Invasive breast carcinoma - IARC
Invasive breast carcinoma - IARC
Invasive breast carcinoma - IARC
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A<br />
Fig. 2.119 Hepatoid <strong>carcinoma</strong>. A Note the trabecular pattern with thick cords of hepatoid cells. B Positive staining for alpha-fetoprotein is observed.<br />
B<br />
Immunoprofile<br />
Immunohistochemical markers for neuro n<br />
specific enolase are typically positive,<br />
and a minority of cases were positive for<br />
c h romogranin {761}.<br />
Cytometric studies<br />
The majority of neoplasms are aneuploid<br />
by flow cytometry {761}.<br />
Prognosis and predictive factors<br />
The neoplasm is highly malignant, and<br />
the behaviour has been aggre s s i v e<br />
regardless of stage {761}.<br />
Large cell neuroendocrine<br />
<strong>carcinoma</strong><br />
Definition<br />
A malignant tumour composed of large<br />
cells that show neuroendocrine differentiation.<br />
Synonym<br />
Undifferentiated <strong>carcinoma</strong> of non-small<br />
cell neuroendocrine type.<br />
Clinical features<br />
Two series of ovarian neuroendocrine<br />
<strong>carcinoma</strong>s of non-small cell type have<br />
been reported {455,756}. The patients<br />
were in the reproductive age group or<br />
beyond (mean 56 years) and presented<br />
with symptoms related to a pelvic mass<br />
in the majority of cases {756}.<br />
Histopathology<br />
These tumours have in all the re p o rt e d<br />
cases been associated with a tumour of<br />
s u rface epithelial-stromal type, either<br />
benign or malignant {455,542,756}. The<br />
n e u roendocrine component consisted<br />
of medium to large cells. Nuclei contained<br />
prominent nucleoli, and mitoses<br />
w e re frequent. The solid component<br />
stained for chromogranin, and neuropeptides<br />
were demonstrated in some<br />
cases.<br />
Prognosis and predictive factors<br />
This type of tumour appears to be highly<br />
a g g ressive; only the neuroendocrine <strong>carcinoma</strong><br />
component was present in the<br />
metastatic sites {455}.<br />
Hepatoid <strong>carcinoma</strong><br />
Definition<br />
A primary ovarian neoplasm that histologically<br />
resembles hepatocellular carc i n o-<br />
ma and is positive for alpha-fetoprotein.<br />
Epidemiology<br />
Hepatoid <strong>carcinoma</strong> of the ovary is a<br />
r a re tumour; only 12 cases have been<br />
re p o rted {1798,2629,2951}. It mainly<br />
occurs in postmenopausal women with<br />
a mean age of 59.6 years (range, 35-78<br />
years).<br />
Clinical features<br />
The symptoms are not specific and are<br />
related to an ovarian mass {2629}.<br />
Elevation of serum alpha-fetopro t e i n<br />
(AFP) is characteristic, and CA125 is elevated<br />
in most cases.<br />
Macroscopy<br />
Tumours vary from 4-20 cm in maximum<br />
dimension with no distinctive macroscopic<br />
features {1798,2629,2951}. In<br />
some cases, formalin fixation re v e a l s<br />
green-coloured areas suggestive of bile<br />
production {2629}.<br />
Histopathology<br />
The tumour cells are arranged in sheets,<br />
c o rds and trabeculae with moderate to<br />
abundant amounts of eosinophilic cytoplasm<br />
and distinctive cell borders re s e m-<br />
bling hepatocellular <strong>carcinoma</strong>. Mitoses<br />
a re generally conspicuous. PA S - p o s i t i v e ,<br />
d i a s t a s e - resistant hyaline globules and<br />
Hall stain-positive bile pigment can be<br />
seen. The presence of immunore a c t i v e<br />
AFP and protein induced by vitamin K<br />
absence or antagonist II (PIVKA-II)<br />
shows functional diff e rentiation toward<br />
hepatocytes {1307,2629}. CA125 is positive<br />
in one-half of the tumours {2629}.<br />
Differential diagnosis<br />
Metastatic hepatocellular <strong>carcinoma</strong> and<br />
hepatoid yolk sac tumour must be ruled<br />
out {3197}.<br />
Histogenesis<br />
Tumours admixed with serous <strong>carcinoma</strong><br />
and tumour cells positive for CA125 suggest<br />
an ovarian surface epithelial origin<br />
{1307,2610,2629}.<br />
Prognosis and predictive factors<br />
Clinical outcome is poor. Seven out of 12<br />
patients died between 4 months and 5<br />
years (mean, 19 months) after initial diagnosis,<br />
and 2 patients had a tumour re c u r-<br />
rence after 6-7 months {1798,2629,2 9 5 1 } .<br />
Tumours resembling adenoid cystic<br />
<strong>carcinoma</strong> and basal cell tumour<br />
Definition<br />
A group of primary ovarian tumours that<br />
histologically resemble certain tumours<br />
of the salivary glands or cutaneous basal<br />
cell <strong>carcinoma</strong>.<br />
184 Tumours of the ovary and peritoneum