Familial SDHB gene mutation in disseminated non-hypoxia-related malignant paraganglioma treated with [<sup>90</sup>Y]Y/[<sup>177</sup>Lu]Lu-DOTATATE-Reference-Cited by-同舟云学术

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Familial SDHB gene mutation in disseminated non-hypoxia-related malignant paraganglioma treated with [⁹⁰Y]Y/[¹⁷⁷Lu]Lu-DOTATATE

Published:2021-08-31 Issue:3 Volume:10 Page:207-213
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Łoń Izabela¹,Kunikowska Jolanta²,Jędrusik Piotr¹,Góra Jarosław¹,Toutounchi Sadegh³,Placha Grzegorz¹,Gaciong Zbigniew¹

Affiliation:

1. Department of Internal Medicine, Hypertension and Vascular Diseases, Medical University of Warsaw, Warsaw, Poland.

2. Department of Nuclear Medicine, Medical University of Warsaw, Warsaw, Poland.

3. Department of General and Endocrine Surgery, Medical University of Warsaw, Warsaw, Poland.

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/10/3/10_2021.01047/_pdf

Reference30 articles.

1. 1. Chen H, Sippel RS, O'Dorisio MS, Vinik AI, Lloyd RV, Pacak K, North American Neuroendocrine Tumor Society. The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma and medullary thyroid cancer. Pancreas. 2010; 39:775-783.

2. 2. Lenders JW, Duh QY, Eisenhofer G, Gimenez-Roqueplo AP, Grebe SK, Murad MH, Naruse M, Pacak K, Young WF Jr; Endocrine Society. Pheochromocytoma and paraganglioma: An Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2014; 99:1915-1942.

3. 3. Mannelli M, Castellano M, Schiavi F, et al. Clinically guided genetic screening in a large cohort of Italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas. J Clin Endocrinol Metab. 2009; 94:1541-1547.

4. 4. Fishbein L, Merrill S, Fraker DL, Cohen DL, Nathanson KL. Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. Ann Surg Oncol. 2013; 20:1444-1450.

5. 5. Vicha A, Musil Z, Pacak K. Genetics of pheochromocytoma and paraganglioma syndromes: new advances and future treatment options. Curr Opin Endocrinol Diabetes Obes. 2013; 20:186-191.

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