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Epithelioid pituicytoma: An unusual case report
BACKGROUND: Pituicytomas are considered World Health Organization Grade I malignancies. Until September 2017, a total of 81 cases of pituicytomas were diagnosed and described in literature. We present such a case in which histopathology shows an epithelioid pattern, a rare variant of pituicytoma. As...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069369/ https://www.ncbi.nlm.nih.gov/pubmed/30105139 http://dx.doi.org/10.4103/sni.sni_319_17 |
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author | Vellutini, Eduardo de Arnaldo Silva Becker, Pedro Henrique Petit Godoy, Luis Felipe Guerreiro, Nicolau Faria Correia Mattedi, Romulo Loss de de Oliveira, Matheus Fernandes |
author_facet | Vellutini, Eduardo de Arnaldo Silva Becker, Pedro Henrique Petit Godoy, Luis Felipe Guerreiro, Nicolau Faria Correia Mattedi, Romulo Loss de de Oliveira, Matheus Fernandes |
author_sort | Vellutini, Eduardo de Arnaldo Silva |
collection | PubMed |
description | BACKGROUND: Pituicytomas are considered World Health Organization Grade I malignancies. Until September 2017, a total of 81 cases of pituicytomas were diagnosed and described in literature. We present such a case in which histopathology shows an epithelioid pattern, a rare variant of pituicytoma. As far as we know, this is only the second such case described in the literature. CASE DESCRIPTION: A 61-year-old male patient presented with complaints of progressive decrease in visual acuity for about 7 months, worse on the left side. Laboratory and endocrinological investigation returned normal values. Magnetic resonance imaging revealed a mixed solid-cystic lesion, measuring about 3.1 × 2.2 × 2.9 cm. The lesion presented with intermediate signal intensity in T1 and T2 sequences and showed avid postcontrast enhancement. The patient underwent resection through a left pterional approach. Pathology revealed a glial neoplasm with an epithelioid pattern and moderate cellularity with rounded-elongated cell nuclei and with a broad eosinophilic cytoplasm. Absence of cellular pleomorphism, any mitotic figures, or areas of necrosis was noted. CONCLUSION: The epithelioid variant of pituicytomas differs from the commonly encountered forms of this tumor which typically present in a fascicular pattern. Microsurgical resection is the treatment of choice. However, in many cases, subtotal resection was performed because of a considerable risk for neurovascular injuries. |
format | Online Article Text |
id | pubmed-6069369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60693692018-08-13 Epithelioid pituicytoma: An unusual case report Vellutini, Eduardo de Arnaldo Silva Becker, Pedro Henrique Petit Godoy, Luis Felipe Guerreiro, Nicolau Faria Correia Mattedi, Romulo Loss de de Oliveira, Matheus Fernandes Surg Neurol Int Neuro-Oncology: Case Report BACKGROUND: Pituicytomas are considered World Health Organization Grade I malignancies. Until September 2017, a total of 81 cases of pituicytomas were diagnosed and described in literature. We present such a case in which histopathology shows an epithelioid pattern, a rare variant of pituicytoma. As far as we know, this is only the second such case described in the literature. CASE DESCRIPTION: A 61-year-old male patient presented with complaints of progressive decrease in visual acuity for about 7 months, worse on the left side. Laboratory and endocrinological investigation returned normal values. Magnetic resonance imaging revealed a mixed solid-cystic lesion, measuring about 3.1 × 2.2 × 2.9 cm. The lesion presented with intermediate signal intensity in T1 and T2 sequences and showed avid postcontrast enhancement. The patient underwent resection through a left pterional approach. Pathology revealed a glial neoplasm with an epithelioid pattern and moderate cellularity with rounded-elongated cell nuclei and with a broad eosinophilic cytoplasm. Absence of cellular pleomorphism, any mitotic figures, or areas of necrosis was noted. CONCLUSION: The epithelioid variant of pituicytomas differs from the commonly encountered forms of this tumor which typically present in a fascicular pattern. Microsurgical resection is the treatment of choice. However, in many cases, subtotal resection was performed because of a considerable risk for neurovascular injuries. Medknow Publications & Media Pvt Ltd 2018-07-24 /pmc/articles/PMC6069369/ /pubmed/30105139 http://dx.doi.org/10.4103/sni.sni_319_17 Text en Copyright: © 2018 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Neuro-Oncology: Case Report Vellutini, Eduardo de Arnaldo Silva Becker, Pedro Henrique Petit Godoy, Luis Felipe Guerreiro, Nicolau Faria Correia Mattedi, Romulo Loss de de Oliveira, Matheus Fernandes Epithelioid pituicytoma: An unusual case report |
title | Epithelioid pituicytoma: An unusual case report |
title_full | Epithelioid pituicytoma: An unusual case report |
title_fullStr | Epithelioid pituicytoma: An unusual case report |
title_full_unstemmed | Epithelioid pituicytoma: An unusual case report |
title_short | Epithelioid pituicytoma: An unusual case report |
title_sort | epithelioid pituicytoma: an unusual case report |
topic | Neuro-Oncology: Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069369/ https://www.ncbi.nlm.nih.gov/pubmed/30105139 http://dx.doi.org/10.4103/sni.sni_319_17 |
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