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<article xmlns:xlink="http://www.w3.org/1999/xlink">
  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Overview of the ImageCLEF 2015 liver CT annotation task</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Neda B.Marvasti</string-name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>María del Mar Roldán García</string-name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Suzan Uskudarli</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>José F. Aldana</string-name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Burak Acar</string-name>
          <email>acarbu@boun.edu.tr</email>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>Boğaziçi University, Computer Engineering Department</institution>
          ,
          <addr-line>Istanbul</addr-line>
          ,
          <country country="TR">Turkey</country>
        </aff>
        <aff id="aff1">
          <label>1</label>
          <institution>Boğaziçi University, Electrical and Electronics Department</institution>
          ,
          <addr-line>Istanbul</addr-line>
          ,
          <country country="TR">Turkey</country>
        </aff>
        <aff id="aff2">
          <label>2</label>
          <institution>University of Malaga, Computer Languages and Computing Science Department Malaga 29071</institution>
          ,
          <addr-line>Spain vavlab.ee.boun.edu.tr</addr-line>
        </aff>
      </contrib-group>
      <abstract>
        <p>The second Liver CT (Computed tomography) annotation challenge was organized during the 2015 Image-CLEF workshop, hosted by the Institut de Recherche en Informatique de Toulouse (IRIT), University of Toulouse, France. This challenge entailed the annotation of Liver CT scans to generate structured reports. This paper describes the motivations for this task, training and test datasets, the evaluation methods, and discusses the approaches of the participating groups.</p>
      </abstract>
      <kwd-group>
        <kwd>ImageCLEF</kwd>
        <kwd>Liver CT annotation task</kwd>
        <kwd>Automatic annotation</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>INTRODUCTION</title>
      <p>ImageCLEF [7] was part of the Cross Language Evaluation Forum (CLEF) 2015
consisting of four main tasks: Image Annotation, Medical Classification, Medical
Clustering, and Liver CT Annotation. It was the second time that the automatic
annotation of Liver CT images was provided as a challenge. However, there are
two changes compared to the last edition of the challenge. First, the format of
the given UsE (user expressed) features has been changed. Furthermore, there
is no CoG (Computer generated) features provided this year. In the term of UsE
features, LiCO (liver case ontology) is used instead of ONLIRA (ontology of
liver for radiology)[4], which has additional patient and study information.</p>
      <p>The purpose of the Liver CT annotation task is to automatically generate
structured reports with use of computer generated features of liver CT volumes.
Structured reports are highly valuable in medical contexts due to the processing
opportunities they provide, such as reporting, image retrieval, and
computeraided diagnosis systems. However, structured report generation is cumbersome
and time consuming. Furthermore, their creation requires administration of the
domain expert, who is time constrained. Consequently, such structured medical
reports are often not found or are incomplete in practice. This challenge has
been designed to aid the fill a pre-prepared structured report using the imaging
information derived from CT images.</p>
      <p>
        The data provided for this challenge consists of 50 training and 10 test
datasets. Participants were asked to answer a fixed set of multiple-choice
questions about livers. The questions were automatically generated from an
opensource liver case ontology (LiCO) [4] and provided in files with RDF (resource
description framework) format. The answers to the questions describe the
properties of the liver, the hepatic vasculature of the liver, and a specific lesion within
it. During this task, the user is presented with the following training data: (
        <xref ref-type="bibr" rid="ref1">1</xref>
        )
data from a CT scan, (
        <xref ref-type="bibr" rid="ref2">2</xref>
        ) a liver mask, (
        <xref ref-type="bibr" rid="ref3">3</xref>
        ) a volume-of-interest that highlights the
selected lesion, and (
        <xref ref-type="bibr" rid="ref4">4</xref>
        ) a rich set of imaging observations (annotations) provided
in RDF format. The imaging observations are LiCObased annotations that were
manually entered by radiologists. Participants need to extract their own image
features from the CT data and use them to automatically annotate the liver
CT volumes. The results have been evaluated in terms of the completeness and
accuracy of the generated annotations.
      </p>
      <p>The rest of the paper is organized as follows, Section 2 gives a detailed
description of the task and introduces the participants. Section 3 presents the
main results of the task and the results of the participants, and finally, Section 4
concludes the paper.
