증례는, 다발성 악골 낭을 주소로 내원한 소아환자들로, 기저세포모반증후군을 의심하였으나 현재까지 증후군의 다른 증상들은 보이고 있지 않으며, 단지 수년간에 걸쳐서 종양의 재발과 수술을 반복하고 있는 경우이다. 악골의 다발성 낭 이외의 기저세포모반증후군의 증상들이 나타나지 않더라도, 나이가 들면 증후군의 다른 증상들이 나타난 경우의 보고도 있으므로, 소아에서 이러한 다발성 치성종양이 관찰되면, 지속적으로 방사선 및 임상 검사를 시행하여 증후군으로의 진행 여부를 관찰하는 것이 중요한 것으로 사료된다.

• 대한방사선치료학회지
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• 제30권1_2호
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• pp.73-81
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• 2018

목 적 : 다발성 뇌 전이의 방사선치료 시 jaw tracking(JT)과 fixed jawFJ)를 이용한 용적세기조절회전치료(Volumetric Modulated Arc Therapy, VMAT)를 비교하고 유용성을 평가하고자 한다. 대상 및 방법 : JT를 이용하여 치료받은 다발성 뇌 전이(Multiple Brain Metastasis) 환자 중 6개 이상의 종양이 있고 조사면 크기가 $14{\times}14cm^2$ 이상인 환자 10명을 대상으로 하였다. Eclipse(Ver 13.6 Varian, USA)로 JT와 FJ의 전산화치료계획을 각각 수립하였으며, 전자포털영상장치(Electronic Portal Imaging Device, EPID)를 이용하여 감마지수(Gamma Index, 3 mm, 3 %, 95 % 신뢰구간) 및 최대선량차이(Max. Dose Difference)를 측정하였다. 또한 손상위험장기(Organ At Risk, OAR)의 $D_{max}$ 및 $D_{mean}$을 산출하고 비교하였으며 처방선량지수(Conformity Index, CI), 선량균질지수(Homogeneity Index, HI)를 평가하였다. 결 과 : JT와 FJ의 측정값을 평가한 감마지수는 모든 Case에서 허용 기준(3 mm, 3 %, 95 % 신뢰구간)에 충족하였으며, 최대선량차이값은 Leaf End Transmission이 발생하는 영역에서 시계방향(Clockwise, CW)은 최대 98.4 %, 평균 43.6 %, 반시계방향(Counter-Clockwise, CCW)은 최대 67.9 %, 평균 41.0 %로 측정되었다. 손상위험장기는 JT를 사용하였을 때 각 정상장기에 대한 $D_{max}$의 최대값은 15.36 %~74.59 %, 평균값은 2.84 %~39.80 % 감소, $D_{mean}$의 최대값은 27.90 %~65.23 %, 평균값은 7.70 %~41.71 %로 감소하였으며, 처방선량지수와 선량균질지수값은 차이가 없었다. 결 론 : 다발성 뇌 전이에서 VMAT으로 치료할 경우 JT를 이용하면 치료계획용적(Planning Target Volume, PTV)의 선량분포에 영향을 미치지 않으면서 불특정 영역에서 발생하는 방사선의 누설 및 투과로 인한 불필요한 피폭을 감소시키고 정상장기에 더 낮은 선량으로 방사선치료가 가능할 것으로 사료된다.

• 대한소아치과학회지
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• 제41권2호
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• pp.166-173
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• 2014

기저세포 모반 증후군은 상염색체 우성 방식으로 유전되는 질환으로 다발성 각화낭성 치성종양, 대두증 및 두정골 융기, 골격계 기형 등을 보이는 질환이다. 다발성 각화낭성 치성 종양, 두정골 융기, 양안격리증을 가진 만 11세 환자의 하악과 상악에서 발생한 다양한 크기의 낭종에 대한 적출술과 이종골 이식술을 시행 후 교정적 견인을 시행하였다. 낭종에 의한 매복 영구치를 가진 성장중인 기저세포 모반 증후군 환자에서의 보존적인 치료를 하였기에 문헌고찰과 더불어 보고하고자 한다.

• Imaging Science in Dentistry
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• 제42권2호
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• pp.115-119
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• 2012

Today, ultrasound imaging is being widely used to assess soft tissue lesions in the maxillofacial region. However, ultrasound investigations of intra-osseous lesions are rare, especially for tumors of the jaws. This report emphasized the capability of this useful imaging modality in identification of the characteristics of malignant conditions involving the bone. Mesenchymal chondrosarcoama, one of the unusual malignant conditions of the jaw, was presented in a young male with significant facial swelling. Different imaging modalities parallel with the histopathologic investigation confirmed the diagnosis. Interestingly, destruction of the bony cortex and new bone formation with a characteristic "sun ray appearance", highly suggestive of sarcomas, was manifested on the ultrasonograph. Thus, this report presented the ultrasonographic features of chondrosarcoma of mandible and considered the ultrasonography to be a useful imaging modality to evaluate intra-osseous jaw lesions.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제43권2호
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• pp.134-137
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• 2017

