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1.
Eye (Lond) ; 26(4): 583-92, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22193879

ABSTRACT

PURPOSE: To report clinical observations and surgical management in a large series of patients with orbitofacial neurofibromatosis type 1 (OFNF). PATIENTS AND METHODS: Patients were identified and medical records reviewed for demographic data, ophthalmologic examinations, surgical interventions, and procedure outcome to create a retrospective, non-comparative case series of patients with OFNF seen at one medical centre over a 23-year period. RESULTS: Sixty patients with OFNF (31 females and 29 males; mean age, 14 years) were followed for an average of 5.7 years. Presenting signs and symptoms included eyelid swelling in all patients, ptosis in 56 (93.3%), proptosis in 34 (56.6%), dystopia or strabismus in 30 (50%), and decreased visual acuity in 50 (83.3%). Surgical intervention included ptosis repair in 54 (90%; mean 1.6 surgical procedures), facial and orbital tumour debulking in 54 (90%; mean 2.3 surgeries), and canthoplasty in 28 (46.6%) patients. Eleven patients required enucleation or exenteration of a blind eye. CONCLUSION: Patients with OFNF often require multiple procedures to preserve vision, prevent additional disfigurement, and achieve cosmetic rehabilitation. Patients need regular ophthalmological monitoring given the potential for progressive visual and cosmetic consequences.


Subject(s)
Facial Neoplasms/surgery , Neurofibromatosis 1/surgery , Orbital Neoplasms/surgery , Adolescent , Adult , Child , Child, Preschool , Facial Neoplasms/pathology , Female , Follow-Up Studies , Humans , Infant , Magnetic Resonance Imaging , Male , Middle Aged , Neurofibromatosis 1/pathology , Orbital Neoplasms/pathology , Retrospective Studies , Saudi Arabia , Tomography, X-Ray Computed , Visual Acuity , Young Adult
2.
Br J Ophthalmol ; 92(10): 1337-41, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18697809

ABSTRACT

OBJECTIVE: To describe causes of preseptal cellulitis (PSC) and outcome of treatment in patients admitted to a tertiary eye-care centre. METHODS: A 15-year (January 1991 to December 2005) review of inpatients with clinical signs and symptoms or radiological evidence suggestive of PSC was conducted. Patients with infection anterior to the orbital septum which is characterised by acute onset of eyelid oedema, tenderness, erythema, warmth and chemosis were included in the study. RESULTS: Among the 104 patients (male:female 64:40) fulfilling the diagnostic criteria for PSC, acute dacryocystitis (ADC) was the most common predisposing cause in 32.6% patients, followed by sinusitis/upper-respiratory infection (URI) in 28.8% and trauma/recent surgery in 27.8% patients. Fifty-per cent required surgical intervention including dacryocystorhinostomy/probing/stenting in 74% and abscess/chalazian drainage in 28.8%. In 38.5% of the patients who had surgical intervention, microbiological investigations were carried out, cultures were positive in 90%. Most common micro-organisms recovered included Staphylococcus and Streptococcus species followed by Haemophilus influenzae and Klebsiella pneumonia. Blood cultures were positive in two of the 34 patients in whom blood was drawn. Most patients responded to systemic antibiotics with resolution of PSC. Seven patients developed late complications which included subacute lid abscesses, eyelid necrosis and cicatricial ectropion. CONCLUSIONS: Sinusitis/URI, ADC and recent history of trauma/surgery were the most common cause of PSC in admitted patients. Although most patients responded to systemic antibiotics, surgical intervention was necessary in some patients to prevent associated complications.


Subject(s)
Abscess/etiology , Cellulitis/etiology , Eyelid Diseases/etiology , Abscess/microbiology , Abscess/therapy , Adolescent , Adult , Aged , Anti-Bacterial Agents/therapeutic use , Cellulitis/microbiology , Cellulitis/therapy , Child , Child, Preschool , Drainage/methods , Eyelid Diseases/microbiology , Eyelid Diseases/therapy , Female , Haemophilus Infections/microbiology , Humans , Infant , Male , Middle Aged , Postoperative Complications/prevention & control , Severity of Illness Index , Staphylococcal Infections/microbiology , Streptococcal Infections/microbiology , Tomography, X-Ray Computed , Treatment Outcome
3.
Br J Ophthalmol ; 90(7): 844-6, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16556619

ABSTRACT

AIM: To report severe visual loss caused by optic nerve avulsion (ONA) in children with door-handle trauma. METHODS: Clinical records at a tertiary eye care hospital, of 14 children who sustained severe visual loss as a result of door-handle injuries, were reviewed. The data were analysed for location, presenting symptoms and signs, diagnostic studies, intervention, and the cause of visual loss. RESULTS: There were 11 males and three females with an average age of 8 years and an average height of 125 cm. The place of trauma was home in 11 and school in three children. Presenting visual acuity (VA) was light perception (LP) in five patients and no light perception (NLP) in nine. All the 14 children had evidence of ONA and four patients had ruptured eye globes that required initial repair. The diagnosis of ONA was made clinically or by imaging studies and confirmed histopathologically in eyes that were enucleated. Average follow up was 28.8 months (range 4 months to 8 years). Final VA was LP in one patient and NLP in 13 patients, eight eyes required enucleation for painful blind eye or to achieve optimal cosmesis. CONCLUSION: ONA was the common cause of visual loss in children who sustained ocular trauma caused by door-handles.


Subject(s)
Accidents, Home , Blindness/etiology , Optic Nerve Injuries/etiology , Accidents , Blindness/pathology , Blindness/surgery , Child , Eye Enucleation , Eye Injuries/etiology , Eye Injuries/pathology , Eye Injuries/surgery , Female , Follow-Up Studies , Humans , Male , Optic Nerve/pathology , Optic Nerve Injuries/pathology , Optic Nerve Injuries/surgery , Schools , Vitreous Hemorrhage/etiology , Vitreous Hemorrhage/pathology
4.
Am J Ophthalmol ; 129(4): 531-3, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10764866

ABSTRACT

PURPOSE: To report a case of severe bilateral proptosis resulting from orbital hemorrhage in a newborn and to discuss the differential diagnoses and management. METHOD: Case report of a 13-day-old male infant with bilateral proptosis since birth. The proptosis was monitored with clinical examinations and computed tomography as well as magnetic resonance imaging (MRI) scans, and it was managed with antibiotic ointment and patching. The MRI scans demonstrated bilateral subperiosteal orbital hemorrhage. RESULTS: Proptosis decreased, and there was successful, complete recovery without untoward sequelae in 14 days; follow-up indicated no late complications at age 1 year. CONCLUSION: Spontaneous orbital hemorrhage, unilateral or bilateral, is uncommon in an otherwise healthy newborn without apparent history of birth trauma. Magnetic resonance imaging scans are helpful in making the diagnosis of subperiosteal hemorrhage, and conservative management is advised.


Subject(s)
Retrobulbar Hemorrhage/complications , Exophthalmos/diagnosis , Exophthalmos/etiology , Exophthalmos/therapy , Humans , Infant, Newborn , Magnetic Resonance Imaging , Male , Orbit/diagnostic imaging , Orbit/pathology , Retrobulbar Hemorrhage/diagnosis , Retrobulbar Hemorrhage/therapy , Tomography, X-Ray Computed
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