Thymic carcinoma presented with systemic lupus erythematosus like symptoms : a case report

المؤلف

al-Heresh, Ala M.

المصدر

Journal of the Royal Medical Services

العدد

المجلد 18، العدد 1 (31 مارس/آذار 2011)، ص ص. 76-78، 3ص.

الناشر

الخدمات الطبية الملكية الأردنية

تاريخ النشر

2011-03-31

دولة النشر

الأردن

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Thymic carcinoma is a rare, highly malignant, mediastinal neoplasm arising from thymic epithelial cells.

It can be associated with paraneoplastic autoimmune phenomenon.

Thymic carcinoma and systemic lupus erythematosus occurring together with hypertrophic osteoarthropathy is extremely rare in children and has been reported only once in the literature.

We report the case of a young Jordanian boy who presented with features suggestive Systemic Lupus Erythematosus and was found to have highly malignant thymic carcinoma complicated with hypertrophic osteoarthropathy.

This case provides insight in to the pathogenesis of thymic carcinoma and its autoimmune effects.

Thorough literature search for cases with similar presentation was performed and discussed in this case report.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

al-Heresh, Ala M.. 2011. Thymic carcinoma presented with systemic lupus erythematosus like symptoms : a case report. Journal of the Royal Medical Services،Vol. 18, no. 1, pp.76-78.
https://search.emarefa.net/detail/BIM-249949

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

al-Heresh, Ala M.. Thymic carcinoma presented with systemic lupus erythematosus like symptoms : a case report. Journal of the Royal Medical Services Vol. 18, no. 1 (Mar. 2011), pp.76-78.
https://search.emarefa.net/detail/BIM-249949

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

al-Heresh, Ala M.. Thymic carcinoma presented with systemic lupus erythematosus like symptoms : a case report. Journal of the Royal Medical Services. 2011. Vol. 18, no. 1, pp.76-78.
https://search.emarefa.net/detail/BIM-249949

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 78

رقم السجل

BIM-249949