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1.
Pediatr Dermatol ; 41(2): 234-242, 2024.
Article in English | MEDLINE | ID: mdl-38326222

ABSTRACT

BACKGROUND: Despite studies of dermatologic manifestations in adults with inflammatory bowel disease (IBD), little is known about the prevalence of IBD-associated skin lesions and their correlation with IBD severity in children. We aimed to address these knowledge gaps in our single-center cohort of children with IBD. METHODS: Retrospective chart review of 528 children and adolescents (≤18 years old) with IBD and seen at Mayo Clinic (Rochester, MN) between 1999 and 2017 was conducted. The Chi-Square/Fischer's exact test (with p ≤ .05 to signify statistical significance) was applied to compare categorical outcomes between Crohn's disease (CD) and ulcerative colitis (UC) patients. RESULTS: In total, 425 IBD patients (64.9% CD, 53% males) and ≥1 dermatologic diagnosis were included. Presence of ≥1 cutaneous infection was recorded in 42.8% of participants. Acne was the most common non-infectious dermatologic condition (30.8%), followed by eczema (15.8%) and perianal skin tags (14.6%). Angular cheilitis (p = .024), keratosis pilaris (KP, p = .003), and perianal skin complications (i.e., skin tags, fistula, and abscesses; all p < .001) were more frequently diagnosed among children with CD, while fungal skin infections (p = .017) were more frequently diagnosed in UC patients. Severity of IBD correlated with higher prevalence of perianal fistula (p = .003), perianal abscess (p = .041), psoriasis (p < .001), and pyoderma gangrenosum (PG, p = .003). CONCLUSIONS: Both IBD-specific and IBD-nonspecific dermatologic conditions are very prevalent in childhood IBD, the most common being infectious. Children with CD are more likely to experience angular cheilitis, KP, and perianal skin findings than those with UC. Perianal disease, psoriasis, and PG are associated with more severe IBD.


Subject(s)
Cheilitis , Colitis, Ulcerative , Crohn Disease , Fistula , Inflammatory Bowel Diseases , Psoriasis , Skin Diseases , Skin Neoplasms , Adult , Male , Adolescent , Humans , Child , Female , Retrospective Studies , Cheilitis/complications , Inflammatory Bowel Diseases/complications , Inflammatory Bowel Diseases/epidemiology , Crohn Disease/complications , Crohn Disease/epidemiology , Crohn Disease/diagnosis , Colitis, Ulcerative/complications , Colitis, Ulcerative/epidemiology , Colitis, Ulcerative/diagnosis , Abscess , Skin Diseases/etiology , Skin Diseases/complications , Psoriasis/complications , Psoriasis/epidemiology , Skin Neoplasms/complications , Fistula/complications
2.
BMC Microbiol ; 23(1): 130, 2023 05 15.
Article in English | MEDLINE | ID: mdl-37183254

ABSTRACT

BACKGROUND: Atopic dermatitis (AD) is an inflammatory skin condition distinguished by an activated Th2 immune response. The local skin microbial dysbiosis is a contributing factor to the development of AD. The pathogenic coagulase-positive Staphylococcus aureus is the primary species responsible for the progression of AD. Even though Staphylococcus pseudintermedius is an animal-origin pathogen, it is increasingly becoming a source of concern in human diseases. As another coagulase-positive Staphylococci, it is crucial to pay more attention to S. pseudintermedius isolated from the lesion site. RESULTS: In our investigation, we presented a case of cheilitis in a patient with atopic dermatitis (AD). We utilized culture and next-generation genomic sequencing (NGS) to identify the bacteria present on the skin swabs taken from the lip sites both prior to and following treatment. Our findings indicated that the predominant bacteria colonizing the lesion site of AD were S. pseudintermedius and S. aureus, both of which were eradicated after treatment. The Multi-locus sequence typing (MLST) of S. pseudintermedius and S. aureus demonstrated coordinated antibiotic susceptibility, with ST2384 and ST22 being the respective types. Although the skin abscess area resulting from S. pseudintermedius infection was significantly smaller than that caused by S. aureus in mice, the expression of cytokines interleukin-4 (IL-4) and interleukin-5 (IL-5) were significantly higher in the S. pseudintermedius-infected mice. CONCLUSIONS: The S. pseudintermedius strain isolated from the lesion site of the AD patient exhibited a higher expression of IL-4 and IL-5 when colonized on mouse skin, as compared to S. aureus. This observation confirms that S. pseudintermedius can effectively induce the Th2 response in vivo. Our findings suggest that animal-origin S. pseudintermedius may play a role in the development of AD when colonized on the skin, emphasizing the importance of taking preventive measures when in contact with animals.


