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[PMID]:29390315
[Au] Autor:Wang HW; Ma CY; Qin XJ; Zhang CP
[Ad] Endereço:Department of Oral and Maxillofacial-Head and Neck Oncology, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology, Shanghai, China.
[Ti] Título:Management strategy in patient with familial gigantiform cementoma: A case report and analysis of the literature.
[So] Source:Medicine (Baltimore);96(50):e9138, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Familial gigantiform cementoma (FGC) is a rare benign autosomal dominant fibrocemento-osseous lesion generally limited to the facial bones, typically in the anterior portion of the mandible; it is often associated with abnormalities of the long bones and prepubertal pathologic fractures. Owing to the small number of such patients, a uniform treatment criterion has not been established. This paper presents a patient with FGC who was treated in our department, and offers a systematic review of the patients reported in the literature. Our aim was to explore the treatment strategy for patients with FGC. PATIENT CONCERNS: Our patient, a 13-year-old boy, presented with a painless enlargement of the mandible first noted 2 years earlier. It had grown rapidly over the preceding 8 months, affecting both his appearance and ability to chew. DIAGNOSIS: Based on the pathologic, clinical, and radiographic features, FGC was diagnosed. INTERVENTIONS: Mandibuloectomy was performed. The mandibular defect was immediately reconstructed with his right vascularized iliac crest flap. At the same time, a PubMed search was conducted to identify studies reporting on other patients with FGC. OUTCOMES: A 3-dimensional computed tomography (3D-CT) scan demonstrated appropriate height of the new alveolar bone. Follow-up results showed recovery of the patient's appearance and mandibular function. He was free of recurrence at 4-year follow-up. LESSONS: FGC is a rare benign fibrocemento-osseous lesion of the jaws that can cause severe facial deformity. Incomplete removal leads to more rapid growth of the residual lesion. Therefore, extensive resection is a suitable strategy to avoid recurrence. Defects of the facial bones found intraoperatively should be repaired with resort to an appropriate donor site. However, it is important to be aware that patients with FGC always have concomitant abnormalities of skeletal metabolism and structure, as well as a vulnerability to fractures of the long bones of the lower extremity. Therefore, the optimal management strategy should include a review of treatment options for other patients as reported in the literature. An optimal protocol can not only provide sufficient high-quality bone suitable for the reconstruction of bone defects, but also minimize complications and maximize quality of life.
[Mh] Termos MeSH primário: Cementoma/diagnóstico
Cementoma/cirurgia
Neoplasias Maxilomandibulares/diagnóstico
Neoplasias Maxilomandibulares/cirurgia
Neoplasias Mandibulares/diagnóstico
Neoplasias Mandibulares/cirurgia
[Mh] Termos MeSH secundário: Adolescente
Transplante Ósseo
Cementoma/diagnóstico por imagem
Diagnóstico Diferencial
Seres Humanos
Ílio/transplante
Imagem Tridimensional
Neoplasias Maxilomandibulares/diagnóstico por imagem
Masculino
Neoplasias Mandibulares/diagnóstico por imagem
Reconstrução Mandibular
Retalhos Cirúrgicos
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180301
[Lr] Data última revisão:
180301
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009138


