ArticleRadiology case reports2022
Primary nodular chest amyloidoma: A case report and review of literature.
Article in Radiology case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 8 citations in OpenAlex.
- Giant cell tumor of the orbital roof: A case report and brief review of literature.Radiology case reports · 2026Article
- An incidental pulmonary amyloidoma detected duringRadiology case reports · 2025Article
- Localized amyloidoma of the chest wall: diagnostic and surgical perspectives.General thoracic and cardiovascular surgery cases · 2023Article
- Tracheobronchial Amyloidosis: A Case Report.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2023Article
- Isolated pulmonary amyloidoma: A rare cause of solitary pulmonary nodule.Respiratory medicine case reports · 2023Article
- Giant mediastinal bronchial artery aneurysm mimicking mediastinal mass: A case report and brief review of the literature.Radiology case reports · 2022Article
- A Rare Case of Amyloidoma of the Chest Wall Presented with Fever of Unknown Origin.Diagnostics (Basel, Switzerland) · 2022Article
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Primary nodular chest wall amyloidoma, in which a solitary mass of amyloid is deposited in and around the lungs with no evidence of systemic amyloidosis, is extremely rare, most often asymptomatic, and may resemble primary bronchogenic carcinoma. As a result, there are fewer than 100 cases published in the literature and no controlled clinical trials. Primary nodular chest wall amyloidoma is typically diagnosed either as an incidental radiological finding or after very serious and destructive mass growth at which point late-stage respiratory and pain symptoms finally develop, most often in elderly patients. We present imaging studies of a 61-year-old male patient with an unusually massive and destructive chest wall mass, originating in the chest wall, diagnosed as chest wall amyloidoma by histopathology analysis. Our CT, MRI, and PET scan findings are consistent with and contribute to the developing pattern of imaging characteristics seen in other case studies, which can be used to identify amyloidoma before it becomes destructive using non-invasive imaging analyses.
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