Giant cell tumor (GCT) of the craniofacial bones has been reported but they are not common. This tumor occurs more often in women than in men and predominantly affects patients around the third to fifth decade of life. GCTs are generally benign but can be locally aggressive as well. We report a case of GCT involving the temporomandibular joint (TMJ), which was initially thought to be temporomandibular disorder (TMD). A 22-year-old female presented with swelling and pain over the right temporal region for 18 months associated with jaw locking and clicking sounds. On examination, her jaw deviated to the right during opening and there was a $2{\times}2$ cm swelling over the right temporal region. Despite routine treatment for TMD, the swelling increased in size. Computed tomography and magnetic resonance imaging of the brain and TMJ revealed an erosive tumor of the temporal bone involving the TMJ which was displacing the temporal lobe. Surgical excision was done and the tumor removed completely. Histopathological examination was consistent with a GCT. No clinical or radiological recurrence was detected 10 months post-surgery.

• 대한두경부종양학회지
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• 제39권2호
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• pp.35-39
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• 2023

Solitary fibrous tumor (SFT), which was initially believed to be a subtype of mesothelioma, has been reported to occur outside the pleura. In the head and neck region, it primarily manifests in the oral or nasal cavity, with rare occurrences in the facial region. A 40-year-old woman visited our hospital with a mass on her chin. Prior to surgery, involuntary movement was observed in the ipsilateral corner of the mouth upon palpation of the mass. Special care was taken during the surgical procedure to avoid damaging the facial nerve. The mass was excised, and histological examination and immunohistochemical analysis confirmed the diagnosis of an SFT. Here, we present the first reported case of an SFT diagnosed in a jaw mass in Korea. The objective of this study was to highlight the importance of the diagnostic accuracy of SFTs in lower jaw masses.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제38권3호
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• pp.152-159
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• 2012

Objectives: This study evaluated bisphosphonate-related osteonecrosis of the jaws (BRONJ) in patients diagnosed with malignant bone tumors. Demographic findings, laboratory, and radiographic analyses were performed to characterize disease severity and progression. Materials and Methods: Patients who had been diagnosed with BRONJ (2005-2010) at the authors' hospital according to the American Association of Oral and Maxillofacial Surgeons were investigated. Twenty-one patients (12 with multiple myelomas, 7 with breast cancer, and 2 with prostate cancer) who had been treated with bisphosphonates (BPs) for malignant bone tumors were included. Radiographic evaluations with a panorama, computed tomography, whole body bone scan, and laboratory findings were evaluated for erythrocyte sedimentation rate (ESR), c-reactive proteins (CRPs), and c-terminal cross-linked telopeptides (CTXs). Results: The average age of the patients was 64.3 (range 51-80), and they were treated with BPs for an average of $35{\pm}19$ months before BRONJ was diagnosed. Types of BPs were zolendronic acid (81%, intravenous [IV]), pamidronate (4.8%, IV), zoledronic acid+pamidronate (4.8%, IV), alendronate (4.8%, per os [PO]), and ibadronate (4.75%, PO). Extraction (67%) and persistent irritation of dentures (20%) were the most common triggering factors. BRONJ in the mandible was reported in 62% of the cases, in the maxilla 24%, and both 14%. BRONJ occurred more frequently in patients with multiple myelomas (n=12, 57.1%). Most of the patients revealed an advanced BRONJ stage; Stage I (n=2, 9%), Stage II (n=13, 62%), and Stage III (n=6, 29%). Conclusion: The differences of the ESR, CRP, and CTX values between the BRONJ-recurring and non-recurring patients after the treatment were not evident. Later stage BRONJ patients showed lower CTX levels. A drug holiday after the diagnosis of BRONJ did not remarkably influence the surgical outcomes. However, the limited number of patients in the study should be considered.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제47권2호
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• pp.112-119
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• 2021

Objectives: Myxomatous odontogenic tumors (MOTs) are the third most common odontogenic tumors in the oral and maxillofacial region. Due to its slow-growing, but locally invasive nature, the tumor is usually detected by accident or only when it becomes a large mass, which causes facial deformity. Materials and Methods: Current study reports three unusual cases of MOT including huge myxoma involve the mandible in middle-aged man, MOT with ossifying fibroma pattern in mandible, and MOT in maxilla of young female patient. The diagnosis and treatment strategy of MOTs was also summarized and updated. Results: In reported three cases of patients with large MOTs, surgical treatment was indicated with fibular free flap reconstruction in the mandible and plate reconstruction in the maxilla. The tumors were successfully treated with radical resection and did not show signs of recurrence during the follow-up period. Conclusion: Surgical treatment indication depends on size, the position of the lesion, patient systemic condition and surgeon individual experience. In the case of a large tumor, radical resection and reconstruction is the standard surgical strategy. The conservative surgical treatment including enucleation with wide curettage is still under controversy. The recurrence rate for MOTs is significantly high, up to 30%, therefore long-term follow-up is essential.