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Características citogenéticas y detección de anormalidades de alto riesgo en mieloma múltiple / High risk cytogenetic abnormalities in patients with multiple myeloma
Legües, María Eugenia; Morales, Paulina; Valenzuela, Mercedes; Encina, Andrea; Martí, María José; Bascuñán, Claudia; Cornejo, Paulina; Peña, Camila; Undurraga, María Soledad.
  • Legües, María Eugenia; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Morales, Paulina; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Valenzuela, Mercedes; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Encina, Andrea; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Martí, María José; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Bascuñán, Claudia; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Cornejo, Paulina; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
  • Peña, Camila; Hospital del Salvador. Unidad de Hematología Clínica. Santiago. CL
  • Undurraga, María Soledad; Hospital del Salvador. Sección Hematología. Laboratorio de Citogenética. Santiago. CL
Rev. méd. Chile ; 147(1): 61-64, 2019. tab, graf
Article in Spanish | LILACS | ID: biblio-1043152
ABSTRACT

Background:

Cytogenetic abnormalities observed in the bone marrow of patients with multiple myeloma (MM) are an important prognostic factor for risk stratification.

Aim:

To investigate karyotype characteristics and frequency of the high-risk cytogenetic abnormalities t(4;14), t(14;16) and del(17p) in Chilean patients with MM. Material and

Methods:

We studied 30 patients with MM by conventional cytogenetics (CC) and fluorescent in situ hybridization of plasma cells selected using cytoplasmic immunoglobulin staining (cIg-FISH).

Results:

Overall, the two techniques in combination allowed us to identify clonal genetic abnormalities in 47% of patients. The t(4;14) abnormality was observed in 19% of patients, del(17p) was observed in 10% of patients, and t(14;16) was not detected.

Conclusions:

Our results showed frequencies of high-risk abnormalities similar to those reported abroad. Cytogenetic studies should be performed routinely for all MM patients at the moment of diagnosis.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Chromosome Aberrations / Multiple Myeloma Type of study: Etiology study / Prognostic study / Risk factors Limits: Adult / Aged / Female / Humans / Male Country/Region as subject: South America / Chile Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2019 Type: Article Affiliation country: Chile Institution/Affiliation country: Hospital del Salvador/CL

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Full text: Available Index: LILACS (Americas) Main subject: Chromosome Aberrations / Multiple Myeloma Type of study: Etiology study / Prognostic study / Risk factors Limits: Adult / Aged / Female / Humans / Male Country/Region as subject: South America / Chile Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2019 Type: Article Affiliation country: Chile Institution/Affiliation country: Hospital del Salvador/CL