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Invasive breast carcinoma - IARC

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A<br />

mal luteinization, can be confused with a<br />

Sertoli-Leydig cell tumour. Positive mucicarmine<br />

and PAS-stains with diastase<br />

digestion are of great value in establishing<br />

the diagnosis of a Krukenberg<br />

tumour. Occasional Krukenberg tumours<br />

may closely resemble fibromas on<br />

macroscopic examination and may contain<br />

relatively few signet-ring cells.<br />

Bilaterality and positive mucin stains<br />

facilitate the differential diagnosis.<br />

Distinction between a transitional cell<br />

<strong>carcinoma</strong> of the urinary tract metastatic<br />

to the ovary and a primary transitional<br />

cell <strong>carcinoma</strong> may be diff i c u l t<br />

{2100,3220}. Clinical information may be<br />

necessary to resolve the issue.<br />

Renal cell <strong>carcinoma</strong> rarely metastasizes<br />

to the ovaries; however, when it does, it<br />

must be distinguished from a primary<br />

clear cell <strong>carcinoma</strong>. The metastatic<br />

tumour usually shows a sinusoidal vascular<br />

pattern, a homogenous clear cell<br />

p a t t e rn without hobnail cells, the<br />

absence of hyalinized papillae and the<br />

absence of mucin {3226}.<br />

A metastatic carcinoid can be confused<br />

B<br />

C<br />

Fig. 2.137 Burkitt-like lymphoma. A T2 weighted sagital computed tomography scan from an 8-year old girl<br />

shows a large pelvic mass. B Sagital section of the ovarian tumour shows a homogeneous, pale surface.<br />

Notice the enlargement of the fallopian tube (FT). C A starry-sky pattern is apparent (B5 fixation).<br />

FT<br />

with a primary carcinoid, granulosa cell<br />

t u m o u r, Sertoli-Leydig cell tumour,<br />

B renner tumour, adenofibroma or<br />

endometrioid <strong>carcinoma</strong> {2605,3226}.<br />

Bilaterality and extraovarian extension<br />

are important features of metastatic carcinoid.<br />

In the ovary, metastatic malignant<br />

melanoma may be confused with primary<br />

malignant melanoma; the latter is unilateral<br />

and usually associated with a dermoid<br />

cyst. When a melanoma is composed<br />

predominantly of large cells, it<br />

may resemble steroid cell lesions such<br />

as steroid cell tumour or luteoma of pregnancy;<br />

when it is composed predominantly<br />

of small cells it may be confused<br />

with a variety of other tumours characterized<br />

by small cells {3223}. Positive stains<br />

for melanin, S-100 protein, melan A,<br />

and/or HMB-45 should establish the<br />

diagnosis of melanoma.<br />

Sarcomas may metastasize to the ovary<br />

from the uterus or extragenital sites and<br />

may occasionally be discovered before<br />

the primary tumour {3222}. Metastastic<br />

low grade endometrial stromal sarcoma<br />

(ESS) may simulate a primary ovarian<br />

sex cord-stromal tumour. Features helpful<br />

in their distinction include the presence<br />

of extraovarian disease, bilaterality<br />

and the characteristic content of spiral<br />

arterioles in metastatic low grade ESS.<br />

Metastatic epitheliolid leiomyosarc o m a<br />

may have an appearance that simulates<br />

the solid tubular pattern of a Sertoli cell<br />

tumour.<br />

Although lymphoma and leukaemia can<br />

involve the ovaries simulating various primary<br />

tumours, they rarely present clinically<br />

as an ovarian mass. In countries<br />

w h e re Burkitt lymphoma is endemic,<br />

however, it accounts for approximately<br />

half the cases of malignant ovarian<br />

tumours in childhood. Dysgerminoma is<br />

one of the most common and difficult differential<br />

diagnoses. The appearance of<br />

the cell nuclei is very import a n t .<br />

I m m u n o h i s t o c h e m i s t ry for lymphoid<br />

markers and placental alkaline phosphatase<br />

are helpful. Carcinoid, granulosa<br />

cell tumour or small cell <strong>carcinoma</strong><br />

can also resemble lymphoma. In patients<br />

with acute myeloid leukaemia, ovarian<br />

involvement in the form of granulocytic<br />

sarcoma ("chloroma") may rarely constitute<br />

the initial clinical presentation of the<br />

disease. Histological examination<br />

reveals a diffuse growth pattern with a<br />

prominent "single file" arrangement of the<br />

tumour cells. Myeloid differentiation can<br />

be demonstrated by the chloroacetate<br />

esterase stain. Immunoperoxidase stains<br />

for lysozyme, CD68, and LCA are also<br />

helpful.<br />

Recognition of the secondary nature of<br />

an ovarian tumour depends on a complete<br />

clinical history, a careful operative<br />

search for a primary extraovarian tumour,<br />

and accurate evaluation of the macroscopic<br />

and histological features of the<br />

ovarian tumour. In rare cases the primary<br />

tumour is not found until several years<br />

after resection of the ovarian metastases<br />

{2605,3226}.<br />

Prognosis and predictive factors<br />

Ovarian metastases often represent a<br />

late disseminated stage of the disease in<br />

which other haematogenous metastases<br />

are also found. The prognosis is, therefore,<br />

poor.<br />

196 Tumours of the ovary and peritoneum

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