scholarly journals Multiple Unerupted Impacted Supernumerary Teeth: A Rare Case Report of Father and Son

2018 ◽  
Vol 3 (2) ◽  
pp. 863-867
Author(s):  
Ajit Joshi ◽  
Manu Goel ◽  
Nitin Fating ◽  
Pawan Dawane
Keyword(s):  
Case Report ◽  
Family History ◽  
Prevalence Rate ◽  
Rare Case ◽  
Radiographic Examination ◽  
Etiologic Factor ◽  
Supernumerary Teeth ◽  
Rare Case Report ◽  
History Of ◽  
Father And Son

Multiple impacted supernumerary teeth without any associated systemic conditions or syndromes are rare. The prevalence rate of supernumerary teeth in the permanent dentition is between 0.1– 6.9 % as compared to 0.3–0.6% in theprimary dentition. In this article, reporting a rare family history of non-syndromic multiple impacted supernumerary teeth,found incidentally during routine radiographic examination. Though the etiologic factor of multiple impacted supernumerary teeth are still not clearly known especially in cases without any syndrome. However, thorough evaluation is necessary toexclude associated systemic conditions.

scholarly journals Twelve Impacted Supernumerary Teeth in a Nonsyndromic Patient: A Rare Case Report

2017 ◽  
Vol 18 (4) ◽  
pp. 342-344
Author(s):  
Fareedi Mukram Ali
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Panoramic Radiograph ◽  
Deciduous Teeth ◽  
Radiographic Examination ◽  
Dental Arch ◽  
Supernumerary Teeth ◽  
Rare Case Report ◽  
Excess Number ◽  
Maxillary Region

ABSTRACT Teeth in excess number than the normal count are called supernumerary teeth. They can be either unilateral or bilateral and single or multiple, found at any place in the dental arch, but most commonly found in the anterior maxillary region. Supernumerary teeth are commonly associated with syndromes when present in more numbers, but can be idiopathic. The present study shows a case report of a 16-year-old female patient who reported with overretained deciduous teeth. A panoramic radiograph showed multiple impacted supernumerary teeth. Based on clinical features and radiographic examination, a diagnosis of idiopathic hyperdontia was given. In such types of patients, management must be planned by a multidisciplinary approach. How to cite the article Al-Iryani GM, Ali FM. Twelve Impacted Supernumerary Teeth in a Nonsyndromic Patient: A Rare Case Report. J Contemp Dent Pract 2017;18(4):342-344.

CHOREA GRAVIDARUM: A RARE CASE REPORT

2021 ◽  
pp. 71-72
Author(s):  
Aswini Viswanadh ◽  
Sujata Singh ◽  
Vinnisa N. V
Keyword(s):  
Case Report ◽  
Family History ◽  
Gestational Age ◽  
Postpartum Period ◽  
Rare Case ◽  
Third Trimester ◽  
Detailed Evaluation ◽  
Rare Case Report

Chorea gravidarum is the term given to chorea occurring during pregnancy. Here, we report a case of 24 year old primigravida at gestational age 38 weeks 3days ,without any signicant past & family history who presented with chorea gravidarum for the rst time in third trimester. On detailed evaluation no etiology was identied. On follow up in postpartum period, her choreiform movements have reduced in intensity, but is still persisting pointing towards an idiopathic origin.

scholarly journals Non-painful severe variant form of eruptive lingual papillitis: A case report and literature review

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Manal Ahmed Halwani
Keyword(s):  
Emergency Department ◽  
Case Report ◽  
Literature Review ◽  
Oral Hygiene ◽  
Rare Case ◽  
Dorsal Surface ◽  
Variant Form ◽  
Girl Child ◽  
Rare Case Report ◽  
History Of

Eruptive lingual papillitis is a common benign disorder manifested by inflammation of fungiform papillae on the dorsolateral surface of the tongue. Several variants of lingual papillitis have been reported since 1997, most or all of them with painful erythematous papules. Here we report a case of 6 years old girl child with non-painful severe variant form of eruptive lingual papillitis presented to the emergency department. The entire dorsal surface of the tongue was surfaced by 2-3mm by multiple erythematous papules and some with a white or yellowish colour. The papules were excessively inflamed, pigmented, aggregated, and crusted. The cause was idiopathic which resolved within ten days. The parent and patient were reassured with advice to practice oral hygiene. This is a rare case report describing non-painful lingual papillitis without a history of any prior episodes.

scholarly journals A ruptured cornual pregnancy successfully managed in a patient with a history of oophorectomy and salpingectomy: A rare case report

2021 ◽  
Vol 9 (10) ◽  
Author(s):  
Marah Mansour ◽  
Amr Hamza ◽  
AlHomam AlMarzook ◽  
Ilda moafak kanbour ◽  
Tamim Alsuliman ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cornual Pregnancy ◽  
Rare Case Report ◽  
History Of

The fatal cholera like diarrhoea in coronavirus disease 2019(COVID-19)- a rare case report in toddler