Subject(s)
Cheilitis , Coinfection , Dermatitis, Atopic , Staphylococcal Infections , Humans , Animals , Mice , Staphylococcus aureus/physiology , Dermatitis, Atopic/complications , Dermatitis, Atopic/microbiology , Interleukin-4 , Interleukin-5 , Multilocus Sequence Typing , Cheilitis/complications , Cheilitis/pathology , Coagulase , Staphylococcal Infections/complications , Skin/microbiology
3.
Tokai J Exp Clin Med ; 47(4): 199-203, 2022 Dec 20.
Article in English | MEDLINE | ID: mdl-36420553

ABSTRACT

Zinc deficiency has long been known as acrodermatitis enteric dermatitis (congenital zinc deficiency). On the other hand, acquired zinc deficiency has attracted attention as a familiar disease in recent years. Epidemiological studies in Japan have shown that acquired zinc deficiency is more common than expected. It is also known that serum zinc levels fall markedly with age. In this report, several cases of acquired zinc deficiency that caused cheilitis are described. In all cases, the only symptom was cheilitis, the serum zinc level was low, and all cases were relieved by zinc supplementation. Zinc deficiency is associated with a range of pathological conditions, including mucocutaneous symptoms, delayed wound healing, dysgeusia, anemia, impaired immunity, and retarded growth development disorders. However, zinc deficiency may be overlooked even in cases of cheilitis alone. Especially in intractable cases, it is important to suspect zinc deficiency as one at the differential diagnoses.


Subject(s)
Acrodermatitis , Cheilitis , Humans , Cheilitis/etiology , Cheilitis/complications , Acrodermatitis/diagnosis , Acrodermatitis/etiology , Zinc , Intestine, Small , Japan
4.
Article in English | MEDLINE | ID: mdl-35457467

ABSTRACT

Actinic cheilitis (AC) is a chronic inflammation of the lip considered an oral, potentially malignant disorder associated with an increased risk of lip squamous cell carcinoma (SCC) development. Controversies surrounding current therapeutic modalities of AC are under debate, and the implications of laser treatment have not been specifically investigated through a systematic review design. The present study aims to evaluate the degree of evidence of laser for the treatment of AC in terms of efficacy and safety. We searched for primary-level studies published before January 2022 through MEDLINE/PubMed, Embase, Web of Science, Scopus and CENTRAL, with no limitation in publication language or date. We evaluated the methodological quality and risk of bias of the studies included using the updated Cochrane Collaboration's tool for assessing risk of bias (RoB-2). Twenty studies (512 patients) met our eligibility criteria. Laser therapy showed a complete clearance of AC in 92.5% patients, with a maximum recurrence rate of 21.43%, and a very low frequency of malignant transformation to SCC (detected in only 3/20 studies analyzed). In addition, cosmetic outcomes and patient satisfaction were described as excellent. In conclusion, our findings indicate that laser therapy is a high efficacy approach to AC.


Subject(s)
Cheilitis , Laser Therapy , Carcinoma, Squamous Cell/etiology , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/therapy , Cheilitis/complications , Cheilitis/pathology , Cheilitis/therapy , Humans , Lip Neoplasms/etiology , Lip Neoplasms/pathology , Lip Neoplasms/therapy
5.
Einstein (Sao Paulo) ; 20: eRC6151, 2022.
Article in English | MEDLINE | ID: mdl-35195191

ABSTRACT

Propolis is a lipophilic resin extracted from plants by bees. The purpose of this case report was to show the importance of this substance as cause of allergic contact cheilitis. A 21-year-old female patient complained of pruritic perioral eczema for 5 years. In the past months it also affected the neck. After diagnosing contact dermatitis, she was submitted to a patch test with a Latin American baseline series. The result was strongly positive for propolis (++) and weakly positive for perfume mix I (+). After the test, the patient revealed she had been using propolis drops, per oris, for 10 years. The worsening of the condition was due to increased dose, aiming "to improve immunity", during the coronavirus disease 2019 (COVID-19) pandemic. The contact allergy to propolis might be increasing due to the widespread use of natural products. Propolis is a sensitizer to be considered in patients with long-lasting cheilitis.


