Myastheniform syndrome secondary to thymoma. Case report
Keywords:
Muscle weakness, Mediastinoscopy, Myasthenia gravis, TimomaAbstract
Introduction: thymoma represents approximately 20 % of mediastinal neoplasms. This tumor is relatively uncommon in the general population, and its study is of great importance due to its paraneoplastic manifestations; like the case in question (myastheniform syndrome). The majority of patients with thymoma are between 40 and 60 years of age, highlighting the novelty of this case with diagnosis at an early age. There are no known risk factors, although there is a strong association with myasthenia gravis and other paraneoplastic syndromes. Myasthenia gravis is the most common disorder associated with thymoma.
Objective: to describe the case of a young man with myastheniform syndrome secondary to a thymoma at the Military Hospital of Matanzas.
Case presentation: 18-year-old male patient with a history of health, who comes to the consultation because, after pharyngotonsillitis, he presents with difficulty swallowing, easy fatigue, with decreased muscle strength, with marked signs of weakness, upon physical examination neurological system, responds to the interrogation with a hidden voice "Positive" Barré and Minganzini maneuver towards the left upper limb and right lower limb. Left patellar osteotendinous hyporeflexia. Babinski and positive substitutes in lower limbs. Left orbicularis paralysis and presence of bilateral horizontal nystagmus. He is diagnosed with a myastheniform syndrome, the cause being detected as the presence of a thymoma by chest tomography. Thymectomy is performed and the patient's recovery is evident.
Conclusions: myastheniform syndrome as a form of presentation of a thymoma is rare at an early age, so a timely diagnosis favors the recovery of these patients.
Downloads
References
2. Solana López I, Izquierdo Martínez A, Losada Vila B. El síndrome de Eaton Lambert: una presentación clínica inusual que suele preceder al diagnóstico oncológico. Rev Clin Med Fam [Internet]. 2022 [citado 2024 Jun 28]; 15(1): 60-62. Disponible en: https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1699-695X2022000100012
3. García Estévez DA. Prevalence of myasthenia gravis in Colombia. Reply. Rev Neurol. [Internet] 2023 [citado 11/06/2024]; 76(07):247-248. Disponible en: https://neurologia.com/articulo/2023078/eng
4. Milanés Armengol AR, Molina Castellanos K, Pino Mas J, Milanés Molina M, Ojeda Leal ÁM. Una mirada actual a la miastenia gravis. Medir [Internet]. 2020 [citado 11/06/2024]; 18(5):907-918. Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1727-897X2020000500907&lng=es.%20%20Epub%2002-Oct-2020.
5. Cabrera Maqueda JM, Alba Isasi MT, Hernández R, Arroyo Tristán A, Morales Ortiz A. Timectomía en miastenia grave timomatosa y no timomatosa: análisis de una cohorte de 46 pacientes. Rev Neurol. [Internet] 2020 [citado 11/06/2024]; 70(06):213-219. Disponible en: https://neurologia.com/articulo/2019411
6. Rojas Marcos I. Protocolo diagnóstico de la debilidad muscular. Medicine-Programa de Formación Médica Continuada Acreditado 2019;12(76):4515-20.
7. Santiago Cortés E, Cortés Durán PM, Bedoya MJ, Terrón Barbosa R, Innerarity Martínez J. Miastenia gravis de rápida instauración. Rev Clin Med Fam [Internet]. 2021 [citado 11/06/2024]; 14(1):28-30. Disponible en: https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1699-695X2021000100028&lang=es
8. Aguirre F, Villa AM. Miastenia gravis: Registro de 190 casos en un centro único. Medicina (B. Aires) [Internet]. 2020 Feb [citado 11/06/2024]; 80(1): 10-16. Disponible en: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802020000100002&lng=es.
9. PadiNa Londoño N, Martínez Ruiz D, Sánchez Álvaro J., Velásquez M. Descripción de las características clínicas y la respuesta a tratamiento en pacientes con miastenia grave sin timoma sometidos a timectomía en una institución de alta complejidad de Cali, Colombia, 2010-2017. rev. colomb. cir. [Internet]. 2020 [citado 11/06/2024]; 35(3):391-397. Disponible en: http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S2011-75822020000300391&lng=en
Downloads
Published
How to Cite
Issue
Section
License
Those authors who have publications with this journal accept the following terms: The authors will retain their copyright and guarantee the journal the right of first publication of their work, which will be simultaneously subject to the Recognition License. Creative Commons that allows third parties to share the work as long as its author and its first publication in this magazine are indicated. Authors may adopt other non-exclusive license agreements for the distribution of the published version of the work (e.g.: deposit it in an institutional telematic archive or publish it in a monographic volume) as long as the initial publication in this journal is indicated. Authors are allowed and recommended to disseminate their work through the Internet (e.g.: in institutional telematic archives or on your website) before and during the submission process, which can produce interesting exchanges and increase citations of the published work.