Author:
Riester Anna,Weismann Dirk,Quinkler Marcus,Lichtenauer Urs D,Sommerey Sandra,Halbritter Roland,Penning Randolph,Spitzweg Christine,Schopohl Jochen,Beuschlein Felix,Reincke Martin
Abstract
ObjectivePheochromocytomas are rare chromaffin cell-derived tumors causing paroxysmal episodes of headache, palpitation, sweating and hypertension. Life-threatening complications have been described in case reports and small series. Systematic analyses are not available. We took an opportunity of a large series to make a survey.Design and methodsWe analyzed records of patients diagnosed with pheochromocytomas in three geographically spread German referral centers between 2003 and 2012 (n=135).ResultsEleven percent of the patients (ten women, five men) required in-hospital treatment on intensive care units (ICUs) due to complications caused by unsuspected pheochromocytomas. The main reasons for ICU admission were acute catecholamine induced Tako-Tsubo cardiomyopathy (n=4), myocardial infarction (n=2), acute pulmonary edema (n=2), cerebrovascular stroke (n=2), ischemic ileus (n=1), acute renal failure (n=2), and multi organ failure (n=1). One patient required extracorporeal membrane oxygenation due to a hypertensive crisis with lung edema occurring during delivery (n=1). Two patients died of refractory shock and pheochromocytomas were found postmortem. Two patients were treated by emergency surgery. Compared to pheochromocytoma patients without life-threatening events (n=120), patients with complications had a significant larger maximal tumor diameter (7.0 vs 4.5 cm, P<0.01), higher levels of catecholamines (20- vs ninefold upper limit of normal, P<0.01), and tended to be younger (42 vs 51 years, P=0.05).ConclusionAlthough pheochromocytomas are rare, they are likely to be associated with a life-threatening situation. Clinicians have to be aware of these situations and perform a timely diagnosis.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Reference24 articles.
1. Phaeochromocytoma
2. An Overview of Pheochromocytoma: History, Current Concepts, Vagaries, and Diagnostic Challenges
3. Kopetschke R Slisko M Kilisli A Tuschy U Wallaschofski H Fassnacht M Ventz M Beuschlein F Reincke M Reisch N . Frequent incidental discovery of phaeochromocytoma: data from a German cohort of 201 phaeochromocytoma. European Journal of Endocrinology/European Federation of Endocrine Societies 2009 161 355–361. (doi:10.1530/EJE-09-0384).
4. Adrenal pheochromocytoma remains a frequently overlooked diagnosis
5. Platts JK Drew PJ Harvey JN . Death from phaeochromocytoma: lessons from a post-mortem survey. Journal of the Royal College of Physicians of London 1995 29 299–306.
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