Subject(s)
COVID-19 , Cheilitis , Dermatitis, Allergic Contact , Propolis , Cheilitis/chemically induced , Cheilitis/complications , Cheilitis/diagnosis , Dermatitis, Allergic Contact/diagnosis , Dermatitis, Allergic Contact/etiology , Female , Humans , Propolis/adverse effects , SARS-CoV-2
6.
Einstein (São Paulo, Online) ; 20: eRC6151, 2022. graf
Article in English | LILACS | ID: biblio-1360390

ABSTRACT

ABSTRACT Propolis is a lipophilic resin extracted from plants by bees. The purpose of this case report was to show the importance of this substance as cause of allergic contact cheilitis. A 21-year-old female patient complained of pruritic perioral eczema for 5 years. In the past months it also affected the neck. After diagnosing contact dermatitis, she was submitted to a patch test with a Latin American baseline series. The result was strongly positive for propolis (++) and weakly positive for perfume mix I (+). After the test, the patient revealed she had been using propolis drops, per oris, for 10 years. The worsening of the condition was due to increased dose, aiming "to improve immunity", during the coronavirus disease 2019 (COVID-19) pandemic. The contact allergy to propolis might be increasing due to the widespread use of natural products. Propolis is a sensitizer to be considered in patients with long-lasting cheilitis.


Subject(s)
Humans , Female , Propolis/adverse effects , Cheilitis/complications , Cheilitis/diagnosis , Cheilitis/chemically induced , Dermatitis, Allergic Contact/diagnosis , Dermatitis, Allergic Contact/etiology , COVID-19 , SARS-CoV-2
10.
Dermatol Online J ; 23(3)2017 Mar 15.
Article in English | MEDLINE | ID: mdl-28329526

ABSTRACT

Chronic granulomatous disease (CGD) is a primaryimmunodeficiency disorder that affects the phagocyticcells of the innate immune system. It is characterizedby recurrent or persistent infections with granulomaformation. Lupus-like lesions have been reported incarriers of CGD and less frequently, in patients withCGD. Immunological study in these patients areusually negative. We describe the case of an 8-yearoldboy with CGD who developed chronic and acutecutaneous lupus erythematous with angular cheilitis,oral ulcers, Raynaud phenomenon, and positiveserologies for antinuclear, anticentromere, and anti-Saccharomyces cerevisiae antibodies.


Subject(s)
Facial Dermatoses/diagnosis , Foot Dermatoses/diagnosis , Granulomatous Disease, Chronic/immunology , Lupus Erythematosus, Cutaneous/diagnosis , Antibodies, Antinuclear/immunology , Antibodies, Fungal/immunology , Cheilitis/complications , Cheilitis/diagnosis , Cheilitis/immunology , Child , Facial Dermatoses/complications , Facial Dermatoses/immunology , Facial Dermatoses/pathology , Foot Dermatoses/complications , Foot Dermatoses/immunology , Foot Dermatoses/pathology , Granulomatous Disease, Chronic/complications , Humans , Lupus Erythematosus, Cutaneous/complications , Lupus Erythematosus, Cutaneous/immunology , Lupus Erythematosus, Cutaneous/pathology , Male , Oral Ulcer/complications , Oral Ulcer/diagnosis , Oral Ulcer/immunology , Raynaud Disease/complications , Raynaud Disease/diagnosis , Raynaud Disease/immunology , Risk Factors , Saccharomyces cerevisiae/immunology
13.
São Paulo; s.n; 2015. 135 p. ilus, tab. (BR).
Thesis in Portuguese | LILACS, BBO - Dentistry | ID: biblio-867723

