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1.
J Bone Miner Metab ; 41(2): 171-181, 2023 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-36859617

RESUMEN

INTRODUCTION: Periostin, an extracellular matrix protein, plays an important role in osteogenesis and is also known to activate several signals that contribute to chondrogenesis. The absence of periostin in periostin knockout mice leads to several disorders such as craniosynostosis and periostitis. There are several splice variants with different roles in heart disease and myocardial infarction. However, little is known about each variant's role in chondrogenesis, followed by bone formation. Therefore, the aim of this study is to investigate the role of several variants in chondrogenesis differentiation and bone formation in the craniofacial region. Periostin splice variants included a full-length variant (Control), a variant lacking exon 17 (ΔEx17), a variant lacking exon 21 (ΔEx21), and another variant lacking both exon 17 and 21 ***(ΔEx17&21). MATERIALS AND METHODS: We used C56BL6/N mice (n = 6) for the wild type (Control)*** and the three variant type mice (n = 6 each) to identify the effect of each variant morphologically and histologically. Micro-computed tomography demonstrated a smaller craniofacial skeleton in ΔEx17s, ΔEx21s, and ΔEx17&21s compared to Controls, especially the mandibular bone. We, thus, focused on the mandibular condyle. RESULTS: The most distinctive histological observation was that each defected mouse appeared to have more hypertrophic chondrocytes than Controls. Real-time PCR demonstrated the differences among the group. Moreover, the lack of exon 17 or exon 21 in periostin leads to inadequate chondrocyte differentiation and presents in a diminutive craniofacial skeleton. DISCUSSION: Therefore, these findings suggested that each variant has a significant role in chondrocyte hypertrophy, leading to suppression of bone formation.


Asunto(s)
Condrocitos , Condrogénesis , Animales , Ratones , Huesos , Diferenciación Celular/genética , Condrocitos/metabolismo , Condrogénesis/genética , Hipertrofia/genética , Hipertrofia/metabolismo , Hipertrofia/patología , Ratones Noqueados , Osteogénesis/genética , Microtomografía por Rayos X
2.
Am J Orthod Dentofacial Orthop ; 164(1): e1-e13, 2023 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-37191595

RESUMEN

INTRODUCTION: Rapid maxillary expansion (RME) expands the maxillary dentition laterally and improves nasal airway obstruction. However, the incidence of nasal airway obstruction improvement after RME is approximately 60%. This study aimed to clarify the beneficial effects of RME on nasal airway obstruction in specific pathologic nasal airway diseases (nasal mucosa hypertrophy and obstructive adenoids) using computer fluid dynamics. METHODS: Sixty subjects (21 boys; mean age 9.1 years) were divided into 3 groups according to their nasal airway condition (control, nasal mucosa hypertrophy, and obstructive adenoids), and those requiring RME had cone-beam computed tomography images taken before and after RME. These data were used to evaluate the nasal airway ventilation condition (pressure) using computer fluid dynamics and measure the cross-sectional area of the nasal airway. RESULTS: The cross-sectional area of the nasal airway significantly increased after RME in all 3 groups. The pressures in the control and nasal mucosa groups significantly reduced after RME but did not change significantly in the adenoid group. The incidence of improvement in nasal airway obstruction in the control, nasal mucosa, and adenoid groups was 90.0%, 31.6%, and 23.1%, respectively. CONCLUSIONS: The incidence of improvement in nasal airway obstruction after RME depends on the nasal airway condition (nasal mucosa hypertrophy and obstructive adenoids). In patients with nonpathologic nasal airway conditions, the obstruction may be sufficiently improved with RME. Furthermore, to some extent, RME may be effective in treating nasal mucosa hypertrophy. However, because of obstructive adenoids, RME was ineffective in patients with nasal airway obstruction.


Asunto(s)
Tonsila Faríngea , Obstrucción Nasal , Masculino , Humanos , Niño , Obstrucción Nasal/diagnóstico por imagen , Obstrucción Nasal/terapia , Obstrucción Nasal/etiología , Técnica de Expansión Palatina/efectos adversos , Hidrodinámica , Mucosa Nasal , Tomografía Computarizada de Haz Cónico , Hipertrofia/complicaciones , Hipertrofia/patología
3.
HNO ; 71(Suppl 1): 67-72, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-37491540

RESUMEN

Hyperplasia of the pharyngeal tonsils is to be considered pathologic when nasopharyngeal symptoms of mechanical obstruction and/or chronic inflammation occur. Chronic Eustachian tube dysfunction can result in various middle ear diseases such as conductive hearing loss, cholesteatoma, and recurrent acute otitis media. During examination, attention should be paid to the presence of adenoid facies (long face syndrome), with a permanently open mouth and visible tip of the tongue. In the case of severe symptoms and/or failure of conservative treatment, adenoidectomy is usually performed on an outpatient basis. Conventional curettage remains the established standard treatment in Germany. Histologic evaluation is indicated for clinical evidence of mucopolysaccharidoses. Due to the risk of hemorrhage, the preoperative bleeding questionnaire, which is obligatory before every pediatric surgery, is referred to. Recurrence of adenoids is possible despite correct adenoidectomy. Before discharge home, otorhinolaryngologic inspection of the nasopharynx for secondary bleeding should be performed and anesthesiologic clearance obtained.


