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In1969, Clark and Mihm described and correlated the clinical and
histological findings in lentigo maligna and lentigo maligna melanoma
and differentiated lentigo maligna melanoma from superficial spreading
melanoma and melanocytic naevi.
Lentigo maligna
melanoma most frequently occurs on the sun-exposed face and upper
extremities of elderly people.
Lentigo maligna
is the precursor lesion and is characterized by an irregular pigmented
macule which expands slowly . The invasive malignant tumour grossly
presents as a raised plaque or a discrete nodule.
Histologically, there
is proliferation of atypical melanocytes singly and in nests along the
basal layer of the epidermis. The atypical cells are small with
prominent nucleoli and characteristic pericellular halo due to fixation
artifact. Multinucleate cells with dendritic processes are often
present. The melanocytes grow along the upper portion of hair follicle
and extends to the level of sebaceous gland duct. There is often
epidermal atrophy.
The dermal
component may be composed of spindle or epithelioid cells. In some
cases, numerous mitotic figures may be present. The superficial dermis
often shows prominent solar elastosis together with scattered pigment
containing macrophages. Patchy inflammation and fibrosis may be noted in
the upper dermis associated with invasion into superficial dermis.
Lentigo maligna
and lentigo maligna melanoma may clinically resemble other pigmented
lesions such as solar lentigo or a superficial malignant melanoma.
Rarely, amelanotic lentigo maligna may resemble dermatitis or Bowen's
disease.
Histologically,
it may be difficult to outline the lateral borders of the lesion as the
scar damaged skin may have an increased number of melanocytes and may
have occasional atypical melanocytes in the basal layer. Often actinic
keratosis and lentigo maligna co-exist. Atypical keratinocytes in
actinic keratosis may cause further problem in making histological
diagnosis.
It may be
difficult to identify the microinvasive foci even after multiple
levels. Spindled melanocytes may resemble fibrohistiocytic cells and be
obscured by inflammatory cells and heavily pigmented melanophages.
These cells may be highlighted by S100 protein and HMB45 immunostains.
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