Mkrtchyan Hasmik, Garcia Ney Daniela Ribeiro, de Ventura Eliane Soares, Liehr Thomas, Felix Gabriel Rafael, Marques-Salles Terezinha de Jesus, Abdelhay Eliana, Macedo Silva Maria Luiza
Jena University Hospital, Institute of Human Genetics and Anthropology, Jena, Germany.
Cancer Genet Cytogenet. 2010 Feb;197(1):71-4. doi: 10.1016/j.cancergencyto.2009.09.019.
High hyperdiploidy with modal chromosome numbers between 50 and 65 is common in childhood acute lymphoblastic leukemia (ALL), occurring in 25-30% of the cases. This chromosomal constitution is associated with a very good prognosis. By contrast, near triploidy and tetraploidy are found in <1% of childhood ALL. Given the sparseness of this group, the associated chromosomal abnormalities and their prognostic implications have not yet been studied in detail. Here, we describe clinical and molecular cytogenetic findings in a child with ALL who had a near-triploid complex karyotype, with loss and gain of chromosomes, including extra copies of the same derivative chromosomes. These findings suggest a random nondisjunction mechanism for near triploidy in the present case.
在儿童急性淋巴细胞白血病(ALL)中,具有50至65条众数染色体数目的高超二倍体很常见,在25%-30%的病例中出现。这种染色体构成与非常好的预后相关。相比之下,近三倍体和四倍体在<1%的儿童ALL中发现。鉴于该组病例稀少,相关的染色体异常及其预后意义尚未得到详细研究。在此,我们描述了一名患有近三倍体复杂核型ALL儿童的临床和分子细胞遗传学发现,该核型存在染色体的丢失和增加,包括相同衍生染色体的额外拷贝。这些发现提示本病例中近三倍体的随机不分离机制。