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PedAM

Pediatric Disease Annotations & Medicines




Disease pheochromocytoma
Phenotype C0020538|hypertension
Sentences 31
PubMedID- 23776872 In addition to the classical triad, pheochromocytoma is commonly associated with hypertension, cardiomyopathy, myocardial infarction, and cerebrovascular accident.
PubMedID- 22346144 pheochromocytoma, an uncommon cause of hypertension which has been estimated to occur in 0.1–1% of hypertensive patients,[1] may be a potentially lethal disease with protean manifestations.
PubMedID- 25838955 It is of significant importance to clarify that hypertension due to pheochromocytoma is paroxysmal, appearing before the 20th week of pregnancy and it may be followed by orthostatic hypotension, unlike gestational hypertension.
PubMedID- 20734598 pheochromocytoma was associated with hypertension in 6 cases.
PubMedID- 21060667 Bilateral optic disc swelling has been reported in a child with severe hypertension due to pheochromocytoma without any other evidence of grade 4 hypertensive retinopathy.11 in the absence of other causes of papilledema and the resolution of the papilledema with control of hypertension, the papilledema was attributed to severe hypertension.
PubMedID- 26098187 Among patients with arterial hypertension the prevalence of cushing's syndrome or pheochromocytoma is less than 1%.
PubMedID- 24274233 The prevalence of pheochromocytoma in patients with hypertension, its major presenting symptom, is around 0.1%.
PubMedID- 23956724 hypertension due to pheochromocytoma in children tends to be more severe and refractory than in adults.
PubMedID- 22148096 Intraoperative hypertension in a patient with undiagnosed pheochromocytoma under spinal anesthesia.
PubMedID- 22611502 With hindsight this is not a logical choice since beta-blockade can worsen hypertension in the presence of a phaeochromocytoma, by opposing beta-adrenoceptor-activated vasodilatation in skeletal muscle beds.
PubMedID- 20385503 Objective: the aim of the present study was to evaluate the relationship between adiponectin levels and insulin sensitivity in patients with endocrine hypertension due to pheochromocytoma comparing them to these in patients with essential hypertension and healthy subjects.
PubMedID- 21223554 The prevalence of pheochromocytoma in patients with hypertension is 0.1-0.6%, and secretes both epinephrine and norepinephrine in at least 50% of cases.
PubMedID- 24180171 The real challenge for clinicians is differentiating pheochromocytoma from other causes of hypertension (preeclampsia, gestational hypertension, and pre-existing or essential hypertension), from other cause of pulmonary edema (preeclampsia, peripartum cardiomyopathy, stress or takotsubo cardiomyopathy, pre-existing cardiac disease [mitral stenosis], and high doses betamimetics), and from other causes of cardiovascular collapse (pulmonary embolism, and amniotic fluid embolism).
PubMedID- 25140230 Introduction: the prevalence of phaeochromocytoma (pcc) in patients with hypertension is 0.1-0.6% and about 10% of pccs are detected in extra-adrenal tissue.
PubMedID- 24009805 The patient was transferred back to maternity with a diagnosis of secondary hypertension possibly due to pheochromocytoma and eventually discharged via the ward by the obstetric team/internists on oral prazocin 1mg once daily and oral nifedipine extended release 30mg twice daily.
PubMedID- 24009448 All patients should undergo a hormonal evaluation for subclinical cushing syndrome and pheochromocytoma, and those with hypertension should also be evaluated for primary hyperaldosteronism.
PubMedID- 26413481 In summary, both primary hyperaldosteronism and pheochromocytoma are important causes of endocrine hypertension that carry significant mortality and morbidity, if left untreated.
PubMedID- 24950401 It can be used in large doses for the short term control of hypertension in patients with phaeochromocytoma or in the treatment of hypertensive crisis following the abrupt withdrawal of clonidine.
PubMedID- 23984157 Extreme hypertension is frequently associated with phaeochromocytoma and was evident in our patient, which as discussed previously, may have contributed to vessel rupture, increased haemorrhage and pseudoaneurysm formation.
PubMedID- 22336161 The detectable rate of hypertension in patients with malignant pheochromocytomas in adrenal medulla and in extra-adrenal sites were less than that in benign and potentially malignant ones (p < 0.05).
PubMedID- 21887038 Management of paroxysmal hypertension due to incidental pheochromocytoma in pregnancy.
PubMedID- 21632813 All patients should undergo hormonal evaluation for subclinical cushing's syndrome and pheochromocytoma, and those with hypertension should also be evaluated for hyperaldosteronism.
PubMedID- 20930983 We have reported an unusual case of traumatic hemorrhage of occult pheochromocytoma, presenting with severe labile hypertension and associated with septic shock.
PubMedID- 20560377 hypertension due to pheochromocytoma can be masked by excessive reduction of intravascular volume by preoperative hemodialysis.
PubMedID- 23153989 Gestational diastolic hypertension with gene mutation-related pheochromocytoma positive at (1)(8)f-dopa pet/ct: diagnostic and therapeutic implications.
PubMedID- 24447929 Clinically, phenoxybenzamine is fda approved and currently used to treat hypertension and sweating associated with pheochromocytoma, a condition in which the adrenal glands secrete high levels of noradrenaline and adrenaline.
PubMedID- 22584715 The first two affected individuals, i-2 and ii-3, developed huge neck lumps (presumably mtc) and severe hypertension (presumably due to pheochromocytoma), causing aphonia (presumably as a result of recurrent laryngeal nerve invasion) and hemiplegia at the age of 42 years (presumably following cathecholamine excess) in individual ii-3.
PubMedID- 23401807 In evaluating the hormone function of any adrenal incidentaloma, testing for subclinical cushing's, pheochromocytoma, and hyperaldosteronism (in patients with hypertension) should be performed [1, 2].
PubMedID- 20167034 Malignant pheochromocytoma presenting with uncontrolled hypertension after kidney transplant.
PubMedID- 23806076 Β-blocking agents should not be used in isolation in catecholamine-induced severe hypertension seen with pheochromocytoma or stimulant intoxication, because the unopposed peripheral α-effect could further increase blood pressure [17,56].
PubMedID- 20640152 The diagnosis of pheochromocytoma was suspected in patients with poorly controlled hypertension associated with bouts of sweating, headache, palpitations, a high serum concentration of chromogranin a and a high level of metanephrins in urine.

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