ABSTRACT

A queilite actínica (QA) é uma lesão potencialmente maligna importante para identificar indícios precoces de transformação maligna para o carcinoma epidermoide de lábio (CEL), possibilitando a implementação de um tratamento eficiente e menos invasivo, que promova um melhor prognóstico para os pacientes. Pesquisas recentes indicam que os métodos histopatológicos geralmente são falhos em traçar o risco de malignização de casos de QA, pois além de não demonstrar as alterações genéticas presentes nos queratinócitos, não foram realizados estudos de acompanhamento clínico para avaliar se o grau de displaia epitelial da QA está relacionado ao risco de malignização para CE. Assim, a presente pesquisa teve como objetivo caracterizar, a partir dos casos atendidos no Serviço de Patologia Cirúrgica da FOUSP, qual a diferença de perfil clínico-patológico de pacientes de QA com evolução para CEL, pacientes de QA sem informações e sinais presentes de malignização e pacientes apenas diagnosticados com CEL, e também visou analisar a expressão de Ki67 e pRb nesses três grupos. Para isso, os dados dos pacientes como idade, sexo, cor da pele, aspecto clínico da lesão fundamental, coloração, tamanho e tempo de duração das lesões foram resgatados de 998 casos e distribuídos nessas três categorias. Os resultados da análise clínico-epidemiológica revelaram que o único aspecto clínico estatisticamente significante para diferenciar pacientes apenas diagnosticados com CEL dos demais


grupos foi o tempo de duração das lesões. A análise do grau de displasia epitelial nos casos de QA na amostra presente revelou que todos os pacientes de QA posteriormente diagnosticados com CEL foram classificados como lesões de alto risco, e ainda exibiram em maior frequência as atipias: aumento do número de figuras de mitose, variação anormal do tamanho do núcleo, variação anormal do tamanho da célula e alteração da relação núcleo/citoplasma, figuras de mitose anormais e aumento do número e tamanho de nucléolos. Tanto a expressão da proteína Ki-67 como da proteína pRb não demonstraram significância estatística na comparação entre os grupos do estudo. Assim, a avaliação de uma ampla série de casos revelou diferença significante no tempo de duração do CEL com relação à QA. Além disso, algumas alterações morfológicas foram observadas com maior frequência em casos de QA com evolução para CEL. No entanto, outros marcadores biológicos devem ser testados em conjunto, para tentar diagnosticar alterações precoces que levem ao desenvolvimento de CEL.


Actinic cheilitis (AC) is a potentially malignant lesion important to identify early signs of malignant transformation into lip squamous cell carcinoma (LSCC), enabling the implementation of an efficient and less invasive treatment to patients. Recent researches pointed that histopatological methods often fail to trace malignization risk in AC cases, because they are unable to identify genetic damage in keratinocytes and do not exist a clinical follow-up studie to assess if the grading of epithelial dysplasia in AC is related with the malignancy risk to LSCC development. Thus, this research aims to characterize, from cases of Surgical Pathology Service of Universidade de São Paulo, the differences in clinical and pathological profile among AC patients which had evolution to LSCC, AC patients without signs and information about malignization and patients diagnosed only with LSCC. This study also analyzed the expression of Ki-67 and pRb proteins in these three groups. To conduct this study, data as age, gender, race, fundamental lesion aspect, color, size and duration time of the lesion were collected from 998 patients. The clinical-epidemiological analysis revealed that duration time of the lesion was the statistically significant clinical feature to differentiate patients diagnosed only with LSCC from other groups. The grading of epithelial dysplasia analysis showed that all AC patients with


a posterior diagnosis of LSCC were classified as high risk lesions and these cases also exhibited most frequently atypia figures as: increased number of mitotic features, abnormal variation in nuclear size, abnormal variation in cellular size, increased nuclear/cytoplasmic ratio, abnormal mitotic features and increased number and size of nucleoli. The immunohistochemical expression of both Ki-67 and pRb protein demonstrated lack of significant statistical difference among the groups. We concluded that the evaluation of a large serie of cases revealed differences in duration time of lesion in patiens only diagnoses with LSCC and some morphological criteria were most frequent in AC cases with a posterior diagnosis of LSCC. However, other biological markers must be tested together, to try to identify early steps of LSCC development.


