scholarly journals Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report

2015 ◽  
Vol 8 (3) ◽  
pp. 124-126
Author(s):  
Ankita Joshi ◽  
Chinmay Sundarray ◽  
Krishna Arpita Sahoo
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Paranasal Sinuses ◽  
Rare Case ◽  
The Other ◽  
High Rate ◽  
Unknown Etiology ◽  
Structural Variations ◽  
The Third ◽  
Rare Case Report

ABSTRACT Paranasal sinus anatomical anomalies with unknown etiology are common. Paranasal sinus-related diseases are associated with so high rate of morbidities, it becomes essential to identify the structure and pathophysiology of the paranasal sinuses. Computed tomography (CT) is a valuable tool in displaying its anatomy, any anatomic variations and diseases. As paranasal sinus development is a complex and long-lasting process, there are great structural variations between individuals. Maxillary and/or frontal sinus aplasia or hypoplasia are more common than the other types. Several degrees and combinations of aplasias and hypoplasias have been reported; however, there is only two case of total paranasal sinus aplasia in the literature. Here, we present the third case of total paranasal sinus aplasia, and the first ever case reported from India. How to cite this article Joshi A, Sundarray C, Sahoo KA. Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report. Clin Rhinol An Int J 2015;8(3):124-126.

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

scholarly journals Cerebral Coenurosis Masquerading as Malignancy: A Rare Case Report from India

2019 ◽  
Vol 10 (02) ◽  
pp. 367-370
Author(s):  
Shamila Mohamed Ali ◽  
P. Somashekara Reddy ◽  
S. Venugopal ◽  
Manmeet Chhabra ◽  
Anita Mahadevan
Keyword(s):  
Case Report ◽  
Characteristic Feature ◽  
Rare Case ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Hydatid Cysts ◽  
The Third ◽  
Rare Case Report ◽  
Cerebral Coenurosis ◽  
Cuticular Layer

ABSTRACTHuman coenurosis is a rare zoonotic disease caused by the larvae of Tinea multiceps seen in sheep-rearing countries. We report the case of a 63-year-old male who was referred to our hospital with a working diagnosis of skull base chondrosarcoma. Histopathological examination after surgical excision revealed characteristic feature of coenurus with multiple scolices invaginating from the outer cuticular layer. Coenuri are often mistaken for giant cysticercal cysts and hydatid cysts. Despite its wide prevalence in cattle, only two cases of human coenurosis are reported from India till date. We report the third case from India.

scholarly journals Recurrent adenoid cystic carcinoma of paranasal sinuses: A rare case report

2020 ◽  
Vol 24 (4) ◽  
pp. 28
Author(s):  
SarahAbdul Wahed ◽  
Katakam Pradeepthi ◽  
MadalaJaya Kiran ◽  
GuttikondaVenkateswara Rao
Keyword(s):  
Case Report ◽  
Adenoid Cystic Carcinoma ◽  
Paranasal Sinuses ◽  
Rare Case ◽  
Adenoid Cystic ◽  
Rare Case Report

scholarly journals Bilateral Hypodontia of Mandibular Second Premolars and Lateral Incisors in a Nonsyndromic Patient: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 24-26
Author(s):  
Shakun Kanjani
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Permanent Teeth ◽  
Rare Occurrence ◽  
Third Molars ◽  
Missing Teeth ◽  
Dental Anomaly ◽  
Mahatma Gandhi ◽  
The Third ◽  
Rare Case Report

ABSTRACT Hypodontia is the term used to describe the developmental absence of one or more primary or permanent teeth, excluding the third molars. It is the most commonly occurring developmental dental anomaly and can be a challenge to manage clinically. Hypodontia can occur in association with syndrome or it may occur in nonsyndromic patient. Bilateral occurrence is common but it is very rare to see two bilateral congenital missing teeth in a nonsyndromic patient. This case report presents a rare occurrence of congenital bilateral missing mandibular second premolars and mandibular lateral incisors in a nonsyndromic patient. How to cite this article Agarwal N, Chaturvedy S, Marwah N, Mishra P, Kanjani S. Bilateral Hypodontia of Mandibular Second Premolars and Lateral Incisors in a Nonsyndromic Patient: A Rare Case Report. J Mahatma Gandhi Univ Med Sci Tech 2016;1(1):24-26.

