Literature DB >> 3415797

Pheochromocytoma crisis.

K Newell1, R A Prinz, S Braithwaite, M Brooks.   

Abstract

Of 26 patients with pheochromocytoma treated between 1974 and 1986, two presented with pheochromocytoma crisis. This unusual presentation consists of hyper- and/or hypotension, high fevers (greater than 40 degrees C), encephalopathy, and multiple organ system failure. Both patients had large tumors associated with markedly elevated levels of epinephrine. Although hypertension was adequately controlled in both patients with phenoxybenzamine, phentolamine (1 patient) and nitroprusside, both patients deteriorated rapidly. The first patient expired during attempts to identify a source of sepsis. None was found at autopsy. The second patient underwent urgent adrenalectomy which reversed the multiple organ system failure and resulted in patient survival. We conclude from review of these patients and three others in the literature that (a) crisis is an unusual presentation of pheochromocytoma; (b) its manifestations include vascular lability, high fever, encephalopathy and multiple organ system failure; (c) it may be the result of increased epinephrine secretion; (d) successful treatment of pheochromocytoma crisis demands prompt diagnosis, vigorous medical therapy and emergent tumor removal if the patient continues to deteriorate.

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Mesh:

Year:  1988        PMID: 3415797     DOI: 10.1093/ajh/1.3.189s

Source DB:  PubMed          Journal:  Am J Hypertens        ISSN: 0895-7061            Impact factor:   2.689


  5 in total

Review 1.  Evaluation of endoscopic and traditional open approaches to pheochromocytoma.

Authors:  A M Kazaryan; N S Kuznetsov; A M Shulutko; D G Beltsevich; B Edwin
Journal:  Surg Endosc       Date:  2004-04-27       Impact factor: 4.584

2.  Clinical characteristics and outcomes of pheochromocytoma crisis: a literature review of 200 cases.

Authors:  Y Ando; Y Ono; A Sano; N Fujita; S Ono; Y Tanaka
Journal:  J Endocrinol Invest       Date:  2022-07-20       Impact factor: 5.467

3.  Multiple organ failure and coma as initial presentation of pheochromocytoma in a patient with multiple endocrine neoplasia (MEN) type II A.

Authors:  W Lorz; C Cottier; E Imhof; N Gyr
Journal:  Intensive Care Med       Date:  1993       Impact factor: 17.440

4.  VEGF-A/VEGF-B/VEGF-C expressions in non-hereditary, non-metastatic phaeochromocytoma.

Authors:  Ichiro Abe; Farhadul Islam; Chung Yau Lo; Victor Liew; Suja Pillai; Alfred K Lam
Journal:  Histol Histopathol       Date:  2021-03-18       Impact factor: 2.303

Review 5.  Pheochromocytoma multisystem crisis treated with emergency surgery: a case report and literature review.

Authors:  Katsura Kakoki; Yasuyoshi Miyata; Youhei Shida; Tomoaki Hakariya; Kosuke Takehara; Seiya Izumida; Motohiro Sekino; Naoe Kinoshita; Tsukasa Igawa; Junya Fukuoka; Hideki Sakai
Journal:  BMC Res Notes       Date:  2015-12-09
  5 in total

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