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[PMID]:29419674
[Au] Autor:Zhang X; Liu L; Yang X; Wang L; Zhang C; Hu Y
[Ad] Endereço:Department of Oral-maxillofacial Head and Neck Oncology, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology.
[Ti] Título:Expression of TP53 and IL-1α in unicystic ameloblastoma predicts the efficacy of marsupialization treatment.
[So] Source:Medicine (Baltimore);97(6):e9795, 2018 Feb.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:In this study, we evaluated the effects of marsupialization in treating unicystic ameloblastoma (UA) and investigated the relationship between TP53 and interleukin 1 α (IL-1α) expression and the clinical outcome of UA treated with marsupialization.Consecutive patients treated with marsupialization and curettage at Shanghai Ninth People's Hospital were included. According to the unified standard, 48 patients were included in this study. Of these, 20 showed a good response, 10 a partial response, and 18 no response, based on the outcome of the marsupialization procedure. The expression of proteins TP53 and IL-1α was detected with immunohistochemistry (IHC). The clinical and pathological characteristics of the patients were analyzed.Analysis of the clinical and pathological characteristics showed that the effects of marsupialization treatment were significantly associated with lesion location (P < .001) and tumor diameter (P = .01). IHC showed that TP53 expression was significantly higher in the good-response group than in the partial- or no-response group (P = .02), and IL-1α expression was significantly higher in the good-response group than in the partial- and no-response groups (P = .03).Marsupialization is an effective preliminary procedure for treating UA before curettage and peripheral ostectomy. The expression of the TP53 and IL-1α proteins correlates directly with the outcome of UA treated with marsupialization.
[Mh] Termos MeSH primário: Ameloblastoma
Descompressão Cirúrgica
Interleucina-1alfa
Neoplasias Mandibulares
Recidiva Local de Neoplasia
Proteína Supressora de Tumor p53
[Mh] Termos MeSH secundário: Adulto
Ameloblastoma/metabolismo
Ameloblastoma/patologia
Ameloblastoma/cirurgia
China
Curetagem/efeitos adversos
Curetagem/métodos
Descompressão Cirúrgica/efeitos adversos
Descompressão Cirúrgica/métodos
Feminino
Perfilação da Expressão Gênica/métodos
Seres Humanos
Imuno-Histoquímica
Interleucina-1alfa/genética
Interleucina-1alfa/metabolismo
Masculino
Neoplasias Mandibulares/metabolismo
Neoplasias Mandibulares/patologia
Neoplasias Mandibulares/cirurgia
Osteotomia Mandibular/efeitos adversos
Osteotomia Mandibular/métodos
Recidiva Local de Neoplasia/diagnóstico
Recidiva Local de Neoplasia/metabolismo
Prognóstico
Estudos Retrospectivos
Estatística como Assunto
Proteína Supressora de Tumor p53/genética
Proteína Supressora de Tumor p53/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (IL1A protein, human); 0 (Interleukin-1alpha); 0 (TP53 protein, human); 0 (Tumor Suppressor Protein p53)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180216
[Lr] Data última revisão:
180216
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180209
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009795


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[PMID]:29369168
[Au] Autor:Md Radzi AB; Tan SS
[Ad] Endereço:Department of Medicine, Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh Campus, Jalan Hospital, Sungai Buloh.
[Ti] Título:A case report of metastatic hepatocellular carcinoma in the mandible and coracoid process: A rare presentation.
[So] Source:Medicine (Baltimore);97(4):e8884, 2018 Jan.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: We report a rare case of hepatocellular carcinoma (HCC) with metastases to the mandible and coracoid process of scapula without evidence of lung involvement. PATIENTS CONCERNS: The patient was diagnosed with HCC, presented 5 months later with right lower tooth pain, swelling over the right mandible area and right shoulder pain. DIAGNOSES: Histopathological examination of mandible showed findings suggestive of metastatic HCC. Magnetic resonance imaging (MRI) of the right shoulder revealed findings of irregular enhancing lesion at the right coracoid process causing erosion of the coracoid process. INTERVENTIONS: Patient was subsequently referred for palliative medicine care. OUTCOMES: He received adequate analgesia. LESSONS: Oral cavity and scapula metastases from HCC are very rare. Most oral metastases are associated with lung metastases, and they possibly occur by hematogenous route. In our case, the possible pathway of metastasis is an anastomotic network of paravertebral veins that bypasses the pulmonary, inferior caval, and portal venous circulations.
[Mh] Termos MeSH primário: Neoplasias Ósseas/secundário
Carcinoma Hepatocelular/secundário
Processo Coracoide/patologia
Neoplasias Hepáticas/patologia
Neoplasias Mandibulares/secundário
[Mh] Termos MeSH secundário: Seres Humanos
Masculino
Meia-Idade
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180208
[Lr] Data última revisão:
180208
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180126
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008884


