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1.
Scand J Rheumatol ; 52(2): 208-216, 2023 03.
Artigo em Inglês | MEDLINE | ID: mdl-35049421

RESUMO

OBJECTIVES: The aims of the study were to investigate the prevalence of impaired sensation after minor salivary gland biopsy (MSGB) in two Swedish centres [Karolinska University Hospital (KUH) and Skåne University Hospital (SUH)] and to assess its impact on quality of life (QoL) and associated risk factors. METHOD: A questionnaire including questions regarding the presence of impaired sensation, impact on QoL, and impact on everyday life was sent to patients who had undergone MSGB between 2007 and 2016, and their medical notes were scrutinized. RESULTS: The study included 630 patients (505 from KUH and 125 from SUH). In KUH the biopsies were performed by rheumatologists and in SUH by dentists or oral and maxillofacial surgeons (OMSs). Long-standing, probably permanent, impaired sensation after MSGB was reported by 21% of patients, and was associated with lower age and absence of anti-SSA antibodies. Patients with long-standing impaired sensation reported the inconvenience (1-10) of impaired sensation as 4.0 (2.0-7.0) [median (interquartile range)], and 32% reported an influence on their QoL, the reported influence (1-10) on everyday life being 3.0 (1.0-5.0). When comparing the outcomes from KUH and SUH, patients from SUH reported a significantly lower frequency of long-standing impaired sensation (14% vs 23%; p = 0.02). CONCLUSION: A high frequency of long-standing impaired sensation after MSGB was found among patients who had undergone MSGB, although it had a low impact on everyday life. The complication frequency was less pronounced when a dentist or an OMS had performed the biopsy.


Assuntos
Glândulas Salivares Menores , Síndrome de Sjogren , Humanos , Glândulas Salivares Menores/patologia , Síndrome de Sjogren/patologia , Estudos Retrospectivos , Qualidade de Vida , Suécia/epidemiologia , Hipestesia/patologia , Biópsia/efeitos adversos
2.
Cytometry A ; 93(10): 1051-1059, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-30089197

RESUMO

Visual grading of chromogenically stained immunohistochemical (IHC) samples is subjective, time consuming, and predisposed to considerable inter- and intra-observer variations. The open-source digital analysis software, CellProfiler has been extensively used for fluorescently stained cells/tissues; however, chromogenic IHC staining is routinely used in both pathological and research diagnostics. The current investigation aimed to compare CellProfiler quantitative chromogenic IHC analyses against the gold standard manual counting. Oral mucosal biopsies from patients with chronic graft-versus-host disease were stained for CD4. Digitized images were manually counted and subjected to image analysis in CellProfiler. Inter-observer and inter-platform agreements were assessed by scatterplots with linear regression and Bland-Altman plots. Validation comparisons between the manual counters demonstrated strong intra-observer concordance (r2 = 0.979), particularly when cell numbers were less than 100. Scatterplots and Bland-Altman plots demonstrated strong agreement between the manual counters and CellProfiler, with the number of positively stained cells robustly correlating (r2 = 0.938). Furthermore, CellProfiler allowed the determination of multiple variables simultaneously, such as area stained and masking to remove any nonstained tissue and white gaps, which also demonstrated reliable agreement (r2 = >0.9). CellProfiler demonstrated versatility with the ability to assess large numbers of images and allowed additional parameters to be quantified. CellProfiler allowed rapid high processing capacity of chromogenically stained chronic inflammatory tissue that was reliable, accurate, and reproducible and highlights potential applications in research diagnostics.


Assuntos
Compostos Cromogênicos/química , Imuno-Histoquímica/métodos , Biomarcadores Tumorais/metabolismo , Humanos , Processamento de Imagem Assistida por Computador/métodos , Software
3.
Oral Dis ; 24(6): 1001-1011, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29500871

