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Keywords Segmental odontomaxillary dysp...

Segmental odontomaxillary dysplasia

https://read.qxmd.com/read/32893658/case-report-of-segmental-odontomaxillary-dysplasia-with-cutaneous-manifestations
#1
P Castaño, I Varela, J Limeres, M Diniz-Freitas, M T Abeleira, M Outumuro, J F Feijoo, P Diz, L García-Caballero
BACKGROUND: Segmental odontomaxillary dysplasia is an uncommon nonhereditary growth disorder that affects the maxilla, gums and ipsilateral dentition. The disorder is diagnosed mainly based on dental (over-retention of primary teeth, dental agenesis and diastemas) and bone findings (bone sclerosis, irregular trabeculation of immature bone and reduced maxillary sinus). This paper provides a case report. CASE REPORT: A 5-year-old child with skin manifestations including hypertrichosis, facial erythema and pigmented nevus was diagnosed with type II segmental odontomaxillary dysplasia based on clinical, radiographic and histopathological analysis...
September 2020: European Journal of Paediatric Dentistry: Official Journal of European Academy of Paediatric Dentistry
https://read.qxmd.com/read/32500425/segmental-ipsilateral-odontognathic-dysplasia-mandibular-involvement-in-segmental-odontomaxillary-dysplasia-and-identification-of-pik3ca-somatic-variant-in-lesional-mandibular-gingival-tissue
#2
Tanya M Gibson, Keith Rafferty, Elyse Ryan, Arupa Ganguly, Ioannis G Koutlas
Segmental odontomaxillary dysplasia (SOD) is a developmental condition of the middle and posterior maxilla featuring dysplastic bone overgrowth, dental abnormalities and, occasionally, various homolateral cutaneous manifestations. Herein, we describe an individual with maxillary abnormality akin to SOD and associated ipsilateral segmental odontomandibular dysplasia. Also, the result of the evaluation of lesional mandibular gingival tissue for overgrowth-related gene variants is reported. An 8-year-old girl presented clinically with congenital maxillary and mandibular alveolar soft tissue enlargement in the area of the premolars...
June 4, 2020: Head and Neck Pathology
https://read.qxmd.com/read/32151309/diagnosis-management-and-follow-up-of-a-rare-regional-developmental-disorder-segmental-odontomaxillary-dysplasia
#3
C Heggie, L Gartshore
Segmental odontomaxillary dysplasia (SOD) is a rare craniofacial developmental disorder. Clinical features include abnormal growth and maturation of bone, premolar agenesis, delayed eruption of permanent molars, and unilateral posterior maxillary enlargement. Radiographic features include altered bone trabeculae, reduced maxillary sinus, pulp stones, and spontaneous resorption of primary molars. The purpose of this report is to describe the case of a seven-year-old boy who presented with dental pain, erythema of the soft tissues of the right maxillary quadrant, severely infra-occluded primary molars and bony expansion of the maxilla...
January 15, 2020: Journal of Dentistry for Children
https://read.qxmd.com/read/29389339/segmental-odontomaxillary-dysplasia-an-underrecognized-entity
#4
Molly Housley Smith, Donald M Cohen, Joseph Katz, Indraneel Bhattacharyya, Nadim M Islam
BACKGROUND AND OVERVIEW: Segmental odontomaxillary dysplasia (SOD) is a characteristic developmental abnormality that demonstrates posterior maxillary enlargement, dental abnormalities, altered bone trabeculation, and possible cutaneous findings. Only 62 cases have been reported in the English-language literature. CASE DESCRIPTION: The authors described 3 newly diagnosed cases of SOD, all found in the left posterior maxilla in adolescent female patients; they reviewed the literature to elucidate this rare entity...
