Descriptor English: | Pheochromocytoma | ||||||
Descriptor Spanish: |
Feocromocitoma
| ||||||
Descriptor Portuguese: | Feocromocitoma | ||||||
Descriptor French: | Phéochromocytome | ||||||
Entry term(s): |
Extra-Adrenal Pheochromocytoma Extra-Adrenal Pheochromocytomas Pheochromocytoma, Extra Adrenal Pheochromocytoma, Extra-Adrenal Pheochromocytomas Pheochromocytomas, Extra-Adrenal |
||||||
Tree number(s): |
C04.557.465.625.650.700.725 C04.557.580.625.650.700.725 |
||||||
RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D010673 | ||||||
Scope note: | A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) |
||||||
Annotation: | benign or malignant; coord IM with usually ADRENAL GLAND NEOPLASMS (IM) |
||||||
Allowable Qualifiers: |
BL blood BS blood supply CF cerebrospinal fluid CH chemistry CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SC secondary SU surgery TH therapy UL ultrastructure UR urine VE veterinary VI virology |
||||||
Related: |
Multiple Endocrine Neoplasia Type 2a
MeSH Multiple Endocrine Neoplasia Type 2b MeSH | ||||||
DeCS ID: | 10868 | ||||||
Unique ID: | D010673 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1966/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2012/07/03 |
-
-
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms
|
Pheochromocytoma
- Preferred
Pheochromocytoma, Extra-Adrenal
- Narrower
Concept UI |
M0016586 |
Scope note | A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) |
Preferred term | Pheochromocytoma |
Entry term(s) |
Pheochromocytomas |
Concept UI |
M0444542 |
Preferred term | Pheochromocytoma, Extra-Adrenal |
Entry term(s) |
Extra-Adrenal Pheochromocytoma Extra-Adrenal Pheochromocytomas Pheochromocytoma, Extra Adrenal Pheochromocytomas, Extra-Adrenal |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey