Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma
Pheochromocytomas are rare neuroendocrine tumors that originate in chromaffin cells of the adrenal medulla and excessively secrete catecholamines, which leads to a multitude of different symptoms. The most common symptoms include headaches, palpitations, and sweating. Because of a diverse clinica...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Sestre Milosrdnice University hospital, Institute of Clinical Medical Research
2024-01-01
|
| Series: | Acta Clinica Croatica |
| Subjects: | |
| Online Access: | https://hrcak.srce.hr/file/481698 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1849320628841086976 |
|---|---|
| author | Romana Marušić Tajana Turk Tatjana Bačun |
| author_facet | Romana Marušić Tajana Turk Tatjana Bačun |
| author_sort | Romana Marušić |
| collection | DOAJ |
| description | Pheochromocytomas are rare neuroendocrine tumors that originate in chromaffin
cells of the adrenal medulla and excessively secrete catecholamines, which leads to a multitude of different
symptoms. The most common symptoms include headaches, palpitations, and sweating. Because
of a diverse clinical presentation, pheochromocytomas pose a major diagnostic challenge and often go
unidentified. These tumors can occur sporadically or as a part of hereditary syndromes. The diagnosis
is confirmed by measuring plasma and 24-hour urinary metanephrine and normetanephrine. Computed
tomography, magnetic resonance imaging, and functional morphological examinations are used for
tumor localization. The treatment is operative and requires special preoperative patient preparation to
prevent hypertensive crisis and arrhythmias. Due to the possibility of recurrence, the patient needs to
be monitored. Pheochromocytoma has a high fatality rate if not recognized on time due to the effect of
catecholamines on the cardiovascular system. |
| format | Article |
| id | doaj-art-29bdceccf0da4f06b1bd86fec42bca90 |
| institution | Kabale University |
| issn | 0353-9466 1333-9451 |
| language | English |
| publishDate | 2024-01-01 |
| publisher | Sestre Milosrdnice University hospital, Institute of Clinical Medical Research |
| record_format | Article |
| series | Acta Clinica Croatica |
| spelling | doaj-art-29bdceccf0da4f06b1bd86fec42bca902025-08-20T03:50:01ZengSestre Milosrdnice University hospital, Institute of Clinical Medical ResearchActa Clinica Croatica0353-94661333-94512024-01-0163.3-450151110.20471/acc.2024.63.03-04.07Clinical Evaluation, Diagnosis and Treatment of PheochromocytomaRomana Marušić0Tajana Turk1Tatjana Bačun2School of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, CroatiaSchool of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia; Department of Radiology, Osijek University Hospital Center, Osijek, CroatiaSchool of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia; Department of Internal Medicine, Osijek University Hospital Center, Osijek, CroatiaPheochromocytomas are rare neuroendocrine tumors that originate in chromaffin cells of the adrenal medulla and excessively secrete catecholamines, which leads to a multitude of different symptoms. The most common symptoms include headaches, palpitations, and sweating. Because of a diverse clinical presentation, pheochromocytomas pose a major diagnostic challenge and often go unidentified. These tumors can occur sporadically or as a part of hereditary syndromes. The diagnosis is confirmed by measuring plasma and 24-hour urinary metanephrine and normetanephrine. Computed tomography, magnetic resonance imaging, and functional morphological examinations are used for tumor localization. The treatment is operative and requires special preoperative patient preparation to prevent hypertensive crisis and arrhythmias. Due to the possibility of recurrence, the patient needs to be monitored. Pheochromocytoma has a high fatality rate if not recognized on time due to the effect of catecholamines on the cardiovascular system.https://hrcak.srce.hr/file/481698PheochromocytomaHeadacheMultiple endocrine neoplasia type 2PalpitationsParoxysmal hypertension |
| spellingShingle | Romana Marušić Tajana Turk Tatjana Bačun Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma Acta Clinica Croatica Pheochromocytoma Headache Multiple endocrine neoplasia type 2 Palpitations Paroxysmal hypertension |
| title | Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma |
| title_full | Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma |
| title_fullStr | Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma |
| title_full_unstemmed | Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma |
| title_short | Clinical Evaluation, Diagnosis and Treatment of Pheochromocytoma |
| title_sort | clinical evaluation diagnosis and treatment of pheochromocytoma |
| topic | Pheochromocytoma Headache Multiple endocrine neoplasia type 2 Palpitations Paroxysmal hypertension |
| url | https://hrcak.srce.hr/file/481698 |
| work_keys_str_mv | AT romanamarusic clinicalevaluationdiagnosisandtreatmentofpheochromocytoma AT tajanaturk clinicalevaluationdiagnosisandtreatmentofpheochromocytoma AT tatjanabacun clinicalevaluationdiagnosisandtreatmentofpheochromocytoma |