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1.
Am J Case Rep ; 23: e935362, 2022 May 21.
Article in English | MEDLINE | ID: mdl-35642551

ABSTRACT

BACKGROUND The immunomodulatory and pharmacokinetic effects of cyclosporine A are used to treat diverse disease entities in different medical fields, including organ transplantation and/or autoimmune diseases. It is also applied in patients with nephrotic range proteinuria as an adjunct to steroids and supportive antihypertensive/antiproteinuric medications. Cyclosporine has a small therapeutic window and is dosed with respect to the underlying disease entity and severity via trough level adaptations. Among its most frequent adverse effects are hypertension, nephrotoxicity, neurotoxicity, and electrolyte disturbances. Hypertrichosis and gingival hyperplasia are obvious and widely recognized adverse effects. CASE REPORT We report on a 66-year-old woman who was treated with cyclosporine A for primary membranous nephropathy. During treatment with cyclosporine, she developed hirsutism and gingival hyperplasia. Later, she reported having impaired nasal breathing and dyspnea on mild physical exercise. Clinical, rhinoscopic, and radiological evaluations showed marked conchal hyperplasia as a potential cause of her symptoms. An extensive medical work-up did not show evidence of allergic, immunologic, or other drug adverse effects, suggesting cyclosporine-induced hyperplasia of the turbinates as a hypothetical causative factor. Dose reductions did not lead to resolution of symptoms but resulted in increasing proteinuria. Therefore, cyclosporine was stopped, and the patient was treated with rituximab. Thereafter, hirsutism and gingival and conchal hyperplasia gradually regressed over 2-4 months, showing complete resolution of conchal hyperplasia on computed-tomography follow-up after 6 months. CONCLUSIONS Cyclosporine can not only result in gingival hyperplasia but also in hyperplasia of the turbinates leading to impaired nasal breathing and shortness of breath on exertion. An extensive search for many other known causes of conchal swelling is warranted to finally suggest an adverse effect of cyclosporine. Discontinuation of cyclosporine resulted in complete remission of conchal hyperplasia as well as other adverse effects.


Subject(s)
Gingival Hyperplasia , Glomerulonephritis, Membranous , Nasal Obstruction , Aged , Cyclosporine/adverse effects , Female , Gingival Hyperplasia/chemically induced , Gingival Hyperplasia/drug therapy , Glomerulonephritis, Membranous/chemically induced , Glomerulonephritis, Membranous/complications , Glomerulonephritis, Membranous/drug therapy , Hirsutism/chemically induced , Hirsutism/drug therapy , Humans , Hyperplasia , Immunosuppressive Agents/adverse effects , Proteinuria/drug therapy , Turbinates
2.
Clin Adv Periodontics ; 12(2): 130-133, 2022 06.
Article in English | MEDLINE | ID: mdl-32852892

ABSTRACT

INTRODUCTION: Gingival enlargement (GE) due to anti-epileptic drugs (AEDs) shows a high prevalence rate. However, lamotrigine, a newer AED, has not shown to induce GE. The present case report describes a rare case of GE in a patient with epilepsy under lamotrigine therapy for the past 3 years. CASE PRESENTATION: In this report, successful management of lamotrigine-influenced GE in a 24-year-old patient with epilepsy by gingivectomy followed by stringent oral hygiene protocol is presented. CONCLUSION: The present case report suggests that, even this newer AED can cause GE and the oral hygiene status of the patients could be an important triggering factor.


Subject(s)
Epilepsy , Gingival Hyperplasia , Gingival Hypertrophy , Gingival Overgrowth , Anticonvulsants/adverse effects , Epilepsy/chemically induced , Epilepsy/drug therapy , Epilepsy/epidemiology , Gingival Hyperplasia/chemically induced , Gingival Hyperplasia/drug therapy , Gingival Hypertrophy/chemically induced , Gingival Hypertrophy/drug therapy , Gingival Overgrowth/chemically induced , Gingival Overgrowth/drug therapy , Humans , Lamotrigine/adverse effects , Young Adult
4.
Int J Mol Sci ; 21(2)2020 Jan 16.
Article in English | MEDLINE | ID: mdl-31963361

