Multiple endocrine neoplasia 2A with RET mutation p.Cys611Tyr: A case report

RATIONALE: Multiple endocrine neoplasia 2A (MEN2A) is a rare autosomal-dominant genetic syndrome, frequently misdiagnosed or neglected clinically, resulting in delayed therapy to patients. PATIENT CONCERNS: A 47-year-old Chinese male patient underwent laparoscopic right adrenal tumorectomy, and post...

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Detalles Bibliográficos
Autores principales: Li, Yan, Tan, Ya-qin, Tang, Zhi-xiang, Liao, Qing-hui, Guo, Zhong-qiu, Lai, Kang-bao, Wang, Rong, Chen, Yu-hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183697/
https://www.ncbi.nlm.nih.gov/pubmed/34087905
http://dx.doi.org/10.1097/MD.0000000000026230

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183697/
https://www.ncbi.nlm.nih.gov/pubmed/34087905
http://dx.doi.org/10.1097/MD.0000000000026230

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