Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
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408<br />
Fig. 1. Extensive erythematous plaque lesion, 7x5cm sized, with verrucous<br />
and hyperkeratotic surface, centrally ulcerated, sharp margins<br />
and slightly infiltrated. (insert: slightly elevated brownish reddish<br />
tumour with an erosive surface. H&E 4X).<br />
Fig. 2. at the periphery of the tumours anastomosing lobules of small<br />
uniform cuboidal poroid cells with focal ductal structures (intracitoplasmic<br />
lumina formation) had proliferated in the upper third of the<br />
dermis (h&E 10X).<br />
Fig. 3. the poroma component consisted of atypical cuboidal cells<br />
with oval nuclei, scant cytoplasm, intercellular bridges and small<br />
round ductal structures (h&E 20X).<br />
CONGRESSO aNNualE di aNatOmia patOlOGiCa SiapEC – iap • fiRENzE, 25-<strong>27</strong> OttOBRE <strong>2012</strong><br />
ponent consisted of atypical cuboidal cells with oval nuclei, scant<br />
cytoplasm, intercellular bridges and small round ductal structures<br />
(Fig. 3). The ductal component is constituted by ducts with lumina<br />
of variable size, lined by cells with intensely cuticular eosinophilic<br />
cytoplasm. “Decapitation” secretion was evident with<br />
intraluminal amorphous eosinophilic material (Fig. 4). Clear cell<br />
change was found and consisted of ample cytoplasm, hiperchromatic,<br />
irregular nuclei. These cells contained abundant amount of<br />
glycogen (Fig. 5). Focal sebaceous and follicular differentiation<br />
was present (Fig. 6). The comedonecrosis island of tumour cells<br />
contained central areas of neoplastic cell death with inflammatory<br />
debris (Fig. 7). Lymphovascular invasion was absent. Distinct<br />
neovascularization and an infiltrate of inflammatory cells could<br />
be seen all around the tumour.<br />
Discussion. Benign cutaneous appendage tumours are common<br />
and it is surprising that their malignant counterparts are exceedingly<br />
rare. Traditionally poroid neoplasms have been classified<br />
as eccrine tumours, relating to the intraepidermal eccrine coil<br />
epithelium. Poroid neoplasms may show different differentiation,<br />
reflecting the embryological association of follicular sebaceous<br />
and ductal structures (folliculosebaceous apocrine units). In<br />
1963 Pinkus and Mehregan 2 described the first case of eccrine<br />
Fig. 4. “decapitation” secretion was evident with intraluminal amorphous<br />
eosinophilic material (H&E 20X).<br />
Fig. 5. the neoplastic cells contained glycogen (H&E 10X).