ABSTRACT

BACKGROUND: Gingival hyperplasia could occur after the administration of cyclosporine A. Up to 90% of the patients submitted to immunosuppressant drugs have been reported to suffer from this side effect. The role of fibroblasts in gingival hyperplasia has been widely discussed by literature, showing contrasting results. In order to demonstrate the effect of cyclosporine A on the extracellular matrix component of fibroblasts, we investigated the gene expression profile of human fibroblasts after cyclosporine A administration. MATERIALS AND METHODS: Primary gingival fibroblasts were stimulated with 1000 ng/mL cyclosporine A solution for 16 h. Gene expression levels of 57 genes belonging to the "Extracellular Matrix and Adhesion Molecules" pathway were analyzed using real-time PCR in treated cells, compared to untreated cells used as control. RESULTS: Expression levels of different genes were significantly de-regulated. The gene CDH1, which codes for the cell adhesion protein E-cadherin, showed up-regulation. Almost all the extracellular matrix metalloproteases showed down-regulation (MMP8, MMP11, MMP15, MMP16, MMP24, MMP26). The administration of cyclosporine A was followed by down-regulation of other genes: COL7A1, the transmembrane receptors ITGB2 and ITGB4, and the basement membrane constituents LAMA2 and LAMB1. CONCLUSION: Data collected demonstrate that cyclosporine inhibits the secretion of matrix proteases, contributing to the accumulation of extracellular matrix components in the gingival connective tissue, causing gingival overgrowth. Patients affected by gingival overgrowth caused by cyclosporine A need to be further investigated in order to determine the role of this drug on fibroblasts.


Subject(s)
Cyclosporine/pharmacology , Cyclosporine/therapeutic use , Gingiva/drug effects , Gingival Hyperplasia/drug therapy , Cells, Cultured , Fibroblasts/drug effects , Fibroblasts/metabolism , Gingiva/metabolism , Gingival Hyperplasia/metabolism , Humans , Matrix Metalloproteinase 11/metabolism , Matrix Metalloproteinase 15/metabolism , Matrix Metalloproteinase 16/metabolism , Matrix Metalloproteinase 8/metabolism , Matrix Metalloproteinases, Membrane-Associated/metabolism , Matrix Metalloproteinases, Secreted/metabolism
5.
Photobiomodul Photomed Laser Surg ; 37(1): 57-61, 2019 Jan.
Article in English | MEDLINE | ID: mdl-31050937

ABSTRACT

Objective: To describe a clinical case of successful conservative management of Localized Juvenile Spongiotic Gingivitis Hyperplasia (LJSGH) using photodynamic therapy (PDT) and reviews the current literature on this pathology. Background data: LJSGH is a recently described rare disease with controversial treatment results. As of today, 13 publications report surgical treatment approaches. The use of CO2 laser and cryotherapy was reported only in one study. The use of PDT was not previously reported. Patients and methods: A 9-year-old male patient was referred to our institution with the chief complaint of asymptomatic "inflamed gingiva" starting 1 year before. Clinical examination revealed an erythematous line accompanying the gingival contour, with a certain degree of hyperplasia. The diagnosis of LJSGH was performed based on clinical features and later confirmed histopathologically. A novel approach using PDT was then proposed. The photosensitizer was methylene blue, and a semiconductor laser diode was used. Results: One week after starting PDT, gingival hyperplasia was partially reduced. Immediately after the end of treatment, a significant reduction of gingival hyperplasia was observed. PDT proved to be safe, quick and painless, with no esthetic harm. Conclusions: This case illustrates the benefit of a more conservative approach as opposed to surgical procedure, with good clinical response and decreased morbidity over a 2-year follow-up period.


Subject(s)
Gingival Hyperplasia/drug therapy , Photochemotherapy/methods , Child , Humans , Lasers, Semiconductor/therapeutic use , Male , Methylene Blue/therapeutic use , Photosensitizing Agents/therapeutic use
9.
Odonto (Säo Bernardo do Campo) ; 22(43/44): 107-113, jan.-dez.2014. ilus
Article in Portuguese | LILACS | ID: lil-790525

ABSTRACT

Crianças que apresentam insuficiência hepática e transplante de fígado tem uma condição sistêmica comprometida. Algumas alterações bucais podem ocorrer nessas crianças, inclusive hiperplasia gengival. OBJETIVO: Utilizar um gel de clorexidina para controlar e minimizar a hiperplasia gengival ocasionada pelo uso de ciclosporina associada a corticosteróide. RELATO DO CASO: Em uma criança de 2 anos e 8 meses, submetida a transplante de fígado com prescrição de ciclosporina associada à corticosteróide, que apresentava hiperplasia gengival em que a opção de remoção cirúrgica do aumento gengival não foi autorizada, foi aplicado gel inibidor de placa clorexidina, uma vez por semana durante quatro semanas. CONSIDERAÇÕES FINAIS: O gel de clorexidina mostrou-se eficaz como auxiliar na terapêutica de impedir a hiperplasia gengival...


