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Choroid plexus carcinoma in a cow

Carcinoma de plexo coróide em um bovino

Abstracts

A red, firm 3.5x3.0x3.0cm mass was found within the right lateral ventricle, compressing the hippocampus and thalamus of the brain of a 4-year-old cow. The pituitary was enlarged and firm. Histologically, both the brain and pituitary masses consisted of moderately pleomorphic epithelial cells arranged as rosettes or sheets supported by a delicate fibrovascular stroma. Based on anatomical localization, histopathological and immunohistochemical findings, a diagnosis of choroid plexus carcinoma with pituitary metastasis was made.

cattle diseases; neoplasms; neuropathology


Um massa vermelha e firme de 3,5x3,0x3,0cm foi observada no ventrículo lateral, comprimindo o hipocampo e tálamo do cérebro de uma vaca de quatro anos de idade. A pituitária estava aumentada de volume e firme. Histologicamente, tanto a massa do cérebro, quanto da pituitária, consistiam de células epiteliais moderadamente pleomórficas, arranjadas em rosetas ou cordões e apoiadas em um delicado estroma fibrovascular. Com base na localização anatômica e nos achados histopatológicos e imuno-histoquímicos, foi realizado um diagnóstico de carcinoma de plexo coróide com metástase para a pituitária.

doenças de bovinos; neoplasmas; neuropatologia


NOTE

PATOLOGY

Choroid plexus carcinoma in a cow

Carcinoma de plexo coróide em um bovino

Fabiano José Ferreira de Sant'AnaI; Adriane Loy GabrielI; Glaucia Denise KommersII; Claudio Severo Lombardo de BarrosII,1 1 Autor para correspondência.

IPrograma de Pós-graduação em Medicina Veterinária, área de concentração em Patologia Veterinária, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brasil

IILaboratório de Patologia Veterinária, Departamento de Patologia, UFSM, 97105-900, Santa Maria, RS, Brasil. E-mail: claudioslbarros@uol.om.br

ABSTRACT

A red, firm 3.5x3.0x3.0cm mass was found within the right lateral ventricle, compressing the hippocampus and thalamus of the brain of a 4-year-old cow. The pituitary was enlarged and firm. Histologically, both the brain and pituitary masses consisted of moderately pleomorphic epithelial cells arranged as rosettes or sheets supported by a delicate fibrovascular stroma. Based on anatomical localization, histopathological and immunohistochemical findings, a diagnosis of choroid plexus carcinoma with pituitary metastasis was made.

Key words: cattle diseases, neoplasms, neuropathology.

RESUMO

Um massa vermelha e firme de 3,5x3,0x3,0cm foi observada no ventrículo lateral, comprimindo o hipocampo e tálamo do cérebro de uma vaca de quatro anos de idade. A pituitária estava aumentada de volume e firme. Histologicamente, tanto a massa do cérebro, quanto da pituitária, consistiam de células epiteliais moderadamente pleomórficas, arranjadas em rosetas ou cordões e apoiadas em um delicado estroma fibrovascular. Com base na localização anatômica e nos achados histopatológicos e imuno-histoquímicos, foi realizado um diagnóstico de carcinoma de plexo coróide com metástase para a pituitária.

Palavras-chave: doenças de bovinos, neoplasmas, neuropatologia.

Central nervous system (CNS) tumors are infrequently described in cattle (SANCHES et al., 2000; BARROS et al., 2006). According to cellular differentiation, number of mitosis and local invasion, choroid plexus neoplasms can be classified as choroid plexus papillomas or carcinomas (KOESTNER et al., 1999). In dogs, these tumors affect especially middle-aged male animals (RIBAS et al., 1989; SUMMERS et al., 1995) and occur adjacent to or within ventricular cavities (ZAKI & NAFE, 1980; WESTWORTH et al., 2008). In humans, the choroid plexus neoplasms occur more frequently in the lateral ventricles, mainly in children (PENCALET et al., 1998). Choroid plexus carcinomas (CPC) are rare neoplasms in all species and are distinguished from papillomas based on cellular pleomorfism, nuclear atypia, high mitotic rate, local invasion and metastases (KOESTNER & HIGGINS, 2002). The current paper describes the clinical, pathological and immunohistochemical findings of a case of CPC in a cow.

A 4-year-old cow had a history of anorexia, weight loss, uncoordinated gait and corneal opacity of unknown duration. It was found in sternal recumbency within a shallow pond and remained in this position until death. The fresh whole brain and a tissue block formed by the Gasserian ganglia, carotid rete mirabile and pituitary gland were submitted for histopathological evaluation. The right telencephalic hemisphere was slightly larger than the left. The whole 10% formalin fixed brain was sectioned at 1cm interval and both sides of each section were evaluated grossly. A red, firm 3.5x3.0x3.0cm mass was found within the right lateral ventricle compressing the hippocampus and thalamus (Figure 1A). The pituitary was enlarged (2.5x 2.0x2.0cm), firm and its cut surface was pale brown with small yellowish areas.



