Regional odontodysplasia: A classical case report

2013 ◽  
Vol 4 (2) ◽  
pp. 86 ◽  
Author(s):  
Ritika Malhotra ◽  
ND Shashikiran ◽  
Shilpy Singla ◽  
Atul Verma
Keyword(s):  
Case Report ◽  
Classical Case ◽  
Regional Odontodysplasia

scholarly journals Generalised versus Regional Odontodysplasia: Diagnosis, Transitional Management, and Long-Term Followup—A Report of 2 Cases

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Mostafa Ibrahim Mostafa ◽  
Nehad Samir Taha ◽  
Mennat Allah Ismail Mehrez
Keyword(s):  
Case Report ◽  
Conservative Treatment ◽  
Conservative Management ◽  
Tooth Extraction ◽  
Treatment Plan ◽  
Treatment Options ◽  
Uncommon Condition ◽  
Regional Odontodysplasia ◽  
Left Quadrant

Background. Odontodysplasia is an uncommon condition. It can be localised or generalised, isolated or part of a syndrome.Case Report. We first report the case of an 8.5-year-old boy who presented with abnormally shaped teeth and multiple intraoral abscesses. Findings of clinical and radiographic examinations were consistent with those of generalised odontodysplasia. A 2-step, conservative treatment plan was executed with a 10-year followup. Step 1 was root canal treatment of nonvital teeth. Step 2 was crowning without preparation of new vital, erupted, and malformed teeth. The second case is that of a 12-year-old girl who presented with lack of teeth in the upper-left quadrant. The impacted teeth were exposed surgically, and fixed restoration was performed for temporary aesthetic improvement.Conclusion. Instead of tooth extraction, an approach previously used in similar cases, conservative management is feasible and offers better prosthetic treatment options for the future.

scholarly journals Characteristics of regional odontodysplasia: A case report

2012 ◽  
Vol 34 (2) ◽  
Author(s):  
Saulo André de Andrade Lima ◽  
Amilcar Viana de Oliveira ◽  
Luciana Silveira Gonçalves Lima ◽  
Luiz Renato Paranhos ◽  
Renata Pilli Jóias ◽  
...  
Keyword(s):  
Case Report ◽  
Regional Odontodysplasia

scholarly journals Christ-Siemens-Touraine Syndrome: A Case Report and Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Sepideh Mokhtari ◽  
Saeedeh Mokhtari ◽  
Ali Lotfi
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Classical Case ◽  
Common Type ◽  
Rare Disorder ◽  
Review Of The Literature ◽  
Sebaceous Glands ◽  
Dental Abnormalities ◽  
Anhidrotic Ectodermal Dysplasia

Ectodermal dysplasia is a rare disorder with defects in two or more of the following structures: the teeth and the skin and its appendages including hair, nails, eccrine, and sebaceous glands. Anhidrotic ectodermal dysplasia is the most common type of disease. This rare disorder, also known as Christ-Siemens-Touraine syndrome, manifests as a triad of hypotrichosis, asteatosis, and anhidrosis. In view of the rarity of this entity, a classical case of anhidrotic ectodermal dysplasia is reported. We have also provided a review of recent investigations in the area of dental abnormalities in this syndrome.

scholarly journals Regional odontodysplasia: case report

2007 ◽  
Vol 15 (6) ◽  
pp. 465-469 ◽  
Author(s):  
Ana Carolina Magalhães ◽  
Juliano Pelim Pessan ◽  
Robson Frederico Cunha ◽  
Alberto Carlos Botazzo Delbem
Keyword(s):  
Case Report ◽  
Regional Odontodysplasia

scholarly journals The classical case of the treatment of an adult patient with the salt-losing form of congenital adrenal cortical dysfunction

2011 ◽  
Vol 57 (4) ◽  
pp. 25-27
Author(s):  
A I Sazonova ◽  
N V Molashenko ◽  
I S Iarovaia ◽  
N Iu Kalinchenko ◽  
E A Troshina
Keyword(s):  
Case Report ◽  
Adult Patient ◽  
Clinical Course ◽  
Classical Case ◽  
Adult Patients ◽  
Dynamic Observation ◽  
Cortical Dysfunction ◽  
Disease Analysis

This case report illustrates peculiarities of the clinical course of congenital adrenal cortical dysfunction in adult patients presenting with the salt-losing form of the disease. Analysis of this case confirmed the necessity of dynamic observation of adults with this pathology in order to avoid complications that are likely to develop in case of inadequate treatment.

