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dacryocystitis/febre
L'enllaç es desa al porta-retalls
12 resultats
Unilateral acute dacryocystitis associated with oculoglandular tularemia: a case report.
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OBJECTIVE
To describe an unusual case of oculoglandular tularemia associated with unilateral acute dacryocystitis and purulent conjunctivitis with 18 weeks pregnancy.
METHODS
It is difficult to culture francisella tularensis on media so serological tests such as micro-agglutination methods are used
Presentation, Diagnostic Evaluation, Management, and Rates of Serious Bacterial Infection in Infants With Acute Dacryocystitis Presenting to the Emergency Department
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Background: Dacryocystitis is considered benign, yet infants represent a population at risk of complications. The presentation, management, and rates of serious bacterial infection in infants with dacryocystitis have not been
[Tuberculous dacryocystitis].
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BACKGROUND
Acute infection and inflammation of the nasolacrimal sac may complicate congenital obstruction of the nasolacrimal duct. Acute dacryocystitis is uncommon later and tuberculosis is exceptionally responsible for it.
METHODS
A 4 1/2 year-old boy was admitted because he suffered from acute
A Rare Complication of Oropharyngeal Tularemia: Dacryocystitis
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Tularemia is a zoonotic disease caused by Francisella tularensis, a highly virulent gram-negative coccobacillus. Oropharyngeal tularemia, one of the clinical subtypes, is the most common clinical form of the disease in Eastern Europe, including Turkey. This clinical form affects mostly the
Orbital abscess during endodontic treatment: a case report.
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BACKGROUND
Orbital infections may result in permanent morbidity because of the severity of infection. Furthermore, delayed diagnosis or treatment of orbital infections can lead to intracranial complications and even death. The majority of orbital infections develop from paranasal sinus infections,
Inflammation of the lacrimal drainage system--assessment by thermography.
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Thermography is an investigative tool without side effects. To our knowledge thermography has not been evaluated in the assessment of lacrimal passage inflammation and obstruction. It can give an objective assessment of presence and degree of inflammation. An infrared scanning device was used to
Two cases of adult-onset Still's disease with orbital inflammatory lesions originating from the lacrimal gland.
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Orbital inflammation has been rarely associated with adult-onset Still's disease (AOSD). We herein describe two AOSD patients who developed lacrimal gland enlargement with inflammation spreading to the contiguous tissues in the orbit. Case 1 was a 26-year-old woman who developed bilateral eyelid
Hereditary angioedema type 2 presented as an orbital complication of acute rhinosinusitis.
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Hereditary angioedema is an autosomal dominant and life-threatening disorder characterized by recurrent episodes of non-pitting edema affecting the skin, respiratory system and digestive tracts and caused by a congenital deficiency or function defect of the C1 esterase inhibitor. Preseptal
[Orbital cellulitis in children].
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BACKGROUND
Because the potential for complications is great, orbital cellulitis must be recognized promptly and treated aggressively.
METHODS
The files of 38 children admitted from 1988 to 1993 because of orbital or periorbital cellulitis were retrospectively analyzed. Clinical findings included
[Pediatric orbital cellulitis without sinusitis: report of four cases].
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BACKGROUND
Pediatric orbital cellulitis is most often caused by ethmoid sinusitis. We present a description of 4 atypical cases of orbital cellulitis without sinusitis.
METHODS
A 4-day-old girl presented with medical canthal swelling and preseptal cellulitis caused by bilateral congenital
Orbital Pseudotumor
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Orbital pseudotumor, also known as orbital inflammatory pseudotumors (OIP), idiopathic orbital inflammation (IOI), orbital inflammatory syndrome (OIS), idiopathic orbital inflammatory pseudotumor (IOIP), or nonspecific orbital inflammation (NSOI) is a benign, space-occupying, and non-infectious
Complete agenesis of major salivary glands.
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A 4 year-old female patient was treated for persistent right-sided dacryocystitis and xerostomia. MRI was performed to screen for a dry syndrome; which resulted in the diagnosis of agenesis of the parotid and submandibular glands as well as lacrimal duct malformation. An MRI of each parent was
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