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Journal articles on the topic 'Stomatitas'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Maity, Pallab, Anjum N. Rizvi, and Charles R. Bursey. "Nematode parasites of Duttaphrynus stomaticus (Lutken, 1864) (Amphibia: Anura) with description of a new species of Rhabdias Stiles and Hassall, 1905 (Nematoda: Rhabdiasidae) from Dehradun (Uttarakhand), India." Acta Parasitologica 63, no. 1 (March 26, 2018): 175–83. http://dx.doi.org/10.1515/ap-2018-0020.

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Abstract Rhabdias stomatica sp. nov. from the lungs of Duttaphrynus stomaticus (Lutken, 1864) from Dehradun, Uttarakhand, India is described and illustrated. Rhabdias stomatica sp. nov. is the 16th species described from the Oriental biogeographical region and the 8th species from India. The new species is differentiated from the closely related Oriental species in having 4 weakly developed lips, a trapezoidal shaped buccal cavity, different position of nerve ring and in the esophagus/body length ratio. In addition, to the new species found in the lungs, mature specimens of Aplectana macintoshii (Stewart, 1914) Travassos, 1931 and larvae representing two unidentified species of nematode were found in the large intestine of the D. stomaticus.

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2

Hong, Dae Young, Seo Kyu Kim, Young II Moon, and Yoon Ju Chong. "Three cases of Major Aphthous Stomatitis (Sutton’s Disease)." Journal of Clinical Otolaryngology Head and Neck Surgery 6, no. 1 (May 1995): 131–37. http://dx.doi.org/10.35420/jcohns.1995.6.1.131.

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3

Baldwin, Patricia Donahue, and Ruth Van Gerpen. "Stomatitis." Clinical Journal of Oncology Nursing 7, no. 4 (July 1, 2003): 471–74. http://dx.doi.org/10.1188/03.cjon.471-474.

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4

Ganesha, Raziv. "MANAGEMENT OF ALLERGIC STOMATITIS CAUSED BY CHICKEN AND EGG." Interdental Jurnal Kedokteran Gigi (IJKG) 17, no. 1 (June 22, 2021): 34–40. http://dx.doi.org/10.46862/interdental.v17i1.1947.

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Introduction: Allergic stomatitis is a hypersensitivity reaction caused by an allergen such as medicines, foods, dental materials. Chicken and egg are some of the common food we usually consumed. Chicken contains a low amount of protein and fat, while egg contains nutrients and easy to process. Although allergic reactions in poultry products are commonly found in eggs and feathers, chicken is often a cause of the allergic reaction. Case: 28-year-old male patient complained of an ulcer in his mouth. It shows the past 3 days on his upper lips then it shows on his left cheek. Case Treatment: Diagnosis made by anamnesis, clinical examination, and supporting examination such as complete blood count, total IgE, and Skin Prick Test. The patient was prescribed topical anti-inflammatory 2 times daily and after the Skin Prick Test was done the patient was given methylprednisolone 3 times daily for 7 days, the patient was treated in 3 visits. Discussion: A Food allergy usually involved type 1 and 4 hypersensitivity reactions, or both. Skin Prick Test is one of the skin test commonly used by clinicians to prove the presence of specific IgE bound to skin mastocyte cells. Treatment for this case besides medication was advised to avoid food that causes the allergic reaction. Conclusion: Management of this case can be successful if the clinician understands the clinical manifestation of hypersensitivity reaction to food and can make the right diagnosis to provide proper treatment. Furthermore requires patient cooperation to follow the prescribed care instruction

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5

Sudarshan, Ramachandran, RajeshwariG Annigeri, GP Mamatha, and GSree Vijayabala. "Uremic stomatitis." Contemporary Clinical Dentistry 3, no. 1 (2012): 113. http://dx.doi.org/10.4103/0976-237x.94560.

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6

Mavrutenkov, V. V. "Viral Stomatitis." CHILD`S HEALTH, no. 3.63 (July 1, 2015): 63–68. http://dx.doi.org/10.22141/2224-0551.3.63.2015.75204.

