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phaeochromocytoma
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phaeochromocytoma

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Also known as PCC, adrenal gland pheochromocytoma, PHEOCHROMOCYTOMA, Pheochromocytoma, Susceptibility to, Pheochromocytoma

Pheochromocytoma (British English: phaeochromocytoma) is a rare tumor of the adrenal medulla composed of chromaffin cells and is a pharmacologically volatile, potentially lethal catecholamine-containing tumor of chromaffin tissue. It is part of the paraganglioma (PGL). These neuroendocrine tumors can be sympathetic, where they release catecholamines into the bloodstream which cause the most common symptoms, including hypertension (high blood pressure), tachycardia (fast heart rate), sweating, and headaches. Some PGLs may secrete little to no catecholamines, or only secrete paroxysmally (episod

In the Vinony graph

Vinony's link graph records 281 inbound references to phaeochromocytoma, and connects out to fludeoxyglucose (18F), sweat and magnetic resonance imaging.

It sits within the topics Adrenal gland disorders, Endocrine neoplasia and Rare cancers.

Vinony links it to 36 Wikipedia language editions.

Key facts

Medical condition.name
Pheochromocytoma
Medical condition.synonyms
Phaeochromocytoma, adrenal medullary tumor, chromaffin cell tumors, paraganglioma
Medical condition.image
Adrenal paraganglioma clinical Pheochromocytoma.jpg
Medical condition.caption
Normal remnant adrenal gland (left) with a pheochromocytoma (right) involving the adrenal medulla
Medical condition.field
Endocrinology, oncology
Medical condition.symptoms
Hypertension, tachycardia, anxiety, sweating, headache, pallor
Medical condition.complications
Hypertensive crisis
Medical condition.causes
80% genetic
Medical condition.diagnosis
Elevated plasma free metanephrines, plasma catecholamines, urinary catecholamines, MRI, PET Scan
Medical condition.treatment
Surgery, chemotherapy, radiation, medication
Medical condition.medication
Alpha blockers (doxazosin, prazosin, terazosin), beta blockers
Medical condition.frequency
0.8 per 100,000 persons
Medical condition.pronounce
(fee-oh-kroh-moh-sahy-toh-muh)

via Wikipedia infobox

Research

27,121 papers

via PubMed

Wikidata facts

Subclass of
disease
Image
Pheochromocytoma high mag.jpg
Show 8 more facts
Commons category
Pheochromocytoma
drug or therapy used for treatment
metirosine
health specialty
endocrinology
symptoms and signs
arterial hypertension
genetic association
MAX
on focus list of Wikimedia project
WikiProject Medicine
named by
Ludwig Pick
Sources (6)

via Wikidata · CC0

~57 min read

Encyclopedic overview

43 sections
Contents
  • Signs and symptoms
  • Complications
  • Cardiovascular system
  • Nervous system
  • Urinary system
  • Genetics
  • Pediatric considerations
  • Hereditary syndromes
  • Other gene variants
  • Diagnosis
  • Differential
  • Notes
  • Biochemical evaluation
  • Gold standard
  • Alternative tests
  • Biochemical phenotypes
  • Tumor localization
  • Anatomic imaging
  • Functional imaging
  • Pathology
  • Treatment
  • Surgery
  • Pre-operative management
  • Alpha blockade
  • Beta blockade
  • Complications
  • Controversy
  • Perioperative fluid status
  • Post-operative management
  • Metastatic disease
  • Diagnosis and location
  • Treatment
  • Prognosis
  • Epidemiology
  • History
  • Society and culture
  • Zebra culture
  • Media
  • Famous People with Pheochromocytoma
  • Etymology
  • References
  • Further reading
  • External links

Pheochromocytoma (British English: phaeochromocytoma) is a rare tumor of the adrenal medulla composed of chromaffin cells and is a pharmacologically volatile, potentially lethal catecholamine-containing tumor of chromaffin tissue. It is part of the paraganglioma (PGL). These neuroendocrine tumors can be sympathetic, where they release catecholamines into the bloodstream which cause the most common symptoms, including hypertension (high blood pressure), tachycardia (fast heart rate), sweating, and headaches. Some PGLs may secrete little to no catecholamines, or only secrete paroxysmally (episodically), and other than secretions, PGLs can still become clinically relevant through other secretions or mass effect (most common with head and neck PGL). PGLs of the head and neck are typically parasympathetic and their sympathetic counterparts are predominantly located in the abdomen and pelvis, particularly concentrated at the organ of Zuckerkandl at the bifurcation of the aorta.

== Signs and symptoms == The symptoms of a sympathetic pheochromocytoma are related to sympathetic nervous system hyperactivity. The classic triad includes headaches (likely related to elevated blood pressure, or hypertension), tachycardia/elevated heart rate, and hyperhidrosis (excessive sweating, particularly at night). However, patients are unlikely to experience continuous symptoms. Due to the paroxysmal nature of catecholamine synthesis and release, patients may experience "attacks" or "spells" where they are suddenly overwhelmed with signs and symptoms of their tumor. Attacks can occur spontaneously (without warning) or may be triggered by a variety of pharmaceutical agents (including histamine, metoclopramide, glucagon, and adrenocorticotropic hormone), foods that contain tyramine (cheese and wine), intraoperative tumor manipulation, intubation, or during anesthetic induction. thumb|alt=|250x250px|Adrenal gland; the Adrenal medulla|medulla (center, red) is the origin of the pheochromocytoma. thumb|There is an adrenal gland, highlighted in yellow, on top of each of the kidneys. Other clinical manifestations that have been reported include (in no particular order): Pallor Heat intolerance Weight loss Chest or abdominal discomfort Palpitations Nausea/vomiting Constipation Orthostatic hypotension — becoming lightheaded or dizzy after swiftly changing positions Psychiatric manifestations Anxiety, panic attacks, nervousness, tremors Hyperglycemia (high blood sugar)

Excerpted from Wikipedia’s “phaeochromocytoma” article, available under the CC BY-SA 4.0 licence.

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