伴有涉及19号染色体19q13.4带易位的肝间叶性错构瘤：一种复发性异常。
Hepatic mesenchymal hamartoma with translocation involving chromosome band 19q13.4: a recurrent abnormality.
作者信息
Rakheja Dinesh, Margraf Linda R, Tomlinson Gail E, Schneider Nancy R
机构信息
Department of Pathology, Children's Medical Center of Dallas and the University of Texas Southwestern Medical Center, 1935 Motor Street, Dallas, TX 75235, USA.
出版信息
Cancer Genet Cytogenet. 2004 Aug;153(1):60-3. doi: 10.1016/j.cancergencyto.2003.12.004.
We report a case of mesenchymal hamartoma of the liver in an 8-month-old male child, in which the cytogenetic analysis revealed a balanced translocation, t(11;19)(q13;q13.4). This is the fifth description of a cytogenetic abnormality in mesenchymal hamartoma and is similar to the four cases reported previously in that one of the breakpoints involved chromosome band 19q13.4.
我们报告了一例8个月大男童的肝脏间叶性错构瘤病例，其中细胞遗传学分析显示存在一种平衡易位，即t(11;19)(q13;q13.4)。这是间叶性错构瘤细胞遗传学异常的第五例描述，并且与之前报道的四例相似，因为其中一个断点涉及19号染色体q13.4带。
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