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1.
Orphanet J Rare Dis ; 18(1): 33, 2023 02 22.
Artigo em Inglês | MEDLINE | ID: mdl-36814255

RESUMO

BACKGROUND: Long-term sequelae are frequent and often disabling after epidermal necrolysis (Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN)). However, consensus on the modalities of management of these sequelae is lacking. OBJECTIVES: We conducted an international multicentric DELPHI exercise to establish a multidisciplinary expert consensus to standardize recommendations regarding management of SJS/TEN sequelae. METHODS: Participants were sent a survey via the online tool "Survey Monkey" consisting of 54 statements organized into 8 topics: general recommendations, professionals involved, skin, oral mucosa and teeth, eyes, genital area, mental health, and allergy workup. Participants evaluated the level of appropriateness of each statement on a scale of 1 (extremely inappropriate) to 9 (extremely appropriate). Results were analyzed according to the RAND/UCLA Appropriateness Method. RESULTS: Fifty-two healthcare professionals participated. After the first round, a consensus was obtained for 100% of 54 initially proposed statements (disagreement index < 1). Among them, 50 statements were agreed upon as 'appropriate'; four statements were considered 'uncertain', and ultimately finally discarded. CONCLUSIONS: Our DELPHI-based expert consensus should help guide physicians in conducting a prolonged multidisciplinary follow-up of sequelae in SJS-TEN.


Assuntos
Síndrome de Stevens-Johnson , Humanos , Síndrome de Stevens-Johnson/complicações , Consenso , Pele , Progressão da Doença
2.
PLoS One ; 14(12): e0226266, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31846467

RESUMO

OBJECTIVE: This systematic review was to assess the presence of Trichomonas tenax in patients with periodontitis and to elucidate its potential role in the onset and development of this disease. METHOD: Systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and by consulting the five databases: Medline, Science Direct, Web of Science, Dentistry and Oral Science Sources and Cochrane Central Register of Controlled Trials. Following Koch's postulates revisited by Socransky as PICO framework, this collection data was only including full text of clinical trials concerning patients with periodontitis, case-reports and in vitro research published between 1960 and March 2019. RESULTS: On the 376 studies identified, only 25 fulfilled our eligible criteria. Most of these studies were in vitro research articles designed to evaluate potential virulence factors, and others were clinical trials (case-control studies, randomized controlled trial) and case-reports. The analysis of these papers has shown that i) Trichomonas tenax is more frequently detected in dental biofilm from sites with periodontitis than in healthy sites; ii) this live flagellate seems capable of producing diverse enzymes that could participate in periodontal breakdown and has the capacity to adhere to epithelial cells, its lysed form could induce the synthesis of IL-8 from macrophage cell lines; iii) the impact of non-surgical treatment of periodontitis have not been thoroughly evaluated on the presence of T. tenax. CONCLUSIONS: This systematic review has reported the presence of T. tenax more frequently in diseased than healthy sites and the capacity of this flagellate to synthesis enzymes which could participate to the degradation of periodontal tissues. Nevertheless, these data do not meet all the postulates and are not enough to provide firm conclusions about the role of T. tenax in the etiopathogenesis of periodontitis.


Assuntos
Periodontite/etiologia , Periodontite/parasitologia , Trichomonas/fisiologia , Humanos
3.
Ann Dermatol Venereol ; 145(10): 572-577, 2018 Oct.
Artigo em Francês | MEDLINE | ID: mdl-30143321

