Literature DB >> 19114176

Diagnosis and treatment of pheochromocytoma in an academic hospital from 1997 to 2007.

Run Yu1, Nicholas N Nissen, Preeti Chopra, Deepti Dhall, Edward Phillips, Meng Wei.   

Abstract

BACKGROUND: The diagnosis and treatment of pheochromocytoma pose a challenge to physicians. Several trends in the presentation, diagnosis, and surgical treatment of pheochromocytoma have emerged in the last 10 years. The diagnostic accuracy and consequences of misdiagnosis of pheochromocytoma are not well known. We aimed to systemically study the diagnostic accuracy and treatment outcomes of pheochromocytoma and to reveal the causes and consequences of misdiagnosis (including both overdiagnosis and underdiagnosis).
METHODS: We reviewed the electronic and paper charts of 49 patients who underwent adrenalectomy or adrenal biopsy with either preoperative or pathologic diagnosis of pheochromocytoma in a large academic hospital from 1997 to 2007. Three groups of patients (overdiagnosed, correctly diagnosed, and underdiagnosed) were compared on clinical courses, biochemical tests, imaging studies, and surgical outcomes.
RESULTS: Pheochromocytoma was overdiagnosed in 9 patients, correctly diagnosed in 30 patients, and underdiagnosed in 10 patients. The overdiagnosis rate was 23% (9/39), and the underdiagnosis rate was 25% (10/40). The 3 distinct groups of patients exhibited significant differences in clinical presentation, biochemical tests, and imaging characteristics. The most common causes of overdiagnosis were misinterpretation of borderline biochemical test results and overzealous imaging. Overdiagnosis subjected patients to unnecessary adrenalectomy and its complications. The most common cause of underdiagnosis was failure to consider and test for pheochromocytoma. Underdiagnosis resulted in dangerous adrenal biopsy or adrenalectomy with hypertensive crisis and nearly doubled the length of stay in hospital. Surgical resection of correctly diagnosed pheochromocytoma was largely effective and safe, but intraoperative and postoperative complications occurred in some patients.
CONCLUSION: We conclude that misdiagnosis of pheochromocytoma is not uncommon and causes serious adverse effects. Correct interpretation of biochemical tests and imaging is crucial to a correct diagnosis, and pheochromocytoma should always be included in the differential diagnosis of any adrenal mass. Our data suggest that physician education is needed to improve the diagnosis and treatment of pheochromocytoma.

Entities:  

Mesh:

Year:  2009        PMID: 19114176     DOI: 10.1016/j.amjmed.2008.08.021

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  15 in total

1.  Sizable but clinically inapparent adrenal pheochromocytomas.

Authors:  R Yu
Journal:  J Endocrinol Invest       Date:  2012-03       Impact factor: 4.256

Review 2.  Progress and challenges in neuroendocrine and neural crest tumours: molecular imaging and therapy.

Authors:  Giovanni Lucignani; Emilio Bombardieri
Journal:  Eur J Nucl Med Mol Imaging       Date:  2009-12       Impact factor: 9.236

3.  Adrenal venous catecholamine concentrations in patients with adrenal masses other than pheochromocytoma.

Authors:  Yasutaka Baba; Masayuki Nakajo; Sadao Hayashi
Journal:  Endocrine       Date:  2012-09-13       Impact factor: 3.633

Review 4.  Diagnosis and management of pheochromocytoma: a practical guide to clinicians.

Authors:  Joseph M Pappachan; Diana Raskauskiene; Rajagopalan Sriraman; Mahamood Edavalath; Fahmy W Hanna
Journal:  Curr Hypertens Rep       Date:  2014-07       Impact factor: 5.369

Review 5.  Pheochromocytoma and paraganglioma-an update on diagnosis, evaluation, and management.

Authors:  Amrish Jain; Rossana Baracco; Gaurav Kapur
Journal:  Pediatr Nephrol       Date:  2019-01-02       Impact factor: 3.714

Review 6.  Anti-hypertensive treatment in pheochromocytoma and paraganglioma: current management and therapeutic features.

Authors:  Alberto Mazza; Michela Armigliato; Maria Cristina Marzola; Laura Schiavon; Domenico Montemurro; Giorgio Vescovo; Marco Zuin; Sotirios Chondrogiannis; Roberta Ravenni; Giuseppe Opocher; Patrick M Colletti; Domenico Rubello
Journal:  Endocrine       Date:  2013-07-02       Impact factor: 3.633

7.  Cardiac arrest in a patient with asthma: role of hemorrhagic pheochromocytoma discovered at autopsy.

Authors:  Run Yu; Serguei I Bannykh; Alberto Marchevsky
Journal:  J Clin Hypertens (Greenwich)       Date:  2012-05-31       Impact factor: 3.738

8.  Small pheochromocytomas: significance, diagnosis, and outcome.

Authors:  Run Yu; Allison Pitts; Meng Wei
Journal:  J Clin Hypertens (Greenwich)       Date:  2012-03-16       Impact factor: 3.738

9.  Pheochromocytoma: Positive predictive values of mildly elevated urinary fractionated metanephrines in a large cohort of community-dwelling patients.

Authors:  Dania Hirsch; Alon Grossman; Varda Nadler; Sandra Alboim; Gloria Tsvetov
Journal:  J Clin Hypertens (Greenwich)       Date:  2019-09-05       Impact factor: 3.738

10.  A large pheochromocytoma with invasion of multiple local organs.

Authors:  Daming Zhu; Ajith Kumar; William S Weintraub; Ehsanur Rahman
Journal:  J Clin Hypertens (Greenwich)       Date:  2011-01       Impact factor: 3.738

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