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. 1999 Jun;154(6):1841–1847. doi: 10.1016/S0002-9440(10)65441-7

Table 4.

Miscellaneous Tumors

Case ref Diagnosis Karyotype
Lu 287* Myofibroblastic sarcoma 45, XX, del(1)(p13), add(5)(p15),+8, der(9)t(9;12)(p11;p11), der(10;12)(q10;q10),−13,−15, del(15)(q15), −21,+2mar/44, idem,−9
Le 165 Myofibroblastic sarcoma 46, X, der(X)t(X;?22)(p22;q11), t(2;14)(q31;q23),−6, del(15)(q21), der(19)t(11;19)(q13;q13),−22,+2mar
Le 210 Myofibroblastic sarcoma 46, XY
Lu 330 Meningeal hemangiopericytoma 47, XX, +5
Lu 259 Mesenchymal chondrosarcoma 45, XX, der(4)t(4;12)(q35;q13), add(5)(p15),−8,−12, der(20)t(8;20)(q13;p13)/46, XX
Lu 320 Inflammatory myofibroblastic tumor 46, XY
Le 166 Infantile fibrosarcoma 48, X,−X,+11,+11,+17/49, idem,+20/46, XX
Le 136 Myosarcoma NOS 82–87, XX,−X,−X, der(1)add(1)(p11)add(1)(q21), der(2)t(1;2)(p22;q33), add(6)(q15), add(7)(q11), add(19)(q13), dmin, inc/46, XX
Le 206 Spindle-cell sarcoma NOS 46, XY
Le 217 Spindle-cell sarcoma NOS 48–50, XY,+X, add(1)(q44),+add(4)(q35), add(6)(q27),+7, del(12)(q11),−13, −14,+20,+mar
Lu 282 Spindle-cell sarcoma NOS 46, XX

*Published as fibrosarcoma in Ref. 27, corresponding to sample I, piece A. The change in the description of the rearrangement involving chromosomes 10 and 12 is basically technical (due to the new possibilities given in the new nomenclature system ISCN (1995)).

Published in Ref. 25 .