scholarly journals Silent Sinus Syndrome in a Female Child with Enophthalmos and Diplopia

2014 ◽  
Vol 7 (1) ◽  
pp. 40-42
Author(s):  
Sandeep Mohindra ◽  
Satyawati Mohindra

ABSTRACT Opacification of the maxillary sinus was first published by Montgomery in the precomputerized era. The term silent sinus syndrome (SSS) was first used by Soparkar et al2 in 1994. They defined an uncommon disease characterized by enophthalmos secondary to ipsilateral atelectasis of the maxillary sinus, even without nasal symptoms. The pathophysiology of SSS was demonstrated by Eto et al in 1993. In this report, we are presenting a case of silent sinus syndrome in a girl of pediatric age group, an unusual age of presentation. How to cite this article Mohindra S, Mohindra S, Gupta AK. Silent Sinus Syndrome in a Female Child with Enophthalmos and Diplopia. Clin Rhinol An Int J 2014;7(1):40-42.

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Xiao-Hui Ma ◽  
Hai-Chun Zhou ◽  
Can Lai ◽  
Kun Zhu ◽  
Xuan Jia

Schwannomas of the paranasal sinus are uncommon. Less than 4% of schwannomas involve the nasal cavity and paranasal sinuses, even less in the pediatric age group. A case of schwannoma arising in maxillary sinus in a 2.5-year-old Chinese boy is reported. The basis for discussion of this case is the exceptional rarity of sinonasal schwannoma in pediatric patients.


Author(s):  
Lagan Paul ◽  
Manisha Agarwal ◽  
Shalini Singh ◽  
Prashant Katre ◽  
Aman Sumeet Arora

AbstractScleritis is the severe painful inflammation of the sclera, which can be infectious or non-infectious. Tuberculosis (TB) is one of the common causes of infectious scleritis. TB, though endemic in countries like India, is rare in pediatric age group. We report a case of a 9-year-old female child who presented with bilateral non-necrotizing anterior scleritis with unilateral posterior scleritis secondary to TB. To our knowledge, this is a rare presentation in pediatric age group, and she is the youngest of few cases of tuberculous posterior scleritis reported in literature.


2021 ◽  
Vol 8 (8) ◽  
pp. 1435
Author(s):  
Praveen U. ◽  
Datta Jhadav ◽  
Jitesh M. Thakare ◽  
Reshmi G. ◽  
Priyanka Krishnan

Myocarditis is an uncommon disease of adult and pediatric age group, characterized by inflammatory cell infiltrates, myocyte necrosis, or myocyte degeneration due to a myriad of causes and resulting in variable degrees of myocardial dysfunction. Which may be caused by infections, connective tissue disorders, granulomatous diseases, toxic agents or can be idiopathic. Viral infections are the most common etiology accounting for more than 50-60% of cases, particularly enterovirus (Coxsackie virus) and adenovirus groups. The disease is typically sporadic but may be epidemic. Manifestations of myocarditis range from asymptomatic or nonspecific generalized illness to acute cardiogenic shock and sudden death. In our case 10-year-old boy presented with history of fever and cough of 2 days duration. On examination patient found to be having tachycardia and tachypnea without other signs of heart failure. chest x-ray suggestive of bilateral pneumonia, ECG showed features of Myocarditis without any echocardiographic or cardiac enzyme abnormality. Child tested positive for corona virus rapid antigen test. Started on Favipiravir, corticosteroids and managed symptomatically. Child's heart rate normalized over a period of 4 days. Patient subsequently discharged with the advice of follow up echocardiography.


2017 ◽  
pp. 28-31
Author(s):  
Shashi Sharma ◽  
Sakshi Dewan ◽  
Naveen Bhardwaj ◽  
Mir Aziz ◽  
Shilpa Singh ◽  
...  

2021 ◽  
Vol 15 (1) ◽  
pp. 431-435
Author(s):  
Mohamed Mansy ◽  
Mostafa Kotb ◽  
Mohamed Abouheba

Congenital lumbar hernias are uncommonly seen in the pediatric age group, with only about 60 cases reported in the literature. It is usually accompanied by a multitude of congenital anomalies involving different organ systems of the body. For instance, it may involve the ribs, spine, muscles, and the kidneys. Herein, we report a case of congenital lumbar hernia in an 8-month-old boy who underwent an operative repair using a mesh with an uneventful outcome.


2020 ◽  
Vol 16 ◽  
pp. 100199
Author(s):  
Archwin Tanphaichitr ◽  
Songphon Nuchawong ◽  
Dev Kamdar ◽  
Morris C. Edelman ◽  
Dhave Setabutr

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