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Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report
INTRODUCTION: The association of thymoma with myasthenia gravis (MG) is well known. Thymoma with sarcoidosis however, is very rare. We presented an interesting case with coexisting thymoma, MG and sarcoidosis. CASE PRESENTATION: A 59-year-old female patient with a history of sarcoidosis was admitted...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2500026/ https://www.ncbi.nlm.nih.gov/pubmed/18652699 http://dx.doi.org/10.1186/1752-1947-2-245 |
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author | Kurukumbi, Mohankumar Weir, Roger L Kalyanam, Janaki Nasim, Mansoor Jayam-Trouth, Annapurni |
author_facet | Kurukumbi, Mohankumar Weir, Roger L Kalyanam, Janaki Nasim, Mansoor Jayam-Trouth, Annapurni |
author_sort | Kurukumbi, Mohankumar |
collection | PubMed |
description | INTRODUCTION: The association of thymoma with myasthenia gravis (MG) is well known. Thymoma with sarcoidosis however, is very rare. We presented an interesting case with coexisting thymoma, MG and sarcoidosis. CASE PRESENTATION: A 59-year-old female patient with a history of sarcoidosis was admitted to the hospital with a one-day history of sudden onset of right-sided partial ptosis and diplopia. Neurosarcoidosis with cranial nerve involvement was considered, but was ruled out by the clinical findings, and MG was confirmed by the positive tensilon test, electrophysiological findings and positive acetylcholine receptor binding antibodies. On further evaluation, a CT chest scan showed a left anterior mediastinal mass and bilateral lymphadenopathy. Post surgical diagnosis confirmed the thymoma and sarcoidosis in the lymph nodes. CONCLUSION: When two or more diseases of undetermined origin are found together, several interesting questions are raised. It is important to first confirm the diagnoses individually. Immunologic mechanisms triggering the occurrence of these diagnoses together, are difficult to address. Although the coexistence of thymoma, MG and sarcoidosis may be coincidental, it is noteworthy to report this case because of the multiple interesting features observed as well as the rarity of occurrence. |
format | Text |
id | pubmed-2500026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25000262008-08-07 Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report Kurukumbi, Mohankumar Weir, Roger L Kalyanam, Janaki Nasim, Mansoor Jayam-Trouth, Annapurni J Med Case Reports Case Report INTRODUCTION: The association of thymoma with myasthenia gravis (MG) is well known. Thymoma with sarcoidosis however, is very rare. We presented an interesting case with coexisting thymoma, MG and sarcoidosis. CASE PRESENTATION: A 59-year-old female patient with a history of sarcoidosis was admitted to the hospital with a one-day history of sudden onset of right-sided partial ptosis and diplopia. Neurosarcoidosis with cranial nerve involvement was considered, but was ruled out by the clinical findings, and MG was confirmed by the positive tensilon test, electrophysiological findings and positive acetylcholine receptor binding antibodies. On further evaluation, a CT chest scan showed a left anterior mediastinal mass and bilateral lymphadenopathy. Post surgical diagnosis confirmed the thymoma and sarcoidosis in the lymph nodes. CONCLUSION: When two or more diseases of undetermined origin are found together, several interesting questions are raised. It is important to first confirm the diagnoses individually. Immunologic mechanisms triggering the occurrence of these diagnoses together, are difficult to address. Although the coexistence of thymoma, MG and sarcoidosis may be coincidental, it is noteworthy to report this case because of the multiple interesting features observed as well as the rarity of occurrence. BioMed Central 2008-07-25 /pmc/articles/PMC2500026/ /pubmed/18652699 http://dx.doi.org/10.1186/1752-1947-2-245 Text en Copyright © 2008 Kurukumbi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kurukumbi, Mohankumar Weir, Roger L Kalyanam, Janaki Nasim, Mansoor Jayam-Trouth, Annapurni Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
title | Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
title_full | Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
title_fullStr | Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
title_full_unstemmed | Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
title_short | Rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
title_sort | rare association of thymoma, myasthenia gravis and sarcoidosis : a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2500026/ https://www.ncbi.nlm.nih.gov/pubmed/18652699 http://dx.doi.org/10.1186/1752-1947-2-245 |
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