scholarly journals A Frontal Retrobulbar Mucocele with Lytic Lesion at Orbital Plate and Orbital Ridge, Rare Case Report

2014 ◽  
Vol 27 (2) ◽  
pp. 105-107
Author(s):  
Haradhan Deb Nath ◽  
Kanak Kanti Barua
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Rare Case ◽  
Lytic Lesion ◽  
Rare Case Report ◽  
Medical University

Mucoceles can occurs when there is obstruction of drainage passage of mucosa of paranasal sinus. Some time it can cause pressure at eye ball and can cause proptosis. A old man admitted at Bangabandhu Sheikh Mujib Medical University with the complaints of right orbital swelling with proptosis of right eye ball. Also complaints of progressive visual bluring & headache for some time. The mucocele was operated by frontal craniotomy and excised completely. As this is a ran case and so few an reported. Bangladesh Journal of Neuroscience 2011; Vol. 27 (2) : 105-107 DOI: http://dx.doi.org/10.3329/bjn.v27i2.17578

scholarly journals Supratentorial primary neuroectodermal tumor (PNET) inside the third ventricle in adult: an rare case report

2013 ◽  
Vol 32 (02) ◽  
pp. 125-129
Author(s):  
Tiago de Paiva Cavalcante ◽  
Siegfried Pimenta Kuehnitzsch ◽  
George Santos dos Passos ◽  
José Eduardo Souza Dias Júnior ◽  
Tobias Engel Ayer Botrel ◽  
...  
Keyword(s):  
Case Report ◽  
Emergency Room ◽  
Ventriculoperitoneal Shunt ◽  
Rare Case ◽  
Third Ventricle ◽  
Treatment Options ◽  
Neurological Status ◽  
The Third ◽  
Rare Case Report ◽  
Undifferentiated Tumors

AbstractThe PNET of CNS are considered malignant undifferentiated tumors, and it represents about 2,8% of all tumors found on infants and teenagers, more rarely found on adults. In the present article will report the case of a patient, male, 23 years-old, with nodular lesion inside the third ventricle, admitted on emergency room with acute intense headache, drowsiness, vomiting and visual clouding, started three days before. Although there have been advances in diagnosis and treatment of PNET in children, few publications were found on the efficiency of available treatment options on adults. In our patient the lesion was completely removed by a anterosuperior interhemispheric transcallosal craniotomy, and subsequently diagnosed as PNET by anatomopathological. Postoperative hydrocephaly was installed and reverted with a ventriculoperitoneal shunt, with clinical and neurological status improvement. The patient died 18 months after diagnosis, due to respiratory hospitalar infection.

scholarly journals Oral focal mucinosis of gingiva - a rare case report and review of literature

2017 ◽  
Vol 5 (1) ◽  
pp. 26
Author(s):  
Chandini Dabbiru ◽  
Raghavendra Mahadev Naik ◽  
Kishore Moturi ◽  
Govind Rajkumar
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Histopathological Examination ◽  
Excisional Biopsy ◽  
Unknown Etiology ◽  
Review Of Literature ◽  
Soft Tissue Lesion ◽  
Rare Case Report ◽  
Myxoid Degeneration

Oral focal mucinosis (OFM) is a rare soft-tissue lesion of unknown etiology. Clinically it appears as asymptomatic round lesions and histologically, characterized by focal myxoid degeneration of connective tissue with presence of stellate shaped fibroblasts which were also evident in the present case. This case report stresses on the fact that diagnosis of OFM is almost impossible hence diagnosis should be confirmed by histopathological examination following incisional or excisional biopsy. Through this article we present a rare case of one such lesion on the gingiva and enumerate the most characteristic and myxomatous lesions. Thus though rare, OFM must be considered in the differential diagnosis of soft tissue overgrowths in oral cavity. Here, we describe the clinical and histopathological   presentation and subsequent management of OFM in a female patient.

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