The novel translocation of t (1;21) in multiple myeloma with poor prognosis
Abstract
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Objective: Multiple myeloma (MM) is characterized as the neoplastic proliferation of plasma cells producing a monoclonal paraprotein. The aim of this paper is to report complex karyotype that leads to a fatal clinical course in a patient with MM. Case: A 48-year-old male patient was diagnosed as MM free lambda. The karyotype of the patient was 46, XY, t(1;21) (p11;p11), del(3) (q25;q29), del(6) (q24;q26), t(11;14) (q13;q32), del(13) (q14;q21) in cytogenetic evaluation. Vincristine, doxorubicin and dexamethasone were started. The creatinine levels increased after the second course of chemotherapy, the chemotherapy protocol was switched to bortezomib and dexamethasone. Patient was admitted to the emergency department with pneumonia after the second chemotherapy cycle. Despite using broad spectrum antibiotics and oxygen support, he died after the development of sepsis syndrome. Conclusion: The anomaly of t (1;21) (p11;p11), that we detected in this case was detected in a case with MM for the first time and this anomaly has not been detected between these breaking points in any malignancies before. Although the prognostic impact of this unique anomaly may be unclear, further studies are needed to evaluate the effect of cytogenetic anomalies on prognosis of multiple myeloma. |
Keywords
References
- 1. Kyle RA, Gertz MA, Witzig TE, Lust JA, Lacy MQ, Dispenzieri A, Fonseca R, Rajkumar SV, Offord JR, Larson DR, editors. Review of 1027 patients with newly diagnosed multiple myeloma. Mayo Clinic Proceedings; 2003: Elsevier.
- 2. Dias NEM. Acute myeloma kidney. Kidney international. 1995;48:1347-61.
- 3. Binder M, Rajkumar S, Ketterling R, Dispenzieri A, Lacy M, Gertz M, Buadi F, Hayman S, Hwa Y, Zeldenrust S. Occurrence and prognostic significance of cytogenetic evolution in patients with multiple myeloma. Blood cancer journal. 2016;6:3e401.
- 4. Amare PSK, Jain H, Nikalje S, Sengar M, Menon H, Inamdar N, Subramanian P, Gujral S, Shet T, Epari S. Observation on frequency & clinico-pathological significance of various cytogenetic risk groups in multiple myeloma: an experience from India. The Indian journal of medical research. 2016;144:4536.
- 5. Shin S-Y, Eom H-S, Sohn JY, Lee H, Park B, Joo J, Jang J-H, Lee M-N, Kim JK, Kong S-Y. Prognostic Implications of Monosomies in Patients With Multiple Myeloma. Clinical Lymphoma Myeloma and Leukemia. 2017;17:3159-64. e2.
- 6. Govindasamy P, Pandurangan P, Tarigopula A, Mani R, C RS. Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India. Asian Pac J Cancer Prev. 2019;20:1235-41.10.31557/apjcp.2019.20.1.235.
- 7. Wang CB, Wu J, Yang K, Su M, Zhang HY, Pan YZ, Wu T, Xi R, Bai H. [Retrospective Analysis of Genetics Abnormalities in Patients with Multiple Myeloma]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2018;26:61681-7.10.7534/j.issn.1009-2137.2018.06.017.
- 8. Shaffer LG, McGowan-Jordan J, Schmid M. ISCN 2013: an international system for human cytogenetic nomenclature (2013): Karger Medical and Scientific Publishers; 2013.
Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Case Report
Authors
Müfide Okay
*
Türkiye
Süreyya Bozkurt
0000-0002-1765-9894
Türkiye
Mehmet Özgeyik
This is me
0000-0002-8510-3505
Türkiye
İbrahim Haznedaroğlu
This is me
0000-0001-8028-9462
Türkiye
Publication Date
April 30, 2019
Submission Date
February 10, 2019
Acceptance Date
March 31, 2019
Published in Issue
Year 1970 Volume: 6 Number: 4