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A Rare Case of Malignant Peri-Aortic Paraganglioma
Malignancy is rare and the majority of lesions are benign.1 Here we present the case of a 46-year-old male who presented to the ED complaining of nausea, vomiting, left lower quadrant pain, headaches and hypertension that initially was refractory to medications. Adjuvant chemotherapy using cyclophos...
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Published in: | The American surgeon 2019-08, Vol.85 (8), p.370-371 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Malignancy is rare and the majority of lesions are benign.1 Here we present the case of a 46-year-old male who presented to the ED complaining of nausea, vomiting, left lower quadrant pain, headaches and hypertension that initially was refractory to medications. Adjuvant chemotherapy using cyclophosphamide, vincristine, and dacarbazine has shown the most benefit, with 37 per cent tumor burden reduction and 40 per cent having resolution of catecholamine symptoms.2 External beam radiation is showing promise for slowing progression of surgically unresectable disease with 81 per cent of patients showing radiographic local control and 94 per cent being symptom free at five-year follow up.3 Lastly, for extensive metastatic disease, long term radionuclide 131-I metaiodobenzylguanidine (MIBG) therapy may be useful in stabilizing progression of disease in approximately 72 per cent of patients.4, 5 This is primarily being used as a palliative measure. Catecholaminesecreting carotid body paraganglioma: successful preoperative control of hypertension and clinical symptoms using high-dose long-acting octreotide. |
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ISSN: | 0003-1348 1555-9823 |
DOI: | 10.1177/000313481908500801 |