Subject(s)
Humans , Male , Female , Carcinoma, Squamous Cell/classification , Carcinoma, Squamous Cell/complications , Carcinoma, Squamous Cell/diagnosis , Immunohistochemistry/methods , Immunohistochemistry , Retinoblastoma Protein/administration & dosage , Retinoblastoma Protein/therapeutic use , Cheilitis/classification , Cheilitis/complications , Cheilitis/diagnosis
14.
São Paulo; s.n; 2015. 135 p. ilus, tab. (BR).
Thesis in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871120

ABSTRACT

A queilite actínica (QA) é uma lesão potencialmente maligna importante para identificar indícios precoces de transformação maligna para o carcinoma epidermoide de lábio (CEL), possibilitando a implementação de um tratamento eficiente e menos invasivo, que promova um melhor prognóstico para os pacientes. Pesquisas recentes indicam que os métodos histopatológicos geralmente são falhos em traçar o risco de malignização de casos de QA, pois além de não demonstrar as alterações genéticas presentes nos queratinócitos, não foram realizados estudos de acompanhamento clínico para avaliar se o grau de displaia epitelial da QA está relacionado ao risco de malignização para CE. Assim, a presente pesquisa teve como objetivo caracterizar, a partir dos casos atendidos no Serviço de Patologia Cirúrgica da FOUSP, qual a diferença de perfil clínico-patológico de pacientes de QA com evolução para CEL, pacientes de QA sem informações e sinais presentes de malignização e pacientes apenas diagnosticados com CEL, e também visou analisar a expressão de Ki67 e pRb nesses três grupos. Para isso, os dados dos pacientes como idade, sexo, cor da pele, aspecto clínico da lesão fundamental, coloração, tamanho e tempo de duração das lesões foram resgatados de 998 casos e distribuídos nessas três categorias. Os resultados da análise clínico-epidemiológica revelaram que o único aspecto clínico estatisticamente significante para diferenciar pacientes apenas diagnosticados com CEL dos demais grupos foi o tempo de duração das lesões. A análise do grau de displasia epitelial nos casos de QA na amostra presente revelou que todos os pacientes de QA posteriormente diagnosticados com CEL foram classificados como lesões de alto risco, e ainda exibiram em maior frequência as atipias: aumento do número de figuras de mitose, variação anormal do tamanho do núcleo, variação anormal do tamanho da célula e alteração da relação núcleo/citoplasma, figuras de mitose anormais e aumento do número e tamanho de nucléolos. Tanto a expressão da proteína Ki-67 como da proteína pRb não demonstraram significância estatística na comparação entre os grupos do estudo. Assim, a avaliação de uma ampla série de casos revelou diferença significante no tempo de duração do CEL com relação à QA. Além disso, algumas alterações morfológicas foram observadas com maior frequência em casos de QA com evolução para CEL. No entanto, outros marcadores biológicos devem ser testados em conjunto, para tentar diagnosticar alterações precoces que levem ao desenvolvimento de CEL.


Actinic cheilitis (AC) is a potentially malignant lesion important to identify early signs of malignant transformation into lip squamous cell carcinoma (LSCC), enabling the implementation of an efficient and less invasive treatment to patients. Recent researches pointed that histopatological methods often fail to trace malignization risk in AC cases, because they are unable to identify genetic damage in keratinocytes and do not exist a clinical follow-up studie to assess if the grading of epithelial dysplasia in AC is related with the malignancy risk to LSCC development. Thus, this research aims to characterize, from cases of Surgical Pathology Service of Universidade de São Paulo, the differences in clinical and pathological profile among AC patients which had evolution to LSCC, AC patients without signs and information about malignization and patients diagnosed only with LSCC. This study also analyzed the expression of Ki-67 and pRb proteins in these three groups. To conduct this study, data as age, gender, race, fundamental lesion aspect, color, size and duration time of the lesion were collected from 998 patients. The clinical-epidemiological analysis revealed that duration time of the lesion was the statistically significant clinical feature to differentiate patients diagnosed only with LSCC from other groups. The grading of epithelial dysplasia analysis showed that all AC patients with a posterior diagnosis of LSCC were classified as high risk lesions and these cases also exhibited most frequently atypia figures as: increased number of mitotic features, abnormal variation in nuclear size, abnormal variation in cellular size, increased nuclear/cytoplasmic ratio, abnormal mitotic features and increased number and size of nucleoli. The immunohistochemical expression of both Ki-67 and pRb protein demonstrated lack of significant statistical difference among the groups. We concluded that the evaluation of a large serie of cases revealed differences in duration time of lesion in patiens only diagnoses with LSCC and some morphological criteria were most frequent in AC cases with a posterior diagnosis of LSCC. However, other biological markers must be tested together, to try to identify early steps of LSCC development.


