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. 2007 Feb 6;96(4):667–676. doi: 10.1038/sj.bjc.6603602

Table 4. Total number of paediatric (⩽16 years) MGCTs analysed by conventional cytogenetic techniques reported in the literature to date, with relative frequencies of iso(12p) by age range.

  Age < 5 years
Age ⩾5 <16 years
  Case mix iso(12p) Case mix iso(12p)
Oosterhuis et al (1988) 1 (1 YST) 0 0 0
Speleman et al (1990) 0 0 1 (1 Mixed) 1
Shen et al (1990) 0 0 1 (1 Mixed) 0 (but 4 copies of chromosome 12)
Albrecht et al (1993) 0 0 1 (1 Germinoma) 0 (but extra 12p material)
de Bruin et al (1994) 0 0 1 (1 Mixed) 1
Perlman et al (1994) 6 (6 YST) 0 0 0
Stock et al (1994) 6 (2 EC, 2 YST, 2 Mixed) 1 5 (2 DG, 1 Mixed, 2 SE) 1
Jenderny et al (1995) 4 (4 YST) 4a 2 (2 YST) 1a
Stock et al (1995) 8 (6 YST, 2 EC) 1 5 (2 DG, 2 Mixed, 1 EC) 2
Sainati et al (1996) 1 (1 EC) 0 0 0
Lemos et al (1998) 1 (1 Geminoma) 0 0 0
Losi et al. (1994) 0 0 1 (1 Mixed) 1
Bussey et al (1999) 21 (11 YST, 7 Mixed, 3 UK) 0 23 (16 Mixed, 3 YST, 2 UK, 1 Germinoma, 1 Malignant teratoma) 2+2 other 12p structural abnormalities
Okada et al (2002) 0 0 10 (6 Germinoma, 3 Mixed, 1 YST) 2
Van Ecten et al (2002) 3 (3 YST) 0 0 0
Poulos et al (2006) 1 (1 Mixed) 1 2 (2 Mixed) 2
         
Total 52 7 (13.5%) 52 13 (25%)+4 others

Case mix includes mixed malignant germ cell tumour (mixed), yolk sac tumour (YST), embryonal carcinoma (EC), dysgerminoma (DG), seminoma (SE) and unknown germ cell tumour (UK).

a

Gain of chromosome 12 by in situ hybridisation – iso(12p) status unclear, but one case in each age range almost certainly iso(12p).