Invasive breast carcinoma - IARC
Invasive breast carcinoma - IARC
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