phaeochromocytoma
Sign in to saveAlso 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- Phaeochromocytoma.Lancet (London, England) · 2005
- Phaeochromocytoma and paraganglioma.Journal of clinical pathology · 2024
- [Phaeochromocytoma and paraganglioma].La Revue de medecine interne · 2019
- Paediatric phaeochromocytoma and paraganglioma: A clinical update.Clinical endocrinology · 2024
- Pathological grading for predicting metastasis in phaeochromocytoma and paraganglioma.Endocrine-related cancer · 2014
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
- exact match
- www.orpha.net/ORDO/Orphanet_29072
- 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 sectionsContents
- 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.