Differentiation of primary ovarian carcinoma from metastatic breast carcinoma

This differential may be difficult if both tumours have similar morphology, the prior breast carcinoma is not available for comparison or the ovarian sampling is limited.

Immunohistochemistry

The useful markers are WT1 (specificity 100%, sensitivity 76%), CA125 (specificity 85%, sensitivity 90%) for ovarian primaries, and GCDFP (specificity 100%, sensitivity 43%) for metastatic breast carcinoma1.

 

 

Primary ovarian carcinoma

Primary breast carcinoma

Breast carcinoma metastatic to ovary

p

 

serous

other

WT1

31/331

1/91

0/361

0/391

<0.0011

CA125

32/33

 

6/361

5/391

<0.0011

GCDFP

0/331

0/91

5/361

17/391

<0.0011

CEA

7/331

2/91

8/361

13/391

NS1

MUC1

33/331

9/91

36/361

37/391

NS1

MUC2

6/331

4/91

3/361

12/391

0.051

           

Reference 1: threshold for positivity was 1% of tumour cells staining. Positivity for WT1 and CA125 with negativity for GCDFP

See also An immunohistochemical panel to determine the site of origin of a mucinosu adenocarcinoma

 

Management

Primary ovarian carcinoma requires debulking and chemotherapy. Metastatic breast carcinoma does not require debulking and requires a different chemotherapeutic regimen.

Prognosis

The five-year survival of primary ovarian carcinoma varies from 5% to 90%, depending on stage and resectability, compared with less than 10% five-year survival for patients with breast carcinoma metastatic to the ovary.

References

1 Tornos C, Soslow R, Chen S, et al. Expression of WT1, CA 125, and GCDFP-15 as useful markers in the differential diagnosis of primary ovarian carcinomas versus metastatic breast cancer to the ovary. Am J Surg Pathol 2005; 29:1482-9

This page last revised 21.1.2006.

©SMUHT/PW Bishop