Association of temporal arteritis, retinal vasculitis, and xanthomatosis with multiple myeloma: case report and literature review.

1998 ◽  
Vol 73 (7) ◽  
pp. 657-660 ◽  
Author(s):  
Y K Keung ◽  
C Yung ◽  
J W Wong ◽  
F Shah ◽  
E Cobos
Keyword(s):  
Multiple Myeloma ◽  
Case Report ◽  
Literature Review ◽  
Temporal Arteritis ◽  
Retinal Vasculitis

scholarly journals Association of Temporal Arteritis, Retinal Vasculitis, and Xanthomatosis With Multiple Myeloma: Case Report and Literature Review

1998 ◽  
Vol 73 (7) ◽  
pp. 657-660 ◽  
Author(s):  
Yi-Kong Keung ◽  
Christianne Yung ◽  
Jacqueline W. Wong ◽  
Farah Shah ◽  
Everardo Cobos
Keyword(s):  
Multiple Myeloma ◽  
Case Report ◽  
Literature Review ◽  
Temporal Arteritis ◽  
Retinal Vasculitis

Multiple myeloma and chronic myelogenous leukemia: a case report with literature review

1993 ◽  
Vol 34 (3) ◽  
pp. 293 ◽  
Author(s):  
Philip J. Klenn ◽  
Bong H. Hyun ◽  
Young Hee Lee ◽  
Wen Yu Zheng
Keyword(s):  
Multiple Myeloma ◽  
Case Report ◽  
Literature Review ◽  
Chronic Myelogenous Leukemia ◽  
Myelogenous Leukemia

scholarly journals Percutaneous vertebroplasty at C2: case report of a patient with multiple myeloma and a literature review

2006 ◽  
Vol 16 (S3) ◽  
pp. 242-249 ◽  
Author(s):  
Miriam Rodriguez-Catarino ◽  
Cecilie Blimark ◽  
Jan Willén ◽  
Ulf-H Mellqvist ◽  
Stig Rödjer
Keyword(s):  
Multiple Myeloma ◽  
Case Report ◽  
Literature Review ◽  
Percutaneous Vertebroplasty

scholarly journals Macroglossia Secondary to Systemic Amyloidosis: Case Report and Literature Review

2005 ◽  
Vol 84 (6) ◽  
pp. 358-361 ◽  
Author(s):  
Sandra Doria Xavier ◽  
Ivo Bussoloti Filho ◽  
Helena Müller
Keyword(s):  
Multiple Myeloma ◽  
Case Report ◽  
Literature Review ◽  
Clinical Condition ◽  
Abdominal Fat ◽  
Systemic Amyloidosis ◽  
Systemic Nature ◽  
Lost To Follow Up ◽  
Different Tissues

Amyloidosis is characterized by an abnormal extracellular deposition of amyloid in different tissues and organs, where it usually causes some type of dysfunction. Its cause is unknown. The two main forms of amyloidosis are systemic and localized; the latter is rare. No satisfactory treatment for systemic amyloidosis has been discovered, and mean survival is poor, ranging from 5 to 15 months depending on the presence or absence of multiple myeloma. We report a case of primary systemic amyloidosis in a 71-year-old man. The diagnosis of amyloidosis was established by tongue biopsy, and its systemic nature was identified by analysis of aspirated abdominal fat. At the 1-year follow-up, the patient's clinical condition had not changed, and he was thereafter lost to follow-up.

scholarly journals Crohn's disease and smoldering multiple myeloma: a case report and literature review

2017 ◽  
Vol 15 (2) ◽  
pp. 249 ◽  
Author(s):  
So Young Park ◽  
Jae Min Kim ◽  
Hyun Joon Kang ◽  
Minje Kim ◽  
Jae Joon Han ◽  
...  
Keyword(s):  
Multiple Myeloma ◽  
Crohn’S Disease ◽  
Case Report ◽  
Crohn's Disease ◽  
Literature Review ◽  
Smoldering Multiple Myeloma
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