Oroantral communication is a pathological communication that occurs between the oral cavity and the maxillary sinus. When this communication suffers epithelialization it is called oroantral fistula. It can occur mainly after extraction of posterior maxillary teeth, due to the close relationship between their roots and the maxillary sinus floor. Aim: To present the surgical options for the treatment of oroantral communication and report a case of a large oroantral fistula, explaining the technique step. Case Report: Female patient female, 37-year-old, presented bucossinusal fistula in the left upper molars area and was surgically treated for its closure. Under local anesthesia an incision was made around the fistula, cutting epithelial tissue to allow the union of the wound edges, and it was sutured by layers: initially sinus mucosa with 4-0 catgut and then the gums, with nylon. The suture was removed 10 days later and by this time the complete closure of the fistula was observed. Conclusion: The decision of which treatment modality to use for oroantral communication is influenced by many factors, such as its size, the tissue conditions and the surgeon’s skills. The surgical technique presented in this case proved effective and easy to perform, with a confortable postoperative period for the patient and with no recurrence of the communication...


Subject(s)
Humans , Male , Child, Preschool , Anti-Infective Agents, Local/therapeutic use , Cyclosporine/adverse effects , Chlorhexidine/therapeutic use , Gingival Hyperplasia/chemically induced , Gingival Hyperplasia/drug therapy , Immunosuppressive Agents/adverse effects , Biliary Atresia/drug therapy , Adrenal Cortex Hormones/adverse effects , Gels , Treatment Outcome
10.
Quintessence Int ; 45(2): 109-13, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24389562

ABSTRACT

Cases of idiopathic gingival enlargement are so infrequent that the etiology and treatment are subjects of discussion. The case of a 49-year-old woman who presented with a rapidly diffuse enlargement of gingiva, clusters of patches on the buccal mucosa, and a furry-coated tongue within 2 months is reported. Results of various laboratory investigations and additional tests, such as the antineutrophil cytoplasmic antibodies (ANCA) and autoantibody to nuclear antigen (ANA) tests, were all negative. Histopathologic examination showed hyperplasia of inflammatory granulation tissues. Oral steroid therapy was effective. Although cases of multiple hyperplasia of inflammatory granulation in the oral cavity are very rare, clinicians should be aware of such cases and understand the efforts to further delineate the etiology, the management, and the prevention of the recurrence of this condition.


Subject(s)
Gingival Hyperplasia/diagnosis , Inflammation/complications , Mouth/pathology , Anti-Infective Agents/administration & dosage , Gingival Hyperplasia/complications , Gingival Hyperplasia/drug therapy , Humans , Male , Middle Aged , Prednisone/administration & dosage
12.
J Formos Med Assoc ; 112(3): 131-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23473525

ABSTRACT

BACKGROUND/PURPOSE: Gingival overgrowth can be induced in patients treated with cyclosporine-A (CsA), an immunosuppressant often used following organ transplantation. A pre-existing rat model designed to mimic CsA-induced gingival overgrowth in humans was used to test the effectiveness of frequent application of a chlorhexidine antiplaque solution in reducing the overgrowth. METHODS: Four groups of rats were fed CsA. One group received chlorhexidine mouthwash twice a day, the second group received chlorhexidine mouthwash once a day, the third group received chlorhexidine mouthwash every other day, and the fourth group did not receive chlorhexidine mouthwash all. A fifth negative control group received only mineral oil. Overgrowth was determined by measuring the changes in the gingival probing depth and the keratinized gingival width on molars. A gingival histological examination was performed. RESULTS: Rats treated with mouthwash twice daily exhibited decreased probing depths and gingival widths without statistical significance. Histological examination revealed that CsA treatment caused gingival enlargement, whereas chlorhexidine treatment twice a day diminished the enlargement. CONCLUSION: These findings suggest that chlorhexidine mouthwash used twice daily may reduce the severity of CsA-induced gingival overgrowth. Further research is warranted to determine the optimal dose and treatment regimen.


