Amyloidosis and vascular thrombosis

المؤلف

Adamu, Bappa

المصدر

Saudi Journal of Kidney Diseases and Transplantation

العدد

المجلد 19، العدد 1 (28 فبراير/شباط 2008)، ص ص. 137-141، 5ص.

الناشر

المركز السعودي لزراعة الأعضاء

تاريخ النشر

2008-02-28

دولة النشر

السعودية

عدد الصفحات

5

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Amyloidosis is a rare systemic disorder of protein metabolism with progressive extracellular deposition of insoluble fibrillary protein, disorganization of tissue architecture, and subsequent organ dysfunction.

Primary amyloidosis is the most common form of this disorder, however, it can develop secondary to plasma cell dyscrasias such as multiple myeloma (MM); 10-15% of MM patients may develop amyloidosis of vital organs.

Amyloidosis is usually associated with bleeding, but less commonly with thrombosis.

We present a 52-year-old Saudi female with amyloidosis secondary to multiple myeloma.

She presented with both venous and extensive arterial thrombosis.

Although relatively rare, plasma cell dyscrasias such as amyloidosis and multiple myeloma could present with thrombotic rather than hemorrhagic complications.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Adamu, Bappa. 2008. Amyloidosis and vascular thrombosis. Saudi Journal of Kidney Diseases and Transplantation،Vol. 19, no. 1, pp.137-141.
https://search.emarefa.net/detail/BIM-38040

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Adamu, Bappa. Amyloidosis and vascular thrombosis. Saudi Journal of Kidney Diseases and Transplantation Vol. 19, no. 1 (Feb. 2008), pp.137-141.
https://search.emarefa.net/detail/BIM-38040

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Adamu, Bappa. Amyloidosis and vascular thrombosis. Saudi Journal of Kidney Diseases and Transplantation. 2008. Vol. 19, no. 1, pp.137-141.
https://search.emarefa.net/detail/BIM-38040

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 141

رقم السجل

BIM-38040