Paraganglioma as a risk factor for bone metastasis

Author:

Yokomoto-Umakoshi Maki1,Umakoshi Hironobu1,Tsuiki Mika1,Ogasawara Tatsuki1,Hamanaka‑Hiroshima Kaho1,Tanabe Akiyo2,Tagami Tetsuya1,Shimatsu Akira1,Naruse Mitsuhide1

Affiliation:

1. Department of Endocrinology and Metabolism, National Hospital Organization Kyoto Medical Center, Kyoto, Japan

2. Division of Endocrinology, National Center for Global Health and Medicine, Tokyo, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference24 articles.

1. 1 Zarnegar R, Kebebew E, Duh QY, Clark OH (2006) Malignant pheochromocytoma. Surg Oncol Clin N Am 15: 555–571.

2. 2 Plouin PF, Amar L, Dekkers OM, Fassnacht M, Gimenez-Roqueplo AP, et al. (2016) European society of endocrinology clinical practice guideline for long-term follow-up of patients operated on for a pheochromocytoma or a paraganglioma. Eur J Endocrinol 174: G1–G10.

3. 3 Naruse M & PHEO-J Group. Nation-wide survey and PHEO network for the study of pheochromocytoma/paraganglioma in Japan (PHEO-J) (2011) Endocrine Reviews. 32 Meeting Abstracts: 2–631. The Endocrine Society’s 93rd annual meeting & expo, abstract No. P2–631.

4. 4 Abdel-Aziz TE, Prete F, Conway G, Gaze M, Bomanji J, et al. (2015) Pheochromocytomas and paragangliomas: a difference in disease behaviour and clinical outcomes. J Surg Oncol 112: 486–491.

5. 5 Choi YM, Sung TY, Kim WG, Lee JJ, Ryu JS, et al. (2015) Clinical course and prognostic factors in patients with malignant pheochromocutoma and paraganglioma: a single institution experience. J Surg Oncol 112: 815–821.

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