Metabolikusan nem megítélhető

English translation: metabolic activity cannot be confirmed, CT recommended

GLOSSARY ENTRY (DERIVED FROM QUESTION BELOW)
Hungarian term or phrase:Metabolikusan nem megítélhető
English translation:metabolic activity cannot be confirmed, CT recommended
Entered by: Jilt

13:49 Feb 22, 2016
Hungarian to English translations [PRO]
Medical - Medical (general)
Hungarian term or phrase: Metabolikusan nem megítélhető
Kedves forum,

Ezt mit jelent?

Kontextus (PET/CT lelet):
Osszefoglalo velemeny:
A presacralis hegszovetben koros, elsosorban gyulladasos eredetunek imponalo FDG-halmozas lathato gazzarvanyok kornyezeteben. A halmozas ugyanakkor malignus folyamat dusitasat elfedheti. A tudokapukban reaktiv folyamat FDG-felvetele. A bal csipoizuletben bursitis lehetosege. Lumbalisan Baastrup-jelenseg. Egyebekben koros dusitas nem abrazolodott. Pulmonalisan koteges maradvanyok es egy METABOLIKUSAN biztonsaggal NEM MEGITELHETO goc, utobbi CT-kovetese javasolt.

Jilt
Jilt
Netherlands
Local time: 18:12
metabolic activity cannot be confirmed, CT recommended
Explanation:
https://en.wikipedia.org/wiki/Positron_emission_tomography

PET scanning with the tracer fluorine-18 (F-18) fluorodeoxyglucose (FDG), called FDG-PET, is widely used in clinical oncology. This tracer is a glucose analog that is taken up by glucose-using cells and phosphorylated by hexokinase (whose mitochondrial form is greatly elevated in rapidly growing malignant tumours). A typical dose of FDG used in an oncological scan has an effective radiation dose of 14 mSv.[3] Because the oxygen atom that is replaced by F-18 to generate FDG is required for the next step in glucose metabolism in all cells, no further reactions occur in FDG. Furthermore, most tissues (with the notable exception of liver and kidneys) cannot remove the phosphate added by hexokinase. This means that FDG is trapped in any cell that takes it up, until it decays, since phosphorylated sugars, due to their ionic charge, cannot exit from the cell. This results in intense radiolabeling of tissues with high glucose uptake, such as the brain, the liver, and most cancers. As a result, FDG-PET can be used for diagnosis, staging, and monitoring treatment of cancers, particularly in Hodgkin's lymphoma, non-Hodgkin lymphoma, and lung cancer. Many other types of solid tumors will be found to be very highly labeled on a case-by-case basis—a fact that becomes especially useful in searching for tumor metastasis, or for recurrence after a known highly active primary tumor is removed. Because individual PET scans are more expensive than "conventional" imaging with computed tomography (CT) and magnetic resonance imaging (MRI), expansion of FDG-PET in cost-constrained health services will depend on proper health technology assessment; this problem is a difficult one because structural and functional imaging often cannot be directly compared, as they provide different information. Oncology scans using FDG make up over 90% of all PET scans in current practice[citation needed].

A few other isotopes and radiotracers are slowly being introduced into oncology for specific purposes. For example, 11C-labelled metomidate (11C-metomidate), has been used to detect tumors of adrenocortical origin.[4][5] Also, FDOPA PET-CT, in centers which offer it, has proven to be a more sensitive alternative to finding, and also localizing, pheochromocytoma than the MIBG scan.[6][7][8]

magyarul itt:

http://www.citymed.hu/cikkreszletes.php?actmenu=5&actsubmenu...
Selected response from:

Attila Cselenyák
Hungary
Local time: 18:12
Grading comment
Koszonom!
4 KudoZ points were awarded for this answer



Summary of answers provided
4 +1metabolic activity cannot be confirmed, CT recommended
Attila Cselenyák
4 +1Ld.lent
hollowman2


Discussion entries: 3





  

Answers


37 mins   confidence: Answerer confidence 4/5Answerer confidence 4/5 peer agreement (net): +1
metabolic activity cannot be confirmed, CT recommended