RESUMO

BACKGROUND: Gingival expression of autoimmune bullous diseases (AIBD) may be inaugural, exclusive or dominant (mucous membrane pemphigoid, pemphigus vulgaris). Histology and direct immunofluorescence are essential to diagnosis. The location of the biopsy and the surgical technique determine the histological quality of the tissue sample. However, gingival tissue is often considered fragile and easily impaired during biopsy. We suggest an original biopsy protocol for the gingival papillae that is simple to perform, non-iatrogenic, and readily accessible to all practitioners who usually treat AIBD patients presenting isolated gingival expression (dermatologists, stomatologists, odontology specialists, ENT specialists). PATIENTS AND METHODS: We conducted a retrospective study from 2012 to 2017 identifying all patients presenting AIBD with gingival expression for whom we performed papillary gingival biopsy for diagnostic ends. Our main objective was to determine the diagnostic efficacy and safety of this surgical technique. RESULTS: Over the study period, 34 papillary gingival biopsies were taken from 19 patients : 15 for histopathological examination and 19 for direct immunofluorescence. Of the 34 biopsies, only one could not be properly analyzed due to lack of epithelium and a second tissue sample was therefore necessary. No short- or long-term complications occurred during post-operative follow-up. CONCLUSION: Gingival papilla biopsy is perfectly suited to the histopathological and immunohistochemical examinations needed for diagnosis of AIBD with isolated gingival expression. This surgical technique shows great efficacy and very good safety. However, additional studies are necessary to confirm our preliminary results, in particular the absence of iatrogenic effects.


Assuntos
Doenças Autoimunes/patologia , Biópsia/métodos , Gengiva/patologia , Doenças da Gengiva/patologia , Dermatopatias Vesiculobolhosas/patologia , Adulto , Idoso , Doenças Autoimunes/diagnóstico , Biópsia/efeitos adversos , Cicatriz/etiologia , Feminino , Técnica Direta de Fluorescência para Anticorpo , Doenças da Gengiva/diagnóstico , Hemorragia Gengival/etiologia , Humanos , Masculino , Pessoa de Meia-Idade , Dor/etiologia , Estudos Retrospectivos , Dermatopatias Vesiculobolhosas/diagnóstico
4.
Ann Dermatol Venereol ; 144(3): 182-190, 2017 Mar.
Artigo em Francês | MEDLINE | ID: mdl-28011091

RESUMO

BACKGROUND: Autoimmune bullous diseases (AIBD) may cause chronic oral lesions that progress insidiously. AIMS: To provide recommendations for optimal oral-dental management of patients presenting AIBD with oral involvement. PATIENTS AND METHODS: In the absence of scientific studies with high levels of proof, these recommendations have been drawn up at two meetings by a committee of experts on AIBD comprising 7 dermatologists, 1 stomatologist, 1 maxillofacial surgeon, 2 odontologists and 4 parodontologists. RESULTS: The oral lesions associated with AIBD may be classified into three grades of severity: severe (generalised erosive gingivitis affecting at least 30% of dental sites), moderate (localised erosive gingivitis affecting less than 30% of dental sites) and controlled (no erosive oral lesions). Good oral-dental hygiene suited to the severity of the oral lesions, must be practised continually by these patients so as to avoid the formation of dental plaque, which aggravates symptoms. Dental and parodontal care must be considered in accordance with the severity grade of the oral lesions: in severe cases, the dental plaque must be eliminated manually with a curette, but several types of care (descaling, treatment for tooth decay, non-urgent extractions, etc.) must be suspended until the grade of severity is moderate or until the disease is stabilised.


Assuntos
Doenças da Boca/patologia , Doenças da Boca/terapia , Higiene Bucal , Penfigoide Bolhoso/patologia , Penfigoide Bolhoso/terapia , Consenso , França , Humanos , Doenças da Boca/imunologia , Higiene Bucal/métodos , Índice de Higiene Oral , Educação de Pacientes como Assunto/métodos , Penfigoide Bolhoso/imunologia , Índice de Gravidade de Doença
5.
Lasers Med Sci ; 25(6): 855-9, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19685196

