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Invasive breast carcinoma - IARC

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yet others at 90% {97,2147}. For pragmatic<br />

reasons, a 90% purity re q u i re m e n t<br />

o ffers a practical solution.<br />

Tumours exhibiting between 50 and 90%<br />

tubular growth pattern with other types<br />

should be regarded as mixed type of<br />

<strong>carcinoma</strong> (see Mixed type <strong>carcinoma</strong>s).<br />

Differential diagnosis<br />

Sclerosing adenosis (SA) can be distinguished<br />

from tubular <strong>carcinoma</strong> by its<br />

overall lobular arc h i t e c t u re and the<br />

marked compression and distortion of<br />

the glandular structures. Myoepithelial<br />

cells are always present in sclerosing<br />

adenosis and can be highlighted by<br />

immunostaining for actin. Similarly, a fully<br />

retained basement membrane can be<br />

shown by immunohistological staining for<br />

collagen IV and laminin in tubules of SA.<br />

Microglandular adenosis (MA) can be<br />

more difficult to differentiate because of<br />

the rather haphazard arrangement of the<br />

tubules, and lack of myoepithelial cells in<br />

the tubules. However, the tubules of MA<br />

are more rounded and regular and often<br />

contain colloid-like secretory material, at<br />

least focally, compared to the often angulated<br />

tubules of tubular carc i n o m a .<br />

Furthermore a ring of basement membrane<br />

is present around tubules of MA.<br />

Complex sclerosing lesions/radial scars<br />

have a typical arc h i t e c t u re with central<br />

f i b rosis and elastosis containing a few<br />

small, often distorted, tubular structures in<br />

which myoepithelial cells can be demonstrated.<br />

The surrounding glandular struct<br />

u res show varying degrees of dilatation<br />

and ductal epithelial hyperplasia.<br />

Immunophenotype<br />

Tubular <strong>carcinoma</strong> is nearly always<br />

e s t rogen and pro g e s t e rone re c e p t o r<br />

positive, has a low growth fraction, and<br />

is ERBB2 and EGFR negative {691,<br />

1 3 7 9 , 2 1 6 6 } .<br />

Genetics<br />

Tubular <strong>carcinoma</strong>s of the <strong>breast</strong> have a<br />

low frequency of genetic alterations<br />

when compared to other types of bre a s t<br />

c a rcinoma. Using LOH and CGH techniques,<br />

alterations have been found<br />

most frequently at chromosomes 16q<br />

(loss), 1q (gain), 8p (loss), 3p FHIT<br />

gene locus, and 11q ATM gene locus<br />

{1754,1779,2476, 3046}. Of part i c u l a r<br />

i n t e rest is the observation that other<br />

sites of chromosomal alteration pre v i-<br />

ously found at high levels in other types<br />

Fig. 1.25 <strong>Invasive</strong> cribriform <strong>carcinoma</strong>. The haphazard distribution of irregularly shaped and angulated invasive<br />

areas is in contrast with the rounded configuration of the ducts with cribriform DCIS on the left side of the field.<br />

of <strong>breast</strong> cancer are not seen, which<br />

implies that tubular <strong>carcinoma</strong> of the<br />

b reast is genetically distinct.<br />

Prognosis and predictive factors<br />

Pure tubular <strong>carcinoma</strong> has an excellent<br />

long term prognosis {409,410,552,771,<br />

1829,2081,2224} which in some series is<br />

similar to age matched women without<br />

<strong>breast</strong> cancer {691}. Recurrence following<br />

mastectomy or <strong>breast</strong> conservation<br />

treatment is rare and localized tubular<br />

<strong>carcinoma</strong>s are considered to be ideal<br />

candidates for <strong>breast</strong> conservation techniques.<br />

Following <strong>breast</strong> conservation,<br />

the risk of local recurrence is so low that<br />

some centres consider adjuvant radiotherapy<br />

unnecessary. Axillary node<br />

metastases occur infrequently, and when<br />

observed rarely involve more than one<br />

low axillary lymph node. There is little<br />

adverse effect of node positivity in tubular<br />

<strong>carcinoma</strong> {691,1471} and the use of<br />

systemic adjuvant therapy and axillary<br />

node dissection are considered unnecessary<br />

by some groups {691,2166}.<br />

<strong>Invasive</strong> cribriform <strong>carcinoma</strong><br />

Definition<br />

An invasive <strong>carcinoma</strong> with an excellent<br />

prognosis that grows in a cribriform pattern<br />

similar to that seen in intraductal<br />

cribriform <strong>carcinoma</strong>; a minor (90%) of an invasive cribriform patt<br />

e rn. The tumour is arranged as invasive<br />

islands, often angulated, in which<br />

well defined spaces are formed by<br />

a rches of cells (a sieve-like or cribrif<br />

o rm pattern). Apical snouts are a re g-<br />

ular feature. The tumour cells are small<br />

and show a low or moderate degree of<br />

nuclear pleomorphism. Mitoses are<br />

r a re. A prominent, reactive appearing,<br />

f i b roblastic stroma is present in many<br />

ICC. Intraductal <strong>carcinoma</strong>, generally<br />

of the cribriform type, is observed in as<br />

many as 80% of cases {2148}. Axillary<br />

lymph node metastases occur in 14.3%<br />

{2148}, the cribriform pattern being<br />

retained at these sites. Lesions showing<br />

a predominantly cribriform arrange-<br />

<strong>Invasive</strong> <strong>breast</strong> cancer<br />

27

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