| DC Field | Value | Language |
|---|
| dc.contributor.author | Chelban, Viorica | - |
| dc.date.accessioned | 2022-02-07T09:53:26Z | - |
| dc.date.available | 2022-02-07T09:53:26Z | - |
| dc.date.issued | 2012 | - |
| dc.identifier.citation | CHELBAN, Viorica. Multiple plasmocytoma - a rare case of three atypical presentations. In: MedEspera: the 4th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2012, p. 67. | en_US |
| dc.identifier.uri | http://repository.usmf.md/handle/20.500.12710/20028 | - |
| dc.description.abstract | Introduction: The solitary plasmocytoma represents less than 5% of all plasma cell neoplasms. The
multiple plasmocytoma is 20 times rarer than solitary plasmocytoma. Progression to multiple myeloma
is common.
Methods: Case study
Results: We report a very rare case of multiple plasmocytoma developed in the bone and two atypical
sites - renal and gastric. The patient was treated with radiotherapy, surgery and chemotherapy. The case
is presented due to its rarity.
Conclusion: The high risk of a progression towards a multiple myeloma justifies a comprehensive initial assessment and regular monitoring of all plasmocytomas. The management of a patient with multiple
plasmocytomas will be determined by the sensitivity and the site of the tumor. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association, Scientific Association of Students and Young Doctors | en_US |
| dc.relation.ispartof | MedEspera: The 4th International Medical Congress for Students and Young Doctors, May 17-19, 2012, Chisinau, Republic of Moldova | en_US |
| dc.subject | Multiple plasmocitoma | en_US |
| dc.subject | extramedullaryplasmocitoma | en_US |
| dc.title | Multiple plasmocytoma - a rare case of three atypical presentations | en_US |
| dc.type | Other | en_US |
| Appears in Collections: | MedEspera 2012
|