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7

Piqué-Duran, E., S. Palacios-Llopis, and J. A. Pérez-Cejudo. "Geographic Stomatitis." Actas Dermo-Sifiliográficas (English Edition) 101, no. 4 (2010): 359–61. http://dx.doi.org/10.1016/s1578-2190(10)70649-1.

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8

Plosay, John J., and Walter C. Robey. "Mouthwash stomatitis." Annals of Emergency Medicine 18, no. 6 (June 1989): 709–10. http://dx.doi.org/10.1016/s0196-0644(89)80540-2.

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9

LeSueur, Benjamin W., and James A. Yiannias. "Contact stomatitis." Dermatologic Clinics 21, no. 1 (January 2003): 105–14. http://dx.doi.org/10.1016/s0733-8635(02)00070-0.

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10

Schmitt, Beverly. "Vesicular stomatitis." Veterinary Clinics of North America: Food Animal Practice 18, no. 3 (November 2002): 453–59. http://dx.doi.org/10.1016/s0749-0720(02)00031-2.

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11

Donaldson, A. I., and N. P. Ferris. "Vesicular stomatitis." Equine Veterinary Education 7, no. 4 (August 1995): 205–7. http://dx.doi.org/10.1111/j.2042-3292.1995.tb01226.x.

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12

Donaldson, A. I., and N. P. Ferris. "Vesicular stomatitis." Equine Veterinary Education 8, S2 (June 10, 2010): 44–46. http://dx.doi.org/10.1111/j.2042-3292.1996.tb01856.x.

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13

Fisher, Alexander A. "Contact Stomatitis." Dermatologic Clinics 5, no. 4 (October 1987): 709–17. http://dx.doi.org/10.1016/s0733-8635(18)30714-9.

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14

LETCHWORTH, G. J., L. L. RODRIGUEZ, and J. DEL CBARRERA. "Vesicular Stomatitis." Veterinary Journal 157, no. 3 (May 1999): 239–60. http://dx.doi.org/10.1053/tvjl.1998.0303.

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15

Talish, Mishaal, and Ashley M. DiLorenzo. "Uremic Stomatitis." New England Journal of Medicine 382, no. 26 (June 25, 2020): 2556. http://dx.doi.org/10.1056/nejmicm1914867.

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16

Timoney, Peter. "Vesicular stomatitis." Veterinary Record 179, no. 5 (July 28, 2016): 119–20. http://dx.doi.org/10.1136/vr.i4075.

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17

Yano, Hiroyuki, and Mitsuyo Kinjo. "Uraemic stomatitis." BMJ Case Reports 12, no. 10 (October 2019): e231948. http://dx.doi.org/10.1136/bcr-2019-231948.

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18

Chen, Yuntzu-Yen, and Matthew J. Zirwas. "Denture Stomatitis." SKINmed 6, no. 2 (March 2007): 92–94. http://dx.doi.org/10.1111/j.1540-9740.2007.05867.x.

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19

van Rijswijk, Ingrid. "Stomatitis prothetica." Tandartspraktijk 35, no. 11 (November 2014): 29–32. http://dx.doi.org/10.1007/s12496-014-0126-5.

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20

. "Stomatitis aphthosa." Medisch-Farmaceutische Mededelingen 40, no. 4 (April 2002): 119. http://dx.doi.org/10.1007/bf03057920.

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21

Littner, M. M., D. Dayan, M. Gorsky, D. Moskona, and M. Harel-Raviv. "Migratory stomatitis." Oral Surgery, Oral Medicine, Oral Pathology 63, no. 5 (May 1987): 555–59. http://dx.doi.org/10.1016/0030-4220(87)90227-1.

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22

Shah, Kena, Juan Guarderas, and Guha Krishnaswamy. "Aphthous stomatitis." Annals of Allergy, Asthma & Immunology 117, no. 4 (October 2016): 341–43. http://dx.doi.org/10.1016/j.anai.2016.07.005.

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23

Cifuentes, Mirtha, Parastoo Davari, and Roy S. Rogers. "Contact stomatitis." Clinics in Dermatology 35, no. 5 (September 2017): 435–40. http://dx.doi.org/10.1016/j.clindermatol.2017.06.007.