Asunto(s)
Tonsila Faríngea , Otitis Media con Derrame , Otitis Media , Niño , Humanos , Tonsila Faríngea/cirugía , Tonsila Faríngea/patología , Adenoidectomía , Inflamación , Hipertrofia/patología , Hipertrofia/cirugía
4.
J Oral Maxillofac Surg ; 80(9): 1534-1543, 2022 09.
Artículo en Inglés | MEDLINE | ID: mdl-35577016

RESUMEN

Enlargement of an inferior alveolar nerve canal (IANC) on radiographic imaging can indicate the presence of a wide variety of pathologic entities. Oral and maxillofacial surgeons have the unique opportunity to regularly examine panoramic radiographs and must exercise proficient clinical judgment when noting abnormal findings on imaging. While malignant processes associated with IANC enlargement are uncommon, these pathologies do occur and may be associated with significant sequelae, especially when accompanied by a delay in diagnosis and in treatment. The purpose of this case report is to describe a case in which a patient presented with mental nerve neuropathy associated with unilateral IANC enlargement on radiography, which was found to be a B-cell lymphoma on biopsy. More importantly, we aim to remind oral and maxillofacial surgeons of this rare presentation of a malignant process so as to promote prompt recognition and referral for appropriate treatment.


Asunto(s)
Linfoma de Células B , Nervio Mandibular , Humanos , Hipertrofia/patología , Linfoma de Células B/complicaciones , Linfoma de Células B/diagnóstico por imagen , Linfoma de Células B/patología , Mandíbula , Nervio Mandibular/diagnóstico por imagen , Nervio Mandibular/patología , Radiografía , Radiografía Panorámica
5.
J Oral Maxillofac Surg ; 79(5): 1122-1132, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-33493432

RESUMEN

PURPOSE: Our current understanding of unilateral condylar hyperplasia (UCH) was put forth by Obwegeser. He hypothesized that UCH is 2 separate conditions: hemimandibular hyperplasia and hemimandibular elongation. This hypothesis was based on the following 3 assumptions: 1) the direction of overgrowth, in UCH, is bimodal-vertical or horizontal, with rare cases growing obliquely; 2) UCH can expand a hemimandible with and without significant condylar enlargement; and 3) there is an association between the condylar expansion and the direction of overgrowth-minimal expansion resulting in horizontal growth and significant enlargement causing vertical displacement. The purpose of this study was to test these assumptions. PATIENTS AND METHODS: We analyzed the computed tomography scans of 40 patients with UCH. First, we used a Silverman Cluster analysis to determine how the direction of overgrowth is distributed in the UCH population. Next, we evaluated the relationship between hemimandibular overgrowth and condylar enlargement to confirm that overgrowth can occur independently of condylar expansion. Finally, we assessed the relationship between the degree of condylar enlargement and the direction of overgrowth to ascertain if condylar expansion determines the direction of growth. RESULTS: Our first investigation demonstrates that the general impression that UCH is bimodal is wrong. The growth vectors in UCH are unimodally distributed, with the vast majority of cases growing diagonally. Our second investigation confirms the observation that UCH can expand a hemimandible with and without significant condylar enlargement. Our last investigation determined that in UCH, there is no association between the degree of condylar expansion and the direction of the overgrowth. CONCLUSIONS: The results of this study disprove the idea that UCH is 2 different conditions: hemimandibular hyperplasia and hemimandibular elongation. It also provides new insights about the pathophysiology of UCH.