RESUMO

The purpose of this study was to compare the tensile bond strength of composite resin bonded to erbium:yttrium-aluminium-garnet (Er:YAG) laser-prepared dentine after different durations of acid etching. The occlusal third of 68 human third molars was removed in order to expose the dentine surface. The teeth were randomly divided into five groups: group B (control group), prepared with bur and total etch system with 15 s acid etching [37% orthophosphoric acid (H(3)PO(4))]; group L15, laser photo-ablated dentine (200 mJ) (laser irradiation conditions: pulse duration 100 micros, air-water spray, fluence 31.45 J/ cm(2), 10 Hz, non-contact hand pieces, beam spot size 0.9 mm, irradiation speed 3 mm/s, and total irradiation time 2 x 40 s); group L30, laser prepared, laser conditioned and 30 s acid etching; group L60, laser prepared, laser conditioned and 60 s acid etching; group L90, laser prepared, laser conditioned and 90 s acid etching. A plot of composite resin was bonded onto each exposed dentine and then tested for tensile bond strength. The values obtained were statistically analysed by analysis of variance (ANOVA) coupled with the Tukey-Kramer test at the 95% level. A 90 s acid etching before bonding showed the best bonding value (P < 0.05) when compared with all the other groups including the control group. There is no significance difference between other groups, nor within each group and the control group. There was a significant increase in tensile bond strength of the samples acid etched for 90 s.


Assuntos
Condicionamento Ácido do Dente/métodos , Colagem Dentária/métodos , Lasers de Estado Sólido/uso terapêutico , Terapia com Luz de Baixa Intensidade/métodos , Resinas Compostas , Corrosão Dentária/métodos , Análise do Estresse Dentário , Dentina/fisiologia , Dentina/efeitos da radiação , Humanos , Técnicas In Vitro , Resistência à Tração , Fatores de Tempo
6.
Eur Arch Paediatr Dent ; 9(3): 142-7, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18793597

RESUMO

BACKGROUND: Williams Beuren syndrome (WBS) is an unusual hereditary connective tissue disease caused by a microdeletion at position 7q11-23 and a haploinsufficiency at the elastin gene. The most frequent specific features are elf-like face, alteration of cognitive functions and cardiovascular diseases including isolated supravalvular aortic stenosis. A number of clinical findings have been reported, but none of the studies evaluating this syndrome consider the oral cavity. It is equally surprising that the gingival tissue, which carries a perfectly structured elastic fibre network, has not yet been investigated. It is important to verify whether subjects affected by WBS are more susceptible to periodontal disease than healthy subjects who are not that much affected, for periodontal disease may have deleterious effects on the cardiovascular system. METHODS: In an attempt to address this issue, the oral manifestations of 8 patients (ages from 5 to 12 years) with WBS have been investigated: dental examination, periodontal examination (gingival phenotype, plaque control record, gingival index, bone quality). RESULTS: All patients had oral parafunction, tooth number abnormalities and malocclusions. Average gingival height and width were greater than normal. Plaque index was always very high except for one patient, but the gingival inflammation was not linked to the quantity of clinical plaque index. There was no obvious loss of attachment. CONCLUSION: As with collagen, elastin is a structural macromolecule of the gingiva. These components play an important role in gingival function and in the resistance of the periodontium to daily aggressions. Unlike genetic diseases characterized by impairment of collagen macrofibrils, it is suggested that the hemizygous gene encoding elastin does not result in periodontal disease. In addition there is an existence of a possible concordance between the elastin gene haploinsufficiency and the periodontal phenotype. There might be some adaptive process to this deficiency.


Assuntos
Anodontia/complicações , Doenças da Gengiva/complicações , Má Oclusão/complicações , Doenças Periodontais/complicações , Síndrome de Williams/complicações , Anodontia/genética , Criança , Pré-Escolar , Elastina/genética , Feminino , Doenças da Gengiva/genética , Humanos , Masculino , Má Oclusão/genética , Doenças Periodontais/genética , Índice Periodontal , Síndrome de Williams/genética
7.
J Vasc Res ; 42(3): 190-201, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15832055

