Delayed eruption of premolars with periodontitis of primary predecessors and a cystic lesion: a case report

2002 ◽  
Vol 12 (1) ◽  
pp. 53-60 ◽  
Author(s):  
Y. Yawaka ◽  
M. Kaga ◽  
M. Osanai ◽  
A. Fukui ◽  
H. Oguchi
Keyword(s):  
Case Report ◽  
Cystic Lesion ◽  
Delayed Eruption

scholarly journals Concomitant cemento-osseous dysplasia and aneurysmal bone cyst of the mandible: a rare case report with literature review

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Han-Gyeol Yeom ◽  
Jung-Hoon Yoon
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Aneurysmal Bone Cyst ◽  
Cystic Lesion ◽  
Bone Cyst ◽  
Neck Region ◽  
Diagnostic Process ◽  
Simultaneous Occurrence ◽  
Head And Neck Region ◽  
Osseous Dysplasia

Abstract Background Concomitant cemento-osseous dysplasia (COD) and aneurysmal bone cyst (ABC) are rare in the head and neck region. In our search of the English language literature, we found only one case report describing the simultaneous occurrence of COD and ABC in the head and neck region. Here, we report a case of COD associated with ABC. Further, we performed a systematic search of the literature to identify studies on patients with COD associated with nonepithelial lined cysts of the jaws. Case presentation The patient was a 32-year-old woman who was referred from a private dental clinic because of a cystic lesion below the mandibular right first molar. She had no pain or significant systemic disease. After performing panoramic radiography and cone-beam computed tomography, the imaging diagnosis was COD with a cystic lesion, such as ABC or solitary bone cyst. Excisional biopsy was performed, which revealed concomitant COD and ABC. Conclusion This case of ABC associated with COD provides insight for the diagnostic process of radiographically mixed lesions with cystic changes.

Peri-Implant Cystic Lesion With Unusual Cellular Changes: A Case Report

2014 ◽  
Vol 4 (4) ◽  
pp. 240-245 ◽  
Author(s):  
Bryan J. Frantz ◽  
Jack G. Caton ◽  
Fred J. Bonacci ◽  
Alessandro Geminiani ◽  
Remì Arseneau ◽  
...  
Keyword(s):  
Case Report ◽  
Cystic Lesion ◽  
Cellular Changes

Lymphoepithelial cyst of the pancreas. A case report

2007 ◽  
Vol 52 (3) ◽  
pp. 53-53
Author(s):  
L Fraser ◽  
OO Komolafe ◽  
JR Anderson
Keyword(s):  
Case Report ◽  
Cystic Lesion ◽  
Cystic Lesions ◽  
Lymphoepithelial Cyst ◽  
Invasive Procedures ◽  
Diagnostic Challenge ◽  
Distal Pancreas ◽  
Ct And Mri ◽  
Diagnostic Investigations ◽  
The Ideal

We present the case of a 63 year-old male who presented with a cystic lesion of the distal pancreas. Excision and histology showed this to be a lymphoepithelial cyst. Cystic lesions of the pancreas represent a diagnostic challenge, especially when pseudocyst secondary to pancreatitis is excluded. These lesions can be broadly classified into benign, pre-malignant and malignant. Widely used imaging modalities such as CT and MRI are not able to categorically differentiate between these. More invasive procedures such as endoscopic US and FNA again do not give a cast-iron diagnosis. Our patient had a symptomatic cystic lesion in his pancreas which was excised after cross-specialty discussion. We advocate that this is the ideal way to treat patients with cystic lesions of the pancreas, with each case considered on its own merits as all current diagnostic investigations have their limitations.

scholarly journals Vallecular cyst in an infant with stridor: a case report

2018 ◽  
Vol 6 (1) ◽  
pp. 58-62
Author(s):  
Nabin Lageju ◽  
Rajendra Prasad Sharma Guragain
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Cystic Lesion ◽  
Failure To Thrive ◽  
Surgical Excision ◽  
Infants And Children ◽  
Solid Component ◽  
Feeding Difficulties ◽  
The Right ◽  
In Infants And Children

