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Tytuł pozycji:

Bilateral idiopathic orbital pseudotumour in a child: a case report

Tytuł:
Bilateral idiopathic orbital pseudotumour in a child: a case report
Autorzy:
Fangyuan Chen
Junjie Tang
Qing Zhou
Temat:
Bilateral
Idiopathic orbital pseudotumor
Paediatric
Case report
Ophthalmology
RE1-994
Źródło:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-6 (2020)
Wydawca:
BMC, 2020.
Rok publikacji:
2020
Kolekcja:
LCC:Ophthalmology
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
1471-2415
Relacje:
http://link.springer.com/article/10.1186/s12886-020-01718-0; https://doaj.org/toc/1471-2415
DOI:
10.1186/s12886-020-01718-0
Dostęp URL:
https://doaj.org/article/6c788cbbe90e49d4b0021ed6dc2dd2fa  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.6c788cbbe90e49d4b0021ed6dc2dd2fa
Czasopismo naukowe
Abstract Background Idiopathic orbital pseudotumour is rare in children. We report a case of bilateral paediatric idiopathic orbital pseudotumour and review the characteristics of this case. Case presentation A 14-year-old female patient presented at our Department of Pulmonary and Critical Care Medicine (PCCM) with complaints of recurrent severe cold and cough for 3 weeks, which had been treated with an intravenous antibiotic. Meanwhile, the patient developed swelling of both eyelids during the period of cold and cough, but her symptoms did not improve after the ocular administration of tobramycin dexamethasone eye drops. The patient was referred from the respiratory medicine ward to our department because of gradually worsening ocular pain, visual deterioration, increased intraocular pressure and serious nausea/vomiting within 24 h of hospitalization. The diagnosis of bilateral idiopathic orbital pseudotumour was made ultimately because of the course of the disease, exclusion of diagnoses such as bacterial ocular infection or malignant tumours and subsequent evidence from orbital magnetic resonance imaging (MRI). Favourable progress in the ocular tension and eyelid swelling was achieved through treatment with intravenous dexamethasone. The binocular intraocular pressure gradually declined to approximately 15 mmHg, and there was favourable progression in the patient’s vision to 20/40 in both eyes on the ninth day of hospitalization. Conclusions Our patient developed rapidly progressive acute orbital signs and symptoms and anterior inflammation, such as pain, proptosis, limited ductions, periorbital oedema, chemosis, vision loss and high intraocular pressure. This case highlights that idiopathic orbital pseudotumour is an uncommon but important cause of acute orbital syndrome in children.

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