Cutaneous
lymphadenoma is a rare tumour with distinctive histologic features. This
entity was originally described as lymphoepithelial tumour of the skin by Santa Cruz
and Barr in 1987. It was renamed cutaneous lymphadenoma in 1991.Cutaneous
lymphadenoma.Am
J Surg Pathol. 1991
Feb;15(2):101-10.
Ackerman et al considered that cutaneous lymphadenoma is a
variant of trichoblastoma
("adamantinoid trichoblastoma").
Clinical presentation:
A
single, small, non-ulcerated, dome-shaped, flesh-colored,
well-circumscribed, slowly enlarging nodule. The lesion has usually been
present for many months or years.
Age & sex:
Usually between 21 and 75
years without a sex predominance.
Site:
Face and
scalp regions or legs.
Microscopic features:
Multiple rounded islands
or nests of epithelial cells ;
Tumour lobules consist
of an outer rim of palisading basaloid cells surrounding a central zone
of large cells with clear cytoplasm and large vesicular cells
; Dense
infiltrate of small, mature lymphocytes within the islands ; Tumour
lobules embedded in a loose-to-dense fibrous stroma
; Few scattered lymphocytes in the stroma
; Focal follicular differentiation and sometimes sebaceous
differentiation; Focal mucinosis, osteoma
formation or prominent sweat gland duct component in some cases ;
Central keratinization
in some lobules.
Immunohistochemistry:
Clear epithelial cells in
the lobules and the basaloid peripheral cells:
Cytokeratin positive.
Lymphoid component reacted
with common leukocyte
antigen (CLA) and
T-cell markers (UCHL-1, CD3).
Some
CD30+
large clear cells may be
present. Many large epithelial cells in the lobules and some
dendritic cells in the stroma :
S-100 positive.
Differential diagnosis:
Clear cell syringoma ; clear cell basal
cell carcinoma ; lymphoepithelioma-like carcinoma of
skin.
Article
Cutaneous lymphadenoma
does not tend to recur after surgical excision. Image
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