RESUMO

OBJECTIVE: To determine the levels of antithyroid antibodies and thyroid hormones in the sera of patients with oral lichen planus (OLP), and to quantify the expression of thyroid proteins in OLP lesions. SUBJECTS AND METHODS: Venous blood samples were drawn from 110 patients with OLP who had no history of thyroid disease or levothyroxine supplementation (OLP+/LT4 -). A random population sample of 657 healthy subjects was used as the control group. Two additional groups were used as comparators. Immunohistochemical and qPCR analyses were performed on tissue specimens collected from the patients with OLP and thyroid disease and healthy subjects. RESULTS: No association was found between the presence of antithyroid antibodies and OLP. More patients in the OLP+/LT4 - group showed high levels of thyroid-stimulating hormone and low levels of free thyroxine than were seen in the control group. Thyroid-stimulating hormone receptor was more highly expressed in the OLP lesions of patients with thyroid disease than in the healthy oral mucosa. CONCLUSIONS: A significant number of patients with OLP who are not previously diagnosed with thyroid disease have thyroid parameters that are compatible with hypothyroidism. The expression of thyroid-stimulating hormone receptor in OLP lesions suggests that mechanisms related to autoimmune thyroid disease are involved in the aetiology of OLP.


Assuntos
Líquen Plano Bucal/sangue , Adulto , Idoso , Idoso de 80 Anos ou mais , Autoanticorpos/sangue , Doenças Autoimunes/imunologia , Estudos de Casos e Controles , Feminino , Humanos , Líquen Plano Bucal/imunologia , Líquen Plano Bucal/metabolismo , Masculino , Pessoa de Meia-Idade , Mucosa Bucal/metabolismo , Receptores da Tireotropina/imunologia , Receptores da Tireotropina/metabolismo , Doenças da Glândula Tireoide/imunologia , Tireotropina/sangue , Tiroxina/sangue
4.
Clin Oral Implants Res ; 24(10): 1088-93, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22697486

RESUMO

PURPOSE: To estimate and compare the costs of maxillary sinus augmentation performed with autologous bone graft either from the iliac crest or from local bone harvested from the mandibula. To evaluate post-operative health-related quality-of-life parameters for patients subjected to sinus augmentation and iliac bone surgery. MATERIAL AND METHODS: The hospital records of 14 patients subjected to sinus augmentation with iliac autograft, and 14 patients treated with local autograft, were analysed with regard to costs related to surgery, hospitalization and sick leave. Post-operative health parameters were assessed with a questionnaire. RESULTS: Mean hospital costs, administration excluded, for sinus augmentation with iliac autograft was €3447. Policlinic treatment alternatives e.g. local bone autograft with or without bone substitutes, rendered costs of approximately 42% thereof. The loss of production for a worker was 41% of the total cost (€9285). With regard to health-related quality-of-life and post-operative morbidity, most of the patients had recovered 14 days after the iliac graft surgery. CONCLUSION: The cost for a sinus augmentation with iliac surgery exceeds that of a policlinic procedure manifold. Provided that a policlinic operation with local bone, with or without bone substitute, renders an adequate end result, the economic gain would be substantial and post-operative morbidity would be greatly reduced.


Assuntos
Transplante Ósseo/economia , Transplante Ósseo/métodos , Custos Hospitalares/estatística & dados numéricos , Ílio/transplante , Levantamento do Assoalho do Seio Maxilar/economia , Levantamento do Assoalho do Seio Maxilar/métodos , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Autoenxertos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Complicações Pós-Operatórias/epidemiologia , Qualidade de Vida , Licença Médica/economia , Licença Médica/estatística & dados numéricos , Inquéritos e Questionários
5.
Heliyon ; 9(4): e15517, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-37128306

RESUMO

The oral cavity commonly displays mucosal lichenoid lesions and salivary gland dysfunction, which are considered different chronic Graft-versus-Host Disease (cGVHD) pathophysiology's. However, diagnostics of salivary gland (sg-)cGVHD are limited. The objectives of the current study are to evaluate the minor salivary gland (MSG) histo-immunopathological profiles post allogenic hematopoietic cell transplantation based on sg-cGVHD criteria. Design: Histopathology was characterized according to two published grading strategies. Firstly, the National Institute of Health (NIH) assessed peri-ductal/acinar infiltration, exocytosis, damage, and fibrosis, and a points-based grading scheme was established (0-16 points, Grade (G) 0 to IV). Second, a modified Sjögren's Syndrome focus-score with parenchymal damage was also adapted, (0-10 points, Score 0 to 2). 146 MSG biopsies from 79 patients were compared, using the histopathological specific criteria for sg-cGVHD pathology. Quantitative immunohistochemistry for T-cells (CD4, CD8), B-cells (CD19, CD20), monocytic cells (CD68) and dendritic cells (CD1a) were also assessed. Results: The large-scale cohort validated the use of both grading schemes. GIII-GIV and score 2 signified a histopathological diagnosis of "likely" sg-cGVHD. Immunopathological severity was associated with increased T-cells (CD4 and CD8) and monocytic (CD68) infiltrate, with minimal involvement of B-cells (CD19 and CD20), and Langerhans cells (CD1a). Conclusions: Both schemes were verified as being suitable for histological grading to improve assessment and diagnosis of sg-cGVHD. The NIH cGVHD grading appears to be more beneficial for research purposes, including final diagnostics of "no/inactive", "possible" or "likely" cGVHD. The study highlights the intricacies of sg-cGVHD pathology; and the need for standardized assessment to improve patient management associated to sg-cGVHD.