Asunto(s)
Asimetría Facial , Cóndilo Mandibular , Asimetría Facial/diagnóstico por imagen , Asimetría Facial/etiología , Asimetría Facial/patología , Humanos , Hiperplasia , Hipertrofia/patología , Masculino , Mandíbula/diagnóstico por imagen , Mandíbula/patología , Cóndilo Mandibular/diagnóstico por imagen , Cóndilo Mandibular/patología
6.
J Oral Maxillofac Surg ; 76(8): 1785.e1-1785.e4, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29654776

RESUMEN

PURPOSE: Enlarged mental tubercles are rare benign exostoses that occur in children. The purpose of this study was to report a case series of patients with hypertrophic mental tubercles and propose a theory for their etiopathogenesis. PATIENTS AND METHODS: In this retrospective case series of patients with hypertrophic mental tubercles, we reviewed patients' medical records for age, gender, clinical presentation, findings on physical examination and radiographic images, and management details. Descriptive data were summarized. RESULTS: The sample included 14 patients (71% of whom were male patients) who presented at a mean age of 12.9 ± 4.8 years (range, 6 to 21 years). Most patients had bilaterally enlarged mental tubercles (n = 8); unilateral cases were primarily on the left side (5 of 6 patients). On clinical examination, a bony prominence in the parasymphyseal region was noted on palpation and occasionally by visual inspection. No tenderness to palpation or overlying skin changes were noted. Typical radiographic features included asymmetry along the inferior border of the mandible in the parasymphyseal region on panoramic radiographs and prominence and/or enlargement of the mental tubercles on computed tomography scans. No evidence of cortical expansion, perforation, or periosteal reaction was found. Three patients requested contouring of the hypertrophied tubercles. CONCLUSIONS: Hypertrophic mental tubercles are rare bony exostoses that occur in children in a region where a confluence of facial muscles attach to the mandible. The etiology likely involves bone deposition occurring in an area of muscle pull.


Asunto(s)
Exostosis/diagnóstico por imagen , Mandíbula/diagnóstico por imagen , Mandíbula/patología , Enfermedades Mandibulares/diagnóstico por imagen , Adolescente , Niño , Femenino , Humanos , Hipertrofia/diagnóstico por imagen , Hipertrofia/patología , Masculino , Radiografía Panorámica , Estudios Retrospectivos , Tomografía Computarizada por Rayos X , Adulto Joven
7.
J Sleep Res ; 26(4): 415-421, 2017 08.
Artículo en Inglés | MEDLINE | ID: mdl-27996170

RESUMEN

The aim of this study was to investigate the association between patterns of jaw motor activity during sleep and clinical signs and symptoms of sleep bruxism. A total of 35 university students and staff members participated in this study after providing informed consent. All participants were divided into either a sleep bruxism group (n = 21) or a control group (n = 14), based on the following clinical diagnostic criteria: (1) reports of tooth-grinding sounds for at least two nights a week during the preceding 6 months by their sleep partner; (2) presence of tooth attrition with exposed dentin; (3) reports of morning masticatory muscle fatigue or tenderness; and (4) presence of masseter muscle hypertrophy. Video-polysomnography was performed in the sleep laboratory for two nights. Sleep bruxism episodes were measured using masseter electromyography, visually inspected and then categorized into phasic or tonic episodes. Phasic episodes were categorized further into episodes with or without grinding sounds as evaluated by audio signals. Sleep bruxism subjects with reported grinding sounds had a significantly higher total number of phasic episodes with grinding sounds than subjects without reported grinding sounds or controls (Kruskal-Wallis/Steel-Dwass tests; P < 0.05). Similarly, sleep bruxism subjects with tooth attrition exhibited significantly longer phasic burst durations than those without or controls (Kruskal-Wallis/Steel-Dwass tests; P < 0.05). Furthermore, sleep bruxism subjects with morning masticatory muscle fatigue or tenderness exhibited significantly longer tonic burst durations than those without or controls (Kruskal-Wallis/Steel-Dwass tests; P < 0.05). These results suggest that each clinical sign and symptom of sleep bruxism represents different aspects of jaw motor activity during sleep.


Asunto(s)
Maxilares/fisiopatología , Músculos Masticadores/fisiopatología , Actividad Motora , Bruxismo del Sueño/diagnóstico , Bruxismo del Sueño/fisiopatología , Sueño/fisiología , Adulto , Electromiografía , Femenino , Humanos , Hipertrofia/patología , Hipertrofia/fisiopatología , Masculino , Músculo Masetero/anomalías , Músculo Masetero/patología , Músculo Masetero/fisiopatología , Músculos Masticadores/patología , Polisomnografía , Bruxismo del Sueño/patología , Sonido , Diente
8.
J Am Acad Dermatol ; 75(1): 64-8, 2016 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-27004804

RESUMEN

BACKGROUND: There is limited information regarding early development of soft-tissue and/or bone hypertrophy with facial port-wine stains (PWS). OBJECTIVE: We sought to characterize patients with hypertrophic PWS presenting during childhood. METHODS: Patients with a facial PWS and underlying hypertrophy that developed before the age of 18 years were included in a multicenter retrospective study. Age at onset of the hypertrophy, its location, association with odontologic problems, presence of other associated complications, and response to laser treatment were recorded. RESULTS: A total of 98 patients were included. The mean age at onset of hypertrophy, retrieved for 77 of 98 patients, was 5.6 years. The hypertrophy was congenital in 26%. Odontologic problems were noted in 39.8% of cases. Other complications, including cataract, asymmetric development of the maxillary bone, and speech delay/disorders, were reported in 18.4%. In all, 67 patients received laser treatment. Only 3% achieved complete or nearly complete clearance of the PWS. LIMITATIONS: As only cases of PWS with early-onset hypertrophy were included, we were unable to calculate the prevalence of this manifestation. CONCLUSION: PWS with early-onset hypertrophy are associated with a high rate of complications and a poor response to laser treatment. Periodic monitoring is recommended for early detection and treatment of complications.


