Malignant hypertension after adrenalectomy
Author(s) -
K.-M. Chow
Publication year - 2004
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfh335
Subject(s) - medicine , adrenalectomy , cardiology
A 48-year-old Chinese presented with bilateral blurred vision, and was found to have accelerated hypertension and funduscopic manifestation of papilloedema. He had been diagnosed as having a left adrenal tumour 2 months previously, when he first reported anorexia and left upper quadrant pain. Computed tomography (Figure 1) and subsequent laparotomy excision revealed a large adrenocortical carcinoma characterized by moderate pleomorphism of tumour cells and mitosis. Preoperative investigation details were not known to the patient, who was thought to be normotensive at that time. He never reported paroxysmal palpitation or symptoms related to catecholamine excess. His plasma potassium level was 2.7mmol/l (normal range 3.5–5.1mmol/l), with a bicarbonate level of 29mmol/l and corresponding urinary potassium of 51mmol/l. Urinary cortisol and catecholamines were within normal range. Questions
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom