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BRAF(V600E) and TERT promoter C228T mutations on ThyroSeq v3 analysis of delayed skin metastasis from papillary thyroid cancer: a case report and literature review

BACKGROUND: Skin metastasis from papillary thyroid cancer (PTC) is a rare entity that can occur up to decades after treatment of the primary tumor. Here, we present a patient who developed skin metastasis 10 years after treatment of her primary tumor and describe the molecular findings of the metast...

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Detalles Bibliográficos
Autores principales: Choi, Jee-Hye, Yu, Hyeong Won, Lee, Ja Kyung, Kim, Woochul, Choi, June Young, Na, Hee Young, Park, So Yeon, Ahn, Chang Ho, Moon, Jae Hoon, Choi, Sang Il, Lee, Ho-Young, Lee, Won Woo, Cha, Wonjae, Jeong, Woo-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936773/
https://www.ncbi.nlm.nih.gov/pubmed/36804879
http://dx.doi.org/10.1186/s12957-023-02937-7
Descripción
Sumario:BACKGROUND: Skin metastasis from papillary thyroid cancer (PTC) is a rare entity that can occur up to decades after treatment of the primary tumor. Here, we present a patient who developed skin metastasis 10 years after treatment of her primary tumor and describe the molecular findings of the metastatic lesion. CASE PRESENTATION: A 44-year-old female with a history of PTC who underwent a total thyroidectomy and radioactive iodine (RAI) treatment 10 years ago presented with a 1.3-cm skin lesion along the prior thyroidectomy scar. A biopsy revealed metastatic PTC, and the patient underwent surgical excision of the lesion. ThyroSeq molecular testing showed the copresence of BRAF(V600E) mutation and TERT promoter C228T mutation. The patient subsequently received one round of adjuvant RAI therapy. CONCLUSIONS: A high index of suspicion is warranted in patients with a history of PTC who develop a skin lesion, even several years after remission of the primary disease. In patients with high-risk mutations, such as BRAF(V600E) and TERT promoter C228T mutations, long-term surveillance of disease recurrence is particularly important.