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Paraganglioma of the Middle Mediastinum

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Date 2020 Sep 21
PMID 32953448
Citations 2
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Abstract

A 60-year-old female was evaluated for significant weight loss, nausea, vomiting, and dysphagia. A computed tomography (CT) of the chest showed a 3 cm mass in the middle mediastinum. CT scan of the abdomen and pelvis revealed no abnormality. Positron emission tomography (PET) of the whole body revealed tracer uptake in the pre-carinal nodal mass. There were no other suspicious foci of tracer uptake. Mediastinoscopy and biopsy revealed a well-differentiated low-grade neuroendocrine tumor. She underwent sternotomy, and after careful mobilization of the great vessels, the middle mediastinal mass was successfully resected. Final pathology revealed a paraganglioma with no morphological signs to suggest malignancy. The right lower paratracheal lymph node did not show any tumor cells. She did well postoperatively.

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References
1.
Lamy A, Fradet G, Luoma A, Nelems B . Anterior and middle mediastinum paraganglioma: complete resection is the treatment of choice. Ann Thorac Surg. 1994; 57(1):249-52. DOI: 10.1016/0003-4975(94)90419-7. View

2.
Takashima Y, Kamitani T, Kawanami S, Nagao M, Yonezawa M, Yamasaki Y . Mediastinal paraganglioma. Jpn J Radiol. 2015; 33(7):433-6. DOI: 10.1007/s11604-015-0436-z. View

3.
Mehta C, Gillespie C, Lin X, Yeldandi A, Decamp M, Bharat A . Rare Middle Mediastinal Paraganglioma Mimicking Metastatic Neuroendocrine Tumor. Ann Thorac Surg. 2015; 100(2):702-5. DOI: 10.1016/j.athoracsur.2014.09.068. View

4.
Amar L, Servais A, Gimenez-Roqueplo A, Zinzindohoue F, Chatellier G, Plouin P . Year of diagnosis, features at presentation, and risk of recurrence in patients with pheochromocytoma or secreting paraganglioma. J Clin Endocrinol Metab. 2005; 90(4):2110-6. DOI: 10.1210/jc.2004-1398. View

5.
Hamidi O, Young Jr W, Iniguez-Ariza N, Kittah N, Gruber L, Bancos C . Malignant Pheochromocytoma and Paraganglioma: 272 Patients Over 55 Years. J Clin Endocrinol Metab. 2017; 102(9):3296-3305. PMC: 5587061. DOI: 10.1210/jc.2017-00992. View