2020 ◽  
Vol 11 (SPL1) ◽  
pp. 1894-1897
Author(s):  
Varsha Gajbhiye ◽  
Shubhangi Patil (Ganvir) ◽  
Sarika Gaikwad
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Digestive System ◽  
Gastrointestinal Symptoms ◽  
Female Child ◽  
Multiple Organ ◽  
Mild Case ◽  
Severe Dehydration ◽  
Rare Case Report ◽  
History Of

A 14-month female child came with complain of cholera like watery loose stool 10-12 times and vomiting 6-7 times, 24 hrs before admission. She was in severe dehydration, hypotension, unconscious with no recorded fever during her stay in hospital and no history of contact with COVID-19. Patient was COVID-19 positive Dehydration and hypotension was corrected, metabolic acidosis continued and eventually patient succumb due to multiple organ failure. This case report should arouse us to suspect COVID infection in every acute Gastroenteritis child who may not have any common symptoms as seen in COVID patient, also who have no history of significant contact with COVID positive patient in family. Some people with COVID-19 develop gastrointestinal symptoms either alone or with respiratory symptoms. Recently, researchers at Stanford University found that a third of patients they studied with a mild case of COVID-19 had symptoms affecting the digestive system. Another recent study Trusted Source published by researchers in Beijing found that anywhere from 3 to 79 percent of people with COVID-19 develop gastrointestinal symptoms.

Rare case of perforated appendicitis presenting as persistent perineal discharge following laparoscopic abdominoperinal excision of rectum (APER)

2021 ◽  
Vol 14 (1) ◽  
pp. e236312
Author(s):  
Tanmoy Mukherjee ◽  
Shantata Jayant Kudchadkar ◽  
Jayesh Sagar ◽  
Shashank Gurjar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Perforated Appendicitis ◽  
Perineal Wound ◽  
Abdominoperineal Excision ◽  
Major Surgery ◽  
Salvage Procedure ◽  
Uncommon Presentation ◽  
Rare Case Report ◽  
History Of

Abdominoperineal excision of rectum (APER) is one of the widely used surgical procedures to treat low rectal cancer, benign conditions like Crohn’s proctitis with anal involvement and as a salvage procedure for anal cancer. Perineal wound infection is a well-recognised complication following such major surgery. Occurrence of appendicitis in a few weeks’ time following such a major surgery is uncommon. However, here we present a rare case report of perforated appendicitis presenting as persistent perineal discharge in an elderly man, following laparoscopic APER for a low rectal tumour. To our knowledge, this is the first time such a rare clinical presentation of appendicitis is reported in the history of medical literature. Through this case report, we aim to highlight the importance of considering such an uncommon presentation in patients with perineal discharge, following APER.

Occurrence of bilaterally impacted mandibular supernumerary teeth: A rare case report and review of literature

2016 ◽  
Vol 7 (3) ◽  
pp. 198
Author(s):  
PraveshKumar Jhingta ◽  
VinayKumar Bhardwaj ◽  
Deepak Sharma ◽  
Nishant Negi ◽  
Sanjeev Vaid ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Supernumerary Teeth ◽  
Rare Case Report

Bizarre extensive erythematous plaques on the abdomen

2018 ◽  
Vol 49 (1) ◽  
pp. 39-42
Author(s):  
Sidharth Tandon ◽  
Surabhi Sinha ◽  
Jasmeet Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
History Of ◽  
Erythematous Plaques

We present a rare case report of a 28-year-old man with a five-month history of bizarre extensive erythematous plaques on the abdomen extending in a dermatomal fashion to the left upper back.

scholarly journals HETEROZYGOUS HEMOCHROMATOSIS: A RARE CASE REPORT

2021 ◽  
Author(s):  
Nirmit Patel ◽  
Aneri Patel ◽  
Viral Patel ◽  
Sakshar Patel ◽  
Dhrushi Patel ◽  
...  
Keyword(s):  
Case Report ◽  
Family History ◽  
Iron Overload ◽  
Rare Case ◽  
First Report ◽  
Rare Case Report

To our knowledge,this is the first report of 31 Y F has no family history and usually,patients do not manifest symptoms if they are heterozygous.Individuals heterozygous for C282Y who have a coexisting insult to the liver,associated with the use of medications,may present with overt manifestations of iron overload.

scholarly journals Bilateral multiple supernumerary premolars in a non-syndromic patient: A rare case report

2019 ◽  
pp. 17-22
Author(s):  
Kriti Garg ◽  
Shiv Shing ◽  
Rohan Sachdeva ◽  
Vishal Mehrotra
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Occurrence ◽  
Supernumerary Teeth ◽  
Developmental Anomalies ◽  
Rare Case Report ◽  
Maxilla And Mandible

Supernumerary teeth are extra teeth above the normal erupted teeth number. Supernumerary premolars are rare developmental anomalies when compared to mesiodens and other supernumerary teeth. Supernumerary premolars are more common in the mandible than the maxilla. This article reports a rare occurrence of supplemental premolars bilaterally present in the maxilla and mandible arches in a non-syndromic patient. Keywords: Supernumerary teeth, premolars, bilateral, maxilla, mandible

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