Table 1 Clinicopathologic and molecular information of the cases.

From: Toward a unifying entity that encompasses most, but perhaps not all, inflammatory leiomyosarcomas and histiocyte-rich rhabdomyoblastic tumors

Case#

Age

Sex

Location

Max. dimension

Tumor border

Mitosis

Necrosis

Resection Margin

Positive immunostaininga

Follow-up (weeks)

OncoScan-inferred karyotypeb

FISH-derived average copy number: chr# (copy number)

Note

1

38

M

Thigh

6.8 cm

Encapsulated

2/50 HPF

Present

Close (<1 mm)

Desmin, SMA, MyoD1, myogenin

NED (9)

54, X, +X, −Y, +5, +5, +12, +12, +20, +20, +22, +22

Chr5q (3.225), Chr9 (1.75), Chr12 (2.825), Chr13 (1.675), Chr17 (1.625), Chr18q (1.5), Chr20q (3.025), Chr22q (3.325)

Trauma 1 year before

2

35

F

Hip

11 cm

Encapsulated, focally infiltrative

1/50 HPF

Present

Positive

Desmin, MyoD1, myogenin

NED (6)

46, XY (with a gain of 5q14.3-q35.3)

Chr5q (3.3), Chr9 (1.95), Chr12 (1.9), Chr17 (1.9), Chr18q (1.875), Chr20q (1.775), Chr22q (1.85)

Adjuvant radiotherapy

3

23

M

Thigh

7.2 cm

Encapsulated

5/50 HPF

Absent

Close (<1 mm)

Desmin, SMA, MyoD1, myogenin

NED (146)

52, XY, +X, +Y, +5, +5, +22, +22

Not performed

Adjuvant radiotherapy. Previously reported (ref. 6)

4

18

M

Back

5.3 cm

Encapsulated, focally infiltrative

2/50 HPF

Absent

Close (<1 mm)

Desmin, SMA, MyoD1, myogenin

NED (6)

58, XY, +X, +Y, +5, +5, +18, +18, +20, +20, +21, +21, +22, +22

Not performed

Neurofibromatosis type 1

  1. NED no evidence of disease.
  2. aOnly desmin was diffusely and strongly positive, while the others were focal.
  3. bHeterozygous chromosomes shown in bold numbers.