A retrospective study of 30 basal cell adenomas of the salivary gland in a Brazilian population and literature review.

PURPOSE: The present study aimed to provide the clinicopathological data of Brazilian patients with basal cell adenoma (BCA). METHODS: Records of BCA cases were retrospectively gathered from the Brazilian National Cancer Institute database between 1996 and 2006. All cases were histopathologically reviewed, and the clinicopathological data were collected from the patients' medical files. In addition, an English literature review about this tumor is also presented. RESULTS: Of 1127 salivary gland tumors identified, 30 were BCAs (2.7%). Women were more affected than men (70.0% vs. 30.0%), and the majority (60.0%) were elderly (> 65 years old). The parotid gland was the most frequent location affected (93.3%), followed by the upper lip (3.3%) and submandibular gland (3.3%). Fine-needle aspiration was the main procedure applied to establish a preoperative diagnosis of tumor; however, the results were not always consistent. Histopathologically, the trabecular pattern was the most common type seen (50.0%) among our BCA samples. Most patients underwent superficial or partial parotidectomy. Frey's syndrome was reported only in one case during the follow-up. No recurrence was noted in the present series. The literature review revealed a total of 213 reported cases of BCA in the period investigated. CONCLUSIONS: This is the first case series of BCA reported in Brazil. As occurred in other previously reported series, the clinicopathological data of BCAs are similar and confirm that this type of tumor is rare, develops predominantly in the parotid gland, frequently affects older women, has an indolent behavior, and the affected patients have an excellent prognosis.

Mantle cell lymphoma: involvement of nodal and extranodal sites in the head and neck, with multifocal oral lesions.

Mantle cell lymphoma (MCL) is a malignant B-cell neoplasm, which comprises monomorphic and small- to medium-sized mantle zone-derived lymphoid cells. It is characterized by chromosomal translocation t(11;14)(q13;q32) and CCND1 truncation, resulting in cell cycle deregulation. It is an aggressive type of non-Hodgkin lymphoma with a propensity to present with extranodal involvement. This study shows the case of an 80-year-old Caucasian male who complained of a 2-month progressive swelling on the right side of his face. The magnetic resonance imaging exam showed multifocal involvement of the head and neck, including oral manifestations, bilateral parotid glands, palate, tongue, and floor of the mouth. An incisional biopsy of the tumor mass was performed. The morphological and immunophenotypic findings were consistent with the diagnosis of MCL. The patient died 4 months later, without any chance of undergoing a therapeutic approach. Although MCL is a rare condition, it should be subjected to a differential diagnosis when affecting the maxillofacial area. Imaging exams and both immunohistochemical and morphological analyses are needed to reach the correct diagnosis. Here, we present an unusual MCL with multifocal involvement of the head and neck.

Mantle cell lymphoma: involvement of nodal and extranodal sites in the head and neck, with multifocal oral lesions

Mantle cell lymphoma (MCL) is a malignant B-cell neoplasm, which comprises monomorphic and small- to medium-sized mantle zone-derived lymphoid cells. It is characterized by chromosomal translocation t(11;14)(q13;q32) and CCND1 truncation, resulting in cell cycle deregulation. It is an aggressive type of non-Hodgkin lymphoma with a propensity to present with extranodal involvement. This study shows the case of an 80-year-old Caucasian male who complained of a 2-month progressive swelling on the right side of his face. The magnetic resonance imaging exam showed multifocal involvement of the head and neck, including oral manifestations, bilateral parotid glands, palate, tongue, and floor of the mouth. An incisional biopsy of the tumor mass was performed. The morphological and immunophenotypic findings were consistent with the diagnosis of MCL. The patient died 4 months later, without any chance of undergoing a therapeutic approach. Although MCL is a rare condition, it should be subjected to a differential diagnosis when affecting the maxillofacial area. Imaging exams and both immunohistochemical and morphological analyses are needed to reach the correct diagnosis. Here, we present an unusual MCL with multifocal involvement of the head and neck.

Orthokeratinized odontogenic cysts presenting as a periapical lesion: report of a case and literature review.

INTRODUCTION: Inflammatory cysts, granulomas, abscesses, and fibrous scars represent most periapical radiolucencies. However, other less common lesions, such as orthokeratinized odontogenic cysts (OOCs), can be found at this region, and they deserve to be discussed because the prognosis for an OOC is different from that expected for the ordinary inflammatory periapical diseases. METHODS: An interesting case of OOC associated with a nonvital tooth in a 40-year-old woman is described. After a previous clinical diagnosis of a radicular cyst, the tooth was extracted, and the lesion was enucleated and submitted to microscopy examination. RESULTS: Because of the detection of an orthokeratinized epithelium lining, a diagnosis of OOC was concluded. After 2 years of periodic follow-up, no signs of recurrence were detected. CONCLUSIONS: The presence of keratin in radicular lesions must be carefully evaluated to eliminate the diagnosis of lesions with more aggressive behavior, such as an OOC or even a keratocystic odontogenic tumor. Hence, histopathologic examination is mandatory to confirm the type of lesion and to differentiate other pathologic conditions, therefore establishing patients' prognoses precisely.