Asunto(s)
Anomalías Múltiples , Láseres de Colorantes/uso terapéutico , Mancha Vino de Oporto/patología , Mancha Vino de Oporto/cirugía , Anomalías Múltiples/diagnóstico , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Preescolar , Cara , Femenino , Humanos , Hipertrofia/congénito , Hipertrofia/patología , Hipertrofia/cirugía , Lactante , Masculino , Persona de Mediana Edad , Cuello , Mancha Vino de Oporto/complicaciones , Pronóstico , Estudios Retrospectivos , Adulto Joven
9.
Dermatol Surg ; 41(11): 1241-5, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26506066

RESUMEN

BACKGROUND: A percentage of patients with capillary malformation (CM) develop soft tissue hypertrophy, bony hypertrophy, and/or nodule formation. OBJECTIVE: To determine the incidence, age of onset, anatomic distribution of soft tissue/bony hypertrophy, and nodule formation in patients with untreated CM. METHODS: A retrospective medical records review of head and neck CM patients presenting to a tertiary referral center over a 7-year period (2004-2011) was performed. RESULTS: Of the 160 patients with CM, 96 demonstrated progression of disease to include either soft tissue/bony hypertrophy or nodule formation. Of these, 87 patients had not received previous treatment and met the inclusion criteria for analysis. On average, soft tissue hypertrophy began at 9 years of age. The V2/maxillary segment was most commonly involved with upper lip hypertrophy being the most prominent. Fourteen percent of the patients also presented with bony hypertrophy, which began at an average age of 15 years. Nodules were present in 38/87 (44%) of patients with an average age of onset of 22 years. CONCLUSION: This study demonstrates the nature progression of CM and quantifies the clinical characteristics of hypertrophy and nodule formation with untreated head and neck CM. Early and continuous treatment is recommended in hopes of preventing CM progression.


Asunto(s)
Cara/patología , Mandíbula/patología , Maxilar/patología , Mancha Vino de Oporto/complicaciones , Adolescente , Adulto , Edad de Inicio , Niño , Preescolar , Femenino , Humanos , Hipertrofia/epidemiología , Hipertrofia/etiología , Hipertrofia/patología , Incidencia , Lactante , Masculino , Boca/patología , Cuello , Estudios Retrospectivos , Factores Sexuales , Adulto Joven
10.
Med Princ Pract ; 23(3): 286-8, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-23969546

RESUMEN

OBJECTIVE: To describe an unusual case of bilateral masseter and pterygoid muscle hypertrophy. CLINICAL PRESENTATION AND INTERVENTION: A 53-year-old female patient presented with a bilateral, painless swelling at the parotid areas without improvement after using antibiotics/systemic corticosteroids/nonsteroidal anti-inflammatory agents. Her medical history included thyroid nodules, but no dental/occlusal disorders were observed. The initial differential diagnosis included salivary gland/jaw bone/masseter pathology, but the CT/MRI revealed only an increase in the size of the masseter and pterygoid muscles. The patient was informed of the benign nature of the swelling and was advised to discontinue the use of nonsteroidal anti-inflammatory agents. CONCLUSION: The bilateral hypertrophy of masseter muscles should be considered in differential diagnosis in cases of unilateral or bilateral swelling of the parotid or lateral mandible area.


Asunto(s)
Hipertrofia/diagnóstico , Músculo Masetero/patología , Músculos Pterigoideos/patología , Diagnóstico Diferencial , Femenino , Humanos , Hipertrofia/patología , Imagen por Resonancia Magnética , Persona de Mediana Edad , Tomografía Computarizada por Rayos X
11.
J Stomatol Oral Maxillofac Surg ; 125(5S1): 101955, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38950733

