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A Case Report of Feline Pituitary Carcinoma with Hypercortisolism

Feline pituitary tumors are rare. An 8-year-old male Japanese domestic cat presented with anorexia and emaciation. The cat died 17 days after admission from progressive neurological symptoms. At necropsy, a pituitary tumor measuring 25 × 18 × 15 mm was found. Microscopically, the tumor was divided i...

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Autores principales: KIMITSUKI, Kazunori, BOONSRIROJ, Hassadin, KOJIMA, Daisuke, PARK, Chun-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979955/
https://www.ncbi.nlm.nih.gov/pubmed/24025433
http://dx.doi.org/10.1292/jvms.13-0373
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author KIMITSUKI, Kazunori
BOONSRIROJ, Hassadin
KOJIMA, Daisuke
PARK, Chun-Ho
author_facet KIMITSUKI, Kazunori
BOONSRIROJ, Hassadin
KOJIMA, Daisuke
PARK, Chun-Ho
author_sort KIMITSUKI, Kazunori
collection PubMed
description Feline pituitary tumors are rare. An 8-year-old male Japanese domestic cat presented with anorexia and emaciation. The cat died 17 days after admission from progressive neurological symptoms. At necropsy, a pituitary tumor measuring 25 × 18 × 15 mm was found. Microscopically, the tumor was divided into multiple lobules and had grown invasively into the adjacent brain tissue and sphenoid bone. Tumor cells had pleomorphic nuclei with prominent centrally located nucleoli and abundant amphophilic polygonal cytoplasm. Immunohistochemically, the tumor cells stained with anti-adrenocorticotropic hormone (ACTH), α-melanin-stimulating hormone (MSH) and β-endorphin antibodies. Ultrastructurally, the cytoplasm of the tumor cells contained various sized secretory granules. Based on these pathological findings, this tumor was diagnosed as pituitary carcinoma originated from pars intermedia cells.
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spelling pubmed-39799552014-04-22 A Case Report of Feline Pituitary Carcinoma with Hypercortisolism KIMITSUKI, Kazunori BOONSRIROJ, Hassadin KOJIMA, Daisuke PARK, Chun-Ho J Vet Med Sci Pathology Feline pituitary tumors are rare. An 8-year-old male Japanese domestic cat presented with anorexia and emaciation. The cat died 17 days after admission from progressive neurological symptoms. At necropsy, a pituitary tumor measuring 25 × 18 × 15 mm was found. Microscopically, the tumor was divided into multiple lobules and had grown invasively into the adjacent brain tissue and sphenoid bone. Tumor cells had pleomorphic nuclei with prominent centrally located nucleoli and abundant amphophilic polygonal cytoplasm. Immunohistochemically, the tumor cells stained with anti-adrenocorticotropic hormone (ACTH), α-melanin-stimulating hormone (MSH) and β-endorphin antibodies. Ultrastructurally, the cytoplasm of the tumor cells contained various sized secretory granules. Based on these pathological findings, this tumor was diagnosed as pituitary carcinoma originated from pars intermedia cells. The Japanese Society of Veterinary Science 2013-09-10 2014-01 /pmc/articles/PMC3979955/ /pubmed/24025433 http://dx.doi.org/10.1292/jvms.13-0373 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Pathology
KIMITSUKI, Kazunori
BOONSRIROJ, Hassadin
KOJIMA, Daisuke
PARK, Chun-Ho
A Case Report of Feline Pituitary Carcinoma with Hypercortisolism
title A Case Report of Feline Pituitary Carcinoma with Hypercortisolism
title_full A Case Report of Feline Pituitary Carcinoma with Hypercortisolism
title_fullStr A Case Report of Feline Pituitary Carcinoma with Hypercortisolism
title_full_unstemmed A Case Report of Feline Pituitary Carcinoma with Hypercortisolism
title_short A Case Report of Feline Pituitary Carcinoma with Hypercortisolism
title_sort case report of feline pituitary carcinoma with hypercortisolism
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979955/
https://www.ncbi.nlm.nih.gov/pubmed/24025433
http://dx.doi.org/10.1292/jvms.13-0373
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