식품의약품안전처는 효율적인 식중독 예방 교육·홍보를 위하여 모바일 증강현실 게임인 ‘식중독잡GO’를 개발 하고 식품안전의 날 등 11개 행사에서 시범운영을 하였다. 행사장에서 ‘식중독잡GO’를 체험한 사람을 대상으로 식중독에 대한 인지정도를 설문조사를 통해 살펴보았다. 설문조사 결과 ‘식중독잡GO’ 게임 전후대비 식중독예방 3대 요령 인지도는 게임 전 51.8%에서 게임 후 78.8%로 향상되었고, 개별 식중독균 인지도는 평균 2.1배 향상되었 다. 설문조사자의 95%가 식중독 이해에 도움이 되었다고 응답하였으며, 90%가 게임이 재미있었다고 응답하였다. 따라서, ‘식중독잡GO’를 유·초·중·고등 교육에 적용을 하면 식중독균의 주요증상, 원인식품 등 식중독 예방 요령의 다양한 교육적 효과를 기대할 수 있을 것으로 사료된다.

Carcinoma ex pleomorphic adenoma (Ca ex PA) is an uncommon malignant tumor. It is an aggressive salivary carcinoma, arising from a primary or recurrent benign pleomorphic adenoma (PA). The most common clinical presentation of Ca ex PA is a firm mass in the parotid gland. Here we report a case of Ca ex PA, arising from a recurrent benign PA in the right parotid gland, in a 70-year old female patient. The lesion was first diagnosed as a PA and a superficial parotidectomy was performed. Re-operation was performed for recurrent PA. The second recurrence was diagnosed as Ca ex PA.

Neurilemmomas, also known as schwannomas, are typically benign, well-encapsulated, slow-growing tumors originating from Schwann cells which encompass peripheral motor and sensory nerves. Neurilemmomas in parapharyngeal space (PPS) are very rare, but they can occasionally originate from the last four cranial nerves and autonomic nerves. In this article, we report the rare case of a 47-year-old male presenting solitary neck swelling and hoarseness. After computed tomography and magnetic resonance imaging, we performed complete surgical excision by a transcervical approach under general anesthesia. In the histologic examination, Neurilemmoma was diagnosed. The patient did not complain of any specific complications, showed good prognosis without recurrence or pain up to date.

Warthin tumor, also known as papillary cystadenoma lymphomatosum is a benign neoplasm which occurs mostly in the parotid gland. It is the second most common benign neoplasm of the parotid gland, following pleomorphic adenoma. In occasion, the size of neoplasm grows slowly, and there is no symptom, except swelling. To prevent the recurrence, some surgeons prefer superficial parotidectomy, but the others prefer local resection with minimal surrounding tissue due to its low recurrence rate. We present a case of Warthin tumor of 55-year-old male.

Schwannoma, benign neoplasia derived from schwann cell, is rare tumor, and prevalent in tongue, palate, floor of mouth and buccal mucosa. Thirty-six-year-old male with asymptomatic protrusion of mandible angle was evaluated. We surgically removed the mass and histological examination gave the diagnosis of ancient schwannoma. We report a case of ancient schwannoma in masseter muscle and review of literature.

융모막암은 임신과 연관되어 융모막조직이 비정상적으로 성장하는 종양으로 난소, 고환, 자궁 등 생식기관에 주로 발현 되며 주변장기로의 침범이나 원격전이를 잘하는 특징이 있다. 융모막암이 생식기관이 아닌 장기에서 발생하는 경우는 매우 드물며 대부분 나쁜 예후를 보인다. 저자들은 중년 여성에서 급성 췌장염과 뇌출혈로 발현되고 다발 장기전이를 동반한 췌장 융모막암 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

Pilomatricoma is the second most common benign dermal-subcutaneous tumor of the head and neck region, after epidermoid cyst, originating from the outer sheath cells of the hair follicle. It can be easily treated with surgical excision. However, it is a relatively unknown skin lesion to maxillofacial surgeons. Therefore, we report a case of pilomatricoma occuring inferolateral area of the parotid gland in a 54-year-old man; with a review of the relevant literature.

External root resorption is one of the rare pathological condition of tooth. It is occurred when periodontal ligament or cementum on the root surface are either damaged or denuded. The causes and classifications have been variously described. Because of the various causes and patterns, and absence of sufficient and consistent evidence for treatment, proper diagnosis and treatment plan based on clinician’s experience and close communication with patient is important. This case report represents the rare case of external root resorption and the treatment. The tooth was retained functionally in oral cavity showing good healing state in 2-year follow-up.