RESUMEN

OBJECTIVES: Botulinum toxin is used in human in repeatedly masticatory muscles injections. A single BTX injection in animal induces mandibular bone loss with a muscle enthesis hypertrophic metaplasia. Our aim was to evaluate mandibular bone changes after unilateral repeated injections of BTX in adult rats. STUDY DESIGN: Mature male rats were randomized into 3 groups: one, two or three injections. Each rat received injections in right masseter and temporalis muscles. The left side was the control side. Microcomputed tomography was used to perform 2D and 3D analyses. RESULTS: Bone loss was evidenced on the right sides of alveolar and condylar bone. Alveolar bone volume increased in both control left side and injected right side whereas condylar bone volume remained constant in all groups, for both sides. Enthesis bone hypertrophic metaplasias were evidenced on the BTX injected sides without any modification with the number of injections. CONCLUSION: BTX repeated injections in masticatory muscles lead to major mandibular condylar and alveolar bone loss that does not worsen. They lead to the occurrence of an enthesis bone proliferation that is not dependent on the number of injections. These results are an argument for the safety of BTX injections in masticatory muscles in human.


Asunto(s)
Pérdida de Hueso Alveolar , Cóndilo Mandibular , Microtomografía por Rayos X , Animales , Ratas , Masculino , Pérdida de Hueso Alveolar/patología , Pérdida de Hueso Alveolar/tratamiento farmacológico , Cóndilo Mandibular/efectos de los fármacos , Cóndilo Mandibular/patología , Inyecciones Intramusculares , Distribución Aleatoria , Músculos Masticadores/efectos de los fármacos , Músculos Masticadores/patología , Ratas Wistar , Toxinas Botulínicas Tipo A/administración & dosificación , Toxinas Botulínicas/administración & dosificación , Músculo Masetero/efectos de los fármacos , Músculo Masetero/patología , Hipertrofia/tratamiento farmacológico , Hipertrofia/patología
12.
J Stomatol Oral Maxillofac Surg ; 125(4): 101751, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38145836

RESUMEN

OBJECTIVE: To compare the dentofacial characteristics of children with and without adenoid and/or tonsillar hypertrophy. METHODS: A consecutive sample of orthodontic patients aged 6-12 that took pre-treatment lateral cephalograms were included in this study. Those with history of previous orthodontic treatment, adenoidectomy or tonsillectomy, or craniofacial anomalies were excluded. The diagnosis of adenoid and tonsillar hypertrophy was based on Fujioka's and Baroni's methods, according to which the subjects were divided into four groups: the adenoid hypertrophy only (AHO) group; tonsillar hypertrophy only (THO) group; combined adenoid and tonsillar hypertrophy (AH+TH) group; and no adenoid or tonsillar hypertrophy (NH) group. Cephalograms were used for skeletal and dental measurement. Data were analyzed using one-way ANOVA, LSD post-hoc tests and Chi-square test. RESULTS: A total of 598 patients were included. Compared with the NH group, the THO group had significantly larger SNB angle (P < 0.001), as well as significantly smaller ANB angle (P<0.001) and Wits value (P = 0.001). The U1-L1 angle of AHO group was significantly smaller than that in the NH group (P = 0.035). The proportion of adenoid hypertrophy in Class II patients was significantly higher than that in Class III patients (P = 0.001). The proportion of tonsillar hypertrophy in Class III patients was significantly higher than that in Class I patients (P < 0.001) and Class II patients (P < 0.001). CONCLUSION: Over 80 % of children seeking orthodontic treatment had either adenoid or tonsillar hypertrophy. Children with adenoid hypertrophy tend to have skeletal Class II malocclusion, while those with tonsillar hypertrophy tend to have skeletal Class III malocclusion.


Asunto(s)
Tonsila Faríngea , Cefalometría , Hipertrofia , Tonsila Palatina , Humanos , Hipertrofia/patología , Hipertrofia/diagnóstico , Hipertrofia/epidemiología , Niño , Tonsila Faríngea/patología , Tonsila Faríngea/cirugía , Tonsila Palatina/patología , Tonsila Palatina/cirugía , Estudios Transversales , Femenino , Masculino , Ortodoncia Correctiva/estadística & datos numéricos , Ortodoncia Correctiva/métodos , Maloclusión/epidemiología , Maloclusión/patología , Maloclusión/diagnóstico , Maloclusión/terapia
13.
Am J Respir Crit Care Med ; 185(8): 805-16, 2012 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-22135346

RESUMEN

Obstructive sleep apnea in infants has a distinctive pathophysiology, natural history, and treatment compared with that of older children and adults. Infants have both anatomical and physiological predispositions toward airway obstruction and gas exchange abnormalities; including a superiorly placed larynx, increased chest wall compliance, ventilation-perfusion mismatching, and ventilatory control instability. Congenital abnormalities of the airway, such as laryngomalacia, hemangiomas, pyriform aperture stenosis, choanal atresia, and laryngeal webs, may also have adverse effects on airway patency. Additional exacerbating factors predisposing infants toward airway collapse include neck flexion, airway secretions, gastroesophageal reflux, and sleep deprivation. Obstructive sleep apnea in infants has been associated with failure to thrive, behavioral deficits, and sudden infant death. The proper interpretation of infant polysomnography requires an understanding of normative data related to gestation and postconceptual age for apnea, arousal, and oxygenation. Direct visualization of the upper airway is an important diagnostic modality in infants with obstructive apnea. Treatment options for infant obstructive sleep apnea are predicated on the underlying etiology, including supraglottoplasty for severe laryngomalacia, mandibular distraction for micrognathia, tonsillectomy and/or adenoidectomy, choanal atresia repair, and/or treatment of gastroesophageal reflux.


