Number of the records: 1
sarkóm synoviálny
SYS d013584 LBL 00000cy--a2200000n--4500 005 20250606214058.2 008 990101|-|anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C04.557.450.565.835 065 $a C04.557.450.795.875 066 $a 01 $c 03 150 $a sarkóm synoviálny $x BL $x BS $x CF $x CH $x CI $x CL $x CN $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SC $x SU $x TH $x UL $x UR $x VE $x VI $2 slo 450 $w v $a Synovioma $2 eng 450 $w v $a sarkóm synoviový $2 slo 450 $w v $a synovióm $2 slo 665 $a 94; was SYNOVIOMA 1963-93 $2 eng 680 9-
$i A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) $2 eng 680 $a coordinate with precoordinated organ/neoplasm term $2 eng 750 $a Sarcoma, Synovial $2 eng 980 $x M
Number of the records: 1