• 제목/요약/키워드: Jaw neoplasm

검색결과 29건 처리시간 0.021초

Leiomyosarcoma of the jaw: case series

  • Choi, Yong-Suk;Almansoori, Akram Abdo;Jung, Tae-Young;Lee, Jae-Il;Kim, Soung Min;Lee, Jong-Ho
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제46권4호
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    • pp.275-281
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    • 2020
  • Objectives: Leiomyosarcoma is a malignant neoplasm that affects smooth muscle tissue and it is very rare in the field of oral and maxillofcial surgery. The purpose of this study was to obtain information on diagnosis of and treatment methods for leiomyosarcoma by retrospectively reviewing of the cases. Patients and Methods: The study included nine patients who were diagnosed with leiomyosarcoma in the Department of Oral and Maxillofacial Surgery at Seoul National University Dental Hospital. The subjects were analyzed with respect to sex, age, clinical features, primary site of disease, treatment method, recurrence, and metastasis. Results: Particular clinical features included pain, edema, mouth-opening limitations, dysesthesia, and enlarged lymph nodes. All cases except one were surgically treated, and recurrence was found in two cases. Four of nine patients were followed up without recurrence and one patient underwent additional surgery due to recurrence. Conclusion: In our case series, notable symptoms included pain, edema, mouth-opening limitations, and dysesthesia; however, it was difficult to label these as specific symptoms of leiomyosarcoma. Considering the aggressive characteristics of the disease and poor prognosis, surgical treatment is necessary with careful consideration of postoperative radiotherapy and chemotherapy.

하악지치 발치 후 우측 교근에 발생한 방선균증의 치험례 (ACTINOMYCOSIS OF THE RIGHT MASSETER FOLLOWING THE EXTRACTION OF LOWER THIRD MOLAR)

  • 이은영;김경원
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제30권3호
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    • pp.296-301
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    • 2008
  • Actinomyces is a part of the normal oral flora, but under certain circumstances it may become pathogenic. Actinomycosis is a chronic granulomatous infective disease caused by microaerophilic Gram-positive bacteria of the genus actinomyces. It can involve almost any system, but principally affects the head and neck. Because the lesions in the submandibular region and the angle of the jaw give the face a swollen, indurated appearance, actinomycosis of mandible can be easily misdiagnosed in its acute or early state of infection. In these cases the disease usually presented as a swelling suggestive of an abscess or mimicking a neoplasm. The yield from standard cultures was poor and repeated sampling and anaerobic culture may be needed to obtain a positive culture. So actinomycosis should always be considered in a differential diagnosis of all infections of the cervicofacial area. Diagnosis of actinomycosis is made based on the histopathology, the clinical presentation and past dental history. We experienced a case of actinomycosis in the masseter muscle and present the case with review of literature.

하악에 발생한 중심성 점액표피양암종: 증례보고 (Central Mucoepidermoid Carcinoma of the Mandible: Case Report)

  • 이충상;김소미;남웅;차인호;김형준
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제33권5호
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    • pp.440-444
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    • 2011
  • Mucoepidermoid carcinoma generally arises from salivary glands and represents 5~10% of all salivary tumors. Arising within the jaws as primary central bony lesions, central mucoepidermoid carcinomas are extremely rare, accounting for only 2~3% of all mucoepidermoid tumors. Central mucoepidermoid carcinoma of the mandible was first reported in 1939 and since then approximately 100 cases have been documented in the literature. Several hypotheses have been proposed to explain the pathogenesis of intraosseous salivary tumors. The most likely source of most intraosseous tumors is odontogenic epithelium. Waldron and Mustoe suggested that central mucoepidermoid carcinoma be included in primary intraosseous carcinoma of the jaw. We report here on a case of central mucoepidermoid carcinoma affecting the mandible and discuss the clinical, radiographic, and histological findings.

하악골에 전이된 위암에 대한 증례 보고 (METASTATIC CANCER OF THE MANDIBLE: A CASE REPORT)

  • 서고은;정지아;송준호;정태영;이수운;박상준
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제32권1호
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    • pp.86-88
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    • 2010
  • Oral metastatic tumors are uncommon and account for about 1% of malignant oral neoplasm. The metastatic lesions are common in breast, lung, kidney and thyroid cancer. About 20% of oral mucosal metastasis is founded before detection of primary lesions. Usually, the metastatic lesions of the oral cavity are involved in the jaw bone, especially mandible more than the oral soft tissues. We report a case diagnosed as the stomach cancer with mandible metastatic lesion looking like TMJ abscess.

악골 골종 2례 : 증례보고 (UNUSUAL PERIPHERAL OSTEOMAS: REPORT OF 2 CASES)

  • 서창호;이두희;김형순;배정수;주현호;원동환;김일현
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제27권3호
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    • pp.276-279
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    • 2001
  • 저자등은 Gardner 증후군과는 연관없이 단독으로 하악의 우각 하연부 내측에서 특이하게 발생한 치밀골 형태의 외골종과 상악의 잔존 치조능상에서 매우 드물게 전체적으로 균일한 해면골 형태의 조직학적 소견을 보이며 발생한 외골종을 치험 하였기에 문헌 고찰과 함께 증례들을 보고하였다.

