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Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review

OBJECT: Exclusively dopamine-producing pheochromocytoma/paraganglioma (PPGL) is an extremely rare subtype. In this condition, intratumoral dopamine β-hydroxylase (DBH), which controls the conversion of norepinephrine from dopamine, is impaired, resulting in suppressed norepinephrine and epinephrine...

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Autores principales: Nezu, Masahiro, Hirotsu, Yosuke, Amemiya, Kenji, Tateno, Toru, Takizawa, Soichi, Inoue, Masaharu, Mochizuki, Hitoshi, Hosaka, Kyoko, Chik, Constance, Oyama, Toshio, Omata, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372287/
https://www.ncbi.nlm.nih.gov/pubmed/36384901
http://dx.doi.org/10.2169/internalmedicine.0743-22
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author Nezu, Masahiro
Hirotsu, Yosuke
Amemiya, Kenji
Tateno, Toru
Takizawa, Soichi
Inoue, Masaharu
Mochizuki, Hitoshi
Hosaka, Kyoko
Chik, Constance
Oyama, Toshio
Omata, Masao
author_facet Nezu, Masahiro
Hirotsu, Yosuke
Amemiya, Kenji
Tateno, Toru
Takizawa, Soichi
Inoue, Masaharu
Mochizuki, Hitoshi
Hosaka, Kyoko
Chik, Constance
Oyama, Toshio
Omata, Masao
author_sort Nezu, Masahiro
collection PubMed
description OBJECT: Exclusively dopamine-producing pheochromocytoma/paraganglioma (PPGL) is an extremely rare subtype. In this condition, intratumoral dopamine β-hydroxylase (DBH), which controls the conversion of norepinephrine from dopamine, is impaired, resulting in suppressed norepinephrine and epinephrine production. However, the rarity of this type of PPGL hampers the understanding of its pathophysiology. We therefore conducted genetic and immunohistological analyses of a patient with an exclusively dopamine-producing paraganglioma. METHODS: Paraganglioma samples from a 52-year-old woman who presented with a 29.6- and 41.5-fold increase in plasma and 24-h urinary dopamine, respectively, but only a minor elevation in the plasma norepinephrine level was subjected to immunohistological and gene expression analyses of catecholamine synthases. Three tumors carrying known somatic PPGL-related gene variants (HRAS, EPAS1) were used as controls. Whole-exome sequencing (WES) was also performed using the patient's blood and tumor tissue. RESULTS: Surprisingly, the protein expression of DBH was not suppressed, and its mRNA expression was clearly higher in the patient than in the controls. Furthermore, dopa decarboxylase (DDC), which governs the conversion of 3,4-dihydroxyphenyl-(L)-alanine ((L)-DOPA) to dopamine, was downregulated at the protein and gene levels. In addition, melanin, which is synthesized by (L)-DOPA, accumulated in the tumor. WES revealed no PPGL-associated pathogenic germline variants, but a missense somatic variant (c.1798G>T) in CSDE1 was identified. CONCLUSION: Although pre-operative plasma (L)-DOPA was not measured, our histological and gene expression analyses suggest that (L)-DOPA, rather than dopamine, might have been overproduced in the tumor. This raises the possibility of pathophysiological heterogeneity in exclusively dopamine-producing PPGL.
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spelling pubmed-103722872023-07-28 Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review Nezu, Masahiro Hirotsu, Yosuke Amemiya, Kenji Tateno, Toru Takizawa, Soichi Inoue, Masaharu Mochizuki, Hitoshi Hosaka, Kyoko Chik, Constance Oyama, Toshio Omata, Masao Intern Med Original Article OBJECT: Exclusively dopamine-producing pheochromocytoma/paraganglioma (PPGL) is an extremely rare subtype. In this condition, intratumoral dopamine β-hydroxylase (DBH), which controls the conversion of norepinephrine from dopamine, is impaired, resulting in suppressed norepinephrine and epinephrine production. However, the rarity of this type of PPGL hampers the understanding of its pathophysiology. We therefore conducted genetic and immunohistological analyses of a patient with an exclusively dopamine-producing paraganglioma. METHODS: Paraganglioma samples from a 52-year-old woman who presented with a 29.6- and 41.5-fold increase in plasma and 24-h urinary dopamine, respectively, but only a minor elevation in the plasma norepinephrine level was subjected to immunohistological and gene expression analyses of catecholamine synthases. Three tumors carrying known somatic PPGL-related gene variants (HRAS, EPAS1) were used as controls. Whole-exome sequencing (WES) was also performed using the patient's blood and tumor tissue. RESULTS: Surprisingly, the protein expression of DBH was not suppressed, and its mRNA expression was clearly higher in the patient than in the controls. Furthermore, dopa decarboxylase (DDC), which governs the conversion of 3,4-dihydroxyphenyl-(L)-alanine ((L)-DOPA) to dopamine, was downregulated at the protein and gene levels. In addition, melanin, which is synthesized by (L)-DOPA, accumulated in the tumor. WES revealed no PPGL-associated pathogenic germline variants, but a missense somatic variant (c.1798G>T) in CSDE1 was identified. CONCLUSION: Although pre-operative plasma (L)-DOPA was not measured, our histological and gene expression analyses suggest that (L)-DOPA, rather than dopamine, might have been overproduced in the tumor. This raises the possibility of pathophysiological heterogeneity in exclusively dopamine-producing PPGL. The Japanese Society of Internal Medicine 2022-11-16 2023-07-01 /pmc/articles/PMC10372287/ /pubmed/36384901 http://dx.doi.org/10.2169/internalmedicine.0743-22 Text en Copyright © 2023 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Nezu, Masahiro
Hirotsu, Yosuke
Amemiya, Kenji
Tateno, Toru
Takizawa, Soichi
Inoue, Masaharu
Mochizuki, Hitoshi
Hosaka, Kyoko
Chik, Constance
Oyama, Toshio
Omata, Masao
Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review
title Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review
title_full Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review
title_fullStr Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review
title_full_unstemmed Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review
title_short Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine β-hydroxylase Upregulation and Intra-tumoral Melanin Accumulation: A Case Report with a Literature Review
title_sort paraganglioma with high levels of dopamine, dopa decarboxylase suppression, dopamine β-hydroxylase upregulation and intra-tumoral melanin accumulation: a case report with a literature review
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372287/
https://www.ncbi.nlm.nih.gov/pubmed/36384901
http://dx.doi.org/10.2169/internalmedicine.0743-22
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