Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Amyloidosis
- Radiologic Findings
- Chest radiograph shows widening of both main bronchi, bulging contour of aorto-pulmonary window, suggesting mediastinal lymphadenopathy
Bilateral pleural effusions are also noted. Contrast enhanced chest CT shows multiple enlarged lymph nodes in the mediastinum and both hilar area.
Multiple tiny calcified nodules are also noted in both lungs. There is another incidental finding, smooth interlobular septal thickening due to interstitial pulmonary edema.
Lymph node, supracarinal, endobronchial ultrasound-guided needle biopsy - Amorphous eosiniphilic materials, consistent with amyloidisis, light (AL) chain-related,
Congo-red stain, Apple-green birefringence
Kidney, native, biopsy - Amyloidosis, light (AL) chain-related, Congo-red positive in mesangium
Bone marrow, needle biopsy - Overall 30% cellularity marrow showing small aggregation of CD 138 (+) plasma cells, consistent with plasma cell myeloma.

- Brief Review
- Amyloidosis is a group of diseases resulting from the extracellular accumulation of abnormal protein in tissues and organs throughout the body. Amyloid protein deposits characteristically retain the dye Congo red, giving a pathognomonic red-green birefringence when viewed with a microscope under polarized light.
Amyloidosis can be classified on the basis of its anatomic distribution or the structure of the protein deposits: systemic or localized. The biochemical classification system, according to the type of the fibrillar component in amyloid deposits, has over two dozen subtypes. The fibrillar proteins amyloid light chain (AL) and serum amyloid A (AA) are present in the vast majority of cases.
Pulmonary involvement- Pulmonary amyloidosis is more often a localized process rather than a part of systemic disease.Two patterns of involvement exist: nodular parenchymal and alveolar septal forms. Nodular parenchymal amyloidosis may manifest as solitary or multiple pulmonary nodules and may mimic a variety of diseases from granulomatous disease to malignancy. Alveolar septal pulmonary amyloidosis is characterized by well-defined 2
- References
- 1. Czeyda-Pommersheim F. et al, Amyloidosis: Modern Crosssectional Imaging, Radiographics. 2015 Sep-Oct;35(5):1381-92.
2. Mitchell PD. et al, A case of pulmonary amyloidosis. Thorax 2014;69(6):600.
3. Fiorelli A. et al, Isolated mediastinal amyloidosis mimicking a neoplastic lesion. Gen Thorac Cardiovasc Surg 2014;62(5):324
- Please refer to
- Case 998 Case 985 Case 982 Case 939 Case 834 Case 794 Case 738 Case 664 Case 509 Case 478 Case 298
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- Keywords
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Amyloidosis, Lymph node,