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아프리카 피그미 고슴도치에서 발생한 편평상피세포암종 (Squamous Cell Carcinoma in an African Pigmy Hedgehog (Atelerix Albiventris))

  • 김완희;김방현;박우람;장동우;정성목;윤정희;김대용;남치주
    • 한국수의병리학회지
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    • 제5권1호
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    • pp.1-4
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    • 2001
  • Squamous cell carcinoma was diagnosed in a 4.5-year-old male African hedgehog (Atelerix albiventris). The patient was referred to Seoul National University, Veterinary Medical Teaching Hospital after 5 days history of left eye exophthalmos and corneal trauma. He had enlarged upper and lower jaw at the left part of the face and endophthalmitis of the left eye. On radiographic examinations, loss of bone density at the left zygomatic arch and sun-burst type periosteal reaction of left mandible with decreased bone density was noted. Histologically, the neoplastic mass consisted of markedly invasive, cords of nests of squamous epithelial cells. Intercellular bridges and keratin pearl formation were also noted.

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Beyond the mouth: Uncovering non-secretory multiple myeloma through oral symptoms

  • Pedro Henrique Chaves Isaias;Fabio Wildson Gurgel Costa;Pedro Henrique Goncalves Holanda Amorim;Raul Anderson Domingues Alves da Silva;Fabrício Bitu Sousa;Karuza Maria Alves Pereira;Ana Paula Negreiros Nunes Alves;Mario Rogério Lima Mota
    • Imaging Science in Dentistry
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    • 제54권2호
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    • pp.211-220
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    • 2024
  • Non-secretory multiple myeloma (NSMM) is a rare cancer of plasma cells characterized by the absence of detectable monoclonal M protein in the blood or urine. A 57-year-old woman presented with mandibular pain but without intraoral swelling. Imaging studies revealed multiple osteolytic lesions in her mandible and pronounced root resorption of the left mandibular second molar. Biopsy results showed atypical plasmacytoid cells positive for anti-kappa, CD138, MUM1, and CD79a antibodies, but negative for anti-lambda and CD20. These results were indicative of a malignant plasma cell neoplasm. No abnormalities were revealed by free light chain assay or by serum or urine protein electrophoresis, leading to a diagnosis of NSMM. The patient began chemotherapy in conjunction with bisphosphonate therapy and achieved remission following treatment. This case underscores the critical role of dentists in the early detection and prevention of NSMM complications, as the disease can initially present in the oral cavity.

DESMOPLASTIC AMELOBLASTOMA의 치험 1례 (A CASE REPORT OF DESMOPLASTIC AMELOBLASTIOMA)

  • 김영미;장현중;김진수;박희경;신홍인;김성국
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제18권1호
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    • pp.144-152
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    • 1996
  • 저자는 desmoplastic ameloblastoma의 문헌 고찰 및 일례의 치험례를 통하여 이 병소의 독특한 임상, 방사선학적 및 병리조직학적 소견을 보고하는 바이다. 1. 임상적 특징으로는 매우 드물게 발생하며, 일반적인 법랑모세포종에 비해 상악 및 악골의 전방부에 호발한다. 2. 방사선학적 특징으로는 경계가 불명확한 방사선 투과상의 병소로, 방사선 불투과상이 혼재되어 나타나 오히려 섬유골화병소와 유사하다. 3. 병리조직학적 특징으로 종양상피도는 압축되어져 모양이 불규칙하고 가장자리세포층은 일반적인 원주세포대신 입방체 또는 편평세포로 이루어져 있고 중심부는 방추형이나 다각형의 세포들이 특징적으로 나타나며 극세포화가 관찰된다. 이들은 교원섬유가 풍부한 결합조직 형성을 동반한다. 4. 재발률은 일반적인 법랑모세포종과 유사할 것으로 사료된다.

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드물게 발생한 얼굴 연조직의 점액섬유종에 대한 증례보고 (A Myxofibroma of the Soft Tissue of Face: A Rare Case Report)

  • 김결희;이동현;정소연;정철훈;조성진;장용준
    • 대한두경부종양학회지
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    • 제40권1호
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    • pp.55-58
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    • 2024
  • Myxoma is a locally invasive neoplasm usually involving the jaw bones, typically occurs between the second and fourth decades. This tumor may comprise 3%-6% of odontogenic tumors. Myxomas of the soft tissue of the face are very rare. We present an unusual case of myxofibroma occurring in a 13-year-old man involving the soft tissue of the face. It congenitally occurred and was a 1 cm sized, ovoid in shape, swelling located on the glabella without any symptoms. An excisional biopsy was performed. A well encapsulated ovoid mass was attached to the corrugator supercilli muscle below the frontalis muscle. It was measured 1.1 × 1 × 0.8 cm and completely excised. Histological examination revealed myxofibroma showing stellate and spinde-shaped cells throughout myxoid ground substance. The unusual features of this case are the site of the tumor, which was localized to the non-tooth bearing area of the mandible and its congenital occurrence history.