February 2018: Journal of the American Dental Association
https://read.qxmd.com/read/24748310/unilateral-segmental-odontomaxillary-dysplasia-a-rare-entity-of-3-cases-and-review
#5
REVIEW
Shalu Rai, Rohit Malik, Sapna Panjwani, Deepankar Misra, Sankalp Verma
Segmental odontomaxillary dysplasia (SOD) is an uncommon, nonhereditary, rare developmental disorder primarily involving the posterior part of the maxilla and related dental components. It is a rare condition of uncertain etiology that results in painless unilateral expansion of the posterior dentoalveolar complex, gingival hyperplasia, lack of one or both premolars in the affected area, delayed eruption of adjacent teeth and malformations of the primary molars. Radiographically, the affected bone is thickened and irregular in outline, with a coarse trabecular pattern that is vertically oriented resulting in a relatively radioopaque granular appearance...
January 2014: Indian Journal of Dental Research: Official Publication of Indian Society for Dental Research
https://read.qxmd.com/read/24531610/segmental-odontomaxillary-dysplasia
#6
Arti Agrawal, Jonathan Daniel, Vasudevan Vijeev
Segmental odontomaxillary dysplasia is a type of hemi-maxillofacial dysplasia. It is a sporadic, mesoectodermal dysplasia that presents early in life, possibly as early as in utero and exhibits male gender predominance (1.7:1.0). Its features include enlargement of the soft tissue and/or bone of one hemimaxilla that may produce mild facial asymmetry, sclerotic radiographic bone changes and dental developmental abnormalities. The dense bone, which often exhibits a radiographic vertical orientation of the trabecular bone pattern, is generally associated with delayed eruption of the teeth...
January 2014: Journal of the Indian Society of Pedodontics and Preventive Dentistry
https://read.qxmd.com/read/24042594/segmental-odontomaxillary-dysplasia-report-of-a-case-emphasizing-histopathological-immunohistochemical-and-scanning-electron-microscopic-features
#7
Rebeca S Azevedo, Luísa J da Silveira, Luis Flávio M Moliterno, Águida Maria M A Miranda, Oslei P de Almeida, Fábio R Pires
Segmental odontomaxillary dysplasia (SOD) is a rare developmental disorder of the maxilla, and there is little information on its morphological features. Thus, the present article describes a case of SOD focusing on its histopathological, immunohistochemical and scanning electron microscopic features. Several dental abnormalities were present, including numerous dentin and pulp defects, altered composition of hard tissue, and proliferation of myofibroblasts in the pulp and the soft tissue surrounding affected teeth...
September 2013: Journal of Oral Science
https://read.qxmd.com/read/23745055/combined-cutaneous-findings-with-segmental-odontomaxillary-dysplasia-review-of-the-literature-and-proposal-of-a-new-clinical-classification
#8
Othman M Yassin, Farouk B Rihani
Segmental odontomaxillary dysplasia is characterized by variability of its clinical and radiological features, and may mimic other fibro-osseous lesions. We describe the case of a segmental odontomaxillary dysplasia in a 12-year-old male comprising of dermal, gingival, bony, and dental abnormalities. He presented with left midfacial diffuse hyperkeratotic erythematous lesion, ipsilateral hypopigmentation of upper lip with indistinct vermilion border, left-sided facial swelling, unilateral maxillary enlargement and ipsilateral failure of eruption of permanent teeth...
2008: International Medical Case Reports Journal
https://read.qxmd.com/read/23483745/midline-segmental-odontomaxillary-dysplasia
#9
Ajaz Shah, Suhail Latoo, Irshad Ahmed, Altaf H Malik, Shahid Hassan, Abraar Bhat, Shazia Mir, Nitul Jain
Segmental odontomaxillary dysplasia (SOD) is a rare developmental disorder of the maxilla, characterized by variability of its clinical and radiological features and may mimic other fibro-osseous lesions. Clinically, the disorder is often diagnosed in early childhood due to a unilateral buccolingual expansion of the posterior alveolar process, gingival enlargement, absence of one or both premolars in the affected region, delayed eruption of the adjacent teeth, and malformations of the primary molars. We describe a rare case of a SOD in a 19-year-old female comprising findings similar to earlier reports, but for the first time SOD is reported along midline...
