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The Annals of Thoracic Surgery, Vol 57, 249-252, Copyright © 1994 by The Society of Thoracic Surgeons
AL Lamy, GJ Fradet, A Luoma and B Nelems
Paraganglioma of the mediastinum is described to be an indolent and
slow-growing tumor. After a patient presented to our center, we reviewed
the world literature to evaluate the prognosis of this tumor. This review
showed that paragangliomas are locally invasive and have a high local
recurrence rate (44/79 or 55.7%) with a true metastatic capacity (21/79 or
26.6%). The overall survival is 62.0% (49/79), but only 36.7% (29/79) of
patients could be considered as free of disease, with survival time of 98.2
+/- 11.7 months (mean +/- standard error). The survival with a complete
resection is 84.6% (125.7 +/- 18.7 months) versus 50.0% (71.5 +/- 13.8
months) for patients with a biopsy or a partial excision and adjuvant
treatment (p < 0.01). We acknowledge the limitation of this
retrospective study, but a prospective trial is not possible because of the
rarity of the tumor. We want to emphasize that paraganglioma of the
anterior and middle mediastinum is an aggressive tumor, and complete
surgical resection, using cardiopulmonary bypass if necessary, is highly
recommended.
ARTICLES
Anterior and middle mediastinum paraganglioma: complete resection is the treatment of choice
Department of Surgery, Vancouver General Hospital, British Columbia, Canada.
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