Feline cutaneous nerve sheath tumours: Histological features and immunohistochemical evaluations

• Published in: Research in veterinary science Vol. 95; no. 2; pp. 548 - 555
• Main Authors: Mandara, M.T., Fabriani, E., Pavone, S., Pumarola, M.
• Format: Journal Article
• Language: English
• Published: England Elsevier India Pvt Ltd 01.10.2013; Elsevier Limited
• Subjects: Animals; Cat; Cat Diseases - pathology; Cats; Collagen; Cutaneous tumour; cytoplasm; Female; giant cells; Immunohistochemistry; Immunohistochemistry - veterinary; laminin; Male; Medical research; metaplasia; necrosis; neoplasms; Nerve Sheath Neoplasms - pathology; Nerve Sheath Neoplasms - veterinary; nerve tissue; Peripheral nerve sheath tumour; Skin Neoplasms - pathology; Skin Neoplasms - veterinary; Tissue Fixation; Tumors; Veterinary medicine; vimentin; Immunohistochemistry; Cutaneous tumour; Peripheral nerve sheath tumour; Cat
• ISSN: 0034-5288; 1532-2661
• DOI: 10.1016/j.rvsc.2013.04.009

Feline cutaneous nerve sheath tumours (CNSTs) are uncommonly reported in the skin, since they are underestimated relative to the more common spindle cell tumours of soft tissue. In this study, 26 nerve sheath tumours selected from 337 skin neoplasms of cats were examined. Histologically, they were classified into malignant (MPNSTs) and benign tumours (BPNSTs) based on degree of cellular atypia and polymorphism as well as mitotic rate and diffuse necrosis. CPNSTs were tipically characterised by Antoni A pattern, in some cases associated with Antoni B pattern. In the malignant peripheral nerve sheath tumours (MPNSTs) the polymorphism was marked, while it was mild to moderate in the benign forms (BPNSTs). In the MPNSTs the mitotic activity was generally higher than in the BPNSTs. In five cases, including three MPNSTs and two BPNSTs, there were multinucleated giant cells. Necrotic foci occurred in a BPNST and in two MPNSTs, while osseous/chondroid metaplasia was found in two cases. Immunohistochemically, all the tumours showed a marked diffuse vimentin expression. S-100 protein was expressed in 17 cases, including 81.8% of BPNSTs and 57.14% of MPNSTs. Twenty-five tumours expressed NSE and twenty-four cases showed immunoreaction for laminin. Thirteen tumours were positive for GFAP, while five tumours were positive for SMA. PGP 9.5 expression was detected in all cases, except for two MPNSTs. NGFR was expressed in eleven cases, including four MPNSTs and seven BPNSTs. Ki67 was expressed in twenty tumours without any relationship with morphologic malignancy of the neoplasm. In this case series we confirmed neoplastic spindloid cells with wavy cytoplasm arranged in compact areas, with occasional nuclear palisading or whirls, and interchanged with loosely arranged areas, as the morphological features supporting a diagnosis of CPNST. A constant concurrent expression of vimentin, NSE, and laminin might confirm the diagnosis of PNST in the absence of clear S-100 protein positivity, especially in the malignant forms. In this study, conclusive data were not obtained on the diagnostic relevance of NGFR- and PGP 9.5-expression in feline CPNSTs.