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Invasive breast carcinoma - IARC

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endometrioid adeno<strong>carcinoma</strong> fro m<br />

atypical complex hyperplasia is best provided<br />

by stromal disappearance<br />

between adjacent glands, i.e. confluent,<br />

c r i b r i f o rm or villoglandular pattern s<br />

{1433,1689,2688,2691}. Other feature s<br />

that may be helpful include a stromal<br />

desmoplastic response and/or tumour<br />

n e c rosis. Stromal foam cells may be<br />

associated with adeno<strong>carcinoma</strong> or its<br />

precursors.<br />

Variants of endometrioid<br />

adeno<strong>carcinoma</strong><br />

Endometrial proliferations may exhibit a<br />

variety of differentiated epithelial types<br />

including squamous/morules, mucinous,<br />

ciliated, cleared or eosinophilic cells,<br />

and architectural variations including<br />

papillary formations. These cell types are<br />

often called metaplasias and may be<br />

e n c o u n t e red in benign, pre m a l i g n a n t<br />

and malignant epithelia. When prominent<br />

in a <strong>carcinoma</strong> the neoplasm is termed a<br />

"special variant" <strong>carcinoma</strong>.<br />

Variant with squamous differentiation<br />

From 20-50% or more of endometrioid<br />

a d e n o c a rcinomas contain vary i n g<br />

amounts of neoplastic epithelium showing<br />

squamous differentiation. Although<br />

the distinction between endometrioid<br />

adeno<strong>carcinoma</strong> with and without squamous<br />

diff e rentiation is not clinically<br />

important, the recognition of squamous<br />

differentiation is nevertheless essential<br />

because the squamous or morular elements<br />

should not be considered a part of<br />

the solid component that increases the<br />

grade of an endometrioid <strong>carcinoma</strong>.<br />

The criteria for squamous differentiation<br />

{2691} are as follows:<br />

(1) Keratinization demonstrated with<br />

standard staining techniques.<br />

(2) Intercellular bridges and/or<br />

(3) Three or more of the following four criteria:<br />

(a) Sheet-like growth without gland formation<br />

or palisading.<br />

(b) Sharp cell margins.<br />

(c) Eosinophilic and thick or glassy cytoplasm.<br />

(d) A decreased nuclear to cytoplasmic<br />

ratio as compared with foci elsewhere in<br />

the same tumour.<br />

Fig. 4.03 Endometrioid adeno<strong>carcinoma</strong>. The bizarre nuclear atypia raises the tumour grade but should also<br />

prompt consideration of a serous adeno<strong>carcinoma</strong>.<br />

Fig. 4.04 Well differentiated endometrioid adeno<strong>carcinoma</strong>, ciliated cell variant. Cilia lining the neoplastic<br />

glands are prominent.<br />

Villoglandular variant<br />

This type is the next most commonly<br />

encountered endometrioid adeno<strong>carcinoma</strong><br />

variant and is usually seen involving<br />

part of a low grade endometrioid <strong>carcinoma</strong><br />

but not the entire tumour. In this<br />

pattern numerous villous fronds are seen,<br />

but their central cores are delicate, and<br />

cells with the usual cytological features<br />

(including stratification perpendicular to<br />

the basement membrane) line the villi.<br />

These features are in contrast to the<br />

more complex papillary architecture and<br />

high grade nuclear features that are typical<br />

of serous and clear cell adeno<strong>carcinoma</strong>s<br />

growing in a papillary pattern.<br />

Secretory variant<br />

Occasional endometrioid adeno<strong>carcinoma</strong>s<br />

are composed of glands lined by<br />

epithelium with voluminous, usually subnuclear,<br />

glycogen vacuoles reminiscent<br />

of early secretory endometrium. These<br />

tumours have minimal nuclear atypia and<br />

are diagnosable as <strong>carcinoma</strong> only by<br />

virtue of a confluent, cribriform or villoglandular<br />

pattern. As with the other variants,<br />

this pattern may be seen as the<br />

only one in an endometrioid adenocarci-<br />

Epithelial tumours and related lesions 223

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