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24

Pechnikov, Y. "Honorrhoid stomatitis." Kazan medical journal 22, no. 2 (December 24, 2020): 248. http://dx.doi.org/10.17816/kazmj52947.

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Klepper (Derm. Woch., 1925, no. 39) describes an interesting case of gonorrhoid stomatitis in a hospital nurse with a history of recurrent aphthous stomatitis. 4 days after the usual relapse, the patient began to care for the child suffering from gonoblenorrhea, and after the next 4 days, she had a sudden deterioration of the usual process in the mouth: severe pain while eating, swelling of the tongue, fever, sores near the tip of the tongue, in the corner of the mouth and along the edge of the lower gum, with severe inflammation. Gonococci were found in smears and cultures of ulcer discharge. This case is interesting, as it contradicts the old ideas about the immunity of the oral mucosa of adults in relation to gonorrhoid infection.

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25

Büyükcam, Ayşe. "Toplum Kaynaklı Pnömoniye Eşlik Eden Ülseratif Stomatit ve Vezikülobüllöz Lezyonlar." Journal of Pediatric Infection 12, no. 3 (September 29, 2018): 126–28. http://dx.doi.org/10.5578/ced.201839.

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26

Arya, Deeksha, Aditi Verma, Saumyendra Vikram Singh, Prashant Gupta, Anupama Pathak, and Shuchi Tripathi. "A study to evaluate etiology of denture stomatitis and to determine interrelationship with trauma and candida albicans count." IP Annals of Prosthodontics and Restorative Dentistry 7, no. 3 (September 15, 2021): 151–56. http://dx.doi.org/10.18231/j.aprd.2021.031.

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Denture stomatitis (DS) is a disease characterized by inflammation and erythema of the oral mucosa areas covered by the denture. Multifactorial etiological factors contribute to denture stomatitis. The purpose of this study is to identify the etiology of denture stomatitis and to establish the role of trauma and fungal infection in denture stomatitis.Subjects wearing previously fabricated removable partial or complete denture who were diagnosed with denture stomatitis were included. It is a cross sectional questionnaire-based study, for mycological study swab sample was smeared, Sabouraud Dextrose Agar (SDA) was used as culture media. Germ tube test was used to identify Candida albicans. To test significance between different variablesKruskal-Wallis test was used. Out of 195 subjects’ slight stomatitis was present in 52.80% patients, followed by moderate stomatitis in 32.31% and no stomatitis in 2.56% subjects. Candida was present in 25.64% patients. Candida significantly more common in moderate stomatitis than others.This study has suggested that there is a significant relation in denture stomatitis and Candida albicans in north Indian population. No significant role of trauma was noticed. Strong correlation has been found in Denture hygiene, cleaning habits and Denture Stomatitis.

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27

Rugo, Hope S., James C. Yao, Marianne Pavel, Alain Ravaud, David Neal Franz, Tanya Taran, Jorge Gallo, Nicolas Rouyrre, Oezlem Anak, and Robert J. Motzer. "Stomatitis incidence and its relationship with efficacy: A meta-analysis of everolimus clinical studies." Journal of Clinical Oncology 32, no. 26_suppl (September 10, 2014): 151. http://dx.doi.org/10.1200/jco.2014.32.26_suppl.151.

