Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Amyloidosis
- Radiologic Findings
- The serial CT scans show progressive findings of diffuse smooth interlobular septal thickening in both lungs. The 5.23 CT scan show the new finding of peribronchial consolidation with suspicious focal calcification and ground-glass opacity in Rt. middle and both lower lobes.
Differential diagnosis are lymphangitic tumor spread, interstitial edema or storage disease such as Niemann-Pick disease. PET-CT scan didn't show primary malignant site.
- Brief Review
- Amyloidosis occurs when proteins accumulate in organs such as the heart, kidney, liver, or intestines. There are three major types of amyloidosis: primary, secondary, and hereditary. Each type of amyloidosis is classified by its underlying causes and the type of protein that accumulates in organs.
Multiple myeloma is a cancer of the plasma cells. These cells are an important part of the immune system responsible for the production of antibodies. In multiple myeloma, the plasma cells overproduce one type of abnormal antibody. The overproduction of abnormal antibodies puts myeloma patients at risk for developing amyloidosis.
Not all multiple myeloma patients will develop amyloidosis. It is estimated that 10 to 15 percent of multiple myeloma patients will experience symptoms from the development of amyloidosis during the course of their disease. However, as many as 38 percent of myeloma patients may develop amyloidosis but experience none of its symptoms.
- References
- 1. Ege E et al. Primary pulmonary amyloidosis associated with multiple myeloma. Tuberk Toraks. 2006;54(1);65-70.
2. Chim et al. Pulmonary Interstitial Amyloidosis Complicating Multiple Myeloma. Journal of Clinical Oncology 2008;26(3);504-506
- Keywords
- Lung, Metabolic and storage lung disesae,