SOLITARY PLASMACYTOMA OF BONE AND EXTRAMEDULLARY PLASMACYTOMA - 2 DIFFERENT ENTITIES

Citation
P. Galieni et al., SOLITARY PLASMACYTOMA OF BONE AND EXTRAMEDULLARY PLASMACYTOMA - 2 DIFFERENT ENTITIES, Annals of oncology, 6(7), 1995, pp. 687-691
Citations number
15
Categorie Soggetti
Oncology
Journal title
ISSN journal
09237534
Volume
6
Issue
7
Year of publication
1995
Pages
687 - 691
Database
ISI
SICI code
0923-7534(1995)6:7<687:SPOBAE>2.0.ZU;2-2
Abstract
Background: The objective of this study was to evaluate the similariti es between solitary plasmacytoma of bone (SPB) and extramedullary plas macytoma (EP). Patients and methods: The clinical features, treatment and survival of 54 patients with localized plasmacytoma (LP) seen at 4 Italian institutions between May 1968 and February 1990 were carefull y reviewed. Follow-up was expected to continue until June 1993. Result s: Thirty-two patients were classified as having SPB and 22 EP. Most o f the patients were males, particularly those in the SPB group. Their median age at diagnosis was 54 years and no significant difference bet ween the two groups was observed. SPB occurred most frequently in the vertebral column (42%) and EP in the upper respiratory tract (73%). Fi fteen patients with SPB and 2 with EP had paraproteinemia at diagnosis , multiple myeloma (MM) became evident in 75% of the patients with per sistent paraprotein after therapy, and in only 22% of those in whom it disappeared. Four patients in the SPB group had immunoparesis, and 3 developed MM. Disease progression toward MM was significantly differen t (p = 0.003) in the two groups, while overall survival differences we re not significant (p = 0.07) unless unrelated causes were excluded (p = 0.02). Adjuvant chemotherapy did not seem to limit diffusion of the disease. Conclusions: Although EP and SPB are both localized forms of plasma cell dyscrasias, SPB seems to have a greater tendency to progr ess in MM. II appears, however, that the apparent stronger propensity of SPB to progress is actually due to the great number of cases that a t diagnosis conceal an occult MM.