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Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports

BACKGROUND: Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with a heterogeneous prognosis, while adrenal metastasis from other primary cancers, including melanoma, may occur more frequently. ACC may rarely occur as part of familial cancer syndromes, but even in sporadic cases, a signi...

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Autores principales: Ko, Ye Lynn, Kumar, Vaishnavi, Lippert, Juliane, Diaz-Cano, Salvador, Skordilis, Kassiani, Kimpel, Otilia, Kircher, Stefan, Asia, Miriam, Elhassan, Yasir S., Altieri, Barbara, Ronchi, Cristina L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817389/
https://www.ncbi.nlm.nih.gov/pubmed/36604647
http://dx.doi.org/10.1186/s12902-022-01253-7
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author Ko, Ye Lynn
Kumar, Vaishnavi
Lippert, Juliane
Diaz-Cano, Salvador
Skordilis, Kassiani
Kimpel, Otilia
Kircher, Stefan
Asia, Miriam
Elhassan, Yasir S.
Altieri, Barbara
Ronchi, Cristina L.
author_facet Ko, Ye Lynn
Kumar, Vaishnavi
Lippert, Juliane
Diaz-Cano, Salvador
Skordilis, Kassiani
Kimpel, Otilia
Kircher, Stefan
Asia, Miriam
Elhassan, Yasir S.
Altieri, Barbara
Ronchi, Cristina L.
author_sort Ko, Ye Lynn
collection PubMed
description BACKGROUND: Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with a heterogeneous prognosis, while adrenal metastasis from other primary cancers, including melanoma, may occur more frequently. ACC may rarely occur as part of familial cancer syndromes, but even in sporadic cases, a significant proportion of patients had other malignancies before or after diagnosis of ACC. Herein we present three cases where sporadic ACC was identified in patients with coexistent or previous history of melanoma. CASE DESCRIPTION: Patient 1 - A 37-yr-old man with a superficial spreading BRAF-positive melanoma was found to harbour a progressively growing left adrenal mass. Initially, he was suspected of having adrenal metastasis, but the histology after adrenalectomy confirmed ACC. Patient 2 - A 68-year-old man with a history of recurrent BRAF-positive melanoma was diagnosed with disseminated metastatic melanoma recurrence, including a rapidly enlarging left adrenal mass. Consequently, he underwent left adrenalectomy, and histology again confirmed ACC. Patient 3 – A 50-yr-old man was referred with histological diagnosis of metastatic ACC. He had a background history of pT1 melanoma. We undertook targeted sequencing of ACC tissue samples in all cases. Somatic variants were observed in the known driver genes CTNNB1 (Patient 1), APC and KMT2D (Patient 2), and APC and TP53 (Patient 3). Germline TP53 variants (Li-Fraumeni syndrome) were excluded in all cases. Retrospective review of our patient cohort in the last 21 years revealed a frequency of 0.5% of histologically diagnosed melanoma metastasis among patients referred for adrenal masses. On the other hand, 1.6% of patients with histologically confirmed ACC had a previous history of melanoma. CONCLUSION: Sporadic ACC can occur in the background of melanoma, even if adrenal metastasis might appear to be the most likely diagnosis. Coexistent primary adrenal malignancy should be considered and investigated for in all patients with a history of melanoma with suspicious adrenal lesions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12902-022-01253-7.
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spelling pubmed-98173892023-01-07 Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports Ko, Ye Lynn Kumar, Vaishnavi Lippert, Juliane Diaz-Cano, Salvador Skordilis, Kassiani Kimpel, Otilia Kircher, Stefan Asia, Miriam Elhassan, Yasir S. Altieri, Barbara Ronchi, Cristina L. BMC Endocr Disord Case Report BACKGROUND: Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with a heterogeneous prognosis, while adrenal metastasis from other primary cancers, including melanoma, may occur more frequently. ACC may rarely occur as part of familial cancer syndromes, but even in sporadic cases, a significant proportion of patients had other malignancies before or after diagnosis of ACC. Herein we present three cases where sporadic ACC was identified in patients with coexistent or previous history of melanoma. CASE DESCRIPTION: Patient 1 - A 37-yr-old man with a superficial spreading BRAF-positive melanoma was found to harbour a progressively growing left adrenal mass. Initially, he was suspected of having adrenal metastasis, but the histology after adrenalectomy confirmed ACC. Patient 2 - A 68-year-old man with a history of recurrent BRAF-positive melanoma was diagnosed with disseminated metastatic melanoma recurrence, including a rapidly enlarging left adrenal mass. Consequently, he underwent left adrenalectomy, and histology again confirmed ACC. Patient 3 – A 50-yr-old man was referred with histological diagnosis of metastatic ACC. He had a background history of pT1 melanoma. We undertook targeted sequencing of ACC tissue samples in all cases. Somatic variants were observed in the known driver genes CTNNB1 (Patient 1), APC and KMT2D (Patient 2), and APC and TP53 (Patient 3). Germline TP53 variants (Li-Fraumeni syndrome) were excluded in all cases. Retrospective review of our patient cohort in the last 21 years revealed a frequency of 0.5% of histologically diagnosed melanoma metastasis among patients referred for adrenal masses. On the other hand, 1.6% of patients with histologically confirmed ACC had a previous history of melanoma. CONCLUSION: Sporadic ACC can occur in the background of melanoma, even if adrenal metastasis might appear to be the most likely diagnosis. Coexistent primary adrenal malignancy should be considered and investigated for in all patients with a history of melanoma with suspicious adrenal lesions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12902-022-01253-7. BioMed Central 2023-01-06 /pmc/articles/PMC9817389/ /pubmed/36604647 http://dx.doi.org/10.1186/s12902-022-01253-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Ko, Ye Lynn
Kumar, Vaishnavi
Lippert, Juliane
Diaz-Cano, Salvador
Skordilis, Kassiani
Kimpel, Otilia
Kircher, Stefan
Asia, Miriam
Elhassan, Yasir S.
Altieri, Barbara
Ronchi, Cristina L.
Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports
title Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports
title_full Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports
title_fullStr Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports
title_full_unstemmed Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports
title_short Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports
title_sort coincidence of primary adrenocortical carcinoma and melanoma: three case reports
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817389/
https://www.ncbi.nlm.nih.gov/pubmed/36604647
http://dx.doi.org/10.1186/s12902-022-01253-7
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