6.
Eur J Dent Educ ; 16(4): 246-53, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23050507

RESUMO

In Scandinavia, as in many European countries, most patients consult their general dentist once a year or more. This gives the dentist a unique opportunity and an obligation to make an early diagnosis of oral diseases, which is beneficial for both the patient and the society. Thus, the dentist must have knowledge of clinical symptoms, local and systemic signs and clinical differential diagnoses to make an accurate diagnosis. The dentist must be competent in selecting appropriate diagnostic tests, for example, tissue biopsy and microbiological samples, and conducting them correctly, as well as in interpreting test results and taking appropriate action accordingly. Furthermore, the dentist must be aware of diseases demanding multidisciplinary cooperation and be able to recognise his/her professional limitation, and to refer to other specialists when required. The dental curriculum changes over time as new approaches, treatments and diagnostic possibilities develop. Likewise, the role of the dentist in the community changes and may vary in different countries. As members of the Scandinavian Fellowship for Oral Pathology and Oral Medicine and subject representatives of oral pathology and oral medicine, we feel obliged to contribute to the discussion of how the guidelines of the dental curriculum support the highest possible standards of dental education. This article is meant to delineate a reasonable standard of oral pathology and oral medicine in the European dental curriculum and to guide subject representatives in curriculum development and planning. We have created an advisory topic list in oral pathology and oral medicine.


Assuntos
Educação em Odontologia/métodos , Medicina Bucal/educação , Patologia Bucal/educação , Competência Clínica , Currículo , Europa (Continente) , Humanos , Países Escandinavos e Nórdicos
7.
J Oral Pathol Med ; 39(10): 800-e1, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20819133

RESUMO

BACKGROUND: For many years, dentists have migrated between the Scandinavian countries without an intentionally harmonized dental education. The free movement of the workforce in the European Union has clarified that a certain degree of standardization or harmonization of the European higher education acts, including the dental education, is required. As a result of the Bologna process, the Association for Dental Education in Europe and the thematic network DentEd have generated guidelines in the document 'Profile and Competences for the European Dentist' (PCD). This document is meant to act as the leading source in revisions of dental curricula throughout Europe converging towards a European Dental Curriculum. In order to render the best conditions for future curriculum revisions providing the best quality dentist we feel obliged to analyse and comment the outlines of oral pathology and oral medicine in the PCD. METHODS: The representatives agreed upon definitions of oral pathology and oral medicine, and competences in oral pathology and oral medicine that a contemporary European dentist should master. The competences directly related to oral pathology and oral medicine were identified, within the PCD. RESULTS: The subject representatives suggested eighteen additions and two rewordings of the PCD, which all were substantiated by thorough argumentation. PERSPECTIVES: Hopefully, this contribution will find support in future revisions of the PCD in order to secure the best quality dental education.