Caracterização da displasia fibrosa em imagens de tomografia computadorizada helicoidal empregando a análise da lacunaridade / Characterization of fibrous dysplasia in helical computed tomography images employing the analysis of lacunarity

A displasia fibrosa é uma alteração de desenvolvimento caracterizada pela substituição do osso normal por tecido conjuntivo denso e trabéculas ósseas imaturas, geralmente encontrada em adolescentes e adultos jovens. Uma alteração genética que envolve a proteína Gs-alfa parece ser a base do processo. A exata incidência e prevalência são difíceis de estabelecer, mas as lesões representam cerca de 5% a 7% dos tumores ósseos benignos. Nos ossos craniofaciais tem predileção pela maxila, podendo causar deformidade grave e assimetria, afetando igualmente ambos os sexos. Radiograficamente, pode apresentar diferentes padrões de imagem dependendo do grau de mineralização e maturação da lesão. .A avaliação da displasia fibrosa nas radiografias da região craniofacial pode ser difícil por causa das aparências variáveis e das estruturas que se sobrepõem, de modo que a tomografia computadorizada é um recurso relevante para o seu correto diagnóstico e planejamento de tratamento. O objetivo deste estudo foi caracterizar a displasia fibrosa através da análise da lacunaridade, um método multiescala para descrever padrões de dispersão espacial. Foram avaliados 10 pacientes (6 homens e 4 mulheres) comprometendo a maxila em sua grande maioria.

Para a análise da lacunaridade, empregou-se cortes tomográficos axiais e coronais e, posteriormente, selecionou-se as regiões de interesse das áreas displásicas e do osso normal contralateral por meio do software MATLAB®. Após testes e análises estatísticas, concluiu-se que os cortes coronais, com ampliação de 3x do seu tamanho original, mostraram superioridade em relação aos axiais e, que a lacunaridade foi menor nas áreas da região displásica em relação ao osso normal, ou seja, a primeira apresentou uma maior homogeneidade de textura que a segunda. Mediante isso, pela técnica da validação cruzada leave-one-out é possível separar os grupos com uma alta acurácia (94,75%) concluindo-se que a lacunaridade é um método de análise de imagens contributivo na caracterização da displasia fibrosa.

Fibrous dysplasia is an alteration of development characterized by replacing normal bone for dense connective tissue and immature trabecular bones, typically found in teenagers and young adults. Genetic modification which involves alpha-Gs protein appears to be the basis of the process. The exact incidence and prevalence are difficult to be established, but injuries represent about 5% to 7% of benign bone tumors. On the craniofacial bones, the tumors have a predilection for the maxilla and often can cause severe deformity and asymmetry affecting both sexes equally. Radiographically, it may have different patterns depending on the image degree of mineralization and maturation of the lesion. The evaluation of radiographs of fibrous dysplasia in the craniofacial region can be difficult because of the different appearances and structures that overlaps, however, CT is an important resource for proper diagnosis and treatment planning.

The aim of this study was to characterize the fibrous dysplasia by analyzing the lacunarity which is a multiscale method to describe patterns of spatial dispersion. We evaluated 10 patients (6 males and 4 females) and the maxillary was the most affected area. To the lacunarity analysis, we used an axial and coronal view and then were selected the regions of interest in the areas of dysplastic and contralateral normal bone by means of MATLAB® software. After tests and statistical analysis can be conclued that the coronal magnification 3x its original size showed superiority compared to thrust, and that the lacunarity was lower in the areas of dysplastic region in relation to normal bone, namely the first presented a more uniform texture than the second. Through this, the technique of cross-validation "leave-one-out" is possible to separate the groups with a high accuracy (94.75%) concluding that the lacunarity is a method of image analysis to characterize the contributory fibrous dysplasia.

Anemia falciforme: aspectos clínicos, laboratoriais e radiográficos de interesse para o cirurgião dentista / Sickle cell anemia: clinical, laboratorial and radiographic aspects of interest to the dentist

A anemia de células falciformes é uma hemoglobinopatia que representa um dos mais graves distúrbios genéticos da síntese de hemoglobina. O fenômeno da falcização dos eritrócitos, observado na anemia falciforme, é responsável por quadros clínicos de isquemia e de infarto tecidual, gerando sinais e sintomas característicos da doença, compromentendo vários órgãos e áreas do organismo, inclusive a região dento-maxilo-facial. Os autores, enfocando uma abordagem multiciplinar, fazem uma revisão da literatura da doença das células falciformes, ressaltando seus aspectos clínicos, laboratoriais e radiográficos de interesse para o cirurgião-dentista.