2</p>
    </sec>
    <sec id="sec-2">
      <title>The Liver CT Annotation Challenge</title>
      <p>This section describes the task and introduces the participants.
2.1</p>
      <p>Task Definition and Datasets
The Liver CT annotation task is proposed towards the generation of structured
reports describing the semantic features of the liver, its vascularity, and the types
of its lesions. The goal of this task is to develop automated mechanisms to assist
medical experts in difficult and practically infeasible task of annotating medical
records.</p>
      <p>The training dataset includes 50 cases, each consisting of:
– a cropped CT image of the liver – a 3D matrix with the same size as cropped</p>
      <p>CT image,
– a liver mask that specifies the part corresponding to the liver – a 3D matrix
indicating the liver areas with a 1 and nonliver areas with a 0,
– a bounding box (ROI) corresponding to the region of the selected lesion
within the liver – as a vector of 6 numbers corresponding to the coordinates
of two opposite corners,
– An RDF file generated using LiCOrepresenting manually entered imaging
observations by a radiologist. In total, there are 73 UsE features. If a feature
is not applicable for a case, it will not be represented in the corresponding
RDF file.</p>
      <p>In the training set, 50 ".mat" files, each containing the first three of above data,
as well as an RDF file representing the imaging observations, have been given to
the participants. In the test set, there is no RDF file and imaging observations are
missing and participants are asked to predict them. The participants have been
asked to extract and use their own image features to complete the task. RFD
files include information of patient, study, and imaging observation. Participants
are expected to predict the only imaging information, same as the last year’s
challenge.</p>
      <p>The resolution of CT images may vary in the range of (x : 190 308 pixels,
y : 213 238 pixels, and z : 41 588 slices). The spacing may also vary in the
range of (x; y : 0:674 1:007 mm, slice : 0:399 2:5 mm).</p>
      <p>It is important to note that, this dataset is partially available through
imageCLEF2015 system (http://medgift.hevs.ch:8080/CLEF2015/faces/Login.
jsp), for academic use only. If you are interested in using this dataset, you need
to properly cite this paper.</p>
      <p>User Expressed Features Imaging observations of a radiologist for the liver
domain are represented with LiCO. A web-based data collection application,
called CaReRa-Web (case retrieval in radiological databases), which can be
accessed for academic use from the CaReRa project website http://www.vavlab.
ee.boun.edu.tr.</p>
      <p>For each case, there are 73 UsE features represented in RDF format. These
features clinically characterize the liver, hepatic vascularity, and liver’s lesions. In
the training set, the UsE features are manually entered by an expert radiologist.
Every UsE feature corresponds to a question answered by a radiologist. Some UsE
features may take on more than one values. Such features are represented with
a multi-choice answers. Features with value marked as "NA" are not included in
the RDF file.</p>
      <p>In the test phase, the participants are expected to predict the UsE features
in the following format (73 4 UsE data):</p>
      <p>Column Annotation Features Type
1 Group string
2 Concept string
3 Properties string
4 Values bar separated list of strings</p>
      <p>The "Group" and "Concept" are the LiCO-based concepts. Each concept may
have several properties. Each property may have multiple values, whose indices
and meaning are given in Table 4 under "Possible values" column. Properties
deemed irrelevant are marked as NA by the radiologist. Note that, UsE features
are grouped as: Liver, Vessel, General, and Lesion. Table 4 lists every group
and its corresponding concepts, properties, possible values, and their assigned
indices.</p>
      <p>In every RDF file, there is a patient which has a study and a set of data
properties same as Name, age and gender, as well as a set of object properties
same as disease and drugs. Each study has a set of data properties including ID
and dates as well as a set of object properties same as laboratory results and
physical examinations. Also each study has a liver, which has a set of imaging
observation. Each liver also has a lesion, which has relevant imaging observation.
2.2</p>
      <p>Evaluation methodology
The evaluation is performed on the basis of completeness and accuracy of the
predicted annotations with reference to the manual annotations of the test dataset.
