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Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia

(1) Background: Plasma cell neoplasia can be separated into independent subtypes including multiple myeloma (MM) and solitary plasmacytoma of the bone (SBP). The first clinical signs patients present with are skeletal pain, most commonly involving ribs and vertebrae. (2) Methods: Retrospective analy...

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Autores principales: Baumgart, Lea, Barz, Melanie, Delbridge, Claire, Aftahy, Amir Kaywan, Janssen, Insa Katrin, Jost, Philipp J., Ryang, Yu-Mi, Meyer, Bernhard, Gempt, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497614/
https://www.ncbi.nlm.nih.gov/pubmed/36135059
http://dx.doi.org/10.3390/curroncol29090490
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author Baumgart, Lea
Barz, Melanie
Delbridge, Claire
Aftahy, Amir Kaywan
Janssen, Insa Katrin
Jost, Philipp J.
Ryang, Yu-Mi
Meyer, Bernhard
Gempt, Jens
author_facet Baumgart, Lea
Barz, Melanie
Delbridge, Claire
Aftahy, Amir Kaywan
Janssen, Insa Katrin
Jost, Philipp J.
Ryang, Yu-Mi
Meyer, Bernhard
Gempt, Jens
author_sort Baumgart, Lea
collection PubMed
description (1) Background: Plasma cell neoplasia can be separated into independent subtypes including multiple myeloma (MM) and solitary plasmacytoma of the bone (SBP). The first clinical signs patients present with are skeletal pain, most commonly involving ribs and vertebrae. (2) Methods: Retrospective analysis of 114 patients (38 female, 76 male) receiving spinal surgery from March 2006 until April 2020. Neurological impairments and surgical instability were the criteria for intervention in this cohort. Analysis was based on demographic data, Spinal Instability Neoplastic Score (SINS), location of the lesion, spinal levels of tumor involvement, surgical treatment, histopathological workup, adjuvant therapy, functional outcome, and overall survival (OS). (3) Results: The following surgical procedures were performed: posterior stabilization only in 9 patients, posterior stabilization and decompression without vertebral body replacement in 56 patients, tumor debulking and decompression only in 8 patients, anterior approach in combined approach without vertebral body replacement and without biopsy and/or without kyphoplasty in 33 patients, 3 patients received biopsies only, and 5 patients received kyphoplasty only. The histopathology diagnoses were MM in 94 cases and SBP in 20 cases. Median OS was 72 months (53.4–90.6 months). Preoperative KPSS was 80% (range 40–100%), the postoperative KPSS was 80% (range 50–100%). (4) Conclusions: Surgery for patients with plasma cell neoplasia is beneficial in case of neurological impairment and spinal instability. Moreover, we were able to show that patients with MM and a low number of spinal levels to be supplied have a better prognosis as well as a younger age at the time of the surgical intervention.
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spelling pubmed-94976142022-09-23 Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia Baumgart, Lea Barz, Melanie Delbridge, Claire Aftahy, Amir Kaywan Janssen, Insa Katrin Jost, Philipp J. Ryang, Yu-Mi Meyer, Bernhard Gempt, Jens Curr Oncol Article (1) Background: Plasma cell neoplasia can be separated into independent subtypes including multiple myeloma (MM) and solitary plasmacytoma of the bone (SBP). The first clinical signs patients present with are skeletal pain, most commonly involving ribs and vertebrae. (2) Methods: Retrospective analysis of 114 patients (38 female, 76 male) receiving spinal surgery from March 2006 until April 2020. Neurological impairments and surgical instability were the criteria for intervention in this cohort. Analysis was based on demographic data, Spinal Instability Neoplastic Score (SINS), location of the lesion, spinal levels of tumor involvement, surgical treatment, histopathological workup, adjuvant therapy, functional outcome, and overall survival (OS). (3) Results: The following surgical procedures were performed: posterior stabilization only in 9 patients, posterior stabilization and decompression without vertebral body replacement in 56 patients, tumor debulking and decompression only in 8 patients, anterior approach in combined approach without vertebral body replacement and without biopsy and/or without kyphoplasty in 33 patients, 3 patients received biopsies only, and 5 patients received kyphoplasty only. The histopathology diagnoses were MM in 94 cases and SBP in 20 cases. Median OS was 72 months (53.4–90.6 months). Preoperative KPSS was 80% (range 40–100%), the postoperative KPSS was 80% (range 50–100%). (4) Conclusions: Surgery for patients with plasma cell neoplasia is beneficial in case of neurological impairment and spinal instability. Moreover, we were able to show that patients with MM and a low number of spinal levels to be supplied have a better prognosis as well as a younger age at the time of the surgical intervention. MDPI 2022-08-29 /pmc/articles/PMC9497614/ /pubmed/36135059 http://dx.doi.org/10.3390/curroncol29090490 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Baumgart, Lea
Barz, Melanie
Delbridge, Claire
Aftahy, Amir Kaywan
Janssen, Insa Katrin
Jost, Philipp J.
Ryang, Yu-Mi
Meyer, Bernhard
Gempt, Jens
Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia
title Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia
title_full Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia
title_fullStr Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia
title_full_unstemmed Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia
title_short Spinal Lesions as Clinical Manifestations of Plasma Cell Neoplasia
title_sort spinal lesions as clinical manifestations of plasma cell neoplasia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497614/
https://www.ncbi.nlm.nih.gov/pubmed/36135059
http://dx.doi.org/10.3390/curroncol29090490
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