Explanation:
https://en.wikipedia.org/wiki/Positron_emission_tomography

PET scanning with the tracer fluorine-18 (F-18) fluorodeoxyglucose (FDG), called FDG-PET, is widely used in clinical oncology. This tracer is a glucose analog that is taken up by glucose-using cells and phosphorylated by hexokinase (whose mitochondrial form is greatly elevated in rapidly growing malignant tumours). A typical dose of FDG used in an oncological scan has an effective radiation dose of 14 mSv.[3] Because the oxygen atom that is replaced by F-18 to generate FDG is required for the next step in glucose metabolism in all cells, no further reactions occur in FDG. Furthermore, most tissues (with the notable exception of liver and kidneys) cannot remove the phosphate added by hexokinase. This means that FDG is trapped in any cell that takes it up, until it decays, since phosphorylated sugars, due to their ionic charge, cannot exit from the cell. This results in intense radiolabeling of tissues with high glucose uptake, such as the brain, the liver, and most cancers. As a result, FDG-PET can be used for diagnosis, staging, and monitoring treatment of cancers, particularly in Hodgkin's lymphoma, non-Hodgkin lymphoma, and lung cancer. Many other types of solid tumors will be found to be very highly labeled on a case-by-case basis—a fact that becomes especially useful in searching for tumor metastasis, or for recurrence after a known highly active primary tumor is removed. Because individual PET scans are more expensive than "conventional" imaging with computed tomography (CT) and magnetic resonance imaging (MRI), expansion of FDG-PET in cost-constrained health services will depend on proper health technology assessment; this problem is a difficult one because structural and functional imaging often cannot be directly compared, as they provide different information. Oncology scans using FDG make up over 90% of all PET scans in current practice[citation needed].

A few other isotopes and radiotracers are slowly being introduced into oncology for specific purposes. For example, 11C-labelled metomidate (11C-metomidate), has been used to detect tumors of adrenocortical origin.[4][5] Also, FDOPA PET-CT, in centers which offer it, has proven to be a more sensitive alternative to finding, and also localizing, pheochromocytoma than the MIBG scan.[6][7][8]

magyarul itt:

http://www.citymed.hu/cikkreszletes.php?actmenu=5&actsubmenu...


    Reference: http://www.citymed.hu/cikkreszletes.php?actmenu=5&actsubmenu...
    Reference: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1255942/
Attila Cselenyák
Hungary
Local time: 18:12
Specializes in field
Native speaker of: Native in HungarianHungarian
PRO pts in category: 28
Grading comment
Koszonom!

Peer comments on this answer (and responses from the answerer)
agree  Erzsébet Czopyk
42 mins
  -> Köszönöm!

neutral  Ildiko Santana: Magyar-magyar volt a kérdés, de én még a Citymed.hu referenciában sem találom a magyarázatot (mármint hogy mit jelent a "metabolikusan nem megítélhető" kifejezés.)
19 hrs
  -> Kedves Ildikó! válaszom a vitafórumban
Login to enter a peer comment (or grade)

1 hr   confidence: Answerer confidence 4/5Answerer confidence 4/5 peer agreement (net): +1
Ld.lent


Explanation:
Az elváltozások (góc) anyagcseréje nem különíthető el a környezetétől, ezért metabolikusan biztonsággal nem állapítható meg a gócról, hogy jóindulatú-e vagy sem, így (a fennálló bizonytalanság miatt) CT-követése javasolt.

hollowman2
Specializes in field
Native speaker of: Native in HungarianHungarian
PRO pts in category: 7

Peer comments on this answer (and responses from the answerer)
agree  Ildiko Santana: Szerintem is. Ld. "A kicsiny elváltozások anyagcseréjét nem lehet elkülöníteni a környezetüktől, ezért írták a leletben azt, hogy metabolikusan nem karakterizálható az elváltozás" http://rakgyogyitas.hu/kerdes/benignus-micronodulus-a-tudobe...
18 hrs
  -> Köszönöm!
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