Completeness is defined as the number of predicted features divided by the total
number of features, while accuracy is the number of correctly-predicted features
divided by the total number of predicted features.</p>
      <p>For answers that allow multiple values to a question, the correct prediction
of a single feature is considered as the correct annotation.</p>
      <p>Completeness =
number of predicted U sE f eatures</p>
      <p>T otal number of U sE f eatures
Accuracy =
number of correctly predicted U sE f eatures</p>
      <p>N umber of predicted U sE f eatures
T otalScore = pCompleteness</p>
      <p>
        Accuracy
(
        <xref ref-type="bibr" rid="ref1">1</xref>
        )
(
        <xref ref-type="bibr" rid="ref2">2</xref>
        )
(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
2.3
      </p>
      <p>Participation
Among 32 groups, which registered for the task and signed the license agreement
to access the datasets, only 1 of them submitted his results. The group name
is "CREDOM", from Biomedical Engineering Laboratory, Tlemcen University,
Algeria. They have submitted three runs to the task.
3
3.1</p>
    </sec>
    <sec id="sec-3">
      <title>Results</title>
      <p>Runs submitted in 2014
Last year in 2014 [1], three groups submitted their results. Their prediction were
based on classifiers, image retrieval, and generalized-coupled tensor
factorization (GCTF). Last year a set of computer generated (CoG) features were also
provided for the participants as an optional data.</p>
      <p>The best performance was achieved by the BMET group [5] submitting 8
runs using two different methods: classifier-based approach using SVM (support
vector machine) and image retrieval algorithm. They also used two different sets
of feature: the prepared CoG features from the database and a bag of visual
words (BoVW). Their classification methods outperformed the other methods,
when they employed their expanded feature set. However, their retrieval method
gave the best results, when the given CoG features were employed. This
observation suggests that the nature of feature sets are important for utilizing different
methods.</p>
      <p>The second best performance was achieved by CASMIP group [2] submitting
only one run to the task. They tried four different classifiers in the learning
phase: linear discriminant analysis (LDA), logistic regression (LR), K-nearest
neighbors (KNN), and finally SVM to predict UsE features. For each UsE feature
the best classifier and its related features were learnt by using exhaustive search.
They used only a certain part of provided CoG features, as well as 9 additional
features extracted in the lesion ROI. As a result, for most of the UsE features,
they achieved the same performance using any classifier and any combination of
image features.</p>
      <p>piLabVAVlab group [3] considered the dataset as heterogeneous data and
GCTF approach was applied to predict UsE features. They considered both
KLdivergence and Euclidean-distance-based cost functions, as well as the coupled
matrix factorization models using GCTF framework.</p>
      <p>The BMET group achieved the highest scores with completeness of %98 (See
Table 3. In terms of accuracy, BMET group has also attained the best score by
using an image retrieval method.
3.2</p>
      <p>Runs submitted this year in 2015
This year in 2015, three runs has been submitted by the "CREDOM" group
[6]. They used two different methods: classification by using random forest (RF)
classifier, and retrieval by considering the specific signature of the liver (See
Table 1.</p>
      <p>For the classification-based method (run 1 and run 2), they have employed
two different sets of features. The first set contains 115 liver texture features
in addition to 9 lesion geometric features, and the second set includes 214
lesion texture features, in addition to 9 lesion geometric features. Classification
is performed by using supervised multi-class RF classifier. In this method, they
divided the UsE features into two groups. For the first group, they have used the
RF classifier, but for the second group, they have used a retrieval based method
with their proposed similarity metric. The reason of proposing this separation is
the unbalanced dataset.</p>
      <p>Second method (run 3) is a retrieval-based method. Basically, they have
encoded the 2D image extracted from the central slice of the lesion by applying
1D Log-Gabor filter, and then break the output of the filter into small blocks
and quantize the dominant angular direction of each block to four levels by
using Daugman method. Afterward, the Hamming distance has been employed
as the similarity metric to retrieve the five most similar images to the test image.
Finally, for each UsE feature, they have used majority voting between retrieved
images.</p>
      <p>Among 73 UsE features, 7 of them were excluded from the evaluation because
of their unbounded labels (numeric continuous values). Table 1, compares the
results of three submitted runs in terms of completeness, accuracy and total
scores.</p>
      <p>
        Table 2 compares the results of different runs in predicting different groups
of UsE features. We divide UsE features into 5 groups: liver, vessels and three
lesion groups with area, lesion and component concepts. Results show that all
runs have completed UsE features of the liver and vessel with high accuracy.