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[PMID]:29197363
[Au] Autor:Wang P; Li YJ; Zhang SB; Cheng QL; Zhang Q; He LS
[Ad] Endereço:Department of Ophthalmology, Tangdu Hospital of Fourth Military Medical University, Xi'an, Shaanxi, China.
[Ti] Título:Metastatic retinoblastoma of the parotid and submandibular glands: a rare case report.
[So] Source:BMC Ophthalmol;17(1):229, 2017 Dec 02.
[Is] ISSN:1471-2415
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Retinoblastoma is the most common intraocular malignancy occurring in children. It can metastasize to the regional lymph nodes, central nervous system and distant organs usually the bones and bone marrow and very rarely to the soft tissue. Here, we report a case of unilateral retinoblastoma in a 4-year-old girl accompanied by a large metastasis of the parotid and submandibular glands that developed about 6 months previously and gradually increased in size 5 months after enucleation of the left eye. CASE PRESENTATION: A 4-year-old girl with a history of unilateral retinoblastoma presented with a large, painful and worsening mass (about 20 × 23 cm) of the left side of the neck. Following surgery, the orbital tumour was completely resected, and the large tumour invasion range in the left side of the neck was not resected completely. Histopathological examination revealed retinoblastoma of the orbit and the parotid and submandibular glands. After chemotherapy and additional local radiotherapy on the parotid and submandibular glands, the tumour was inactive and stable. CONCLUSIONS: Delayed detection and inappropriate management contribute to poor outcomes. Fundus examinations, education regarding the early signs of RB, and optimization of the therapeutic strategy for RB may play important roles in ocular health.
[Mh] Termos MeSH primário: Neoplasias Mandibulares/secundário
Neoplasias Orbitárias/patologia
Neoplasias Parotídeas/secundário
Neoplasias da Retina/patologia
Retinoblastoma/patologia
[Mh] Termos MeSH secundário: Pré-Escolar
Feminino
Seres Humanos
Glândula Submandibular/patologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171220
[Lr] Data última revisão:
171220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171204
[St] Status:MEDLINE
[do] DOI:10.1186/s12886-017-0627-8


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[PMID]:29058856
[Au] Autor:Jaishankar HP; Patil K; Mahima VG; Keshari D
[Ti] Título:Giant Cell Tumor of Mandibular Condyle: A Rarity.
[So] Source:J Calif Dent Assoc;45(2):81-4, 2017 02.
[Is] ISSN:1043-2256
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Tumor de Células Gigantes do Osso/diagnóstico
Côndilo Mandibular/patologia
Neoplasias Mandibulares/diagnóstico
Neoplasias Mandibulares/cirurgia
[Mh] Termos MeSH secundário: Adulto
Diagnóstico Diferencial
Tumor de Células Gigantes do Osso/patologia
Tumor de Células Gigantes do Osso/cirurgia
Seres Humanos
Masculino
Neoplasias Mandibulares/patologia
Radiografia Panorâmica
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171113
[Lr] Data última revisão:
171113
[Sb] Subgrupo de revista:D
[Da] Data de entrada para processamento:171024
[St] Status:MEDLINE


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Mendonça, Elismauro Francisco de
Texto completo SciELO Brasil
[PMID]:28877285
[Au] Autor:Yamamoto-Silva FP; Silva BSF; Batista AC; Mendonça EF; Pinto-Júnior DDS; Estrela C
[Ad] Endereço:Universidade Federal de Goiás, Departamento de Ciências Estomatológicas, Goiânia, GO, Brasil.
[Ti] Título:Chondroblastic osteosarcoma mimicking periapical abscess.
[So] Source:J Appl Oral Sci;25(4):455-461, 2017 Jul-Aug.
[Is] ISSN:1678-7765
[Cp] País de publicação:Brazil
[La] Idioma:eng
[Ab] Resumo:Case report: The present report describes a case of chondroblastic osteosarcoma in the periapical region of teeth #29, #30, and #31 of an 18-year-old male. Clinical history showed self-reported discomfort in the right posterior gingiva for over a month. Physical examination showed a small expansion and redness of the right mandibular buccal and lingual cortical plates, but no signs of pain or inflammation were observed. All the teeth responded positively to pulp sensibility. Periapical and panoramic radiographs showed slight periapical radiolucency in the roots of teeth #29 and #30, clear periodontal ligament space widening, and evident loss of lamina dura. Incisional biopsy was performed, and based on microscopic findings the diagnosis of chondroblastic osteosarcoma was confirmed. Conclusions: Non-endodontic diseases associated with tooth root apex, such as chondroblastic osteosarcoma, should be included in differential diagnosis of jaw lesions that resemble periapical abscess.
[Mh] Termos MeSH primário: Condrócitos/patologia
Neoplasias Mandibulares/patologia
Osteossarcoma/patologia
Abscesso Periapical/patologia
[Mh] Termos MeSH secundário: Adolescente
Biópsia
Tomografia Computadorizada de Feixe Cônico
Diagnóstico Diferencial
Seres Humanos
Imuno-Histoquímica
Masculino
Neoplasias Mandibulares/diagnóstico por imagem
Osteossarcoma/diagnóstico por imagem
Abscesso Periapical/diagnóstico por imagem
Radiografia Panorâmica
[Pt] Tipo de publicação:CASE REPORTS
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171006
[Lr] Data última revisão:
171006
[Sb] Subgrupo de revista:D; IM
[Da] Data de entrada para processamento:170907
[St] Status:MEDLINE


