An unusual presentation of cavernous sinus syndrome in a pediatric patient

العناوين الأخرى

تظاهر نادر لمتلازمة الجيب الكهفي عند طفلة

المؤلفون المشاركون

Nasr, Zayd
Stasheff, Steven
Packer, Roger
Whitehead, Matthew
Latif, Tarannum

المصدر

Journal of the Arab Board of Health Specializations

العدد

المجلد 23، العدد 1 (30 يونيو/حزيران 2022)، ص ص. 47-49، 3ص.

الناشر

المجلس العربي للاختصاصات الصحية

تاريخ النشر

2022-06-30

دولة النشر

سوريا

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص EN

Cavernous sinus syndrome in pediatrics is a rare condition with poorly understood epidemiology.

Tolosa Hunt syndrome is characterized by severe and unilateral periorbital headaches accompanied by restricted and painful eye movements.

We present a 6-year-old female patient with symptoms of right eye ptosis, diplopia, and recurrent headaches of varying duration.

Initial non-contrast MRI showed 2.8 x 2.1 cm mass expanding the right cavernous sinus with extension into Meckel’s cave and Dorello’s canal.

Patient was started on IV corticosteroids on hospital admission and after 2-3 days, eye movements improved.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Nasr, Zayd& Stasheff, Steven& Packer, Roger& Whitehead, Matthew& Latif, Tarannum. 2022. An unusual presentation of cavernous sinus syndrome in a pediatric patient. Journal of the Arab Board of Health Specializations،Vol. 23, no. 1, pp.47-49.
https://search.emarefa.net/detail/BIM-1431369

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Nasr, Zayd…[et al.]. An unusual presentation of cavernous sinus syndrome in a pediatric patient. Journal of the Arab Board of Health Specializations Vol. 23, no. 1 (2022), pp.47-49.
https://search.emarefa.net/detail/BIM-1431369

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Nasr, Zayd& Stasheff, Steven& Packer, Roger& Whitehead, Matthew& Latif, Tarannum. An unusual presentation of cavernous sinus syndrome in a pediatric patient. Journal of the Arab Board of Health Specializations. 2022. Vol. 23, no. 1, pp.47-49.
https://search.emarefa.net/detail/BIM-1431369

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 49

رقم السجل

BIM-1431369