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Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review

The diagnosis and management of the alteration of the normal function of the oculomotor nerve (third cranial nerve) varies depending on the characteristics of the paralysis, the age of the patient, and the associated symptoms and signs. Oculomotor nerve palsy may be caused by lesions located anywher...

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Autores principales: Pavel, Irina Andreea, Costea, Claudia Florida, Anton, Cătălin Constantin, Măriuţa, Ioana Roxana, Ciobanu Apostol, Delia Gabriela, Sava, Anca, Cucu, Andrei Ionuţ, Nicoară, Simona Delia, Turliuc, Mihaela Dana, Schmitzer, Speranța, Tănase, Daniela Maria, Scripcariu, Dragoş Viorel, Bogdănici, Camelia Margareta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926139/
https://www.ncbi.nlm.nih.gov/pubmed/36588497
http://dx.doi.org/10.47162/RJME.63.3.13
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author Pavel, Irina Andreea
Costea, Claudia Florida
Anton, Cătălin Constantin
Măriuţa, Ioana Roxana
Ciobanu Apostol, Delia Gabriela
Sava, Anca
Cucu, Andrei Ionuţ
Nicoară, Simona Delia
Turliuc, Mihaela Dana
Schmitzer, Speranța
Tănase, Daniela Maria
Scripcariu, Dragoş Viorel
Bogdănici, Camelia Margareta
author_facet Pavel, Irina Andreea
Costea, Claudia Florida
Anton, Cătălin Constantin
Măriuţa, Ioana Roxana
Ciobanu Apostol, Delia Gabriela
Sava, Anca
Cucu, Andrei Ionuţ
Nicoară, Simona Delia
Turliuc, Mihaela Dana
Schmitzer, Speranța
Tănase, Daniela Maria
Scripcariu, Dragoş Viorel
Bogdănici, Camelia Margareta
author_sort Pavel, Irina Andreea
collection PubMed
description The diagnosis and management of the alteration of the normal function of the oculomotor nerve (third cranial nerve) varies depending on the characteristics of the paralysis, the age of the patient, and the associated symptoms and signs. Oculomotor nerve palsy may be caused by lesions located anywhere from the oculomotor nucleus to the termination of the third nerve in the extraocular muscles. Although there have been significant advances in neuroimaging to facilitate early diagnosis, the management of a patient presenting with isolated oculomotor palsy is still challenging. This review tackles the case of a 52-year-old patient, with a history of pulmonary tuberculosis (at the age of five), referred to the Department of Ophthalmology, St. Spiridon Emergency Clinical Hospital, Iaşi, Romania. The patient had diplopia accompanied by right eyelid ptosis, symptoms that began suddenly 10 days before hospitalization. The clinical examination showed right eye grade II palpebral ptosis, exotropia with limitation of eyeball movements in adduction, supra-/infraduction. Biomicroscopic examination of the anterior pole revealed the presence of anisocoria and light-near dissociation on the affected side. Numerous investigations were performed to identify the cause, starting with tumoral markers, which were within normal limits. Magnetic resonance angiography (MRA) was performed, and posterior communicating artery aneurysm was ruled out. The endocrinology examination and hormonal laboratory tests were also within normal parameters. Due to suspicions of generalized tuberculosis raised by the infectious disease doctor or presence of secondary lesions, thoraco-abdomino-pelvic computed tomography (CT) scan with contrast agent was done and its findings required gastroenterological exploration. After various explorations, the certainty diagnosis was set by histopathological examination, which revealed gastric adenocarcinoma.
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spelling pubmed-99261392023-02-15 Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review Pavel, Irina Andreea Costea, Claudia Florida Anton, Cătălin Constantin Măriuţa, Ioana Roxana Ciobanu Apostol, Delia Gabriela Sava, Anca Cucu, Andrei Ionuţ Nicoară, Simona Delia Turliuc, Mihaela Dana Schmitzer, Speranța Tănase, Daniela Maria Scripcariu, Dragoş Viorel Bogdănici, Camelia Margareta Rom J Morphol Embryol Case Report The diagnosis and management of the alteration of the normal function of the oculomotor nerve (third cranial nerve) varies depending on the characteristics of the paralysis, the age of the patient, and the associated symptoms and signs. Oculomotor nerve palsy may be caused by lesions located anywhere from the oculomotor nucleus to the termination of the third nerve in the extraocular muscles. Although there have been significant advances in neuroimaging to facilitate early diagnosis, the management of a patient presenting with isolated oculomotor palsy is still challenging. This review tackles the case of a 52-year-old patient, with a history of pulmonary tuberculosis (at the age of five), referred to the Department of Ophthalmology, St. Spiridon Emergency Clinical Hospital, Iaşi, Romania. The patient had diplopia accompanied by right eyelid ptosis, symptoms that began suddenly 10 days before hospitalization. The clinical examination showed right eye grade II palpebral ptosis, exotropia with limitation of eyeball movements in adduction, supra-/infraduction. Biomicroscopic examination of the anterior pole revealed the presence of anisocoria and light-near dissociation on the affected side. Numerous investigations were performed to identify the cause, starting with tumoral markers, which were within normal limits. Magnetic resonance angiography (MRA) was performed, and posterior communicating artery aneurysm was ruled out. The endocrinology examination and hormonal laboratory tests were also within normal parameters. Due to suspicions of generalized tuberculosis raised by the infectious disease doctor or presence of secondary lesions, thoraco-abdomino-pelvic computed tomography (CT) scan with contrast agent was done and its findings required gastroenterological exploration. After various explorations, the certainty diagnosis was set by histopathological examination, which revealed gastric adenocarcinoma. Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2022 2022-09-30 /pmc/articles/PMC9926139/ /pubmed/36588497 http://dx.doi.org/10.47162/RJME.63.3.13 Text en Copyright © 2022, Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Case Report
Pavel, Irina Andreea
Costea, Claudia Florida
Anton, Cătălin Constantin
Măriuţa, Ioana Roxana
Ciobanu Apostol, Delia Gabriela
Sava, Anca
Cucu, Andrei Ionuţ
Nicoară, Simona Delia
Turliuc, Mihaela Dana
Schmitzer, Speranța
Tănase, Daniela Maria
Scripcariu, Dragoş Viorel
Bogdănici, Camelia Margareta
Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
title Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
title_full Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
title_fullStr Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
title_full_unstemmed Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
title_short Complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
title_sort complete oculomotor nerve palsy – first manifestation of gastric adenocarcinoma: clinical experience and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926139/
https://www.ncbi.nlm.nih.gov/pubmed/36588497
http://dx.doi.org/10.47162/RJME.63.3.13
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