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[PMID]:28697347
[Au] Autor:Salman SO; Fernandes RP; Rawal SR
[Ad] Endereço:Associate Program Director and Assistant Professor, Department of Oral and Maxillofacial Surgery, University of Florida-Jacksonville College of Medicine, Jacksonville, FL. Electronic address: Salam.Salman@jax.ufl.edu.
[Ti] Título:Immediate Reconstruction and Dental Rehabilitation of Segmental Mandibular Defects: Description of a Novel Technique.
[So] Source:J Oral Maxillofac Surg;75(10):2270.e1-2270.e8, 2017 Oct.
[Is] ISSN:1531-5053
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The aim of this report is to present a new technique using current technologic advances for immediate reconstruction and dental rehabilitation of segmental mandibular defects with a screw-retained prosthesis. One case is reviewed and a detailed review of surgical and prosthetic techniques used is presented.
[Mh] Termos MeSH primário: Implantação Dentária Endo-Óssea/métodos
Neoplasias Mandibulares/cirurgia
Tumores Odontogênicos/cirurgia
Procedimentos Cirúrgicos Reconstrutivos/métodos
[Mh] Termos MeSH secundário: Seres Humanos
Masculino
Fatores de Tempo
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171012
[Lr] Data última revisão:
171012
[Sb] Subgrupo de revista:AIM; D; IM
[Da] Data de entrada para processamento:170712
[St] Status:MEDLINE


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[PMID]:28670912
[Au] Autor:Sinha P; Yuen SN; Chernock RD; Haughey BH
[Ad] Endereço:1 Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
[Ti] Título:Mandibular Lytic Lesion in Familial Paraganglioma Syndrome Type I: A Clinical Conundrum.
[So] Source:Ann Otol Rhinol Laryngol;126(8):615-618, 2017 Aug.
[Is] ISSN:1943-572X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: The entity of primary mandibular paraganglioma (PGL) is not well accepted within the head and neck. Mandibular PGLs hitherto reported in literature are malignant metastatic lesions, mostly from a pheochromocytoma. METHODS: We report a case of mandibular lytic lesion in a young female with multifocal PGLs but no family history of PGLs. We also performed a literature search to identify published cases of mandibular PGL. RESULTS: Lack of established criteria for malignancy in a PGL made diagnosis and treatment challenging. Testing was negative for a pheochromocytoma and positive for mutation of succinate dehydrogenase gene encoding subunit D (SDHD), thus rendering a diagnosis of familial PGL syndrome type I. Due to the absence of prior published reports of nonmalignant, primary mandibular PGL, patient was treated with surgery and postoperative radiotherapy. Our literature search revealed 4 published cases of mandibular PGL, all of which had an osteoblastic appearance and were malignant. CONCLUSIONS: Isolated mandibular PGL does not always indicate a malignant metastatic lesion. Genetic testing is recommended in patients with early onset of PGL and/or multifocality even without a positive family history. Surgical resection alone with surveillance can be offered for such isolated lesions in the presence of familial PGL syndrome type I.
[Mh] Termos MeSH primário: Neoplasias Mandibulares/diagnóstico por imagem
Síndromes Neoplásicas Hereditárias/diagnóstico por imagem
Paraganglioma/diagnóstico por imagem
[Mh] Termos MeSH secundário: Adulto
Transplante Ósseo
Tumor do Corpo Carotídeo
Feminino
Tumor do Glomo Jugular
Seres Humanos
Ílio/transplante
Imagem Tridimensional
Neoplasias Mandibulares/genética
Neoplasias Mandibulares/patologia
Neoplasias Mandibulares/cirurgia
Neoplasias Primárias Múltiplas
Síndromes Neoplásicas Hereditárias/genética
Paraganglioma/genética
Paraganglioma/patologia
Paraganglioma/cirurgia
Succinato Desidrogenase/genética
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (SDHD protein, human); EC 1.3.99.1 (Succinate Dehydrogenase)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170821
[Lr] Data última revisão:
170821
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170704
[St] Status:MEDLINE
[do] DOI:10.1177/0003489417717502