Assuntos
Competência Clínica/normas , Currículo/normas , Educação em Odontologia/normas , Guias como Assunto , Medicina Bucal/educação , Patologia Bucal/educação , Odontologia/normas , União Europeia , Humanos , Cooperação Internacional , Medicina Bucal/normas , Patologia Bucal/normas
8.
Clin Oral Implants Res ; 21(4): 424-9, 2010 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-20443795

RESUMO

OBJECTIVES: To investigate the capacity of Cerament, an injectable bone substitute, to guide bone generation from a cortical surface. MATERIALS AND METHOD: Cerament was applied to the cortical surface of rat tibiae and investigated histologically after 3, 6 and 12 weeks, using a procedure similar to that performed in sham-operated rats. RESULTS: In both groups, the thickness of the bone cortex increased significantly from 473 + or - 58 microm (mean + or - SD) at day 0 to 1193 + or - 255 microm (Cerament) and 942 + or - 323 microm (sham) after 3 weeks. In the Cerament group, the new bone thickness remained constant (1258 + or - 288 microm) until the end of the experiment at 12 weeks, while the sham group demonstrated a return to initial cortical thickness (591 + or - 73 microm) at 12 weeks. The newly formed bone in the Cerament group was highly trabecular after 3 weeks but attained a normal trabecular structure of the cortex after 12 weeks. CONCLUSION: Cerament may guide bone generation from an intact cortical bone surface. Although bone remodeling speed may differ between rats and humans, our study indicates that Cerament may become a useful alternative to autologous bone, both to fill defects and to increase bone volume by cortical augmentation.


Assuntos
Substitutos Ósseos , Animais , Regeneração Óssea , Masculino , Ratos , Ratos Sprague-Dawley , Tíbia/cirurgia
9.
J Dent Res ; 98(1): 54-60, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30216733

RESUMO

BRAF V600E is the most common mutation in conventional ameloblastoma (AM) of the mandible. In contrast, maxillary AMs appear to harbor more frequently RAS, FGFR2, or SMO mutations. Unicystic ameloblastoma (UAM) is considered a less aggressive variant of ameloblastoma, amenable to more conservative treatment, and classified as a distinct entity. The aim of this study was to characterize the mutation profile of UAM ( n = 39) and to compare it to conventional AM ( n = 39). The associations between mutation status and recurrence probability were also analyzed. In the mandible, 94% of UAMs (29/31, including 8/8 luminal, 6/8 intraluminal, and 15/15 mural subtypes) and 74% of AMs (28/38) revealed BRAF V600E mutations. Among the BRAF wild-type cases, 1 UAM showed a missense SMO mutation (p.L412F), whereas 2 NRAS (p.Q61R), 2 HRAS (p.Q61R), and 2 FGFR2 (p.C383R) activating mutations were identified in AM. Of the 3 maxillary UAMs, only 1 revealed a BRAF V600E mutation. Taken together, our findings demonstrate high frequency of activating BRAF V600E mutations in both UAM and AM of the mandible. In maxillary UAMs, the BRAF V600E mutation prevalence appears to be lower as was shown for AM previously. It could therefore be argued that UAM and AM are part of the spectrum of the same disease. AMs without BRAF V600E mutations were associated with an increased rate of local recurrence ( P = 0.0003), which might indicate that routine mutation testing also has an impact on prognosis.


Assuntos
Ameloblastoma/genética , Neoplasias Maxilomandibulares/genética , Tumores Odontogênicos/genética , Proteínas Proto-Oncogênicas B-raf/genética , Ameloblastoma/metabolismo , Marcadores Genéticos , Humanos , Neoplasias Maxilomandibulares/metabolismo , Quinases de Proteína Quinase Ativadas por Mitógeno , Mutação , Recidiva Local de Neoplasia , Tumores Odontogênicos/metabolismo , Prognóstico
10.
Eur J Cancer Prev ; 14(6): 525-9, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16284497

RESUMO

The purpose was to identify cases of squamous cell carcinoma (SCC) of the tongue, in which a biopsy taken at the site preceding the cancer could be verified to show a lichenoid contact type of reaction (LCR). We retrieved all 724 SCC of the tongue from the Swedish Cancer Registry in the period 1995-2000. These cases were cross-searched with our own oral biopsy data files from 1988 to 1994, in order to identify biopsies with LCR-type lesions preceding the cancer. We found four verified and some additional tentative cases. The study demonstrated that there is a low incidence of malignant transformation in LCR-type oral lesions, not much different from what has been previously reported in oral lichen planus.