None of the runs can completely annotate the component-related concepts of
lesions. Lesion-related concepts of lesion are fully completed, while showing a
very low accuracy. Results show that the third run (retrieval based method),
outperforms the other runs.
This was the second time that the liver CT annotation task was organized.
We provided liver patient data collected via a hybrid patient information entry
system, whose liver characteristics are based on the LiCO ontology. The challenge
was to predict UsE features of patient records, given in RDF format. This year
in 2015, in contrast to last year’s edition, users have not been provided with
CoG features. Also, they were free to use any set of image features to perform
the task. As this was the first time that UsE features were provided in RDF
formats, it was not surprising that few groups were finally able to submit their
runs for this complex task. Out of 32 teams, 1 team submitted its runs. The
approaches and results were reviewed and documented in this paper. Since the
dataset was exactly the same as last year’s, comparison of the results of all runs
submitted to the liver CT annotation task in both 2014 and 2015 is also provided
in this paper. The main challenge of the task was due to the unbalanced dataset
and participants tried to overcome this issue with different methods. Among all
methods, image retrieval obtained the best performance. It was observed that
feature selection is important for the best performance of the prediction method.
Acknowledgments The Liver CT Annotation task is supported by TÜBİTAK
Grant # 110E264 (CaReRa project), and in part by COST Action IC1302
(KEYSTONE).
Group Concept Properties Possible values(assigned indices)
Liver Placement downward displacement(0), normal placement(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),
left
      </p>
      <p>
        ward displacement(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), upward displacement(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), other(
        <xref ref-type="bibr" rid="ref4">4</xref>
        )
Liver Liver LLiivveerr SCioznetCouhrange iodrterhceergeru(al4sa)erd(0(0),), inlcorbeualsaetde(d1()1,)n,ormnoald(u2l)a,ro(t2h),er(3r)egular(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ),
Liver Craniocaudal The amount change in size of liver(mm)
Dimension(mm)
Density Type heterogeneous(0), homogeneous(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), other(
        <xref ref-type="bibr" rid="ref2">2</xref>
        )
      </p>
      <p>
        Density Change decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Right Lobe iRoicgahutdalLobe DCimraenn-- The amount change in size of right lobe(mm)
sion(mm)
Right Lobe Size decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
      </p>
      <p>Change
Left Lobe dLaelftDLiombeenCsiroann(imocma)u- The amount change in size of left lobe(mm)</p>
      <p>
        Left Lobe Size decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
      </p>
      <p>
        Change
Caudate Lobe CCraaundiaotceaudal LoDbie- The amount change in size of caudate lobe(mm)
mension(mm)
Caudate Lobe Size decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Change
      </p>
      <p>
        Hepatic Artery Lu- decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Vessel Hepatic Arterymen Diameter
      </p>
      <p>
        Hepatic Artery Lu- obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
men Type
Hepatic Hepatic Portal V. decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Portal Vein Lumen Diam.
      </p>
      <p>
        Hepatic Portal V. obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Lumen Type
is Cavernous Trans- NA(-1),True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0),NA(-1)
formation
Observed?(Hepatic
      </p>
      <p>
        Portal Vein)
Left Portal Left Portal V. Lumen decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Vein Diam.
      </p>
      <p>
        Left Portal V. Lumen obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Type
is Cavernous Trans- NA(-1),True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0),NA(-1)
formation
Observed?(Left Portal
      </p>
      <p>
        Vein)
Right Portal Right Portal V. Lu- decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Vein men Diam.