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[PMID]:28654767
[Au] Autor:Cervenka PD; Perez L; Perez DE; Jones B
[Ad] Endereço:Second-Year Resident, National Capital Consortium Oral and Maxillofacial Surgery Residency Program, Walter Reed National Military Medical Center, Bethesda, MD. Electronic address: peter.d.cervenka.mil@mail.mil.
[Ti] Título:Melanoma Metastasis to the Mandible-Case Report and Comprehensive Literature Review.
[So] Source:J Oral Maxillofac Surg;75(9):2025.e1-2025.e12, 2017 Sep.
[Is] ISSN:1531-5053
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:With the incidence of melanoma increasing yearly, there is a need for heightened awareness of its metastatic potential and for screening with appropriate referral for identification of pre-metastatic lesions. Melanoma has a 16- to 25-month period to metastasize from a localized disease to one with a median survival no longer than 12 months once metastasis occurs. Nearly one third of oral metastases are found to be the first indication of occult malignancy from a distant site. This report describes the case of a 54-year-old woman with a longstanding undiagnosed acral lentiginous melanoma with metastasis to the maxillofacial region. She underwent resection and died 7 months later. The authors analyzed case reports and the current literature for biological mechanisms of metastasis, risk factors, clinical presentation, classifications, staging, treatment modalities, prognosis, and current therapy modalities.
[Mh] Termos MeSH primário: Neoplasias Mandibulares/secundário
Melanoma/secundário
Neoplasias Cutâneas/patologia
[Mh] Termos MeSH secundário: Diagnóstico Diferencial
Evolução Fatal
Feminino
Seres Humanos
Imagem Tridimensional
Neoplasias Mandibulares/diagnóstico por imagem
Neoplasias Mandibulares/terapia
Melanoma/diagnóstico por imagem
Melanoma/terapia
Meia-Idade
Radiografia Panorâmica
Neoplasias Cutâneas/diagnóstico por imagem
Neoplasias Cutâneas/terapia
Polegar/patologia
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170920
[Lr] Data última revisão:
170920
[Sb] Subgrupo de revista:AIM; D; IM
[Da] Data de entrada para processamento:170628
[St] Status:MEDLINE


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[PMID]:28650783
[Au] Autor:Kim SH; Oh MS; Seo YS; Kim JY; Nam SH; Lim SM
[Ti] Título:Conservative Treatment of Multiple Keratocystic Odontogenic Tumors in a Young Patient with Nevoid Basal Cell Carcinoma Syndrome by Decompression: A 7-year Follow-up Study.
[So] Source:J Clin Pediatr Dent;41(4):300-304, 2017.
[Is] ISSN:1053-4628
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Multiple keratocystic odontogenic tumors (KCOT) occurred in a young child is challenging problem in the field of pediatric dentistry, and might have been related to nevoid basal cell carcinoma syndrome (NBCCS). Because of high recurrence rate of KCOTs, complete surgical resection is generally accepted as definitive treatment. However, complete surgical resection could induce negative effect on the development of permanent teeth and growth of jaw. Herein, we reported successful treatment case of young KCOT patient with NBCCS. Although multiple KCOTs occurred continually, the majority of the lesions healed well by decompression and important anatomical structures and permanent teeth were successfully preserved. The purpose of this paper is to report more conservative treatment of multiple keratocystic odontogenic tumors (KCOTs) by repeated decompressions with later peripheral ostectomy during a 7-year follow-up.
[Mh] Termos MeSH primário: Síndrome do Nevo Basocelular/cirurgia
Descompressão Cirúrgica/métodos
Neoplasias Mandibulares/cirurgia
Neoplasias Primárias Múltiplas/cirurgia
Tumores Odontogênicos/cirurgia
[Mh] Termos MeSH secundário: Síndrome do Nevo Basocelular/patologia
Criança
Feminino
Seres Humanos
Neoplasias Mandibulares/patologia
Recidiva Local de Neoplasia/patologia
Recidiva Local de Neoplasia/cirurgia
Neoplasias Primárias Múltiplas/patologia
Tumores Odontogênicos/patologia
Osteotomia
Radiografia Panorâmica
Reoperação
Extração Dentária
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170914
[Lr] Data última revisão:
170914
[Sb] Subgrupo de revista:D
[Da] Data de entrada para processamento:170627
[St] Status:MEDLINE
[do] DOI:10.17796/1053-4628-41.4.300



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