RESUMO

Supravalvular aortic stenosis (SVAS) and Williams Beuren syndrome (WBS) can be considered as inherited diseases affecting the whole arterial tree and causing narrowing of the vessels. It has been reported that abnormal deposition of elastin in arterial walls of patients with SVAS and WBS leads to increased proliferation of arterial smooth muscle cells (SMC), which result in the formation of hyperplastic intimal lesions. In this work, we conducted morphological and morphometrical analysis with stenotic aortas from patients suffering from SVAS and WBS and from healthy control subjects and demonstrated that the amount of elastic fibers and the loss of integrity of vascular elastic fibers in the aortas reflect similar changes in the skin of patients with SVAS or WBS, as reported in our previous work conducted on skin in these pathological states. On the other hand, we conducted investigations on metalloproteinases (MMP2, MMP9, MMP7) and their specific tissue inhibitors TIMP1 and TIMP2 to verify their possible involvement in the etiopathogeny of SVAS and WBS. We particularly evidenced an altered MMP9/TIMP1 balance in favor of matrix degradation which could facilitate SMC migration and neointimal hyperplasia. Our findings suggest that elastinolytic enzymes secreted by arterial SMC, possibly including matrilysin 1, are critical for the development of arterial lesions in SVAS and WBS and contribute to perpetuate arterial stenosis in either SVAS or WBS.


Assuntos
Aorta/fisiopatologia , Estenose Aórtica Supravalvular/fisiopatologia , Síndrome de Williams/fisiopatologia , Adulto , Aorta/patologia , Estenose Aórtica Supravalvular/patologia , Estudos de Casos e Controles , Criança , Pré-Escolar , Humanos , Processamento de Imagem Assistida por Computador , Técnicas Imunológicas , Metaloproteases/metabolismo , Distribuição Tecidual , Inibidor Tecidual de Metaloproteinase-1/metabolismo , Inibidor Tecidual de Metaloproteinase-2/metabolismo , Síndrome de Williams/patologia
8.
Arch Dermatol Res ; 296(5): 220-5, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15449075

RESUMO

Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are considered to be drug-induced diseases, and are characterized by extensive mucocutaneous disorder and epidermal necrosis which result in the detachment of the epidermis. Inactive and active forms of metalloproteinases (MMP2 and MMP9) secreted by skin explants maintained in organ culture for 72 h and in blister fluid from two TEN and three SJS patients were investigated. Interestingly, lesional skin from both the TEN and the SJS patients cultured for 3 days in conditioned medium showed high levels of both 72 kDa progelatinase A and 66 kDa activated gelatinase A, and the 66 kDa activated form was not observed in cultures of skin from control individuals. Furthermore, indirect immunodetection showed the presence of MMP2 and MMP9 in TEN and SJS patients' skin. Increased gelatinase activity in the culture medium of TEN and SJS skin maintained in organ culture and in blister fluid indicates that these gelatinases may be responsible for the detachment of the epidermis in these drug-induced necrolyses.


Assuntos
Metaloproteinase 2 da Matriz/metabolismo , Metaloproteinase 9 da Matriz/metabolismo , Síndrome de Stevens-Johnson/enzimologia , Adulto , Idoso , Vesícula/enzimologia , Vesícula/etiologia , Vesícula/patologia , Western Blotting , Líquidos Corporais/enzimologia , Estudos de Casos e Controles , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Técnicas Imunoenzimáticas , Técnicas Imunológicas , Masculino , Pessoa de Meia-Idade , Técnicas de Cultura de Órgãos , Pele/enzimologia , Pele/patologia , Coloração e Rotulagem , Síndrome de Stevens-Johnson/complicações , Síndrome de Stevens-Johnson/patologia
9.
Clin Oral Investig ; 7(4): 198-205, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12802622

