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Horner’s syndrome secondary to thymic adenocarcinoma: Case report

Síndrome de Horner secundario a adenocarcinoma primario de timo: reporte de caso




Section
Case Reports

How to Cite
Gil, M., & Anaya, D. (2017). Horner’s syndrome secondary to thymic adenocarcinoma: Case report. Journal of Medicine and Surgery Repertoire, 26(4), 249-252. https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/61

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Magda Gil
    Denis Anaya

      Objective: To describe the case of a patient suffering from Horner’s syndrome of an unusual cause, that is, a primary thymic adenocarcinoma. She attended the ophthalmology service at Hospital de San José.
      Study design: A case report.
      Methods: A review of the literature was performed on Horner’s syndrome emphasizing on the causes associated with mediastinal lesions particularly thymic carcinomas, given their low incidence and rare occurrence.
      Case report: A 41-year-old woman with a six month history of right hemicranial headache radiating to the neck and right arm, paresthesias and right hemifacial anhidrosis, right upper eyelid ptosis and miosis of the right pupil. A thymic neoplasm classified as an adenocarcinoma was diagnosed by imaging tests and evidencing the presence of Horner’s syndrome. The tumor was resected and followed by adjuvant oncologic therapy.
      Conclusion: A rare cause of Horner’s syndrome is preganglionic compression of the sympathetic pathway by a mediastinal mass such as a thymic adenocarcinoma, one of the most uncommon tumors involving the thymus and the mediastinum.


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      1. Walton KA, Buono LM. Horner syndrome. Curr Opin Ophthalmol. 2003;14:357–63.

      2. Miller N, Newman NJ, Biousse V. Kerrison. Anatomy and physiology of the autonomic nervous system. En: Wilkins LW, editor. Walsh and Hoyt Clinical Neuro-ophthalmology. 6 th ed. Baltimore, United States: Wolters Kluwer; 2005. p. 649.

      3. Salvesen R. Innervation of sweat glands in the forehead. A study in patients with Horner’s syndrome. J Neurol Sci. 2001;183:39–42.

      4. Maloney WF, Younge BR, Moyer NJ. Evaluation of the causes and accuracy of pharmacologic localization in Horner’s syndrome. Am J Ophthalmol. 1980;90:394–402.

      5. Fraile G, Rodriguez-Garcia JL, Monroy C, Fogue L, Millan JM. Thymic cyst presenting as Horner’s syndrome. Chest. 1992;101:1170–1.

      6. Jindal T, Chaudhary R, Sharma N, Meena M, Dutta R, Kumar A. Primary mediastinal chondrosarcoma with Horner’s syndrome. Gen Thorac Cardiovasc Surg. 2011;59:145–7.

      7. Srirajaskanthan R, Toubanakis C, Dusmet M, Caplin ME. A review of thymic tumours. Lung Cancer. 2008;60:4–13.

      8. Ruffini E, Detterbeck F, van Raemdonck D, Rocco G, Thomas P, Weder W, et al., European Society of Thoracic Surgeons Thymic Working Group. Thymic carcinoma: A cohort study of patients from the European society of thoracic surgeons database. J Thorac Oncol. 2014;9:541–8.

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