Fibrolipoma, a variant of lipoma, is rare in oral cavity, and the pathogenesis is uncertain. The diagnosis and differentiation of fibrolipoma with other clinically similar lesions is very essential for proper treatment planning. We present a case of fibrolipoma on palate of a 28-year-old male.

Oral hyperpigmentation is common in patients older 40 years. But lesions in a newborn are unusual and congenital melanotic macule of the tongue has rarely been reported. A 2-month-old infant with 3 pigmented lesion on the right side of the dorsal tongue was evaluated. They were brown black but not homogeneous in color, smooth, nonblanchable, and nonpalpable, with irregular margins. We recommend excisional biopsy under general anesthesia because of possibility of malignancy, but parents refuse invasive procedure. On a following-up examination of the child at the age of 1 year, the pigmented lesions were unchanged. We report a case of congenital melanotic macules on the tongue and a review of literature about the lesion.

Malignant peripheral nerve sheath tumors (MPNSTs) are defined as malignant tumors arising from peripheral nerves or differentiating along the line of the elements of the nerve sheath. MPNSTs that originate from the brain parenchyma are exceptionally rare and are termed malignant intracerebral nerve sheath tumors. We experienced a case of the epithelioid variant of malignant intracerebral nerve sheath tumor (MINST) occurring in the right frontal lobe of a 50-year-old man. He underwent gross total resection of the tumor. Histologically, the tumor cells had round, polygonal, or ovoid nuclei and moderate amounts of eosinophilic cytoplasm, which was defined as epithelioid cells. The tumor cells were arranged in short cords or nests with vaguely nodular patterns embedded in the myxoid stroma. Regarding mitotic activity, 15 mitotic figures were noted per 10 high-power fields. Immunohistochemically, tumor cells were positive for S-100 protein and synaptophysin, but negative for glial fibrillary acidic protein, HMB-45, EMA, and AE1/ AE3. Furthermore, immunostaining for INI1 was negative. Loss of the tumor-suppressor gene product SMARCB1/ INI1 expression has been recognized in epithelioid MPNST, but not in conventional MPNST. Postoperatively, he underwent radiotherapy and was followed for almost 1 year without recurrence. The present case is the first report of the epithelioid MINST.

Extramedullary plasmacytomas (EMPs) are rare soft tissue malignant neoplasms composed of plasma cells. They are sometimes found in soft tissues. The majority of primary EMPs occur in the head and neck region, especially in the upper respiratory tract and oral cavity. We present a case of a 52-year-old female with an EMP. The patient’s initial chief complaint was swelling of the soft palate. An excisional biopsy was performed under general anesthesia. Final pathologic diagnosis was EMP of the soft palate with partial involvement of the resection margin. In order to exclude the possibility of multiple myeloma, a bone marrow exam with chromosomal study was completed. The patient was also referred to the Department of Radiation Oncology for postoperative radiation therapy (PORT); however, the patient refused to undergo PORT. The patient is currently under close observation for signs and symptoms of recurrence or metastases through regular follow-up visits and imaging studies.

Osteochondroma is one of the most common benign tumors of the bone. Although osteochondroma is rarely seen in the facial region, it was reported that the cases occured in the mandibular region, especially around the condyle. Patients complain about malocclusion, temporomandibular disorders and facial asymmetry. The treatments of these cases include total condylectomy or local resection of the lesion. A 48-year-old man visited our hospital. His chief complaints were pain in the left temporomandibular joint (TMJ) and deviation of mandible during mouth opening. Panoramic radiograph showed an enlarged left condyle. A bony proliferation with benign sign was also observed in the computed tomography. Surgical treatment was done by removing the bony mass. Histologically, biopsy result was an osteochondroma. After surgery, there was reduced pain and normal mouth opening. Deviation of the mandible was also observed. We report a case of osteochondroma on the mandibular condyle and a review of literature about the surgical treatment.