Background and Objectives: Vallecular cysts are rare and generally asymptomatic. In infants and children they present with stridor, feeding difficulties, failure to thrive. Treatment is surgical excision with cautery or laser.Presentation of Case: We discuss the clinical, radiological presentation of a 7 months old child with vallecular cyst which was surgically treated with deroofing and marsupialisation with elecrocautery. There was no recurrence even up 2 years of follow-up.Discussion: Flexible nasopharyngolaryngoscopic examination was done which showed present of swelling in the left vallecula pushing the epiglottis posteriorly and to the right with narrowed normal endolarynx. Radiological investigations with CT scan showed cystic lesion noted in left side of neck with no septation and solid component. The lesion was extending to ipsilateral vallecula and paraglottic region with narrowing of endolarynx.Conclusion: Vallecular cyst is rare cause of noisy breathing in infants and children. In adults it is usually asymptomatic. Treatment of choice is marsupialization with electrocautery or laser.

scholarly journals Early Diagnosis of Bilateral Supplemental Primary and Permanent Maxillary Lateral Incisors: A Case Report

2011 ◽  
Vol 05 (02) ◽  
pp. 215-219 ◽  
Author(s):  
Gozde Yildirim ◽  
Sule Bayrak
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Permanent Dentition ◽  
Primary Dentition ◽  
Mixed Dentition ◽  
Diagnosis And Treatment ◽  
Supernumerary Teeth ◽  
Delayed Eruption ◽  
Normal Shape ◽  
Shape And Size

ABSTRACTSupernumerary teeth occur frequently in permanent dentition, but they are rarely found in primary dentition. Supernumerary teeth of orthodox shape and size that resemble normal dentition are called ‘supplemental teeth’. Supplemental teeth are less common than supernumerary teeth and are often overlooked because of their normal shape and size. Supplemental teeth may cause esthetic problems, delayed eruption and crowding, and they require early diagnosis and treatment to prevent complications. The case reported here is one of bilateral supplemental teeth impeding the eruption of permanent maxillary lateral incisors, and it emphasizes the importance of early diagnosis and treatment during early mixed dentition. (Eur J Dent 2011;5:215-219)

Delayed Eruption of a Mandibular Primary Cuspid Associated with Compound Odontoma

2005 ◽  
Vol 6 (4) ◽  
pp. 152-159 ◽  
Author(s):  
Sule Kavaloglu Cildir ◽  
Kemal Sencift ◽  
Vakur Olgac ◽  
Nuket Sandalli
Keyword(s):  
Case Report ◽  
Common Type ◽  
Primary Dentition ◽  
Odontogenic Tumor ◽  
Delayed Eruption ◽  
Compound Odontoma

Abstract Although odontomas are considered to be a common type of odontogenic tumor, they rarely occur solely in the primary dentition. This case report presents an eight and a half-year-old-child with a compound odontoma located in the mandible, which caused the impaction of both primary and permanent canines. Citation Cildir SK, Sencift K, Olgac V, Sandalli N. Delayed Eruption of a Mandibular Primary Cuspid Associated with Compound Odontoma. J Contemp Dent Pract 2005 November;(6)4:152-159.

Dental Findings in a Child with Osteopathia Striata with Cranial Sclerosis (OS-CS): A Case Report

2013 ◽  
Vol 37 (4) ◽  
pp. 411-413
Author(s):  
M Nishiguchi ◽  
K Satoh ◽  
Y Kamasaki ◽  
T Hoshino ◽  
T Fujiwara
Keyword(s):  
Case Report ◽  
Early Stage ◽  
Permanent Teeth ◽  
Dental Anomalies ◽  
Osteopathia Striata ◽  
Dental Management ◽  
Cranial Sclerosis ◽  
Planning Treatment ◽  
Delayed Eruption ◽  
Oral Abnormalities

The dental management of an 8-year-old girl with osteopathia striata with cranial sclerosis (OS-CS) is described. The girl presented with various oral abnormalities. The aim of this case report was to describe in detail the dental findings in a patient with OC-CS and the precautions to be taken when planning treatment. In the present case, many dental anomalies, such as delayed eruption of the permanent teeth, obliteration of the dental pulp, short roots, fused roots and taurodontism, were detected. In patients with OS-CS, routine dental care from an early stage is recommended to manage this anomaly properly.

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