Assuntos
Carcinoma de Células Escamosas/patologia , Erupções Liquenoides/patologia , Lesões Pré-Cancerosas , Neoplasias da Língua/patologia , Idoso , Carcinoma de Células Escamosas/etiologia , Transformação Celular Neoplásica , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Sistema de Registros/estatística & dados numéricos , Fatores de Risco , Neoplasias da Língua/etiologia
11.
Artigo em Inglês | MEDLINE | ID: mdl-25944682

RESUMO

Whether psoriasis can manifest itself in the oral mucosa has been a matter of debate for many years. If an oral version of psoriasis exists, most researchers regard this manifestation as rare. The present report describes two patients who presented with lesions possibly related to cutaneous psoriasis. One patient had patchy erythematous lesions on the gingiva, and one had serpiginous lesions in the hard palate. We discuss these cases in relation to the existing literature, with special emphasis on the clinical and histopathologic criteria for the diagnosis of oral psoriasis.


Assuntos
Doenças da Boca/diagnóstico , Psoríase/diagnóstico , Adulto , Biópsia , Diagnóstico Diferencial , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Mucosa Bucal/patologia
12.
Autoimmunity ; 24(2): 101-11, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-8986322

RESUMO

We analysed inflammatory changes at selected time intervals, of salivary and lacrimal glands in the developing immunostimulatory [BN-->(BN x LEW)F1] model of graft-versus-host (GVH) reaction. A focal mononuclear adenitis in lacrimal and salivary glands developed at day 7 and increased clearly in "onset"-rats. Inflammatory responses in submandibular and parotid glands were less consistent and weaker than in lacrimal glands. There was no significant focus score difference between males and females. The lacrimal infiltrates were characterised immunohistochemically with monoclonal antibodies. Our findings indicate that CD4+ cells of donor origin dominated infiltrates, whereas a moderate number of B cells appeared only in large (late) foci. At stages corresponding to the onset of GVH disease (GVHD) in skin/labial mucosa, numerous CD8+ lymphocytes and NK cells were found in lacrimal glands, adjacent to ductal/ vascular plexa, sometimes forming small foci and with evidence of epithelial damage. We conclude that GVHD-associated T cell migration into rat exocrine glands occurs as a result of the semi-alloantigen-activated phenotype properties of the T cells. This activation occurs initially in lymphoid tissue and migration into glands is secondary to this and unrelated to antigen specificity. We also found evidence of amplification and tissue damage, interpreted as due to local reactivation of the T cells.


Assuntos
Doenças Autoimunes/imunologia , Doenças Autoimunes/patologia , Doença Enxerto-Hospedeiro/induzido quimicamente , Doença Enxerto-Hospedeiro/patologia , Aparelho Lacrimal/patologia , Linfadenite/patologia , Glândulas Salivares/patologia , Animais , Cruzamentos Genéticos , Modelos Animais de Doenças , Feminino , Imuno-Histoquímica , Masculino , Ratos , Ratos Endogâmicos BN , Ratos Endogâmicos Lew
13.
APMIS ; 99(7): 595-601, 1991 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-2069801

RESUMO

Contact hypersensitivity is characterized by an early and specific diapedesis of mononuclear cells into the site of antigenic challenge. In order to study the functional and ultrastructural properties of the endothelium involved in the recruitment of leukocytes, Sprague-Dawley rats were skin sensitized to DNFB; and this was followed by challenge of the oral mucosa. In vitro binding of peripheral blood mononuclear cells to high endothelial venules in lymph nodes was highly specific but no affinity of peripheral blood mononuclear cells to the vessels was observed in normal oral mucosa or in early contact hypersensitivity. However, 10 days after repeated DNFB challenge, occasional vessels bound overlaid peripheral blood mononuclear cells. Ultrastructurally, we identified migration of mononuclear cells through small venules three h after challenge. The vessels involved, however, did not display morphological signs of activation reminiscent of high endothelial venules in lymph nodes. Mast cell degranulation was evident as early as 30 min after challenge, and a possible mechanism for mast cell-mediated leukocyte recruitment is discussed.