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151 Background: The most common adverse event (AE) with everolimus (EVE) is stomatitis. This meta-analysis evaluated the incidence, severity, and possible impact of stomatitis on efficacy in patients (pts) with cancer or tuberous sclerosis complex (TSC) who received EVE. Methods: Stomatitis events from 7 randomized, double-blind, phase 3 EVE studies included: RECORD-1 (RCC), RADIANT-2 (NET), RADIANT-3 (pNET), BOLERO-2 (HR+/HER2- breast cancer [BC]), BOLERO-3 (HER2+BC), and EXIST-1 and -2 (TSC). Time to first stomatitis occurrence and recurrence were analyzed using Kaplan-Meier (KM) methods. Stratified Cox regression analysis adjusted for baseline prognostic factors and corrected for confounding effect of duration of exposure was used to analyze association between stomatitis occurrence (≤ 8 wks of EVE start) and PFS in pts with cancer and response rate in pts with TSC. Results: This evaluation included EVE-treated pts with cancer (n = 1,455) and TSC (n = 157). Pts with cancer had stomatitis incidence of 66.9%, which occurred early, median 0.82 mo (95% CI, 0.7-1.0; 2-mo KM estimate 60.8%). 8.6% were grade 3/4 events. 1.7% of pts discontinued due to stomatitis. Stomatitis recurred in 40% of pts and appeared gradually. In pts with TSC similar results were observed. In EVE-treated pts, development of stomatitis was associated with longer PFS (corrected HR [95% CI]) in BOLERO-2 (0.78 [0.62-1.00]) and RADIANT-3 (0.70 [0.48-1.01]), and similar trend was observed in RECORD-1 (0.90 [0.66-1.22]) and RADIANT-2 (0.87 [0.61-1.22]), but not in BOLERO-3. In TSC, probably due to few pts, relationship between stomatitis and response was not conclusive. In all trials, pts on EVE had longer PFS vs placebo irrespective of stomatitis incidence. Conclusions: Stomatitis is observed frequently in initial wks of EVE therapy. Most AEs were grade 1/2 and manageable, rarely led to pt discontinuation. Stomatitis recurred in < 50% of pts. EVE-treated pts with cancer who had stomatitis achieved stable benefit similar to overall population, suggesting that continuing EVE is helpful. The importance of prophylactic measures in reducing EVE-induced stomatitis incidence and improving its management is being determined by ongoing studies.

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28

Hara, Yaeko, Hiroshi Shiratuchi, Tadayoshi Kaneko, and Hiroshi Sakagami. "Search for Drugs Used in Hospitals to Treat Stomatitis." Medicines 6, no. 1 (January 29, 2019): 19. http://dx.doi.org/10.3390/medicines6010019.

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Stomatitis is an inflammatory disease of the oral mucosa, often accompanied by pain. Usually it is represented by aphthous stomatitis, for which treatment steroid ointment is commonly used. However, in the cases of refractory or recurrent stomatitis, traditional herbal medicines have been used with favorable therapeutic effects. Chemotherapy, especially in the head and neck region, induces stomatitis at higher frequency, which directly affects the patient’s quality of life and treatment schedule. However, effective treatment for stomatitis has yet to be established. This article presents the clinical report of Kampo medicines on the stomatitis patients in the Nihon university, and then reviews the literature of traditional medicines for the treatment of stomatitis. Among eighteen Kampo medicines, Hangeshashinto has been the most popular for the treatment of stomatitis, due to its prominent anti-inflammatory activity. It was unexpected that clinical data of Hangeshashinto on stomatitis from Chinese hospital are not available. Kampo medicines have been most exclusively administered to elder person, as compared to pediatric population. Supplementation of alkaline plant extracts rich in lignin-carbohydrate complex may further extend the applicability of Kampo medicines to viral diseases.

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29

Borotova, Sharifa Abdupattoevna. "Effective Treatment Of Afthous Stomatitis In The Practice Of A Doctor." American Journal of Medical Sciences and Pharmaceutical Research 03, no. 04 (April 28, 2021): 39–42. http://dx.doi.org/10.37547/tajmspr/volume03issue04-05.

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Aphthous stomatitis is a focal inflammation of the oral mucosa, in which round ulcers (aphthae or erosion) form. Aphthae affect the inner surface of the cheeks, palate, tongue, become covered with a gray or yellowish coating, cause pain and discomfort. Usually the disease proceeds chronically, from time to time exacerbates, after 7-10 days it goes into remission.

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30

Indrawati, Erni, and Kus Harijanti. "Management of allergic stomatitis due to dailyfoodconsumption(Penatalaksanaan stomatitis alergika akibat konsumsi makanan sehari-hari)." Journal of Dentomaxillofacial Science 13, no. 2 (June 30, 2014): 129. http://dx.doi.org/10.15562/jdmfs.v13i2.402.

