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Paraganglioma with High Levels of Dopamine, Dopa Decarboxylase Suppression, Dopamine ß-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.
Afiliação
  • Nezu M; Department of Endocrinology and Diabetes, Yamanashi Central Hospital, Japan.
  • Hirotsu Y; Genome Analysis Center, Yamanashi Central Hospital, Japan.
  • Amemiya K; Division of Endocrinology and Metabolism, Department of Medicine, University of Alberta, Canada.
  • Tateno T; Genome Analysis Center, Yamanashi Central Hospital, Japan.
  • Takizawa S; Genome Analysis Center, Yamanashi Central Hospital, Japan.
  • Inoue M; Division of Endocrinology and Metabolism, Department of Medicine, University of Alberta, Canada.
  • Mochizuki H; Department of Endocrinology and Diabetes, Yamanashi Central Hospital, Japan.
  • Hosaka K; Department of Endocrinology and Diabetes, Yamanashi Central Hospital, Japan.
  • Chik C; Genome Analysis Center, Yamanashi Central Hospital, Japan.
  • Oyama T; Department of Urology, Yamanashi Central Hospital, Japan.
  • Omata M; Division of Endocrinology and Metabolism, Department of Medicine, University of Alberta, Canada.
Intern Med ; 62(13): 1895-1905, 2023 Jul 01.
Article em En | MEDLINE | ID: mdl-36384901
ABSTRACT
Object Exclusively dopamine-producing pheochromocytoma/paraganglioma (PPGL) is an extremely rare subtype. In this condition, intratumoral dopamine ß-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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraganglioma / Feocromocitoma / Neoplasias das Glândulas Suprarrenais Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraganglioma / Feocromocitoma / Neoplasias das Glândulas Suprarrenais Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article