Subject(s)
Humans , Male , Female , Carcinoma, Squamous Cell/classification , Carcinoma, Squamous Cell/complications , Carcinoma, Squamous Cell/diagnosis , Immunohistochemistry/methods , Immunohistochemistry , Retinoblastoma Protein/administration & dosage , Retinoblastoma Protein/therapeutic use , Cheilitis/classification , Cheilitis/complications , Cheilitis/diagnosis
15.
Gen Dent ; 62(4): e26-9, 2014.
Article in English | MEDLINE | ID: mdl-24983181

ABSTRACT

Lip cancer is 65 times more likely to occur in kidney transplant patients than in members of the general population. Immunosuppression drugs taken by the transplant patients have been associated with this increased occurrence. This case report shows the progression from actinic cheilosis to squamous cell carcinoma (SCC) in the lower lip of a 58-year-old man receiving immunosuppressive therapy 9 years after undergoing a kidney transplant. Earlier incisional biopsies had resulted in a histological diagnosis of actinic cheilosis. However, the last incisional biopsy showed histological results compatible with SCC, and oncological surgery was performed. Eight months post-surgery, the patient was free of cancer and metastasis. Frequent dental follow-up visits allowed for the early diagnosis, proper treatment, and an improved prognosis for this patient.


Subject(s)
Carcinoma, Squamous Cell/diagnosis , Cheilitis/complications , Kidney Transplantation , Lip Neoplasms/diagnosis , Carcinoma, Squamous Cell/complications , Early Diagnosis , Humans , Immunosuppressive Agents/administration & dosage , Lip Neoplasms/complications , Male , Middle Aged
16.
Ethiop J Health Sci ; 23(2): 183-7, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23950636

ABSTRACT

BACKGROUND: Plasma cell gingivitis (PGC) is a rare disease of gingival tissues which is difficult to treat. It has a higher rate of reoccurrence and needs a detailed and careful analysis of etiology. Further, its association with chelitis is rare, only few cases have been reported and the condition with this presentation poses a diagnostic dilemma. CASE REPORT: This paper reports a 16 year old male with a complaint of bleeding and swelling of gingiva since 3 years. The gingival enlargement occurred on facial aspect of upper and lower anterior teeth involving attached gingival. He also presented with swelling of both lips which was recurrent and for the same duration of 3 years. DISCUSSION: Based on clinical features and histopathological findings, a diagnosis of plasma cell gingivitis with inflammatory chelitis was made. A detailed history of possible allergen exposure was taken and patch test was conducted to identify any such allergens. Other conditions were ruled out by blood investigation, detailed medical and drug history. CONCLUSION: A close collaboration between Periodontist and Dermatologist is essential to manage such a case.


Subject(s)
Cheilitis/complications , Gingiva/pathology , Gingival Hyperplasia/complications , Gingivitis/complications , Lip/pathology , Plasma Cells/pathology , Adolescent , Cheilitis/pathology , Gingivitis/pathology , Humans , Male , Recurrence
17.
Histopathology ; 63(3): 371-7, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23865379

ABSTRACT

AIM: This study investigated the immunohistochemical expression of hMLH1 and hMSH2 proteins in lower lip squamous cell carcinoma (SCC) and actinic cheilitis (AC), to contribute to the understanding of the development of lower lip cancer. METHODS AND RESULTS: Forty cases of lower lip AC and SCC were studied. Quantitative immunohistochemical analysis was undertaken by counting 1000 cells (positive and negative) in each lesion. Statistical evaluation included Student's t-test and one-way ANOVA. For SCC and AC, the mean number of hMLH1- and hMSH2-positive cells decreased with advanced stage of the lesion. The largest mean number of immunostained cells was observed in AC cases without dysplasia or with mild dysplasia (hMLH1: 721.23 ± 88.116; hMHS2: 781.50 ± 156.93). Intermediate values were obtained for AC with moderate or severe dysplasia (hMLH1: 532.86 ± 197.72; hMHS2: 611.14 ± 172.48). Lower lip SSCs presented the smallest number of positive cells (hMLH1: 255.03 ± 199.47; hMHS2: 518.38 ± 265.68). A statistically significant difference was observed between groups (P < 0.001). CONCLUSIONS: The results support the hypothesis that changes in the immunoexpression of these mismatch proteins are related to the process of carcinogenesis of the lower lip.


