S. Watanabe et al., TRICHOBLASTIC FIBROMA - A CASE-REPORT AND AN IMMUNOHISTOCHEMICAL STUDY OF CYTOKERATIN EXPRESSION, The American journal of dermatopathology, 18(3), 1996, pp. 308-313
A 47-year-old woman noticed a nodule on her right shoulder that had be
en gradually increasing in size without symptoms. Histologic features
of the biopsied nodule included round to irregularly shaped epithelial
lobules demarcated by abundant sclerotic stroma located within the lo
wer dermis and extending to the subcutis. The epithelial lobules consi
sted of cuboidal to columnar basaloid cells and were frequently arrang
ed in narrow strands with many bifurcations and branching. Cystic stru
ctures containing lamellar keratinous material were occasionally found
in connection with the lobules. The histologic findings were interpre
ted as trichoblastic fibroma. Immunohistochemical studies with antibod
ies directed against cytokeratins (CK) and involucrin revealed positiv
e staining in most of the tumor cells with RCK102 and 34 beta E12 anti
keratin antibodies, whereas the epithelial cords and the peripheral ce
lls of the cystic structures stained with 170.2.14, 4.1.18, and CAM 5.
2 antikeratin antibodies. However, CK1 or simple epithelial cytokerati
ns were not detected in any neoplastic elements, Based on comparative
immunohistochemical findings in normal hair follicles, we propose that
trichoblastic fibroma may first differentiate toward the outermost ce
ll layer of the outer root sheath between the lower permanent portion
and the upper transient portion and then into various other parts of t
he hair follicle.