Ependymomas as primary
central nervous system neoplasms are occasionally observed in human infants
however; they are rare in animals. A three-year-old male goat was presented
with clinical neurological signs. At necropsy, a 3×2×2 cm, bulging, white-grey-
to red, soft mass extending into the left lateral ventricle of brain was
observed. Microscopically, the mass with densely cellular population was
nonencapsulated, mostly containing cuboidal-columnar neoplastic cells with
pseudo-rosettes formation. Mitotic figures were rare and malignancy indexes
were not observed. Neoplastic cells were immunohistochemically positive for Glial
Fibrillary Acidic Protein (GFAP), S-100, and vimentin; however, they did not
express Cytokeratins. On the basis of the location, histologic and
immunohistochemical findings, the tumor was diagnosed as an ependymoma.
Ependymomas as primary
central nervous system neoplasms are occasionally observed in human infants
however; they are rare in animals. A three-year-old male goat was presented
with clinical neurological signs. At necropsy, a 3×2×2 cm, bulging, white-grey-
to red, soft mass extending into the left lateral ventricle of brain was
observed. Microscopically, the mass with densely cellular population was
nonencapsulated, mostly containing cuboidal-columnar neoplastic cells with
pseudo-rosettes formation. Mitotic figures were rare and malignancy indexes
were not observed. Neoplastic cells were immunohistochemically positive for Glial
Fibrillary Acidic Protein (GFAP), S-100, and vimentin; however, they did not
express Cytokeratins. On the basis of the location, histologic and
immunohistochemical findings, the tumor was diagnosed as an ependymoma.
Konular | Sağlık Kurumları Yönetimi |
---|---|
Bölüm | Olgu Sunumu |
Yazarlar | |
Yayımlanma Tarihi | 1 Ocak 2017 |
Yayımlandığı Sayı | Yıl 2017 Cilt: 43 Sayı: 1 |