PHEOCHROMOCYTOME A LOCALISATION CARDIAQUE. ECHEC DE METHODES DIAGNOSTIQUES NON INVASIVES CLASSIQUES

Translated title of the contribution: Cardiac phaeochromocytoma: Failure of conventional non-invasive diagnostic methods

Annick Haouzi, N. Danchin, E. Renoult, C. Selton-Suty, D. Amrein, P. Mathieu, M. Kessler, F. Cherrier

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

We report an exceptional case of cardiac phaeochromocytoma which raised problems of localization. A 30-year-old man, who for several years had been hypertensive, was admitted for attacks of paroxysmal hypertension. Very high levels of urinary catecholamines suggested a diagnosis of phaeochromocytoma, but no tumour was found at computerized tomography (CT) and metaiodobenzylguanidine (MIBG) scintigraphy. However, regional venous samplings detected 2 para-carotid phaeochromocytomas which were surgically removed. Thereafter, the symptoms persisted and investigations were resumed. As new regional venous samplings showed high levels of catecholamines in the right atrium, a mediastinal and, chiefly, cardiac phaeochromocytoma was suspected. No tumour was visible at CT or ultrasonography and another MIBG scintigraphy proved negative. Coronary angiography showed a very large tumour behind the left atrium, well supplied by the circumflex artery and by a branch of the right coronary artery. The patient was operated upon and is now totally asymptomatic after a 9-month follow-up. This case emphasizes the value of invasive methods (i.e. regional venous sampling and coronary angiography) in the localization of this ectopic tumour. In most cases, however, phaeochromocytomas can be localized by MIBG scintigraphy.

Original languageFrench
Pages (from-to)97-100
Number of pages4
JournalArchives des Maladies du Coeur et des Vaisseaux
Volume82
Issue number1
StatePublished - Jan 1 1989

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Pheochromocytoma
Heart Failure
Radionuclide Imaging
Heart Atria
Coronary Angiography
Catecholamines
Neoplasms
Tomography
Ultrasonography
Coronary Vessels
Arteries
Hypertension

All Science Journal Classification (ASJC) codes

  • Cardiology and Cardiovascular Medicine

Cite this

Haouzi, A., Danchin, N., Renoult, E., Selton-Suty, C., Amrein, D., Mathieu, P., ... Cherrier, F. (1989). PHEOCHROMOCYTOME A LOCALISATION CARDIAQUE. ECHEC DE METHODES DIAGNOSTIQUES NON INVASIVES CLASSIQUES. Archives des Maladies du Coeur et des Vaisseaux, 82(1), 97-100.
Haouzi, Annick ; Danchin, N. ; Renoult, E. ; Selton-Suty, C. ; Amrein, D. ; Mathieu, P. ; Kessler, M. ; Cherrier, F. / PHEOCHROMOCYTOME A LOCALISATION CARDIAQUE. ECHEC DE METHODES DIAGNOSTIQUES NON INVASIVES CLASSIQUES. In: Archives des Maladies du Coeur et des Vaisseaux. 1989 ; Vol. 82, No. 1. pp. 97-100.
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abstract = "We report an exceptional case of cardiac phaeochromocytoma which raised problems of localization. A 30-year-old man, who for several years had been hypertensive, was admitted for attacks of paroxysmal hypertension. Very high levels of urinary catecholamines suggested a diagnosis of phaeochromocytoma, but no tumour was found at computerized tomography (CT) and metaiodobenzylguanidine (MIBG) scintigraphy. However, regional venous samplings detected 2 para-carotid phaeochromocytomas which were surgically removed. Thereafter, the symptoms persisted and investigations were resumed. As new regional venous samplings showed high levels of catecholamines in the right atrium, a mediastinal and, chiefly, cardiac phaeochromocytoma was suspected. No tumour was visible at CT or ultrasonography and another MIBG scintigraphy proved negative. Coronary angiography showed a very large tumour behind the left atrium, well supplied by the circumflex artery and by a branch of the right coronary artery. The patient was operated upon and is now totally asymptomatic after a 9-month follow-up. This case emphasizes the value of invasive methods (i.e. regional venous sampling and coronary angiography) in the localization of this ectopic tumour. In most cases, however, phaeochromocytomas can be localized by MIBG scintigraphy.",
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Haouzi, A, Danchin, N, Renoult, E, Selton-Suty, C, Amrein, D, Mathieu, P, Kessler, M & Cherrier, F 1989, 'PHEOCHROMOCYTOME A LOCALISATION CARDIAQUE. ECHEC DE METHODES DIAGNOSTIQUES NON INVASIVES CLASSIQUES', Archives des Maladies du Coeur et des Vaisseaux, vol. 82, no. 1, pp. 97-100.