Samples from the brain and pituitary were processed by routine methods for histopathological evaluation. Sections were stained with hematoxylin and eosin and immunohistochemistry (IHC) using streptavidin-biotin-peroxidase complexa and 3,3-diaminobenzidinb. For IHC the following antibodies were applied in proper dilutions on the tumor sections: anti-vimentinc (monoclonal, 1:100), anti-glial fibrillary acidic protein (GFAP)c (polyclonal, 1:1.000) and anti-bovine pancytokeratin (polyclonal, 1:500)c. IHC sections were counterstained with Harris hematoxylin. Positive controls for IHC consisted of normal brain tissue including choroid plexus. For negative controls, the primary antibodies were replaced with PBS.

Microscopically, the brain mass consisted of moderately pleomorphic epithelial cells that were arranged as rosettes or sheets supported by a delicate fibrovascular stroma. The cells were columnar, ciliated and exhibited eosinophilic cytoplasm and hipochromatic, oval to round nuclei, localized in the basal domain of the cell, with 2-5 prominent nucleoli. Two to four mitoses per high power field were observed. Numerous and extensive areas of necrosis with hemorrhage were frequent (Figure 1B). In the pituitary an histologically similar markedly invasive neoplasm was observed (Figure 1C). On IHC evaluation of the brain and pituitary neoplasms a moderate multifocal labeling for pancytokeratin mainly in the apical domain of the cell was observed (Figure 1D). There was no labeling for vimentin and GFAP. The labeling for GFAP and pancytokeratin was positive in brain tissue used as control. On the basis of location, histopathological and immunohistochemical findings, a diagnosis of CPC was made.

Clinic signs for cattle with neoplasms of the choroid plexus depend on the anatomical location of the tumor and the resultant compression on adjacent structures. Circling and head tilt to the right side, and ataxia were observed in a case of plexus papilloma of fourth ventricle in a bovine (YAMADA et al., 1998) and progressive ataxia, ventromedial strabismus and hyperaesthesia were reported in a cow with choroid plexus papilloma of the third ventricle (HOENERHOFF et al., 2006). In the present case, the affected cow presented anorexia, weight loss, incoordination and corneal opacity.

Features such as high mitotic rate, marked necrosis, nuclear atypia and solid growth are considered as malignancy indicators for choroid plexus neoplasms (RIBAS et al., 1989; KOESTNER & HIGGINS, 2002). Metastasis and invasion along the neuraxis should be used as diagnostic criterion for malignancy of choroid plexus neoplasms (KOESTNER et al., 1999). In dogs, this neoplasm metastatize frequently within the ventricular spaces or the meninges (CANTILE et al., 2002). In the present case, high mitotic index, marked cellular pleomorfism, extensive areas of necrosis and hemorrhage and the occurrence of tumor cells in the pituitary similar to those found in the brain tumor were considered critical in favoring the diagnosis of CPC. The pituitary neoplasm was considered metastasis from the CPC, based on the similar cellular features and lack of anatomical continuity between the pituitary and the brain tumor. CPC may spread along cerebrospinal fluid pathways (SHORTRIDGE, 1971; KOESTNER & HIGGINS, 2002). In these case, no secondary tumor implantation was not observed in any locus along the ventricular system and metastasis could be explained by embolic dissemination.

The differential diagnosis between CPC and papillary ependymoma may be difficult since some histological features of both neoplasms are similar (RIBAS et al., 1989; KOESTNER & HIGGINS, 2002) which is not since choroid plexus epithelial cells are modified ependymal cells (DELLMANN & EURELL, 1998). Choroid plexus tumors however have a fibrovascular stroma, while ependymomas possess a fibrillar, non-collagenous background (RIBAS et al., 1989). IHC is the most reliable diagnostic criterion to set apart these two neoplasms. Tumor cells of choroid plexus tumors express cytokeratin while ependymoma cells will express GFAP and vimentin (KOESTNER & HIGGINS, 2002). Many reports mention the absence cytokeratin immunoreactivity in ependymomas from humans and animals (MIETTINEN et al., 1986; KANEKO et al., 1990; CARRIGAN et al., 1996; KOESTNER & HIGGINS, 2002; VURAL et al., 2006). Usually choroid plexus tumors in humans express cytokeratin, vimentin to a lesser extent, and rarely GFAP. The expression of these same markers in similar tumors from dogs have been described as variable (WILSON et al., 1989; CANTILE et al., 2002).

In the present report, a rare case of choroid plexus carcinoma in a cow is described. The immunohistochemical evaluation was essential in confirming the diagnosis.

SOURCES AND MANUFACTURERS

a-Streptavidin-biotin-peroxidase complex, Dako, Carpinteria, California, United States of America (USA).

b-3,3-diaminobenzidin, Sigma Chemical Co., St. Louis, Missouri, USA.

c-Anti-vimentin, anti-glial fibrillary acidic protein (GFAP), and anti-bovine pancytokeratin, Dako, Carpinteria, California, USA.

Received 02.09.09

Approved 06.10.09

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  • 1
    Autor para correspondência.
  • Publication Dates

    • Publication in this collection
      31 July 2009
    • Date of issue
      Oct 2009

    History

    • Received
      09 Feb 2009
    • Accepted
      10 June 2009
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