Asunto(s)
Anomalías Craneofaciales/complicaciones , Anomalías Craneofaciales/diagnóstico , Apnea Obstructiva del Sueño/etiología , Apnea Obstructiva del Sueño/terapia , Tonsila Faríngea/patología , Tonsila Faríngea/cirugía , Adulto , Factores de Edad , Terapia Combinada , Femenino , Estudios de Seguimiento , Humanos , Hipertrofia/patología , Hipertrofia/cirugía , Incidencia , Lactante , Laringomalacia/complicaciones , Laringomalacia/congénito , Laringe/anomalías , Masculino , Micrognatismo/complicaciones , Micrognatismo/diagnóstico , Tonsila Palatina/patología , Tonsila Palatina/cirugía , Polisomnografía/métodos , Medición de Riesgo , Índice de Severidad de la Enfermedad , Apnea Obstructiva del Sueño/fisiopatología , Resultado del Tratamiento
14.
Eur Rev Med Pharmacol Sci ; 27(5 Suppl): 75-79, 2023 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-37869951

RESUMEN

OBJECTIVE: Narrow maxilla occurring due to various congenital or acquired causes creates major orthodontic problems and complicates prosthetic dental rehabilitation. The etiologic factors are mostly related to upper airway pathologies that restrict breathing and cause negative pressure at the base of the nose and nasopharynx. The upper and lower airway is a whole unit. Regional anomalies or acquired problems affect the entire system. This can lead to developmental issues and permanent disorders in childhood, which will last their real life. This study was planned to investigate the incidence of nasopharyngeal obstruction originating from allergic rhinitis, turbinate hypertrophy, septum deviation, and adenoid vegetation in children scheduled for orthodontic treatment due to maxillary stenosis. PATIENTS AND METHODS: Our study group consists of one hundred children aged 12-16 years who applied to the orthodontist due to dental malalignment and were found to have a narrowing of the maxilla. After the orthodontic evaluation, the patients were referred for an ENT examination to evaluate the etiological factors originating from the upper respiratory tract. In the study group, nasal congestion and allergic rhinitis were first investigated. All symptoms were evaluated and scored. Then, an ENT physical examination was performed in all cases, and nasal cavities, nasopharynx, and oropharynx were assessed with a fiberoptic endoscope. Regarding etiological factors, allergic rhinitis, turbinate hypertrophy, nasal septum deviation, and adenoid vegetation that would prevent breathing were carefully investigated. RESULTS: Firstly, deep palate, narrowed maxillary arch, V-shaped arch, adenoid face type, bilateral posterior crossbite, insufficient lip presence, maxillary incisor protrusion (upper forward thrust), skeletal class 2 division 1 malocclusion, and increased lower face height detected in patients primarily diagnoses were grouped according to their pathologies. Allergic rhinitis was found in 43 cases, turbinate hypertrophy in 30 instances, nasal septum deviation in 18 cases, and adenoid vegetation that prevented respiration in 61 patients. CONCLUSIONS: It is known that increased nasal airway resistance due to allergic rhinitis, septal deviation, turbinate hypertrophy, or adenoid vegetation in the upper respiratory tract may lead to permanent orthodontic disorders in children and adolescents. A multidisciplinary approach, early diagnosis, and treatment should be the first step to prevent this situation. Secondly, it should be planned to correct the anatomical disorders that have occurred with appliances and, if necessary, surgical approaches. Taking precautions before permanent problems arise in childhood is also crucial in prosthetic dentistry.


