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Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma
Olfactory neuroblastomas, or esthesioneuroblastomas, are rare and aggressive malignant tumors that typically arise from the olfactory neuroepithelium in the upper nasal cavity. In rare instances, they can be ectopic originating from areas outside the upper nasal cavity such as the sellar region. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580437/ https://www.ncbi.nlm.nih.gov/pubmed/37908997 http://dx.doi.org/10.1210/jcemcr/luad081 |
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author | Seshan, Nandini Hanft, Simon Goswami, Gayotri Syal, Arjun |
author_facet | Seshan, Nandini Hanft, Simon Goswami, Gayotri Syal, Arjun |
author_sort | Seshan, Nandini |
collection | PubMed |
description | Olfactory neuroblastomas, or esthesioneuroblastomas, are rare and aggressive malignant tumors that typically arise from the olfactory neuroepithelium in the upper nasal cavity. In rare instances, they can be ectopic originating from areas outside the upper nasal cavity such as the sellar region. These tumors, also known as primary sellar neuroblastomas, may be mistaken for pituitary macroadenomas. We present a rare case of a primary sellar neuroblastoma in a 30-year-old woman with a prior diagnosis of presumed prolactinoma, status post transsphenoidal resection, with residual visual deficits, who presented with worsening vision and headaches. Pituitary magnetic resonance imaging showed a large sellar mass causing compression of the optic chiasm, and invasion of the right cavernous sinus and bilateral cavernous internal carotid arteries. The patient underwent a second transsphenoidal resection. Postoperatively, she developed central adrenal insufficiency, central hypothyroidism, central hypogonadism, and transient syndrome of inappropriate antidiuretic hormone secretion. Owing to rapid tumor regrowth, she underwent a craniotomy with plans for radiation treatment. This condition is challenging to diagnose and has poorly defined clinical management guidelines. An early, aggressive approach with surgical intervention is recommended. |
format | Online Article Text |
id | pubmed-10580437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105804372023-10-31 Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma Seshan, Nandini Hanft, Simon Goswami, Gayotri Syal, Arjun JCEM Case Rep Case Report Olfactory neuroblastomas, or esthesioneuroblastomas, are rare and aggressive malignant tumors that typically arise from the olfactory neuroepithelium in the upper nasal cavity. In rare instances, they can be ectopic originating from areas outside the upper nasal cavity such as the sellar region. These tumors, also known as primary sellar neuroblastomas, may be mistaken for pituitary macroadenomas. We present a rare case of a primary sellar neuroblastoma in a 30-year-old woman with a prior diagnosis of presumed prolactinoma, status post transsphenoidal resection, with residual visual deficits, who presented with worsening vision and headaches. Pituitary magnetic resonance imaging showed a large sellar mass causing compression of the optic chiasm, and invasion of the right cavernous sinus and bilateral cavernous internal carotid arteries. The patient underwent a second transsphenoidal resection. Postoperatively, she developed central adrenal insufficiency, central hypothyroidism, central hypogonadism, and transient syndrome of inappropriate antidiuretic hormone secretion. Owing to rapid tumor regrowth, she underwent a craniotomy with plans for radiation treatment. This condition is challenging to diagnose and has poorly defined clinical management guidelines. An early, aggressive approach with surgical intervention is recommended. Oxford University Press 2023-07-12 /pmc/articles/PMC10580437/ /pubmed/37908997 http://dx.doi.org/10.1210/jcemcr/luad081 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Seshan, Nandini Hanft, Simon Goswami, Gayotri Syal, Arjun Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma |
title | Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma |
title_full | Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma |
title_fullStr | Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma |
title_full_unstemmed | Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma |
title_short | Primary Sellar Neuroblastoma Masquerading as a Pituitary Macroadenoma |
title_sort | primary sellar neuroblastoma masquerading as a pituitary macroadenoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580437/ https://www.ncbi.nlm.nih.gov/pubmed/37908997 http://dx.doi.org/10.1210/jcemcr/luad081 |
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