Reiter's Syndrome in Children: Case Report and Review of Literature

1962 ◽  
Vol 1 (3) ◽  
pp. 148-151
Author(s):  
Andrew M. Margileth
Keyword(s):  
Rheumatoid Arthritis ◽  
Case Report ◽  
Juvenile Rheumatoid Arthritis ◽  
No Value ◽  
Recent Literature ◽  
Classical Case ◽  
Review Of Literature ◽  
Reiter's Syndrome ◽  
The Past ◽  
Reiter’S Syndrome

1. Our experience with a six-year-old boy who had diarrhea, urethritis, conjunctivitis and arthritis is presented as a classical case of Reiter's syndrome. The patient recovered fully in a period of five months and has remained well during the past five years. 2. The cause of Reiter's syndrome remains unknown but in children may be related to Flexner bacillus dysentery. 3. The disease in children is usually less severe than in adults and all 11 children reported have recovered. The recent literature is reviewed. 4. Treatment with antibiotics is of no value and steroid therapy has not prevented exacerbations nor shortened the course of the disease. 5. The nongonococcal triad of urethritis, conjunctivitis, and arthritis is a distinct clinicopathologic entity which differs from known infections and juvenile rheumatoid arthritis.

Comparative case report of segmental odontomaxillary dysplasia and regional odontodysplasia

Dental Update ◽  
2014 ◽  
Vol 41 (9) ◽  
pp. 825-831
Author(s):  
Stephanie L Clark ◽  
Alison M Cairns ◽  
Keith D Hunter
Keyword(s):  
Case Report ◽  
Regional Odontodysplasia ◽  
Segmental Odontomaxillary Dysplasia

scholarly journals A CLASSICAL CASE OF PREGNANCY INDUCED GINGIVAL ENLARGEMENT: A CASE REPORT

2014 ◽  
Vol 3 (45) ◽  
pp. 11104-11108
Author(s):  
Shailendra S Chauhan ◽  
Amit Pandey ◽  
Amrita Raj ◽  
Ankita Raj ◽  
Saket Nigam
Keyword(s):  
Case Report ◽  
Classical Case ◽  
Gingival Enlargement

Congenital Midline Cervical Cleft: A Case Report with Review of Literature

2017 ◽  
Vol 8 (1) ◽  
pp. 25-30 ◽  
Author(s):  
Ashwin A Jaiswal ◽  
Bikram K Behera ◽  
Ravindranath Membally ◽  
Manoj K Mohanty
Keyword(s):  
Case Report ◽  
Cleft Lip ◽  
Classical Case ◽  
Review Of Literature ◽  
Suprasternal Notch ◽  
Anterior Neck ◽  
Thyroglossal Duct Cysts ◽  
Bronchogenic Cysts ◽  
Head Neck ◽  
Midline Cervical Cleft

ABSTRACT Aim To highlight a rare case of a congenital midline cervical cleft (CMCC) in context with embryological theories/hypothesis, presentation, and management along with review of literature. Introduction Congenital midline cervical cleft is a rare but interesting anterior neck anomaly with controversial theories/ hypothesis regarding its embryogenesis. Case report We describe here a classical case of midline cervical cleft that presented at birth with a cephalocaudal orientation, extending from the level below the hyoid bone to the suprasternal notch with a length of 3 cm and width of 0.5 cm. At 6 months of age, the lesion was excised and closure was done by multiple Z-plasty, with satisfactory results. Discussion Although the diagnosis is clinical, it is frequently misdiagnosed. The associated clinical features could include thyroglossal duct cysts, cleft lip/mandible/sternum, cervical contractures, mandibular spurs, microgenia, and/or bronchogenic cysts. If it is not treated at an early age, it can result in complications like webbing of the neck, dental malocclusion, and restricted neck movements. Conclusion Earliest recognition of CMCC and proper intervention can provide better esthetic and functional prognosis. Clinical significance A correct earlier recognition of the lesion and appropriate surgical management are key to avoid longterm complications. How to cite this article Jaiswal AA, Behera BK, Membally R, Mohanty MK. Congenital Midline Cervical Cleft: A Case Report with Review of Literature. Int J Head Neck Surg 2017;8(1):25-30.

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