Bilateral dacryoadenitis

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Bilateral dacryoadenitis complicated by lymphocytic hypophysitis.

Three patients developed dacryoadenitis (DA) or lymphocytic pneumonitis before the diagnosis of lymphocytic hypophysitis (LyH). There were two previous reports of concurrence of DA and LyH. Our patients add support to the idea that DA and LyH are manifestations of a systemic autoimmune disease. We suggest that the discovery of DA should prompt imaging and endocrine investigation of LyH.

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[Epstein-Barr virus bilateral dacryoadenitis: case report].

UNLABELLED The authors present a rare case of acute bilateral dacryoadenitis in association with infectious mononucleosis. A 27 year-old woman had acute bilateral lacrimal gland enlargement with inflammatory signs. The CT scan findings and laboratorial investigations confirmed the diagnosis of infectious mononucleosis. The systemic treatment with intravenous steroids was initiated leading to co...

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Bilateral dacryoadenitis as a presenting symptom of an extra-ocular disease.

A 49-year-old woman, with no medical history, presented with bilateral swollen eyelids, progressive conjunctivitis and proptosis for the last month (figure 1). She was referred by the ophthalmologist because an underlying disease was suspected. Magnetic resonance imaging of the orbitae showed bilateral enlargement of the lacrimal glands (figure 2). Treatment by the ophthalmologist with antihist...

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Acute suppurative dacryoadenitis.

On examination, vision in the right eye was 6/9. There was periorbital edema and tenderness most marked in the lateral upper lid. On lid retraction (Fig. 1) there was localised chemosis, and an enlarged vascular lacrimal swelling with vellow purulent material in the upper temporal fornix. Extreme lateral gaze was slightly limited but there was no fluctuant area in the lid. Systemically he had a...

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IgG4-Related Chronic Sclerosing Dacryoadenitis

dilated fundus examination findings were normal. Blood studies were negative for antinuclear antibodies and rheumatoid factors and showed a normal complete blood count and negative angiotensin-converting enzyme levels. We diagnosed bilateral atypical Cogan syndrome in the patient. The bilateral iritis resolved with cycloplegics and topical steroid drops. The patient has been referred for a coch...

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ژورنال

عنوان ژورنال: Journal of Emergencies, Trauma, and Shock

سال: 2012

ISSN: 0974-2700

DOI: 10.4103/0974-2700.93096