Adrenocortical carcinoma other imaging studies: Difference between revisions

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*MIBG scan
*MIBG scan
*[[Bone scan]]s are used to visualize bone [[metastasis]]
*[[Bone scan]]s are used to visualize bone [[metastasis]]
ACC typically presents as a large, heterogeneous mass
with intense FDG uptake greater than liver background
(Figure 4). In a study of 77 patients with surgically proven
diagnosis of ACA or ACC, [18F]FDG PET/CT had a sensitivity
of 100% and specificity of 88% in distinguishing
benign from malignant lesions by using cutoff value above
1.45 for adrenal to liver maximum standardized uptake
value (SUV). In the same study using a cutoff value of 3.4
for adrenal maximum SUV, the sensitivity was 100% and
specificity70%(108). Assessment of morphological characteristics
such as tumor size, heterogeneity, and irregular
margins as well as attenuation value and metabolic activity
is likely to improve accuracy. [18F]FDG PET/CT, however,
cannot distinguish ACC from metastases, lymphoma,
or pheochromocytoma, which also exhibit high
metabolic activity (109). In a meta-analysis of published
data to determine the diagnostic utility of [18F]FDG
PET/CT for distinguishing benign from malignant adrenal
tumors, [18F]FDG PET/CT had sensitivity of 97% and
specificity of 91% (109). No significant difference in accuracy
was found between visual analysis, SUV analysis,
and standardized uptake ratio (defined as ratio of adrenal
SUV activity to liver SUV activity) analysis.
[18F]FDG PET/CT is a useful modality for stagingACC
and evaluating local recurrence. In a study on 22 patients
with ACC, sensitivity of [18F]FDG PET/CT was 90% for
diagnosis of metastases as compared with 88% for diagnostic
CT. However, they should be considered complementary
imaging modalities because 12% and 10% of
lesions were seen only by [18F]FDG PET/CT or CT, respectively
(110). [18F]FDG PET/CT has low sensitivity for
characterization of smaller lesions, particularly for those lesions less than 10 mm in diameter (111). Intensity of
FDGuptake was found to be related to survival in patients
with ACC, with a maximum SUV of _10 indicating poor
prognosis (111). In a study of 12 patients with previously
resectedACC,[18F]FDGPET/CTcorrectly identified local
tumor recurrence in all patients (112). [18F]FDG is not a
tumor-specific tracer, and increased uptake may be seen in
benign conditions including postoperative changes.
Functional imaging by positron emission tomography
(PET) with [18F]fluorodeoxyglucose (FDG) and [11C]me-tomidate (MTO) or [123I]MTO (where available) may be
used to confirm diagnosis of a malignant lesion or establish
the adrenocortical origin of a tumor. NP59 ([131I]-
iodocholesterol) scans are no longer available.
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 15:23, 20 September 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]

Overview

Adrenal angiography,venography, positron emission tomography and MIBG may be used in the diagnosis of adrenocortical carcinoma.

Other Imaging Studies

Other Imaging studies that may be used in diagnosis of adrenocortical carcinoma are:[1]

ACC typically presents as a large, heterogeneous mass

with intense FDG uptake greater than liver background

(Figure 4). In a study of 77 patients with surgically proven

diagnosis of ACA or ACC, [18F]FDG PET/CT had a sensitivity

of 100% and specificity of 88% in distinguishing

benign from malignant lesions by using cutoff value above

1.45 for adrenal to liver maximum standardized uptake

value (SUV). In the same study using a cutoff value of 3.4

for adrenal maximum SUV, the sensitivity was 100% and

specificity70%(108). Assessment of morphological characteristics

such as tumor size, heterogeneity, and irregular

margins as well as attenuation value and metabolic activity

is likely to improve accuracy. [18F]FDG PET/CT, however,

cannot distinguish ACC from metastases, lymphoma,

or pheochromocytoma, which also exhibit high

metabolic activity (109). In a meta-analysis of published

data to determine the diagnostic utility of [18F]FDG

PET/CT for distinguishing benign from malignant adrenal

tumors, [18F]FDG PET/CT had sensitivity of 97% and

specificity of 91% (109). No significant difference in accuracy

was found between visual analysis, SUV analysis,

and standardized uptake ratio (defined as ratio of adrenal

SUV activity to liver SUV activity) analysis.

[18F]FDG PET/CT is a useful modality for stagingACC

and evaluating local recurrence. In a study on 22 patients

with ACC, sensitivity of [18F]FDG PET/CT was 90% for

diagnosis of metastases as compared with 88% for diagnostic

CT. However, they should be considered complementary

imaging modalities because 12% and 10% of

lesions were seen only by [18F]FDG PET/CT or CT, respectively

(110). [18F]FDG PET/CT has low sensitivity for

characterization of smaller lesions, particularly for those lesions less than 10 mm in diameter (111). Intensity of

FDGuptake was found to be related to survival in patients

with ACC, with a maximum SUV of _10 indicating poor

prognosis (111). In a study of 12 patients with previously

resectedACC,[18F]FDGPET/CTcorrectly identified local

tumor recurrence in all patients (112). [18F]FDG is not a

tumor-specific tracer, and increased uptake may be seen in

benign conditions including postoperative changes.

Functional imaging by positron emission tomography

(PET) with [18F]fluorodeoxyglucose (FDG) and [11C]me-tomidate (MTO) or [123I]MTO (where available) may be

used to confirm diagnosis of a malignant lesion or establish

the adrenocortical origin of a tumor. NP59 ([131I]-

iodocholesterol) scans are no longer available.

References

  1. National Cancer Institute. Physician Data Query Database 2015. http://www.cancer.gov/types/adrenocortical/patient/adrenocortical-treatment-pdq#section/_1

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