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Allergic stomatitis or stomatitis venenata is a hypersensitivity reaction caused by an allergen from medicines, foods,dental materials (restoration material, prosthetic, orthodontic appliance, mercury, acrylic, cobalt). This report willdiscusses the management of food allergic stomatitis. The common cause of food allergy in adult patients are orange(citrus fruit), nuts, fish, marine fish and wheat. Oral manifestations of allergic stomatitis begin with multiple vesiclesand becomes fibrin-covered ulcers with erythematous edges accompanied by inflammation and pain. The patient was a53-year-old woman who has suffered stomatitis since 6 months ago, and had seen dentist in private practice andgovernment dental-practice (hospitals and health centers). The patient has an a allergy history. Intra oral examinationfound the presence of multiple ulcers on the buccal mucosa upper right, cheek mucosa lower right and tongue. Thefinal diagnosis of the case is allergic stomatitis due to daily food alergic base on anamesis, clinical examination andlaboratory tests. Treatment to prevent allergic stomatitis causes, symptomatic therapy, and topical corticosteroids. Itwas concluded that management of allergic stomatitis should avoid the food as primary causes, giving mouthwashcontaining analgesic/anti-inflammatory and topical corticosteroids.

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31

Sivesh Sangar, Jayanth Kumar Vadivel, and Visalakshi Ramanathan. "Prevalence of smoking in patients with aphthous stomatitis: A retrospective case-control study." International Journal of Research in Pharmaceutical Sciences 11, SPL3 (October 22, 2020): 1755–60. http://dx.doi.org/10.26452/ijrps.v11ispl3.3508.

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Apthous stomatitis represents one of the most common ulcerations occurring in the oral cavity. This ulcer has an exclusive predilection of affecting the non-keratinized mucosa only. The aim of this study was to assess the prevalence of smoking in patients with apthous stomatitis. Seventy-six patients with recurrent apthous stomatitis attending Saveetha Dental Hospital, Chennai were included in the study. The data gathered was entered into an excel table, and the data analysis was done in SPSS. The data analysis revealed that the mean age of the collected samples of 76 patients was 32.21 years, and 67.1% of the samples were males. Analyzing the clinical variants, 70 patients had minor apthous stomatitis, five patients had major apthous stomatitis, and one patient had herpetiform apthous stomatitis. Results showed that patients who are not smokers have a higher rate of recurrence of recurrent apthous stomatitis compared to patients who are smokers with 6.6% being the prevalence rate for smokers and 93.4% being the prevalence rate for non-smokers. Data analysis was done using a chi-square analysis between the clinical variants of recurrent apthous stomatitis and smoking habits (chi-square-1.132; df-2; p-0.05) we found the results were statistically significant (P=0.05) which implies there were less self-reported diabetics in this study Prevalence of smoking in patients with recurrent apthous stomatitis is significantly lower than patients who are not smokers. The reason for the decreased occurrence of apthous stomatitis in smokers may be due to the increased keratinization of the mucosa.

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32

Naimer, Sody. "Pseudomembranous Plaque Stomatitis." Investigative Dermatology and Venereology Research 2, no. 3 (2016): 1–5. http://dx.doi.org/10.15436/2381-0858.16.1010.

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33

Chattopadhyay, Amit, and Kishore V. Shetty. "Recurrent Aphthous Stomatitis." Otolaryngologic Clinics of North America 44, no. 1 (February 2011): 79–88. http://dx.doi.org/10.1016/j.otc.2010.09.003.

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34

Paolo, P., A. Ronchi, F. Spadari, G. P. Bombeccari, I. Bolengo, L. Brambilla, S. Ferrucci, and G. Guzzi. "Beryllium-related stomatitis." Toxicology Letters 238, no. 2 (October 2015): S161. http://dx.doi.org/10.1016/j.toxlet.2015.08.499.

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35

Giedlin, Martin A., David N. Cook, and Thomas W. Dubensky. "Vesicular stomatitis virus." Cancer Cell 4, no. 4 (October 2003): 241–43. http://dx.doi.org/10.1016/s1535-6108(03)00251-4.

