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fibroblastic variant, particularly on the elbow or jaw. Differential diagnoses for such<br />

lesions include various forms <strong>of</strong> chronic infectious lymphangitis/lymphadenitis (e.g.<br />

glanders, epizootic lymphangitis and cutaneous histoplasmosis) and metastasising<br />

carcinomas.<br />

Why biopsy?<br />

Histopathology usually permits confirmation <strong>of</strong> a clinical diagnosis <strong>of</strong> equine sarcoid<br />

and elimination <strong>of</strong> the considerable list <strong>of</strong> differential diagnoses. However, nonexcisional<br />

biopsy may provoke transition <strong>of</strong> a quiescent sarcoid into a rapidly<br />

growing aggressive one. For this reason, many equine practitioners are loath to<br />

interfere, particularly with large or poorly demarcated lesions or when a suitable<br />

method <strong>of</strong> treatment is unlikely to be available once the diagnosis is confirmed.<br />

Diagnostic histological features <strong>of</strong> equine sarcoids<br />

Histologically, most sarcoids are characterised by dermal fibroblastic proliferation<br />

and intimately associated, pseudoepitheliomatous hyperplasia <strong>of</strong> the epidermis.<br />

T<strong>here</strong> is usually some degree <strong>of</strong> hyperkeratosis and t<strong>here</strong> may be mild parakeratosis.<br />

Long, narrow, anastomosing rete pegs <strong>of</strong> hyperplastic and at least focally acanthotic<br />

epidermis extend into the proliferating spindle cell component in the dermis.<br />

The infiltrative and poorly demarcated dermal component is usually <strong>of</strong> moderately<br />

high cell density, with the superficial portion tending to be more cellular than the<br />

deep part. The dermal fibroblasts are slender to plump fusiform cells with poorly<br />

defined cytoplasmic boundaries. The nuclei may be slender and elongate or enlarged<br />

and <strong>of</strong> irregular shape. Mitotic figures are usually infrequent (0-1 per high power<br />

field) but may be more numerous (up to 2-3 per high power field) in superficial than<br />

in deep areas <strong>of</strong> sarcoids and adjacent to areas <strong>of</strong> ulceration. Mitoses and<br />

fibroblastic nuclear pleomorphism, anisokaryosis and nucleolar enlargement may be<br />

observed in rapidly growing or recurrent sarcoids; cellular anaplasia is, however, rare.<br />

The fibroblasts are typically arrayed in tight whorls, interweaving bundles, haphazard<br />

tangles and occasionally herringbone and basket weave patterns, with a small to<br />

moderate amount <strong>of</strong> intercellular collagen. In recently developed sarcoids, the<br />

volume <strong>of</strong> intercellular collagen may be minimal. In chronic lesions, the collagen<br />

content increases and the dense fibres may appear hyalinised. Plump dermal<br />

fibroblasts usually directly abut the epidermis and, in a high percentage <strong>of</strong> sarcoids,<br />

are characteristically oriented perpendicular to the epidermal basement membrane in<br />

a picket-fence arrangement. Hair follicles enveloped by fibroblasts may undergo<br />

cystic dilation.<br />

Histological variants<br />

Prominent hyperplasia <strong>of</strong> the epidermis with formation <strong>of</strong> long rete pegs is not<br />

invariably present in sarcoids. It is usually observed in verrucous and mixed forms<br />

and at the margins <strong>of</strong> ulcerated areas in fibroblastic sarcoids. In occult sarcoids, the<br />

80<br />

ACVSC Proceedings Dermatology Chapter Science Week 2005

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