Literature DB >> 21311646

Paraganglioma in a young patient with asymptomatic severe hypertension: a case report and review of the literature.

Ch Koumaras, P Anagnostis, M Tzimou, I Giavanidis, Th Gossios, A Antoniadis, V G Athyros, A Karagiannis.   

Abstract

We present a case of a 19-year old woman who was admitted to our department with a recently, and incidentally, diagnosed severe hypertension [220/140 mmHg systolic/diastolic blood pressure (BP)]. The patient was asymptomatic. The laboratory investigation demonstrated both elevated plasma norepinephrine (1807 pg/ml, normal range 120-350 pg/ml) and 24h urinary free catecholamines (483 µg/24h, normal range <150 µg/24h), making the diagnosis of a catecholamineproducing tumor highly probable. Although magnetic resonance imaging of the abdomen showed normal adrenal glands, it revealed a mass (4x4 cm) anterior to the inferior vena cava. The diagnosis of paraganglioma was confirmed by the (131)Imeta- iodobenzylguanidine scintigraphy. Preoperatively, α- and β-adrenergic receptor blockers were administered. After successful resection of the tumor, the patient's BP was restored to normal and remained stable during the 3-month follow up. Plasma and 24h urinary catecholamine levels were also normalized. In conclusion, it is important to consider paragangliomas as a possible cause of secondary hypertension and proceed to diagnosis and treatment as described above, since surgical removal of the tumor, especially in sporadic cases, may cure the patient.

Entities:  

Keywords:  catecholamines; hypertension; paraganglioma

Year:  2010        PMID: 21311646      PMCID: PMC3031332     

Source DB:  PubMed          Journal:  Hippokratia        ISSN: 1108-4189            Impact factor:   0.471


  18 in total

Review 1.  Pheochromocytoma and functional paraganglioma syndrome: no longer the 10% tumor.

Authors:  Elisabeth Edström Elder; Grahame Elder; Catharina Larsson
Journal:  J Surg Oncol       Date:  2005-03-01       Impact factor: 3.454

2.  Biochemical diagnosis of pheochromocytoma: which test is best?

Authors:  Jacques W M Lenders; Karel Pacak; McClellan M Walther; W Marston Linehan; Massimo Mannelli; Peter Friberg; Harry R Keiser; David S Goldstein; Graeme Eisenhofer
Journal:  JAMA       Date:  2002-03-20       Impact factor: 56.272

3.  High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing.

Authors:  Frederieke M Brouwers; Graeme Eisenhofer; Jessica J Tao; Jeffrey A Kant; Karen T Adams; W Marston Linehan; Karel Pacak
Journal:  J Clin Endocrinol Metab       Date:  2006-08-15       Impact factor: 5.958

4.  Phaeochromocytomas presenting as acute crises after beta blockade therapy.

Authors:  L Sibal; A Jovanovic; S C Agarwal; R T Peaston; R A James; T W J Lennard; R Bliss; A Batchelor; P Perros
Journal:  Clin Endocrinol (Oxf)       Date:  2006-08       Impact factor: 3.478

5.  Pheochromocytoma and paraganglioma in children: a report of 24 cases of the French Society of Pediatric Oncology.

Authors:  Y Perel; M Schlumberger; G Marguerite; N Alos; Y Revillon; D Sommelet; L De Lumley; F Flamant; J F Dyon; P Lutz; H Heloury; J Lemerle
Journal:  Pediatr Hematol Oncol       Date:  1997 Sep-Oct       Impact factor: 1.969

6.  Circulating and urinary catecholamines in pheochromocytoma. Diagnostic and pathophysiologic implications.

Authors:  E L Bravo; R C Tarazi; R W Gifford; B H Stewart
Journal:  N Engl J Med       Date:  1979-09-27       Impact factor: 91.245

Review 7.  The optimal imaging of adrenal tumours: a comparison of different methods.

Authors:  Ioannis Ilias; Anju Sahdev; Rodney H Reznek; Ashley B Grossman; Karel Pacak
Journal:  Endocr Relat Cancer       Date:  2007-09       Impact factor: 5.678

Review 8.  Adrenal incidentaloma: a diagnostic challenge.

Authors:  Panagiotis Anagnostis; Asterios Karagiannis; Konstantinos Tziomalos; Anna I Kakafika; Vasilios G Athyros; Dimitri P Mikhailidis
Journal:  Hormones (Athens)       Date:  2009 Jul-Sep       Impact factor: 2.885

Review 9.  Pheochromocytoma: an update on genetics and management.

Authors:  Asterios Karagiannis; Dimitri P Mikhailidis; Vasilios G Athyros; Faidon Harsoulis
Journal:  Endocr Relat Cancer       Date:  2007-12       Impact factor: 5.678

10.  Prevalence of clinically unsuspected pheochromocytoma. Review of a 50-year autopsy series.

Authors:  M G Sutton; S G Sheps; J T Lie
Journal:  Mayo Clin Proc       Date:  1981-06       Impact factor: 7.616

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  1 in total

1.  Hypertensive crisis during wide excision of gastrointestinal stromal cell tumor (GIST): Undiagnosed paraganglioma -A case report-.

Authors:  Helen Ki Shinn; Jong Kwon Jung; Jay Kim Park; Jong Hoon Kim; In Young Jung; Hong Sik Lee
Journal:  Korean J Anesthesiol       Date:  2012-03-21
  1 in total

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