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DOI: 10.1055/s-2007-966102
© Georg Thieme Verlag KG Stuttgart · New York
Vertebral prosthetic arthrodesis migration to the esophageal lumen: a rare cause of dysphagia
Publication History
Publication Date:
05 July 2007 (online)
A 52-year-old man was referred because of progressive dysphagia. He had a past medical history of recurrent spinal hydatidosis at the D1 - 2 level, which was surgically treated in 2000 and 2002 with a total corporectomy of the D1 vertebrae, removal of cysts, arthrodesis with a Moss prosthesis, and insertion of a titanium implant. In 2004, computed tomography (CT) showed the migration of the prosthesis to the posterior mediastinum. The patient underwent repeat surgery but the prosthetic arthrodesis could be only partially removed. One year later, he complained of moderate dysphagia. An upper endoscopy was performed, showing an extrinsic compression at the level of cervical esophagus with normal appearing mucosa ([Figure 1]). Because of progression of dysphagia, a second upper endoscopy was performed 6 months later, and revealed a foreign body in the lumen of the esophagus, at the level of the previous extrinsic compression, that was impossible to mobilize ([Figure 2]).
Figure 1 Extrinsic compression at the level of cervical esophagus with normal appearing mucosa.
Figure 2 Foreign body in the lumen of the cervical esophagus.
The CT image confirmed that the foreign body was the residual arthrodesis, which had progressed through the posterior mediastinum, and had eroded the esophageal wall ([Figure 3]). Using CT, it was also possible to identify a fistulous tract from the D1 - 2 level to the esophagus, which was the pathway followed by the arthrodesis when migrating to the esophageal lumen. The patient underwent surgery, and the residual arthrodesis was removed without complications.
Figure 3 CT image showing residual arthrodesis partially inserted in the esophageal wall (with a severe inflammatory reaction), and in the interior of the lumen.
Hydatid disease is relatively common in the Mediterranean area, but bone hydatidosis is rare and occurs in 1 - 2.5 % of cases of human hydatidosis [1] [2]. About 50 % of cases of bone hydatidosis are spinal [3] [4]. Surgery is the treatment of choice, with removal of the affected vertebrae combined with prosthetic bone fixation. To our knowledge, this is the first case reported with migration of the vertebral prosthetic arthrodesis eroding the esophageal wall and, therefore, represents an unusual case of dysphagia.
Endoscopy_UCTN_Code_CCL_1AB_2AF
Endoscopy_UCTN_Code_CCL_1AB_2AC_3AH
References
- 1 Szypryt E P, Morris D L, Mulholland R C. Combined chemotherapy and surgery for hydatid bone disease. J Bone Joint Surg Br. 1987; 69 141-144
- 2 Zlitni M, Ezzaouia Z, Lebib H. et al . Hydatid cyst of bone: diagnosis and treatment. World J Surg. 2001; 25 75-82
- 3 Govender T S, Aslam M, Parbhoo A. et al . Hydatid disease of the spine. Clin Orthop Relat Res. 2000; 378 143-147
- 4 Herrera A, Martínez A A, Rodríguez J. Spinal hydatidosis. Spine. 2005; 30 2439-2444
G. Fernández-Esparrach, MD
Endoscopy Unit
Institut de Malalties Digestives
Hospital Clínic
Villarroel 170
08036 Barcelona
Spain
Fax: +34-93-2279387
Email: mgfernan@clinic.ub.es