Subject(s)
Chlorhexidine/administration & dosage , Cyclosporine/adverse effects , Gingival Hyperplasia/drug therapy , Immunosuppressive Agents/adverse effects , Mouthwashes/administration & dosage , Animals , Gingival Hyperplasia/pathology , Male , Rats , Rats, Sprague-Dawley
13.
Transpl Int ; 25(4): 391-400, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22211928

ABSTRACT

This 24-week, open, single-arm, prospective, multicenter study evaluated the effects of conversion from ciclosporin to Tacrolimus QD in adult kidney transplant patients. Stable patients receiving ciclosporin were converted to Tacrolimus QD at 0.1mg/kg/day. Relative change in renal function (primary endpoint) was assessed using estimated creatinine clearance (eCrCl) with a noninferiority margin set at -10%. A total of 346 patients were enrolled; and 301 patients were treated per protocol (PPS) in the hyperlipidemia (n=42), hypertrichosis (n=106), hypertension (n=77) and gingival hyperplasia (n=76) groups. Relative change in eCrCl was -0.6% in all PPS patients (95% CI, -2.2; 0.9) and -5.3% in the hyperlipidemia (CI, -9.59; -0.97), 0.9% in the hypertrichosis (CI, -2.59; 4.45), -0.1% in the hypertension (CI, -3.8; 3.68), and -1% in the gingival hyperplasia groups (CI, -4.63; 2.65) (PPS), meeting noninferiority criteria. There was no acute rejection. Decreases in serum lipids and blood pressure were moderate but without meaningful change in the number of treatment medications. Substantial decreases in severity of ciclosporin-related cosmetic side effects were evident from investigator and patient self-report of symptoms. Renal function remained stable after conversion to Tacrolimus QD. The effect of conversion on cardiovascular parameters was not clinically meaningful, however, marked improvement in ciclosporin-related cosmetic side effects was observed. (ClinicalTrials.gov number: NCT00481481).


Subject(s)
Cyclosporine/adverse effects , Gingival Hyperplasia/chemically induced , Hypertrichosis/chemically induced , Kidney Transplantation/physiology , Tacrolimus/therapeutic use , Adult , Aged , Creatinine/blood , Cyclosporine/therapeutic use , Female , Gingival Hyperplasia/drug therapy , Humans , Hyperlipidemias/chemically induced , Hyperlipidemias/drug therapy , Hypertension/chemically induced , Hypertension/drug therapy , Hypertrichosis/drug therapy , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/therapeutic use , Lipids/blood , Male , Middle Aged , Prospective Studies , Tacrolimus/blood
14.
Afr Health Sci ; 12(4): 576-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23516009

ABSTRACT

Amlodipine is a dihydropyridine calcium channel blocker that is used in the management of both hypertension and angina. Amlodipine induced side effects are headache, dizziness, edema, flushing, palpitations, and rarely gingival hyperplasia. The exact reason of amlodipine-induced gingival hyperplasia is not known. We presented a case with chronic renal failure (CRF) that developed gingival hyperplasia due to amlodipine use, which improved after ceasing the drug.


Subject(s)
Amlodipine/adverse effects , Calcium Channel Blockers/adverse effects , Gingival Hyperplasia/chemically induced , Kidney Failure, Chronic/drug therapy , Adult , Amlodipine/therapeutic use , Calcium Channel Blockers/therapeutic use , Gingival Hyperplasia/drug therapy , Humans , Hypertension/drug therapy , Male , Treatment Outcome
18.
Ren Fail ; 29(3): 265-70, 2007.
Article in English | MEDLINE | ID: mdl-17497438