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36

Preeti, L., KT Magesh, K. Rajkumar, and Raghavendhar Karthik. "Recurrent aphthous stomatitis." Journal of Oral and Maxillofacial Pathology 15, no. 3 (2011): 252. http://dx.doi.org/10.4103/0973-029x.86669.

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37

Zunt, Susan L. "Recurrent aphthous stomatitis." Dermatologic Clinics 21, no. 1 (January 2003): 33–39. http://dx.doi.org/10.1016/s0733-8635(02)00075-x.

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38

Rees, Terry D., and William H. Binnie. "RECURRENT APHTHOUS STOMATITIS." Dermatologic Clinics 14, no. 2 (April 1996): 243–56. http://dx.doi.org/10.1016/s0733-8635(05)70353-3.

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39

Porter, Stephen R., Anne Hegarty, Fotini Kaliakatsou, Tim A. Hodgson, and Crispian Scully. "Recurrent aphthous stomatitis." Clinics in Dermatology 18, no. 5 (September 2000): 569–78. http://dx.doi.org/10.1016/s0738-081x(00)00147-4.

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40

Brown, Carlton G., and Linda H. Yoder. "Stomatitis: An Overview." American Journal of Nursing 102 (April 2002): 20–23. http://dx.doi.org/10.1097/00000446-200204001-00005.

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41

Porter, S. R., C. Scully, and A. Pedersen. "Recurrent Aphthous Stomatitis." Critical Reviews in Oral Biology & Medicine 9, no. 3 (July 1998): 306–21. http://dx.doi.org/10.1177/10454411980090030401.

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Recurrent aphthous stomatitis (RAS) is one of the most common oral mucosal disorders. Nevertheless, while the clinical characteristics of RAS are well-defined, the precise etiology and pathogenesis of RAS remain unclear. The present article provides a detailed review of the current knowledge of the etiology, pathogenesis, and managment of RAS.

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42

Solomon, LW. "Chronic ulcerative stomatitis." Oral Diseases 14, no. 5 (July 2008): 383–89. http://dx.doi.org/10.1111/j.1601-0825.2008.01446.x.

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43

Piantanida, E. Winfield, and Curt P. Samlaska. "Recurrent aphthous stomatitis." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 82, no. 5 (November 1996): 472. http://dx.doi.org/10.1016/s1079-2104(96)80186-7.

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44

Ship, Jonathan A. "Recurrent aphthous stomatitis." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 81, no. 2 (February 1996): 141–47. http://dx.doi.org/10.1016/s1079-2104(96)80403-3.

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45

Generali, Joyce, and Dennis J. Cada. "Pentoxifylline: Aphthous Stomatitis." Hospital Pharmacy 39, no. 10 (October 2004): 958–61. http://dx.doi.org/10.1177/001857870403901006.

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46

Beguerie, Julieta Ruiz, and Mariana Sabas. "Recurrent Aphthous Stomatitis." Journal of the Dermatology Nurses’ Association 7, no. 1 (2015): 8–12. http://dx.doi.org/10.1097/jdn.0000000000000099.

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47

&NA;. "Recurrent Aphthous Stomatitis." Journal of the Dermatology Nurses’ Association 7, no. 1 (2015): 13–14. http://dx.doi.org/10.1097/jdn.0000000000000109.

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48

Ryan, Melody, Robert J. Baumann, Craig S. Miller, and Chris Baker. "Valproate-Associated Stomatitis." Journal of Child Neurology 17, no. 3 (March 2002): 225–27. http://dx.doi.org/10.1177/088307380201700315.

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49

Generali, Joyce, and Dennis J. Cada. "Pentoxifylline: Aphthous Stomatitis." Hospital Pharmacy 42, no. 12 (December 2007): 1117–21. http://dx.doi.org/10.1310/hpj4212-1117.

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50

Rennie, J. S., P. C. Reade, K. D. Hay, and C. Scully. "Recurrent aphthous stomatitis." British Dental Journal 159, no. 11 (December 1985): 361–67. http://dx.doi.org/10.1038/sj.bdj.4805734.

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