Table 2 Clinical and anatomopathological characteristics of oncocytic adrenocortical tumors, good vs. poor outcomes

From: Clinicopathological description of 43 oncocytic adrenocortical tumors: importance of Ki-67 in histoprognostic evaluation

Characteristicsa

Good outcome

Poor outcome

Sex (female)

23 (57.5%)

2 F/1M

Age (years)

47.5 (38.0–55.8)

46, 50, 59

Tumor size (cm)

6.8 (4.5–9.9)

8.5, 10, 21

Tumor weight (g)

161 (59–392)

80, 176, 2940

Hormonal production

20 (54%)

2/3 (1 cortisol, 1 cortisol and androgen)

Pure oncocytic tumors

26 (65%)

2/3

Dominant diffuse architecture

35 (88%)

2/3

Mitotic index > 5/50 HPF

20 (50%)

3/3

Atypical mitosis

21 (53%)

3/3

Capsular invasion

9 (23%)

2/3

Venous invasion

7 (18%)

2/3

Sinusoidal invasion

0 (0%)

1/3

Necrosis

13 (33%)

3/3

Reticulin stain: disrupted

32 (91%)

3/3

Ki-67 PI (%)

3 (1–3.5)

7, 14, 15

ENS@T (III or IV)

3 (8%) (only stage III)

3/3 III, III and IV

Different approaches by scores

  Weiss score

5 (3–6)

7, 7, 8

  Lin–Weiss–Bisceglia score (borderline, malignant)

6 Borderline (15%), 25 Malignant (63%)

3 Malignant

  Reticulin algorithm (malignant)

20 (56%)

3

  Helsinki score

6 (3–9.5)

15, 22, 23

  1. COMETE study, N = 43
  2. aFor “Good outcome” tumors, data are described with group size (%) for categorical data and median (IQR) for quantitative data. For “Poor outcome” tumors, considering the population size (n = 3), we listed the exact distribution or the three corresponding values