Odontomas are mixed odontogenic tumors in which both the epithelial and mesenchymal components have undergone functional differentiation. Two types of odonotma are histomorphologically recognized: complex and compound. Complex odontomas have little or no morphologic similarity to normal tooth formation, and they commonly found in the posterior mandible. They are typically asymptomatic, and the most common presenting symptom is usually lack of eruption of a permanent tooth. The recommended treatment for an odontoma is conservative surgical excision. No tendency for recurrence has been noted. An eight-year-old girl was presented with swollen mouth floor. Radiographically, there were radiopaque mass on anterior mandible with impacted lower left central incisor. Under midazolam intraoral sedation and N2O-O2 inhalation sedation, the odontomas were surgically removed. The diagnosis was complex odontoma. After follow-up of 28 months period, there was no recurrence. The impacted tooth erupted spontaneously and the space for the erupted tooth was regained orthodontically.

내시경 역행 췌담관조영술 중 경췌중격절개술은 선택적 담관 삽관이 어려운 환자에서 성공률을 높일 수 있는 방법으로 알려져 있다. 최근 후향적 연구에서는 경췌중격절개술이 침형절개도를 이용한 조임근절개술보다 효과적이며 안전한 것으로 보고되었다. 그러나 이번 증례에서 담석췌장염 환자에서 경췌중격절개술 후 벽내 십이지장 혈종 및 십이지장 폐쇄가 발생하였고 이로 인해 저혈량쇼크 등 치명적인 합병증이 발생하였다. 따라서 급성 췌장염이 동반된 환자에서 내시 경역행췌담관조영술 중 경췌 중격절개술을 시행한 후에는 벽내 십이지장 혈종과 같은 합병증 발생 여부를 주의 깊게 관찰할 필요가 있다고 생각된다.

Infected walled-off pancreatic necrosis (WOPN) is dangerous complication of acute pancreatitis. Open necrosectomy and post-operative irrigation of necrotic cavity have been conventional treatment for infected pancreatic necrosis, however, recently minimally invasive techniques such as endoscopic necrosectomy has been regarded as preferred treatment method for infected WOPN. Endoscopic necrosectomy provides a targeted approach with a reduction in the systemic inflammatory response and avoidance of wound complications. Non alcohol related Wernicke encephalopathy is rare disease caused by thiamine deficiency due to intravenous feeding, and presented an encephalopathy, oculomotor dysfunction, gait ataxia. We report herein a case of Wernicke encephalopathy after successful endoscopic necrosectomy for infected WOPN.

췌장의 점액성 낭성 종양(mucinous cystic neoplasm)은 국내 다기관 연구에 의하면 전체 췌장 낭성 종양의 약 25%를 차지하고 있다. 대부분 중년 여성에게 호발하고, 병변은 췌장 체부 및 미부에 위치하며, 점액성 낭선암(mucinous cystadenocarcinoma) 으로 악화될 수 있는데, 크기가 서서히 증가하므로 이의 파열은 매우 드문 합병증이다. 저자들은 72세 남성에서 발생한 췌장 점액성 낭선암의 자발 파열 증례를 문헌 고찰과 함께 보고하는 바이다.

The trauma of incisive canal associated dental implant placement in the anterior maxilla can cause the nasopalatine duct cyst. It is difficult to identify the nasopalatine duct cyst or the location of the incisive canal, only using periapical radiograph or panorama radiograph. So it is necessary to take computed tomography scan for an analysis on the relation between the implant and the incisive canal. This case report present the patient had the nasopalatine duct cyst following the placement of dental implant in the anterior maxilla, and was undergone implant removal and cyst enucleation with bone graft.

We report a rare case of intraosseous epidermoid cyst in mandibular body. A non symptomatic patient without trauma history had a cystic lesion on mandible close to the third molar. The lesion was enucleated while extracting of left lower third molar. The microscopic findings were consistent with an epidermoid cyst. Key words：Epidermoid Cyst, Intraosseous, Mandible

This case report describes the effectiveness of cervical corrective exercises in a patient with cervical radiculopathy (CR) who experienced radicular pain, upper limb paresis, and limited functional activity. A 39-year-old male with cervical radiculopathy performed the cervical corrective exercises for reducing pain. Pain intensity, cervical posture, and active range of motion of cervical intersegmental spine motion were measured baseline, after 4 weeks, and after 8 weeks with self-reported questionnaire and radiographs. After 8 weeks of intervention, the patient demonstrated alleviated radicular symptoms, improved neck posture and active range of flexion and extension of the cervical intersegmental spine. Especially in the angle between the cervical vertebra 6 and 7, the angle was changed from -4.69° to 3.30° during resting position after intervention. The present case indicates that the cervical corrective exercises might be a possible treatment to effectively reduce radicular symptoms, improve neck posture, and active cervical intersegmental motion for patient with CR.