Assuntos
Dermatite de Contato/fisiopatologia , Endotélio Linfático/fisiopatologia , Endotélio Vascular/fisiopatologia , Leucócitos/fisiologia , Mucosa Bucal/fisiopatologia , Animais , Adesão Celular , Dermatite de Contato/patologia , Modelos Animais de Doenças , Endotélio Linfático/ultraestrutura , Endotélio Vascular/ultraestrutura , Feminino , Técnicas In Vitro , Masculino , Microscopia Eletrônica , Mucosa Bucal/ultraestrutura , Ratos , Ratos Endogâmicos
14.
Clin Exp Rheumatol ; 9(2): 137-41, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-2060160

RESUMO

The prevalence of primary Sjögren's syndrome (primary SS) among patients with autoimmune thyroiditis (AT), and that of AT among patients with primary SS were studied prospectively. Of 63 patients with AT, one had precipitating antibodies against SS-A/Ro antigen together with objectively verified primary SS, and none had precipitating anti-SS-B/La antibodies; in contrast 17/63 (27%) had above normal values of anti-SS-B/La antibodies, as tested with ELISA. Of 19 AT patients tested objectively for xerostomia and keratoconjunctivitis sicca, six (32%) had keratoconjunctivitis sicca together with xerostomia and four (21%) had autoimmune sialadenitis. The prevalence of AT in patients with primary SS (n = 28) was 18%; of the 28 patients, 64% had an enlarged or abnormal thyroid gland on palpation and four of them (14%) had cytology verified AT. Ten (36%) had anti-thyroglobulin and/or antimicrosomal autoantibodies. Based upon the present investigation we conclude that the prevalence of primary SS is ten times higher among patients with AT, and that of AT is nine times higher among patients with primary SS, compared with the general population.


Assuntos
Doenças Autoimunes/complicações , Síndrome de Sjogren/complicações , Tireoidite/complicações , Adulto , Idoso , Idoso de 80 Anos ou mais , Anticorpos Antinucleares/análise , Doenças Autoimunes/epidemiologia , Doenças Autoimunes/imunologia , Feminino , Humanos , Ceratoconjuntivite Seca/complicações , Masculino , Pessoa de Meia-Idade , Prevalência , Glândulas Salivares/patologia , Síndrome de Sjogren/epidemiologia , Síndrome de Sjogren/fisiopatologia , Glândula Tireoide/fisiopatologia , Tireoidite/epidemiologia , Tireoidite/imunologia , Xerostomia/complicações
15.
Exp Toxicol Pathol ; 46(4-5): 329-34, 1994 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-7894244

RESUMO

BN, but not LEW, rats treated with subcutaneous injections of mercuric chloride (HgCl2) develop an autoimmune syndrome with infiltration of mononuclear cells into various organs including the oral mucosa. In the present study, we have utilized autometallographic techniques to visualize mercury in the oral mucosa, salivary and lacrimal glands of mercury-sensitive BN and -non-sensitive LEW rats injected with HgCl2. Mercury was deposited intracellularly in dendritic cells that were scattered throughout the lamina propria and submucosal connective tissue of both rat strains. In addition, mercury was detected in dendritic cells appearing within small cell clusters in the juxtaepithelial connective tissue of BN oral mucosa. In salivary and lacrimal glands, mercury was found in dendritic cells scattered throughout the stroma as well as in mononuclear cell foci. Mercury was also found in ductal epithelium. No staining was seen in any of the non-mercury-treated controls. Phenotypic analysis revealed that most mercury-laden cells were ED2+ resident macrophages and that some, but not all, of these cells expressed MHC class II antigens (RT1B).


Assuntos
Doenças Autoimunes/induzido quimicamente , Aparelho Lacrimal/química , Cloreto de Mercúrio/toxicidade , Mercúrio/análise , Mucosa Bucal/química , Glândulas Salivares/química , Animais , Doenças Autoimunes/metabolismo , Doenças Autoimunes/patologia , Autoimunidade/efeitos dos fármacos , Autoimunidade/fisiologia , Antígenos de Histocompatibilidade Classe II/análise , Histocitoquímica , Injeções Subcutâneas , Aparelho Lacrimal/imunologia , Macrófagos/citologia , Macrófagos/imunologia , Masculino , Cloreto de Mercúrio/administração & dosagem , Mucosa Bucal/imunologia , Fenótipo , Ratos , Ratos Endogâmicos BN , Ratos Endogâmicos Lew , Glândulas Salivares/imunologia , Síndrome
16.
Int J Oral Maxillofac Surg ; 40(6): 621-7, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21334177

