scholarly journals Pancake Kidney: A Rare Case Report Developmental Anomaly in Child

Med Phoenix ◽  
2017 ◽  
Vol 2 (1) ◽  
pp. 71-73
Author(s):  
Ramjee Bastola ◽  
Pashupati Bhatta ◽  
Akhilesh Kumar Jha ◽  
Shekhar Meheta ◽  
Akash Raya ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Renal Agenesis ◽  
Horseshoe Kidney ◽  
Developmental Anomaly ◽  
Imaging Findings ◽  
Radiological Imaging ◽  
Developmental Anomalies ◽  
Rare Case Report ◽  
Renal Abnormalities

The aim of the study is to present a rare case of incidentally detected pelvic pancake kidney with radiological imaging findings in a 11 year old male child. There are many developmental anomalies of kidney Various types of congenital renal abnormalities such as renal agenesis, ectopic or horseshoe kidney can be encountered where one of the most rarest presentation with a single ureter on pancake kidney is encountered in number that count in fingers worldwide.Med Phoenix Vol.2(1) July 2017, 71-73

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

scholarly journals Fibrous dysplasia of maxilla – A rare case report

2021 ◽  
pp. 485-488
Author(s):  
Vijaya R Kamble ◽  
Shalini N Waghmare ◽  
Aditi V Rangari ◽  
Mangala Meti ◽  
Pritam Pohankar ◽  
...  
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia ◽  
Female Patient ◽  
Malignant Transformation ◽  
Histological Examination ◽  
Rare Case ◽  
Definitive Diagnosis ◽  
Developmental Anomaly ◽  
Rare Case Report ◽  
Examination Methods

Fibrous dysplasia (FD) is a skeletal developmental anomaly, which is non-hereditary in origin and idiopathic in nature. It is a benign fibro-osseous disease that affects one or more bones. It usually affects unilaterally and is seen in the posterior region. Approximately 0.5% of untreated cases show the malignant transformation. We report the case of a 35-year-old female patient with FD involving the maxilla. The clinical diagnostic approach, different imaging modalities, and histological examination methods for definitive diagnosis have been elaborated.

scholarly journals Concrescence of impacted mandibular third molar with a fourth molar

2015 ◽  
Vol 7 (1) ◽  
pp. 48-49
Author(s):  
D Deepa ◽  
K.V Arun Kumar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Third Molar ◽  
Developmental Anomaly ◽  
Permanent Teeth ◽  
Impacted Mandibular Third Molar ◽  
Mandibular Third Molar ◽  
Rare Case Report ◽  
Mandibular Teeth

Abstract Concrescence is a developmental anomaly of tooth in which fusion between two completely formed roots takes place at the cementum. It may involve either deciduous or permanent teeth. Concrescence is mostly observed in maxillary than in mandibular teeth. A rare case of impacted mandibular third molar fused with a supernumerary molar has been reported here. How to cite this article Arun Kumar KV, Deepa D. Concrescence of impacted mandibular third molar with a fourth molar - A Rare Case Report. CODS J Dent 2015;7:48-49.

scholarly journals Mandibular Primary First Molar with Single Root and Single Canal: A Rare Case Report

2020 ◽  
Vol 6 (1) ◽  
pp. 67-71
Author(s):  
Tazdik G Chowdhury ◽  
KM Rowank Jahan ◽  
Tasnim A Jannat ◽  
Ashik Abdullah Imon
Keyword(s):  
Case Report ◽  
Root Morphology ◽  
Rare Case ◽  
Developmental Anomaly ◽  
Single Root ◽  
Rare Case Report ◽  
Radiographic Interpretation ◽  
Mandibular First Molar

An extremely uncommon tooth developmental anomaly seen such as bilateral primary mandibular first molar with a single root and single canal. Various researchers found that due to failure of invagination of HERS leads to various anomalies in root morphology. A 9 year old girl with pain on lower left side of the jaw originated from mandibular left first molar. On right side there was also presence of 84 with single root. The tooth was treated by pulpectomy followed by restoration. Due to unusual morphology, the chance of endodontic mishaps is extremely high in the search of additional canal, which can be overcome by proper knowledge of root morphology and radiographic interpretation. Journal of National Institute of Neurosciences Bangladesh, 2020;6(1): 67-71

scholarly journals A Rare Case Report of Septic Embolism and Infective Endocarditis due to Nocardia farcinia from North India

2020 ◽  
pp. 263246362096054
Author(s):  
Sweta Singh ◽  
Uday Shanker Singh
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Rare Case ◽  
Unusual Case ◽  
Imaging Techniques ◽  
North India ◽  
Radiological Imaging ◽  
Chronic Alcoholic ◽  
Septic Embolism ◽  
Rare Case Report

Nocardia farcinia endocarditis is an extremely rare phenomenon. It is an opportunistic ubiquitously present pathogen in the environment. Here, we present an unusual case of septic embolism with infective endocarditis due to Nocardia spp. in a 55-year-old chronic alcoholic male. Radiological imaging techniques and microbiological investigations helped in the timely diagnosis. Timely institution of treatment based on sensitivity results resulted in favorable outcome in the patient.

P575 Uterus didelphus with blind hemivagina and ipsilateral renal agenesis - a rare case report

2009 ◽  
Vol 107 ◽  
pp. S576-S576
Author(s):  
J. Faria ◽  
S. Soares ◽  
M. Bernardo ◽  
C. Ferreira ◽  
S. Coutinho ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Renal Agenesis ◽  
Rare Case Report

IgA nephropathy in a horseshoe kidney: A rare case report

2017 ◽  
Vol 4 (1) ◽  
pp. 47
Author(s):  
Chandrakala R. Iyer ◽  
Nagendra Katwe ◽  
Srinivas Rao Paladugu
Keyword(s):  
Case Report ◽  
Iga Nephropathy ◽  
Rare Case ◽  
Horseshoe Kidney ◽  
Rare Case Report

scholarly journals A giant retroperitoneal schwannoma in pregnancy: a rare case report and review of literature

2020 ◽  
Vol 7 (6) ◽  
pp. 2052
Author(s):  
Aditya Prasad Padhy ◽  
Prathmesh Mishra ◽  
Deepak Das ◽  
Nishant Agarwal
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Pregnant Female ◽  
Radiological Imaging ◽  
Review Of Literature ◽  
Rare Tumors ◽  
Rare Case Report ◽  
Retroperitoneal Schwannoma ◽  
In Pregnancy

Retroperitoneal schwannomas are though more common among females, are very much rare tumors arising from sheath of nerves. Also, extremely rare during pregnancy. Very few articles till date are there regarding retroperitoneal schwannomas that’s too in pregnant female. Usually these are symptomatic unless causing some compression to other intra-abdominal structures like vessels or bowel and usually malignant. As its retroperitoneal very difficult to diagnose it. So, with proper investigations and radiological imaging, first have to find out the differential diagnosis prior to planning for surgery.

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