Literature DB >> 2899426

Pheochromocytoma multisystem crisis. A surgical emergency.

K A Newell1, R A Prinz, J Pickleman, S Braithwaite, M Brooks, T H Karson, S Glisson.   

Abstract

Three of 27 patients treated for pheochromocytoma between 1974 and 1987 presented with pheochromocytoma multisystem crisis (PMC). This unusual presentation consists of multiple organ system failure, temperature often greater than 40 degrees C, encephalopathy, and hypertension and/or hypotension. Although urgent medical therapy achieved blood pressure control in all three patients, the other manifestations of PMC progressed rapidly in spite of alpha and even beta blockade. The first patient died during attempts to localize a septic focus. The other two patients underwent urgent adrenalectomy and had postoperative improvement in their multiple organ system failure. All three tumors were large and produced markedly elevated levels of epinephrine. In conclusion (1) PMC is an unusual presentation of pheochromocytoma; (2) its manifestations include multiple organ system failure, high fever, encephalopathy, and vascular lability; (3) it may result from increased epinephrine secretion; and (4) successful treatment of PMC demands prompt diagnosis, vigorous medical preparation, and emergency tumor removal if the patient's condition continues to deteriorate.

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Year:  1988        PMID: 2899426     DOI: 10.1001/archsurg.1988.01400320042007

Source DB:  PubMed          Journal:  Arch Surg        ISSN: 0004-0010


  23 in total

Review 1.  Pheochromocytoma as an endocrine emergency.

Authors:  Frederieke M Brouwers; Jacques W M Lenders; Graeme Eisenhofer; Karel Pacak
Journal:  Rev Endocr Metab Disord       Date:  2003-05       Impact factor: 6.514

2.  Pheochromocytoma multisystem crisis successfully treated by emergency surgery: report of a case.

Authors:  Naotaka Uchida; Kiyosuke Ishiguro; Takako Suda; Motonobu Nishimura
Journal:  Surg Today       Date:  2010-09-25       Impact factor: 2.549

3.  Hypertension in pheochromocytoma: characteristics and treatment.

Authors:  Samuel M Zuber; Vitaly Kantorovich; Karel Pacak
Journal:  Endocrinol Metab Clin North Am       Date:  2011-06       Impact factor: 4.741

4.  No evidence for increased mortality in SDHD variant carriers compared with the general population.

Authors:  Leonie T van Hulsteijn; Berdine Heesterman; Jeroen C Jansen; Jean-Pierre Bayley; Frederik J Hes; Eleonora P M Corssmit; Olaf M Dekkers
Journal:  Eur J Hum Genet       Date:  2015-03-11       Impact factor: 4.246

Review 5.  Pheochromocytoma: diagnosis and management update.

Authors:  William M Manger; Graeme Eisenhofer
Journal:  Curr Hypertens Rep       Date:  2004-12       Impact factor: 5.369

Review 6.  Adrenal disorders in pregnancy.

Authors:  Silvia Monticone; Richard J Auchus; William E Rainey
Journal:  Nat Rev Endocrinol       Date:  2012-09-11       Impact factor: 43.330

Review 7.  Adverse drug reactions in patients with phaeochromocytoma: incidence, prevention and management.

Authors:  Graeme Eisenhofer; Graham Rivers; Alejandro L Rosas; Zena Quezado; William M Manger; Karel Pacak
Journal:  Drug Saf       Date:  2007       Impact factor: 5.606

8.  Phaeochromocytoma presenting as acute hyperamylasaemia and multiple organ failure.

Authors:  T J Gan; R F Miller; A R Webb; R C Russell
Journal:  Can J Anaesth       Date:  1994-03       Impact factor: 5.063

9.  Pheochromocytoma multisystem crisis with transient stress cardiomyopathy due to ruptured pheochromocytoma.

Authors:  Kenji Sakamoto; Suano Kojima; Seiji Hokimoto; Hisao Ogawa
Journal:  BMJ Case Rep       Date:  2015-12-09

Review 10.  Pheochromocytoma.

Authors:  William M Manger; Ray W Gifford
Journal:  J Clin Hypertens (Greenwich)       Date:  2002 Jan-Feb       Impact factor: 3.738

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