RESUMO

Recent experimental research demonstrated that non-reducing temporomandibular joint (TMJ) disc displacement in growing rabbits impaired mandibular growth. TMJ disc displacement is also shown to induce histological changes of the condylar cartilage. The authors hypothesized that the severity of these changes would correlate to the magnitude of mandibular growth. Bilateral non-reducing TMJ disc displacement was surgically created in 10 growing New Zealand White rabbits. Ten additional rabbits constituted a sham operated control group. Aided by tantalum implants, growth was cephalometrically determined for each mandibular side during a period equivalent to childhood and adolescence in man. At the end of the growth period, histologically classified cartilage features were correlated with the assessed ipsilateral mandibular growth. Non-reducing displacement of the TMJ disc during the growth period induced histological reactions of the condylar cartilage in the rabbit model. The severity of cartilage changes was inversely correlated to the magnitude and the direction of mandibular growth, which resulted in a retrognathic growth pattern.


Assuntos
Luxações Articulares/complicações , Mandíbula/crescimento & desenvolvimento , Retrognatismo/etiologia , Disco da Articulação Temporomandibular/patologia , Transtornos da Articulação Temporomandibular/complicações , Animais , Atrofia , Remodelação Óssea/fisiologia , Cartilagem Articular/crescimento & desenvolvimento , Cartilagem Articular/patologia , Cefalometria/métodos , Modelos Animais de Doenças , Marcadores Fiduciais , Hiperplasia , Processamento de Imagem Assistida por Computador , Mandíbula/patologia , Côndilo Mandibular/crescimento & desenvolvimento , Côndilo Mandibular/patologia , Osteoartrite/etiologia , Osteoartrite/patologia , Osteogênese/fisiologia , Coelhos , Distribuição Aleatória , Tantálio/química , Fatores de Tempo
17.
Artigo em Inglês | MEDLINE | ID: mdl-21330162

RESUMO

Imatinib mesylate is a tyrosine kinase inhibitor which targets Bcr-Abl-protein, c-Kit, and platelet-derived growth factor receptor. The drug was originally developed for treatment of chronic myeloid leukemia but is also regarded as first-line treatment of patients with metastatic gastrointestinal stromal tumours (GIST). Dermatologic side effects are common, with superficial edema and rash as the most frequent. In addition, imatinib mesylate treatment is often associated with hypopigmentation. Intraoral side effects are very rare. The present paper demonstrates 1 patient with GIST and 2 patients with chronic myeloid leukemia treated with imatinib mesylate for 5-6 years. All 3 patients presented with diffuse solitary bluish-brown pigmentations in the hard palate. The lesions persisted at follow-ups. There were no other pigmentations in the oral mucosa. The histopathologic examination showed depositions of melanin pigment in the lamina propria. The possible relationship between the observed melanotic maculae and imatinib mesylate treatment is discussed.


Assuntos
Antineoplásicos/efeitos adversos , Melanose/induzido quimicamente , Palato Duro/efeitos dos fármacos , Piperazinas/efeitos adversos , Pirimidinas/efeitos adversos , Idoso , Benzamidas , Feminino , Tumores do Estroma Gastrointestinal/tratamento farmacológico , Humanos , Mesilato de Imatinib , Leucemia Mielogênica Crônica BCR-ABL Positiva/tratamento farmacológico , Pessoa de Meia-Idade
18.
Int J Oral Maxillofac Surg ; 40(12): 1441-4, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21764560

RESUMO

A case of osteomyelitis in a 71-year-old woman with paroxysmal nocturnal hemoglobinuria (PNH) is reported. Osteomyelitis of the jaw is a well known condition of the oral and maxillofacial region that may cause severe morbidity. It is well documented that vaso-occlusive crises in sickle cell anaemia, a hemolytic blood disorder, can make the jaw bone susceptible to osteomyelitis. The authors report a case proposing an association between PNH and osteomyelitis of the mandible.


Assuntos
Hemoglobinúria Paroxística/complicações , Doenças Mandibulares/etiologia , Osteomielite/etiologia , Idoso , Anti-Inflamatórios/uso terapêutico , Doença Crônica , Feminino , Seguimentos , Glucocorticoides/uso terapêutico , Humanos , Osteosclerose/etiologia , Prednisolona/uso terapêutico , Radiografia Panorâmica
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