July 2012: Annals of Maxillofacial Surgery
https://read.qxmd.com/read/22677745/clinical-and-radiological-presentation-of-hemimaxillofacial-dysplasia-segmental-odontomaxillary-dysplasia-critical-analysis-and-report-of-a-case
#10
REVIEW
Silvina Friedlander-Barenboim, Kıvanç Kamburoğlu, Israel Kaffe
OBJECTIVES: The purpose of the present study was to critically evaluate the literature, describe the clinical and radiographic features of HD-SOD (hemimaxillofacial dysplasia/segmental odontomaxillary dysplasia), and describe one new case, involving a 12-year-old boy, with detailed radiological, clinical, and histologic characteristics. METHODS: Thirty-six cases published between 1987 and 2010, together with the present case, were evaluated according to criteria that included gender, age, location of the lesion, findings, and symptoms...
February 2012: Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
https://read.qxmd.com/read/22139529/segmental-odontomaxillary-dysplasia-report-of-3-cases-and-literature-review
#11
REVIEW
Wilfredo Alejandro González-Arriagada, Pablo Agustin Vargas, Rodrigo Fuentes-Cortés, Marco Antonio Nasi-Toso, Marcio Ajudarte Lopes
Segmental Odontomaxillary Dysplasia (SOD) is an uncommon developmental disorder of unknown etiology that causes a unilateral alteration of the maxilla associated with an abnormal growth and maturation of bone, lack of one or both premolars and delayed tooth eruption on the affected side, alteration of adjacent gingival tissue with or without facial cutaneous lesions. Radiographically is observed an irregular trabecular pattern and reduction of the maxillary sinus. There are 50 cases reported in the English-language literature...
June 2012: Head and Neck Pathology
https://read.qxmd.com/read/21977473/unilateral-segmental-odontomaxillary-hypoplasia-an-unusual-case-report
#12
Sushma Pandey, Keerthilatha M Pai, Ajay G Nayak, Ravindranath Vineetha
Facial asymmetry is not an uncommon occurrence in day to day dental practice. It can be caused by various etiologic factors ranging from facial trauma to serious hereditary conditions. Here, we report a rare case of non-syndromic facial asymmetry in a young female, who was born with this condition but was not aware of the progression of asymmetry. No relevant family history was recognized. She was also deficient in both deciduous and permanent teeth in the corresponding region of maxilla. Hence, the cause of this asymmetry was believed to be a segmental odontomaxillary hypoplasia of left maxilla accompanied by agenesis of left maxillary premolars and molars and disuse atrophy of corresponding facial musculature...
March 2011: Imaging Science in Dentistry
https://read.qxmd.com/read/21802321/clinical-and-radiological-presentation-of-hemimaxillofacial-dysplasia-segmental-odontomaxillary-dysplasia-critical-analysis-and-report-of-a-case
#13
Silvina Friedlander-Barenboim, Kıvanç Kamburoğlu, Israel Kaffe
OBJECTIVES: The purpose of the present study was to critically evaluate the literature, describe the clinical and radiographic features of HD-SOD (hemimaxillofacial dysplasia/segmental odontomaxillary dysplasia), and describe one new case, involving a 12-year-old boy, with detailed radiological, clinical, and histologic characteristics. METHODS: Thirty-six cases published between 1987 and 2010, together with the present case, were evaluated according to criteria that included gender, age, location of the lesion, findings, and symptoms...
July 28, 2011: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
https://read.qxmd.com/read/21764204/hemimaxillofacial-dysplasia-segmental-odontomaxillary-dysplasia-case-study-with-11-years-of-follow-up-from-primary-to-adult-dentition
#14
Charles P Minett, Tom D Daley
No abstract text is available yet for this article.
May 2012: Journal of Oral and Maxillofacial Surgery
https://read.qxmd.com/read/21684782/segmental-odontomaxillary-dysplasia-report-of-a-series-of-5-cases-with-long-term-follow-up
#15
REVIEW
Joseph C Whitt, James W Rokos, Charles L Dunlap, Bruce F Barker
We report a series of 5 cases of segmental odontomaxillary dysplasia (SOMD) with follow-up periods ranging from 8 to 21 years, bringing the total number of reported cases to 45. SOMD is a sporadic, mesoectodermal dysplasia that presents early in life, possibly as early as in utero and exhibits male gender predominance (1.7:1.0). Its features include enlargement of the soft tissue and/or bone of 1 hemimaxilla that may produce mild facial asymmetry. Subsequent growth of the affected area is proportional to that of the unaffected hemimaxilla...