ABSTRACT

BACKGROUND: It has been shown that azithromycin improves cyclosporine-induced gingival hyperplasia (GH), but its efficacy was never compared against an efficient oral hygiene program (OHP). The aim of this study was to analyze the effects of azithromycin plus OHP versus OHP alone in patients with cyclosporine-induced GH. METHODS: After periodontal evaluation, 20 renal transplant recipients received detailed oral hygiene instructions and a complete OHP, and were randomized to control (OHP) or azithromycin groups (OHP plus azithromycin). Patients were re-evaluated after 15 and 30 days. Both groups were similar in time after transplant, age, gender, cyclosporine dose, and cyclosporine through level and serum creatinine. The control group had fewer patients using calcium cannel blockers (10% vs. 70%, p = 0.02). RESULTS: All patients improved in pain, halitosis, and gum bleeding after OHP. The control group did not improve plaque index (PI) or GH. In contrast, baseline PI decreased from 1.52 +/- 0.28 to 0.50 +/- 0.16 on day 15 (p < 0.01) and to 0.46 +/- 0.14 on day 30 (p < 0.01) in the azithromycin group, and the GH score decreased from 1.9 +/- 0.27 to 0.90 +/- 0.27 on day 15 (p < 0.05) and to 0.70 +/- 0.21 on day 30 (p < 0.01). CONCLUSION: Azithromycin associated to efficient OHP induced a striking reduction in cyclosporine-induced GH, while efficient OHP alone improved oral symptoms but did not decrease cyclosporine-induced GH.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Azithromycin/therapeutic use , Cyclosporine/adverse effects , Gingival Hyperplasia/chemically induced , Gingival Hyperplasia/therapy , Immunosuppressive Agents/adverse effects , Oral Hygiene , Adult , Analysis of Variance , Combined Modality Therapy , Female , Follow-Up Studies , Gingival Hyperplasia/drug therapy , Humans , Kidney Transplantation , Male , Surveys and Questionnaires , Treatment Outcome
19.
J Am Dent Assoc ; 138(3): 338-48; quiz 396, 398, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17332039

ABSTRACT

BACKGROUND: Hyperplastic granular gingivitis or "strawberry gingivitis" is a rare manifestation of Wegener's granulomatosis (WG), but it is nearly pathognomonic for this multisystem autoimmune vasculitis. The dentist may be the first health care professional to see patients with symptoms and findings of this condition. Early diagnosis and treatment is the most important factor in the management of this potentially fatal disease. METHODS: The authors present three case reports that demonstrate the disease spectrum and conducted a literature review focused on current understanding of this disease. RESULTS: The first patient had only the classic gingival manifestations of the disease. The second patient had simultaneous typical gingival lesions, as well as dermatologic findings. The third patient had an atypical oral presentation of aphthous ulcers and erythematous gingiva, as well as respiratory and genital involvement. Reaching a definitive diagnosis sometimes is challenging owing to the subtle onset of the disease and variable clinical and laboratory findings. CONCLUSION AND CLINICAL IMPLICATIONS: Clinicians should be familiar with the broad variety of oral and systemic components of WG, as well as strategies to facilitate prompt disease recognition and to provide continued oral health care to these medically complex patients.


Subject(s)
Gingival Hyperplasia/etiology , Granulomatosis with Polyangiitis/complications , Oral Ulcer/etiology , Adult , Antibodies, Antineutrophil Cytoplasmic/analysis , Diagnosis, Differential , Female , Gingival Hyperplasia/drug therapy , Granulomatosis with Polyangiitis/drug therapy , Granulomatosis with Polyangiitis/pathology , Humans , Male , Middle Aged , Oral Ulcer/drug therapy , Sinusitis/etiology
20.
J. epilepsy clin. neurophysiol ; 13(1): 33-36, Mar. 2007.
Article in Portuguese | LILACS | ID: lil-457663

ABSTRACT

INTRODUÇÃO: A hiperplasia gengival pode ser causada por alguns medicamentos, entre os quais a fenitoína. Torna-se importante a prevenção, o diagnóstico precoce e o seguimento de pessoas com epilepsia por profissional da área odontológica. OBJETIVO: O presente artigo tem o propósito de discutir os aspectos etiológicos, clínicos e terapêuticos da hiperplasia gengival medicamentosa. METODOLOGIA: Revisão da literatura. RESULTADOS: A necessidade de aliar o tratamento odontológico ao tratamento medicamentoso é enfatizada como forma de prevenir e/ou minimizar a hiperplasia gengival medicamentosa conseqüente à ação farmacológica de algumas drogas e fatores irritantes localizados nos tecidos dentais e periodontais.


INTRODUCTION: Gingival hyperplasia may be caused by some drugs including phenytoin. There are very important factors in this area, including prevention, early diagnosis, and follow-up of people with epilepsy by an specialist in odontological area. OBJECTIVE: The aim of this paper is to discuss the etiology, clinical and therapeutic aspects of drug induced gingival hyperplasia. METHODOLOGY: Literature review. RESULTS: The need to combine dental and drug treatment is emphasized as a way to prevent and/or minimize drug induced gingival hyperplasia due to pharmacological action of some drugs, as well as, local dental and periodontal irritants.


Subject(s)
Humans , Phenytoin/adverse effects , Epilepsy/pathology , Gingival Hyperplasia/etiology , Gingival Hyperplasia/drug therapy
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