Frontoethmoidal mucocele presenting as proptosis

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Frontoethmoidal mucocele presenting as proptosis.

To cite: Shang Kuan W-C, Chi C-C. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013202733 DESCRIPTION A 34-year-old man suffered from itching, burning and a foreign body sensation in his left eye for 6 months prior to his first ophthalmology clinic visit, where eye drops were prescribed for presumed keratitis without obvious improvement. Furthermore, his left e...

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Frontoethmoidal Mucocele Presenting as Progressive Enophthalmos

In this case report we describe a 27-year-old man who presented with progressive enophthalmos for 5 months without any other associated ocular symptoms such as pain, diplopia, or visual disturbance. Computed tomography showed that his progressive enophthalmos originated from a frontoethmoidal mucocele and this caused destruction of the lamina papyracea and shrinkage of the ethmoidal air cell. F...

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Fronto-ethmoidal mucocele as a cause of unilateral proptosis.

MUCOCOELE of the frontal or ethmoidal sinuses is an uncommon cause of unilateral proptosis which may produce considerable difficulty in diagnosis. There seems a natural tendency for these cases to be sent to an eye specialist, and a curious reluctance for him to refer the patient to an E.N.T. surgeon, often preferring a neurological opinion which may involve the patient in expensive and unpleas...

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Orbital myeloid sarcoma presenting as massive proptosis.

A 10-year-old boy presented with right proptosis for 8 months. The eyeball was grossly pushed down, with diffuse corneal haze and non-reactive pupil. Systemic examination was normal. Previous investigations in another centre included a computerized tomography scan, which showed a well-defined enhancing retro-bulbar mass, a non-contributory fine needle aspiration cytology and a biopsy showing fi...

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IgDK multiple myeloma presenting as unilateral proptosis.

A 72-year-old woman presented with painful proptosis of the right eye and a large destructive tumour of the middle cranial fossa. A diagnosis of IgDK multiple myeloma was made, based on histopathologic and immunologic studies of the biopsy. Biochemistry and bone marrow examination further confirmed the myeloma as IgDK type. The clinical, radiological, and pathological findings are presented. Th...

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ژورنال

عنوان ژورنال: Case Reports

سال: 2014

ISSN: 1757-790X

DOI: 10.1136/bcr-2013-202733