August 2011: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
https://read.qxmd.com/read/21197434/segmental-odontomaxillary-dysplasia-review-of-the-literature-and-case-report
#16
Riya M Kuklani, Madhu K Nair
Segmental Odontomaxillary Dysplasia (SOD) is an uncommon, nonhereditary, recently recognized developmental disorder affecting the upper jaw and related dental components. It is a rare condition of uncertain etiology that results in painless unilateral expansion of the posterior dentoalveolar complex, gingival hyperplasia, lack of one or both premolars in the affected area, delayed eruption of adjacent teeth and malformations of the primary molars. Radiographically, the affected bone is thickened and irregular in outline, with coarse trabecular pattern that is vertically oriented resulting in a relatively radiopaque granular appearance...
2010: International Journal of Dentistry
https://read.qxmd.com/read/19115802/prosthetic-rehabilitation-of-segmental-odontomaxillary-dysplasia-seven-year-follow-up
#17
Birgül Ozpinar, Bülent Gökçe, Gökhan Uzel, M Erhan Cömlekoğlu
Segmental odontomaxillary dysplasia is an uncommon maxillofacial deformity. Clinically, overgrowth and maturation of the maxillary right or left posterior alveolus and the respective gingiva, lack of premolars, delayed eruption of the adjacent teeth, and malformed primary molars are observed. The purpose of this report was to describe the clinical and radiographic findings of a 47-year-old female with segmental odontomaxillary dysplasia and summarize the prosthetic rehabilitation with fixed and removable partial dentures...
January 2009: Cleft Palate-craniofacial Journal
https://read.qxmd.com/read/19054480/case-report-segmental-odontomaxillary-dysplasia-a-rare-disorder
#18
S K Bhatia, N Drage, A J Cronin, M L Hunter
BACKGROUND: Segmental odontomaxillary dysplasia (SOD) is a rare developmental disorder of the maxilla characterised by abnormal growth and maturation of bone, teeth and gingival of the affected segment. Due to the rarity of the disorder, the full range of clinical manifestations is unknown. Since there are concerns that cases may be subject to misdiagnosis, this report aims to increase awareness of the condition among paediatric dentists. CASE REPORT: A 7-year-old boy was initially referred regarding failure of eruption of maxillary primary molars...
December 2008: European Archives of Paediatric Dentistry: Official Journal of the European Academy of Paediatric Dentistry
https://read.qxmd.com/read/18789102/segmental-odontomaxillary-dysplasia-presenting-with-facial-hypertrichosis-commissural-lip-clefting-and-hyperlinear-palms
#19
Lisa J Koenig, Denis P Lynch, Kim B Yancey
Segmental odontomaxillary dysplasia is a rare disorder that unilaterally affects the maxilla causing facial asymmetry and presenting with hypertrichosis and hypoplastic or missing teeth in the affected area. Lip clefting has only been reported in one other case. We report a case of segmental odontomaxillary dysplasia presenting with hypertrichosis of the face, hyperlinear palms with faint erythema, and commissural lip clefting.
July 2008: Pediatric Dermatology
https://read.qxmd.com/read/15283787/a-syndrome-of-hemimaxillary-enlargement-asymmetry-of-the-face-tooth-abnormalities-and-skin-findings-hats
#20
REVIEW
Michael Jude Welsch, Sarah L Stein
Hemimaxillofacial dysplasia and segmental odontomaxillary dysplasia appear to be the same syndrome, having the common features of unilateral abnormalities of bone, teeth, gums, and skin. Oral manifestations are the hallmark of this condition. Those affected are generally recognized in childhood and may have partial anodontia, abnormal spacing of the teeth, delayed eruption, and gingival thickening of the affected segment. Reported cutaneous manifestations include facial asymmetry, Becker's nevus, "hairy nevus," lip hypopigmentation, discontinuity of the vermilion border, depression of the cheek, and erythema...
July 2004: Pediatric Dermatology
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