Asunto(s)
Maxilar , Rinitis Alérgica , Niño , Adolescente , Humanos , Maxilar/patología , Nariz/patología , Nasofaringe/patología , Rinitis Alérgica/complicaciones , Hipertrofia/patología
15.
J Hazard Mater ; 432: 128654, 2022 06 15.
Artículo en Inglés | MEDLINE | ID: mdl-35286933

RESUMEN

Fluoride at high doses is a well-known toxic agent for the musculoskeletal system, primarily in bone and cartilage cells. Research on fluoride toxicity concerning particularly on the skeletal muscle is scanty. We hypothesized that during skeletal fluorosis, along with bone, muscle is also affected, so we have evaluated the effects of Sodium fluoride (NaF) on mouse skeletal muscles. Sodium fluoride (80 ppm) was administered to 5-week-old C57BL6 mice drinking water for 15 and 60 days, respectively. We carried out histology, primary culture, molecular and proteomic analysis of fluoride administered mouse skeletal muscles. Results indicated an increase in the muscle mass (hypertrophy) in vivo and myotubes ex vivo by activating the IGF1/PI3/Akt/mTOR signalling pathway due to short term NaF exposure. The long-term exposure of mice to NaF caused loss of muscle proteins leading to muscle atrophy due to activation of the ubiquitin-proteasome pathway. Differentially expressed proteins were characterized and mapped using a proteomic approach. Moreover, the factors responsible for protein synthesis and PI3/Akt/mTOR pathway were upregulated, leading to muscle hypertrophy during the short term NaF exposure. Long term exposure to NaF resulted in down-regulation of metabolic pathways. Elevated myostatin resulted in the up-regulation of the muscle-specific E3 ligases-MuRF1, promoting the ubiquitination and proteasome-mediated degradation of critical sarcomeric proteins.


Asunto(s)
Agua Potable , Fluoruro de Sodio , Animales , Fluoruros/toxicidad , Hipertrofia/inducido químicamente , Hipertrofia/metabolismo , Hipertrofia/patología , Ratones , Ratones Endogámicos C57BL , Músculo Esquelético/metabolismo , Atrofia Muscular/inducido químicamente , Atrofia Muscular/metabolismo , Atrofia Muscular/patología , Complejo de la Endopetidasa Proteasomal/metabolismo , Proteómica , Proteínas Proto-Oncogénicas c-akt/metabolismo , Fluoruro de Sodio/metabolismo , Fluoruro de Sodio/toxicidad , Serina-Treonina Quinasas TOR/metabolismo
16.
Am J Otolaryngol ; 32(2): 147-51, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-20392530

RESUMEN

OBJECTIVE: This study was designed for better understanding of the role of different methods of nasal endoscopy in the assessment of adenoid hypertrophy and comparing them with lateral neck radiography and patients' symptoms. SUBJECTS AND METHOD: From August 2007 until January 2009, in the otolaryngology ward of a tertiary referral center, 89 patients who had symptoms related to chronic mouth breathing participated in this study. History of the symptoms related to adenoid hypertrophy was obtained from them. In addition, all patients underwent nasal endoscopy and lateral nasopharynx x-ray. The clinician who did nasal endoscopy was blinded to information about clinical data and x-ray and vice versa. Afterward, the relationship between symptoms and each diagnostic procedure was evaluated. RESULTS: Patients had a mean age of 9.47 ± 4.68 years. In the evaluation of the relationship between symptoms grading and grading in lateral neck radiography, this relationship was significant about snoring. Furthermore, there was a significant relationship between the endoscopic size of adenoid and number of the episodes of acute otitis media. The sum of symptoms grading had a significant relationship with the size of adenoid in lateral neck x-ray, but not in nasal endoscopy. CONCLUSION: The results of the present study indicated that both radiography and nasal endoscopy could define the relationship between adenoid hypertrophy and associated symptoms and therefore are complementary. Between them, despite the popularity of nasal endoscopy, radiography can serve as a better planning tool.


Asunto(s)
Tonsila Faríngea/diagnóstico por imagen , Tonsila Faríngea/patología , Endoscopía/métodos , Adolescente , Niño , Preescolar , Método Doble Ciego , Femenino , Humanos , Hipertrofia/diagnóstico por imagen , Hipertrofia/patología , Masculino , Otitis Media/etiología , Radiografía , Ronquido/etiología
17.
Eur Arch Otorhinolaryngol ; 268(11): 1589-92, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-21607580

RESUMEN

Our objective was to confirm the necessity of nasal endoscopy in the diagnosis and treatment of choanal adenoid in adult patients with persistent bilateral nasal obstruction and recurrent nasal infections that may lead to repeated unsuccessful medical and surgical procedures. We present a series of 64 adult patients (18-37 years: 40 males, 24 females). All patients had persistent bilateral nasal obstruction and recurrent nasal infections. There was history of repeated medical and surgical unsuccessful procedures. Choanal adenoid was confirmed by nasal endoscopy and CT scanning. Absence of adenoid tissues in the nasopharynx was confirmed in all cases. Surgical removal of choanal adenoids was undertaken in all cases endoscopically. Some other surgical procedures like straightening of a deviated septum or reduction of a hypertrophied turbinate were undertaken in some indicated cases. Most of the cases experienced complete relief from obstruction and return of a patent nasal airway, and improvement of associated complaints such as dry mouth and persistent cough. A thorough review of this phenomenon and its clinical relevance, and methods of diagnosis and management are presented. We recommend a thorough nasal endoscopy as a routine in cases of persistent nasal obstruction even in the presence of an apparent cause of obstruction.


