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Myasthenia Gravis Presenting Like Guillain-Barré Syndrome

Authors :
Isha Misra
Frehiwot D. Temesgen
Noha Soleiman
Janaki Kalyanam
Mohankumar Kurukumbi
Source :
Case Reports in Neurology, Vol 4, Iss 3, Pp 137-143 (2012)
Publication Year :
2012
Publisher :
Karger Publishers, 2012.

Abstract

Myasthenia gravis (MG) is an autoimmune disorder characterized by weakness in specific muscle groups, especially the ocular and bulbar muscles. Guillain-Barré syndrome (GBS) presents with ascending paralysis and areflexia, often secondary to an infection. Several theories have been proposed regarding the etiology behind GBS, with many studies pointing to a possible autoimmune cause. If this is in fact true, it is also possible that the two diseases may develop concurrently. While this is unusual, several recently published studies highlight such cases of concurrent MG and GBS. This co-occurrence could involve certain common proteins, as the two diseases can present somewhat similarly. This is an unusual case of a patient with no significant past medical history, presenting with generalized weakness and symptoms of new-onset diabetes, who developed bilateral ptosis, distal weakness, and areflexia while in the hospital, raising the possibility of concurrent MG and GBS. Although the diagnosis of MG was confirmed by the positive anticholinesterase antibodies and tensilon test, several features, including sudden onset of ascending paralysis and areflexia, were more common in GBS than MG. It is possible, albeit rare, that these two syndromes could have developed concurrently and that the untreated diabetes mellitus could have contributed to the neurological symptoms. This case is reported because of the rarity of its features, diagnostic and management challenges.

Details

Language :
English
ISSN :
1662680X
Volume :
4
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Case Reports in Neurology
Publication Type :
Academic Journal
Accession number :
edsdoj.666481b0814b3ca12f8e091c991e61
Document Type :
article
Full Text :
https://doi.org/10.1159/000342448