Extended resection of a plasmocytoma of bone and an amyloidoma of the chest wall

Solitary plasmocytoma of bone is a rare condition of plasma cell neoplasia that presents as a single lesion. Amyloidoma of the chest wall is an uncommon presentation of solitary tissue amyloid deposition in the absence of systemic light-chain amyloidosis. This report describes a patient with both un...

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Main Authors: Safi, Seyer (Author) , Winkel, Jan op den (Author) , Schnabel, Philipp Albert (Author) , Hegenbart, Ute (Author) , Neben, Kai (Author) , Schneider, Thomas (Author) , Dienemann, Hendrik (Author)
Format: Article (Journal)
Language:English
Published: 29 November 2013
In: The annals of thoracic surgery
Year: 2013, Volume: 96, Issue: 6, Pages: 2223-2225
ISSN:1552-6259
DOI:10.1016/j.athoracsur.2013.04.109
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.athoracsur.2013.04.109
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0003497513010230
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Author Notes:Seyer Safi, Jan op den Winkel, Philipp A. Schnabel, Ute Hegenbart, Kai Neben, Thomas Schneider, and Hendrik Dienemann
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Summary:Solitary plasmocytoma of bone is a rare condition of plasma cell neoplasia that presents as a single lesion. Amyloidoma of the chest wall is an uncommon presentation of solitary tissue amyloid deposition in the absence of systemic light-chain amyloidosis. This report describes a patient with both uncommon conditions. The tumor originated from the spine and invaded the right lung. In this exceedingly rare case, radiotherapy and a two-step resection of the right lower lobe, full-thickness chest wall, diaphragm, and vertebral body of T9 provided local control of the tumor. Spondylodesis of T7 to T11 provided spine stability.
Item Description:Gesehen am 25.01.2022
Physical Description:Online Resource
ISSN:1552-6259
DOI:10.1016/j.athoracsur.2013.04.109