RESUMO

This study examined the effects of a vegetable extract from Lupinus albus (LU105) on MMPs and TIMPs secreted by human gingival fibroblasts in culture. LU105 was extracted from seeds of L. albus and is freely soluble in water. Gelatin zymography showed that control human gingival fibroblasts maintained in culture for 48 h express pro-MMP2 (progelatinase A) in the culture medium while the active form of MMP2 (gelatinase A), the active form of MMP9 (gelatinase B), and pro-MMP9 (progelatinase B) are not detected. Fibroblasts derived from inflamed gingiva expressed in the culture medium increased amounts of pro-MMP2 (progelatinase A) compared with controls and significant amounts of pro-MMP9 (progelatinase B). LU105 diminished the expression by gingival fibroblasts derived from inflamed tissue of both pro-MMP2 and pro-MMP9. Furthermore LU105 did not modify the amount of TIMP2 expressed in culture by controls or by gingival fibroblasts derived from inflamed tissue. TIMP1 and MMP1 significantly decreased when LU105 was added in the culture media of gingival fibroblasts derived from inflamed tissue compared with control fibroblasts. Thus LU105 seems to offer an opportunity to restore a correct balance between MMP2, MMP9, MMP1, and their natural inhibitors, i.e., TIMP1 and TIMP2 in human inflamed gingiva.


Assuntos
Gengiva/efeitos dos fármacos , Gengiva/enzimologia , Lupinus , Metaloproteinases da Matriz/efeitos dos fármacos , Oligopeptídeos/farmacologia , Periodontite/enzimologia , Extratos Vegetais/farmacologia , Inibidores de Proteases/farmacologia , Adolescente , Adulto , Análise de Variância , Western Blotting , Células Cultivadas , Eletroforese em Gel de Poliacrilamida , Fibroblastos/efeitos dos fármacos , Fibroblastos/enzimologia , Gengiva/citologia , Humanos , Inibidores de Metaloproteinases de Matriz , Metaloproteinases da Matriz/análise , Metaloproteinases da Matriz/biossíntese , Sementes , Inibidores Teciduais de Metaloproteinases/análise , Inibidores Teciduais de Metaloproteinases/biossíntese , Inibidores Teciduais de Metaloproteinases/efeitos dos fármacos
10.
Am J Med Genet ; 87(2): 134-8, 1999 Nov 19.
Artigo em Inglês | MEDLINE | ID: mdl-10533027

RESUMO

The elastin gene is consistently deleted in Williams syndrome and as this protein represents the major component of the elastic fibers of the dermis, we sought to investigate skin elastic fibers in Williams syndrome as a key to unraveling extracellular matrix disorganization in this condition. Both morphometric parameters analyzed by using automated image analysis and immunofluorescence labeling with monoclonal antibodies against elastin and fibrillin 1 showed a disorganized pre-elastic (oxytalan and elaunin) and mature elastic fibers in the dermis of 10 Williams syndrome patients compared with five healthy children and one patient with isolated supravalvular aortic stenosis. Skin biopsies in Williams syndrome patients provide a simple mean to elucidate extracellular matrix anomalies. Hopefully, this method could give clues to the understanding of the elastic network anomalies in this condition and even to the consequences of these latter on elasticity and resilience of other tissues such as the arterial tree.


Assuntos
Tecido Elástico/anormalidades , Tecido Elástico/química , Anormalidades da Pele/metabolismo , Anormalidades da Pele/patologia , Síndrome de Williams/metabolismo , Síndrome de Williams/patologia , Adolescente , Estenose da Valva Aórtica/genética , Estenose da Valva Aórtica/metabolismo , Estenose da Valva Aórtica/patologia , Criança , Pré-Escolar , Cromossomos Humanos Par 7/genética , Tecido Elástico/patologia , Elastina/análise , Elastina/deficiência , Elastina/genética , Matriz Extracelular/química , Matriz Extracelular/patologia , Fibrilina-1 , Fibrilinas , Técnica Indireta de Fluorescência para Anticorpo , Humanos , Proteínas dos Microfilamentos/análise , Anormalidades da Pele/genética , Síndrome de Williams/genética
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