Asunto(s)
Adenoidectomía/métodos , Tonsila Faríngea/cirugía , Endoscopía/métodos , Errores Médicos/prevención & control , Obstrucción Nasal/diagnóstico , Tonsila Faríngea/diagnóstico por imagen , Tonsila Faríngea/patología , Adolescente , Adulto , Errores Diagnósticos/prevención & control , Femenino , Estudios de Seguimiento , Humanos , Hipertrofia/diagnóstico por imagen , Hipertrofia/patología , Hipertrofia/cirugía , Masculino , Obstrucción Nasal/etiología , Obstrucción Nasal/cirugía , Nasofaringe , Estudios Retrospectivos , Tomografía Computarizada por Rayos X , Resultado del Tratamiento , Adulto Joven
18.
Pediatr Allergy Immunol ; 21(8): 1095-106, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-20609137

RESUMEN

Adenoidal hypertrophy (AH) and adenotonsillar hypertrophy are common disorders in the pediatric population and can cause symptoms such as mouth breathing, nasal congestion, hyponasal speech, snoring, and obstructive sleep apnea (OSA), as well as chronic sinusitis and recurrent otitis media. More serious long-term sequelae, typically secondary to OSA, include neurocognitive abnormalities (e.g. behavioral and learning difficulties, poor attention span, hyperactivity, below average intelligence quotient); cardiovascular morbidity (e.g. decreased right ventricular ejection fraction, left ventricular hypertrophy, elevated diastolic blood pressure); and growth failure. Adenoidectomy (with tonsillectomy in cases of adenotonsillar hypertrophy) is the typical management strategy for patients with AH. Potential complications have prompted the investigation of non-surgical alternatives. Evidence of a pathophysiologic link between AH and allergy suggests a possible role for intranasal corticosteroids (INS) in the management of patients with AH. This article reviews the epidemiology and pathophysiology of AH with a particular focus on evidence of its association with allergy and allergic rhinitis. Current treatment options are briefly considered with discussion on the rationale and evidence for the use of INS.


Asunto(s)
Tonsila Faríngea/patología , Corticoesteroides/uso terapéutico , Hipersensibilidad Inmediata/terapia , Hipertrofia/terapia , Adenoidectomía/efectos adversos , Tonsila Faríngea/efectos de los fármacos , Tonsila Faríngea/inmunología , Tonsila Faríngea/cirugía , Adolescente , Niño , Preescolar , Ensayos Clínicos como Asunto , Humanos , Hipersensibilidad Inmediata/epidemiología , Hipersensibilidad Inmediata/inmunología , Hipersensibilidad Inmediata/patología , Hipertrofia/epidemiología , Hipertrofia/inmunología , Hipertrofia/patología , Inflamación , Riesgo
19.
Neuromuscul Disord ; 30(2): 105-110, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-32001146

RESUMEN

Subjects affected by Duchenne muscular dystrophy (DMD) develop severe malocclusions with the progression of the disease, due to changes in orofacial musculature and function, including tongue hypertrophy. We aimed to evaluate the benefits of maintaining mandibular interarch width with the help of a simple fixed orthodontic appliance. Three adolescent DMD boys were selected consecutively to receive a passive rigid mandibular lingual arch, and followed for 4-5 years. An untreated age-matched control group was chosen and followed for a similar period. Study casts were obtained at baseline and after follow-up. Outcomes measured were overjet, overbite, maxillary and mandibular intermolar widths, mandibular arch depth, molar relationships, and the presence of lateral crossbites and anterior or lateral openbites. Changes in measurements obtained between the two time points were compared in each age-matched pair. There was a clinically important increase in the mandibular intermolar width in the non-treated children ranging from 2.5 mm to 9 mm, but not in those treated. Malocclusions generally deteriorated in untreated children while they remained stable in treated children. The use of a rigid mandibular lingual arch in boys with DMD can help slow down the rapid deterioration of the developing malocclusions that accompanies the progression of the disease.


Asunto(s)
Maloclusión/prevención & control , Distrofia Muscular de Duchenne/complicaciones , Distrofia Muscular de Duchenne/patología , Aparatos Ortodóncicos , Evaluación de Resultado en la Atención de Salud , Lengua/patología , Adolescente , Niño , Estudios de Seguimiento , Humanos , Hipertrofia/patología , Masculino , Maloclusión/etiología , Proyectos Piloto
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