2023
DOI: 10.1016/j.rmcr.2023.101820
|View full text |Cite
|
Sign up to set email alerts
|

Isolated pulmonary amyloidoma: A rare cause of solitary pulmonary nodule

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 18 publications
(40 reference statements)
0
0
0
Order By: Relevance
“…The literature indicates the existence of two amyloid forms with a high potential to affect the respiratory tract. The most common pattern is AL light chain (AL) amyloidosis, with an occurrence consecutive to the deposition of excess immunoglobulin light chain fragments, subsidiarily with a substrate of plasma cell dyscrasia [9,10]. AL amyloidosis accounts for approximately 70% of all systemic amyloidosis cases [9], or 63-80% in other sources [6].…”
mentioning
confidence: 99%
“…The literature indicates the existence of two amyloid forms with a high potential to affect the respiratory tract. The most common pattern is AL light chain (AL) amyloidosis, with an occurrence consecutive to the deposition of excess immunoglobulin light chain fragments, subsidiarily with a substrate of plasma cell dyscrasia [9,10]. AL amyloidosis accounts for approximately 70% of all systemic amyloidosis cases [9], or 63-80% in other sources [6].…”
mentioning
confidence: 99%