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Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome

Pheochromocytomas (PCCs) are rare but potentially lethal tumors that arise from the adrenal medulla. The clinical suspicion and diagnosis of PCC can be challenging due to the non-specific nature of signs and symptoms. In many patients, infection with severe acute respiratory syndrome coronavirus 2 (...

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Autores principales: Ziegler, Christian G., Riediger, Carina, Gruber, Matthias, Kunath, Carola, Ullrich, Martin, Pietzsch, Jens, Nölting, Svenja, Siepmann, Timo, Bornstein, Stefan R., Remde, Hanna, Constantinescu, Georgiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551989/
https://www.ncbi.nlm.nih.gov/pubmed/36237184
http://dx.doi.org/10.3389/fendo.2022.967995
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author Ziegler, Christian G.
Riediger, Carina
Gruber, Matthias
Kunath, Carola
Ullrich, Martin
Pietzsch, Jens
Nölting, Svenja
Siepmann, Timo
Bornstein, Stefan R.
Remde, Hanna
Constantinescu, Georgiana
author_facet Ziegler, Christian G.
Riediger, Carina
Gruber, Matthias
Kunath, Carola
Ullrich, Martin
Pietzsch, Jens
Nölting, Svenja
Siepmann, Timo
Bornstein, Stefan R.
Remde, Hanna
Constantinescu, Georgiana
author_sort Ziegler, Christian G.
collection PubMed
description Pheochromocytomas (PCCs) are rare but potentially lethal tumors that arise from the adrenal medulla. The clinical suspicion and diagnosis of PCC can be challenging due to the non-specific nature of signs and symptoms. In many patients, infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) could lead to long-term symptoms including fatigue, headaches, and cognitive dysfunction. Here, we present the case of a patient incidentally diagnosed with an adrenal mass that proved to be a PCC after imaging was performed due to persisting complaints after coronavirus disease 2019 (COVID-19) infection. A 37-year-old male patient was referred to our center because of a right-sided inhomogeneous adrenal mass, incidentally found during a computed tomographic scan of the thorax performed due to cough and dyspnea that persisted after COVID-19 infection. Other complaints that were present prior to COVID-19 infection included profuse sweating, dizziness, exhaustion with chronic fatigue, and concentration difficulties. The patient had no history of hypertension, his blood pressure was normal, and the 24-h ambulatory blood pressure monitoring confirmed normotension but with the absence of nocturnal dipping. Plasma normetanephrine was 5.7-fold above the upper limit (UL) of reference intervals (738 pg/ml, UL = 129 pg/ml), whereas plasma metanephrine and methoxytyramine were normal at 30 pg/ml (UL = 84 pg/ml) and <4 pg/ml (UL = 16 pg/ml), respectively. Preoperative preparation with phenoxybenzamine was initiated, and a 4-cm tumor was surgically resected. Profuse sweating as well as dizziness was resolved after adrenalectomy pointing toward PCC and not COVID-19-associated patient concerns. Altogether, this case illustrates the difficulties in recognizing the possibility of PCC due to the non-specific nature of signs and symptoms of the tumor, which in this case did not include hypertension and coincided with some of the symptoms of long COVID-19.
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spelling pubmed-95519892022-10-12 Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome Ziegler, Christian G. Riediger, Carina Gruber, Matthias Kunath, Carola Ullrich, Martin Pietzsch, Jens Nölting, Svenja Siepmann, Timo Bornstein, Stefan R. Remde, Hanna Constantinescu, Georgiana Front Endocrinol (Lausanne) Endocrinology Pheochromocytomas (PCCs) are rare but potentially lethal tumors that arise from the adrenal medulla. The clinical suspicion and diagnosis of PCC can be challenging due to the non-specific nature of signs and symptoms. In many patients, infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) could lead to long-term symptoms including fatigue, headaches, and cognitive dysfunction. Here, we present the case of a patient incidentally diagnosed with an adrenal mass that proved to be a PCC after imaging was performed due to persisting complaints after coronavirus disease 2019 (COVID-19) infection. A 37-year-old male patient was referred to our center because of a right-sided inhomogeneous adrenal mass, incidentally found during a computed tomographic scan of the thorax performed due to cough and dyspnea that persisted after COVID-19 infection. Other complaints that were present prior to COVID-19 infection included profuse sweating, dizziness, exhaustion with chronic fatigue, and concentration difficulties. The patient had no history of hypertension, his blood pressure was normal, and the 24-h ambulatory blood pressure monitoring confirmed normotension but with the absence of nocturnal dipping. Plasma normetanephrine was 5.7-fold above the upper limit (UL) of reference intervals (738 pg/ml, UL = 129 pg/ml), whereas plasma metanephrine and methoxytyramine were normal at 30 pg/ml (UL = 84 pg/ml) and <4 pg/ml (UL = 16 pg/ml), respectively. Preoperative preparation with phenoxybenzamine was initiated, and a 4-cm tumor was surgically resected. Profuse sweating as well as dizziness was resolved after adrenalectomy pointing toward PCC and not COVID-19-associated patient concerns. Altogether, this case illustrates the difficulties in recognizing the possibility of PCC due to the non-specific nature of signs and symptoms of the tumor, which in this case did not include hypertension and coincided with some of the symptoms of long COVID-19. Frontiers Media S.A. 2022-09-27 /pmc/articles/PMC9551989/ /pubmed/36237184 http://dx.doi.org/10.3389/fendo.2022.967995 Text en Copyright © 2022 Ziegler, Riediger, Gruber, Kunath, Ullrich, Pietzsch, Nölting, Siepmann, Bornstein, Remde and Constantinescu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Ziegler, Christian G.
Riediger, Carina
Gruber, Matthias
Kunath, Carola
Ullrich, Martin
Pietzsch, Jens
Nölting, Svenja
Siepmann, Timo
Bornstein, Stefan R.
Remde, Hanna
Constantinescu, Georgiana
Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome
title Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome
title_full Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome
title_fullStr Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome
title_full_unstemmed Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome
title_short Case report: Incidentally discovered case of pheochromocytoma as a cause of long COVID-19 syndrome
title_sort case report: incidentally discovered case of pheochromocytoma as a cause of long covid-19 syndrome
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551989/
https://www.ncbi.nlm.nih.gov/pubmed/36237184
http://dx.doi.org/10.3389/fendo.2022.967995
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