PHEOCHROMOCYTOME A LOCALISATION CARDIAQUE. ECHEC DE METHODES DIAGNOSTIQUES NON INVASIVES CLASSIQUES. / Haouzi, Annick; Danchin, N.; Renoult, E.; Selton-Suty, C.; Amrein, D.; Mathieu, P.; Kessler, M.; Cherrier, F.

In: Archives des Maladies du Coeur et des Vaisseaux, Vol. 82, No. 1, 01.01.1989, p. 97-100.

Research output: Contribution to journalArticle

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AU - Haouzi, Annick

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AU - Renoult, E.

AU - Selton-Suty, C.

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AU - Kessler, M.

AU - Cherrier, F.

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N2 - We report an exceptional case of cardiac phaeochromocytoma which raised problems of localization. A 30-year-old man, who for several years had been hypertensive, was admitted for attacks of paroxysmal hypertension. Very high levels of urinary catecholamines suggested a diagnosis of phaeochromocytoma, but no tumour was found at computerized tomography (CT) and metaiodobenzylguanidine (MIBG) scintigraphy. However, regional venous samplings detected 2 para-carotid phaeochromocytomas which were surgically removed. Thereafter, the symptoms persisted and investigations were resumed. As new regional venous samplings showed high levels of catecholamines in the right atrium, a mediastinal and, chiefly, cardiac phaeochromocytoma was suspected. No tumour was visible at CT or ultrasonography and another MIBG scintigraphy proved negative. Coronary angiography showed a very large tumour behind the left atrium, well supplied by the circumflex artery and by a branch of the right coronary artery. The patient was operated upon and is now totally asymptomatic after a 9-month follow-up. This case emphasizes the value of invasive methods (i.e. regional venous sampling and coronary angiography) in the localization of this ectopic tumour. In most cases, however, phaeochromocytomas can be localized by MIBG scintigraphy.

AB - We report an exceptional case of cardiac phaeochromocytoma which raised problems of localization. A 30-year-old man, who for several years had been hypertensive, was admitted for attacks of paroxysmal hypertension. Very high levels of urinary catecholamines suggested a diagnosis of phaeochromocytoma, but no tumour was found at computerized tomography (CT) and metaiodobenzylguanidine (MIBG) scintigraphy. However, regional venous samplings detected 2 para-carotid phaeochromocytomas which were surgically removed. Thereafter, the symptoms persisted and investigations were resumed. As new regional venous samplings showed high levels of catecholamines in the right atrium, a mediastinal and, chiefly, cardiac phaeochromocytoma was suspected. No tumour was visible at CT or ultrasonography and another MIBG scintigraphy proved negative. Coronary angiography showed a very large tumour behind the left atrium, well supplied by the circumflex artery and by a branch of the right coronary artery. The patient was operated upon and is now totally asymptomatic after a 9-month follow-up. This case emphasizes the value of invasive methods (i.e. regional venous sampling and coronary angiography) in the localization of this ectopic tumour. In most cases, however, phaeochromocytomas can be localized by MIBG scintigraphy.

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