Subject(s)
Adaptor Proteins, Signal Transducing/metabolism , Carcinoma, Squamous Cell/metabolism , Lip Neoplasms/metabolism , MutS Homolog 2 Protein/metabolism , Nuclear Proteins/metabolism , Adult , Aged , Aged, 80 and over , Carcinogenesis , Carcinoma, Squamous Cell/etiology , Carcinoma, Squamous Cell/pathology , Cheilitis/complications , Cheilitis/metabolism , Cheilitis/pathology , DNA Mismatch Repair , Female , Humans , Immunohistochemistry , Lip Neoplasms/etiology , Lip Neoplasms/pathology , Male , Middle Aged , MutL Protein Homolog 1 , Precancerous Conditions/metabolism , Precancerous Conditions/pathology , Retrospective Studies
18.
Oral Dis ; 18(7): 667-72, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22548381

ABSTRACT

OBJECTIVE: Heightened interest in oral health has lead to an increase in patients complaining of xerostomia, which is associated with various oral mucosal disorders. In this study, we investigated the relationship between Candida species and oral mucosal disorders in patients with xerostomia. SUBJECTS AND METHODS: We evaluated whole salivary flow rate and presence of oral mucosal disorders in 48 patients with xerostomia and 15 healthy controls. The number of Candida species was measured as colony-forming units after propagation on selective medium. Identification of Candida at the species level was carried out by polymerase chain reaction and restriction fragment length polymorphism analysis. We then examined the relationship between Candida species and oral mucosal symptoms. RESULTS: Compared with controls, patients with xerostomia exhibited significantly decreased whole salivary flow rate, increased rate of oral mucosal symptoms, and higher numbers of Candida. Salivary flow rate negatively correlated with the number Candida. Among patients with oral candidiasis, Candida albicans was isolated from the tongue mucosa and Candida glabrata was isolated from the angle of the mouth. CONCLUSION: These results suggest that particular Candida species are involved in the pathogenesis of oral mucosal disorders in patients with xerostomia.


Subject(s)
Candidiasis, Oral/complications , Mouth Mucosa/microbiology , Xerostomia/complications , Adult , Aged , Candida albicans/isolation & purification , Candida glabrata/isolation & purification , Candidiasis, Oral/microbiology , Case-Control Studies , Cheilitis/complications , Chi-Square Distribution , Colony Count, Microbial , DNA, Fungal/genetics , Female , Humans , Male , Middle Aged , Mouth Mucosa/pathology , Polymorphism, Restriction Fragment Length , Saliva/metabolism , Sjogren's Syndrome/complications , Statistics, Nonparametric , Tongue Diseases/complications
19.
Int J Paediatr Dent ; 22(5): 390-6, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22404234

ABSTRACT

BACKGROUND: This paper aims to review the case of a girl who presented with a number of dental anomalies, in addition to unusual skin, nail and hair conditions. Tragically an undiagnosed cardiomyopathy caused unexpected sudden death. The case is discussed with reference to a number of dermatological and oral conditions which were considered as possible diagnoses. CASE REPORT: AW had been under long term dental care for prepubertal periodontitis, premature root resorption of primary teeth, soft tissue and dental anomalies, and angular cheilitis. Separately she had also been seen by several dermatologists with respect to palmar plantar keratosis, striae keratoderma, wiry hair and abnormal finger nails. Tragically the patient suffered a sudden unexpected death and the subsequent post mortem identified an undiagnosed dilated cardiomyopathy. CONCLUSION: The most likely diagnosis is that this case is a variant of Carvajal Syndrome with additional dental anomalies. To date we have been unable to identify mutations in the desoplakin gene. We aim to emphasise the importance of recognising these dental and dermatological signs when they present together as a potential risk factor for cardiac abnormalities.


Subject(s)
Aggressive Periodontitis/complications , Anodontia/complications , Cardiomyopathies/complications , Hair Diseases/complications , Keratoderma, Palmoplantar/complications , Root Resorption/complications , Tooth Loss/complications , Abnormalities, Multiple , Adolescent , Aggressive Periodontitis/therapy , Cardiomyopathies/diagnosis , Cardiomyopathy, Dilated , Cheilitis/complications , Child , Child, Preschool , Female , Hair Diseases/diagnosis , Humans , Infant , Infant, Newborn , Keratoderma, Palmoplantar/diagnosis , Mouth Mucosa/abnormalities , Tooth Exfoliation/complications , Tooth, Deciduous/physiopathology
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