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1.
Eur J Ophthalmol ; 32(4): NP11-NP16, 2022 Jul.
Article in English | MEDLINE | ID: mdl-33843287

ABSTRACT

PURPOSE: To report two cases of COVID-19 under treatment with a corticosteroid; in one case rhino-orbitocerebral mucormycosis and in another one rhino-orbital mucormycosis developed. CASE PRESENTATION: A 40-year old woman and a 54-year old man with severe COVID-19 underwent corticosteroid therapy for immune-related lung injuries. The first case presented with a bilateral visual loss and complete ophthalmoplegia of the right eye. The second case presented with vision loss, proptosis, orbital inflammation, and complete ophthalmoplegia on the left side. Histopathologic, nasal endoscopic examinations, and radiologic findings confirmed mucormycosis in both patients. The patients denied orbital exenteration and were managed with systemic amphotericin B and daily endoscopic sinus debridement and irrigation with diluted amphotericin B. Because of the intracranial space involvement, the first case died. The second case was successfully managed surgically and medically. CONCLUSION: Rhino-orbital/cerebral mucormycosis may be developed in COVID-19 patients under treatment with corticosteroid, and requires prompt diagnosis and management.


Subject(s)
COVID-19 , Eye Diseases , Eye Infections, Fungal , Mucormycosis , Ophthalmoplegia , Orbital Diseases , Adult , Amphotericin B , Antifungal Agents/therapeutic use , Eye Diseases/drug therapy , Eye Infections, Fungal/diagnosis , Eye Infections, Fungal/drug therapy , Female , Humans , Male , Middle Aged , Mucormycosis/diagnosis , Mucormycosis/drug therapy , Mucormycosis/etiology , Ophthalmoplegia/drug therapy , Orbital Diseases/diagnosis , Orbital Diseases/drug therapy , Orbital Diseases/etiology , Steroids
2.
J Craniofac Surg ; 32(5): e444-e446, 2021.
Article in English | MEDLINE | ID: mdl-33235165

ABSTRACT

ABSTRACT: Intraconal orbital hidrocystoma is a very rare entity. Herein, a 6-month old boy with an intraconal apocrine hidrocystoma will be reported. The patient presented with a left-sided mild proptosis and significant anisometropic hypermetropia. Clinical examinations revealed choroidal folds and optic disc blurring in the left eye. Orbital MRI disclosed an intraconal well-defined cystic lesion that was hypointense in T1 and hyperintense in T2 weighted images. The lesion was excised completely through a lateral orbitotomy and diagnosed histologically as an apocrine hidrocystoma. Excepting partial improvement of anisometropia, other clinical signs were improved after surgery.


Subject(s)
Hidrocystoma , Sweat Gland Neoplasms , Eye , Hidrocystoma/diagnostic imaging , Hidrocystoma/surgery , Humans , Infant , Magnetic Resonance Imaging , Male , Orbit/diagnostic imaging , Orbit/surgery , Sweat Gland Neoplasms/diagnostic imaging , Sweat Gland Neoplasms/surgery
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