      </p>
      <p>
        Right Portal V. Lu- obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
men Type
is Cavernous Trans- NA(-1),True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0),NA(-1)
formation
Observed?(Right Portal
      </p>
      <p>
        Vein)
Hepatic Vein HDeiapmat.ic V. Lumen decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Hepatic V. Lumen obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Type
      </p>
      <p>Diagnosis of given image using ICD10 codes (bar
separated) and in the free text MD’s comments are written
(bar separated).</p>
      <p>
        Cluster Size 1(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), 2(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), 3(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), 4(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), 5(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ), multiple(
        <xref ref-type="bibr" rid="ref6">6</xref>
        )
      </p>
      <p>
        For simple cases this value shows number of lesions inside
the ROI, but in case of having more than one lesions of a
certain type, the biggest lesion is annotated as a sample of
that cluster and number of lesions with same properties
is written here
Contrast Uptake NA(-1), dense(0), heterogeneous(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), homogeneous(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
      </p>
      <p>
        minimal(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), moderate(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
Contrast Pattern NA(-1), central(0), early uptake then wash out(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),
fixing contrast in late phase(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), heterogeneous(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ),
homogeneous(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), peripheric(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ), peripheric nodular(
        <xref ref-type="bibr" rid="ref6">6</xref>
        ), spokes
wheel(
        <xref ref-type="bibr" rid="ref7">7</xref>
        ), undecided(8), other(9)
Lesion Composition SolidCycsticMix(0), Solid(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), SolidWithCystic(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
      </p>
      <p>
        PureSolid(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), PredominantSolid(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), Cystic(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ),
PureCystic(
        <xref ref-type="bibr" rid="ref6">6</xref>
        ), PredominantCystic(
        <xref ref-type="bibr" rid="ref7">7</xref>
        ),
CysticWithSolidComponent(8), CysticWithDebris(9), Abcess(10)
Ob- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0)
,
      </p>
      <p>
        Properties Possible values(assigned indices)
Area Margin Type sgeeropgirgaipnhioiucas(l(40)),,spililcudleafitinveed(5(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),),wierlrledgeufilanre(d2()6, ),loobtuhlearr((73)),
Shape band(0), fusiform(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), irregular(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), linear(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), nodular(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ),
      </p>
      <p>
        ovoid(
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is Contrasted True(
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is Calcified? (Area) True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0),NA(-1)
Area Calcification NA(-1), coarse(0), focal(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), millimetric-fine(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
puncType tate(
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        ), scattered(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
Density NA(-1), hyperdense(0), hypodense(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), isodense(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
      </p>
      <p>
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        )
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      <p>
        Density Type NA(-1), heterogeneous(0), homogeneous(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), other(
        <xref ref-type="bibr" rid="ref2">2</xref>
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Capsule issuleC)alcified? (Cap- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0),NA(-1)
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      <p>
        Capsule Calcification NA(-1), coarse(0), focal(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), millimetric-fine(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
punc
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        Type tate(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), scattered(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
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Polyp iPsoClyaplcifieCda?lc(iPficoalytipo)n TNrAu(e-(11)),,Fcaolsaer(s0e)(,0N),A(f-o1c)al(
        <xref ref-type="bibr" rid="ref1">1</xref>
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puncType tate(
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        ), scattered(
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        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
is Calci- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
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Pseudocapsule fied?(Pseudocapsule)
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        <xref ref-type="bibr" rid="ref1">1</xref>
        ), millimetric-fine(
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punc
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        Type tate(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), scattered(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
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Septa iSsepCtaalcifieCda?lc(iSfiecpattiao)n TNrAu(e-(11)),,Fcaolsaer(s0e)(,0N),A(f-o1c)al(
        <xref ref-type="bibr" rid="ref1">1</xref>
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puncType tate(
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        ), scattered(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
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Diameter Type NA(-1), complete(0), incomplete(
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        <xref ref-type="bibr" rid="ref2">2</xref>
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        Thickness NA(-1), thick(0), thin(
        <xref ref-type="bibr" rid="ref1">1</xref>
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        )
Solid is Calcified? (Solid True(
        <xref ref-type="bibr" rid="ref1">1</xref>
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Component Component)
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      <p>
        Solid Component NA(-1), coarse(0), focal(
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        ), millimetric-fine(
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punc
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        Calcification Type tate(
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        ), scattered(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
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Wall iWsaCllalcifieCda?lc(iWficaaltli)on TNrAu(e-(11)),,Fcaolsaer(s0e)(,0N),A(f-o1c)al(
        <xref ref-type="bibr" rid="ref1">1</xref>
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puncType tate(
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        ), scattered(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
Wall Type NA(-1), thick(0), thin(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), other(
        <xref ref-type="bibr" rid="ref2">2</xref>
        )
is Contrasted?(Wall) True(
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