Chest Film Reading, Lecture 11.
Dr/ ABD ALLAH NAZEER. MD.
Benign tumour of the lung.
Benign lung tumour are a heterogenous group of neoplastic
lesions originating from pulmonary structures.
The term Benign may be misleading because these interface
with lung function.(E. g.. Obstruction of a major bronchus
may occur), depending upon tumour location.
Benign tumours make up 2-5% of all primary lung tumours.
The exact incidence is not known because these tumours are
often asymptomatic and are only detected during
autopathy.
Reported series suggest that benign lung tumours affect
men more frequently than women.
The age range of patients affected is 17-77 years, with a
mean age of 56 years for all types.
Benign lung tumors:
Are not cancerous, so will not spread to other parts of the body , Grow slowly, or
might even stop growing or shrink, Are usually not life-threatening , Usually do
not need to be removed
Can expand and push against nearby tissues but will not invade, destroy, or
replace other tissues
Hamartoma
There are a number of different kinds of benign lung tumors, the most common
being hamartomas. They account for about 55% of all benign lung tumors, and 8%
of all lung tumors.
Characteristics of lung hamartomas:
About 80% are found in the peripheral, or outer, portion of the lung’s connective
tissue. The remainder are found inside the bronchial tubes (the airways leading to
the lungs). Deeper growths may be difficult to distinguish from cancerous nodules.
Are made up of “normal” tissues such as cartilage, connective tissue, fat, and
muscle but in abnormal amounts
Are usually less than 4 centimeters in diameter
Stay within a limited area and are not likely to press against nearby tissue
Usually appear in chest X-rays as a coin-like round growth
May look like fluffy wool or popcorn in about 15% of cases
Are found more often in males than females, and between the ages of 50 and 70
Papilloma
Another type of benign lung tumor is called a papilloma. It grows in the bronchial
tubes, sticking out from the surface area where it is attached. Papillomas are not
very common and are divided into three types.
Categories of pulmonary papillomas:
Squamous
Occur in both children and adults
May appear as just one nodule or many
Result from infection by human papilloma virus (HPV), the same virus that causes
warts and certain sexually transmitted diseases
Glandular
No cause has been identified
Are less common than squamous papillomas
Develop in larger airways than squamous papillomas
Can occur in all ages but mostly adults
Almost always appear as one nodule, centrally located
Mixed squamous and glandular
Contain a mix of squamous and glandular papilloma tissue
Only a small number of cases have been reported
Has the potential to eventually turn cancerous because the squamous cells can
change over time.
Alveolar Adenoma Alveolar adenomas are unusual neoplasms that are
typically identified in the periphery of the lung. Originally described in
1986 by Yousem and these tumors have been identified in adults
ranging in age from 39 to 74 years, usually as an asymptomatic solitary
pulmonary nodule. Alveolar adenomas are soft, multicystic, and
lobulated. No definite gender predilection has been identified.
Solitary Fibrous Tumor of the Lung. Solitary fibrous tumors are
typically pleural-based tumors, but intrapulmonary examples have
been described.50,51 Pulmonary SFTs are generally peripheral; they
are sometimes on the pulmonary parenchymal side of the pleura but in
some instances are completely separate from the pleura. They are firm
and white with a whorled appearance. Solitary fibrous tumors may
derive from submesothelial fibroblasts.
Hemangiomas are a build-up of blood vessel cells in the skin or internal
organs. Hemangiomas are a common type of birthmark, often
occurring in the head, neck or trunk. They may appear red or bluish in
colour. Most go away on their own. Those that interfere with vision,
hearing or eating may require treatment.
Leiomyomas. Primary solitary pulmonary leiomyomas can be endobronchial or
parenchymal. Multiple smooth muscle tumors of the lung in women with history
of uterine leiomyomas are more likely part of the entity of benign metastasizing
leiomyoma.
Chondromas. Chondromas are tumors composed of hyaline or myxohyaline
cartilage without epithelial elements or other mesenchymal elements. Although
these can represent isolated, sporadic tumors, such tumors with myxoid stroma in
young women require examination for the Carney triad (gastric smooth muscle
tumors, paraganglioma, chondromas).
Lipomas. These can be intraparenchymal or endobronchial, the latter being
more common.58 These tumors must be composed solely of adipose tissue; any
component of lobulated cartilage or epithelial ingrowth on cleft like spaces raises
the possibility of an adipose tissue–rich hamartoma.
Granular Cell Tumors. Benign tumor classifications included granular cell
myoblastoma (granular cell tumor), although these do not appear to be common
benign lung tumors. In limited series of cases, these tumors occur in adults
(average age, 40 years) with a male predominance. They are usually central
tumors and therefore more likely to be symptomatic with cough, obstruction, or
hemoptysis. They are often irregular and locally invasive and therefore can recur
after conservative resection, but they do not metastasize.
Pulmonary hamartoma with "popcorn calcifications."
Pulmonary hamartoma with "popcorn calcifications."
Pulmonary hamartoma with "popcorn calcifications."
Respiratory
papillomatosis.
Endoluminal masses
in respiratory
papillomatosis seen
on the axial computed
tomography scan
(black arrow) and on
bronchoscopy (white
arrow).
Coronal multiplanar
reconstruction and the
virtual bronchoscopic
image showing
extensive involvement
of the distal trachea
(arrow) and the right
bronchus in a case of
recurrent respiratory
papillomatosis.
Airway involvement in
Wegner’s granulomatosis.
A: Axial computed
tomography image shows
cavitary lung nodules
(large arrows); B: Coronal
multiplanar reconstruction
in lung window
demonstrates irregular
narrowing of the left main
bronchus (small arrows).
Lung
granuloma.
Alveolar adenoma.
Alveolar adenoma at the left inferior hilum.
Alveolar adenoma.
Bronchial mucous gland adenoma presenting
as massive hemoptysis: A diagnostic dilemma.
Pulmonary capillary hemangiomas.
Pulmonary Sclerosing Hemangioma.
Sclerosing hemangioma of lung.
Solitary fibrous
Tumour of the
pleura.
Solitary fibrous
Tumour of the
pleura.
benign localized
fibrous tumor
originating from
the mediastinal
pleura.
Pulmonary Leiomyoma, CT scan showing multiple well-defined
rounded bilateral lung nodules with no 18F-FDG uptake.
Pulmonary Leiomyoma, MR images show multiple
well-defined rounded bilateral lung nodules
Solitary benign pulmonary leiomyoma.:
Osteochondromatosis of chest wall.:
chest wall
chondrosarcoma.
CT show mediastinal lipoma compressing the lung.
CT scan showing a mass of fatty content in the dorsal region of the left thorax.
Mediastinal lipomatosis with cardiac intracavitary involvement.
Lung cancer, also known as carcinoma of the lung or
pulmonary carcinoma, is a malignant lung tumor
characterized by uncontrolled cell growth in tissues of the
lung.
Signs and symptoms which may suggest lung cancer
include:
respiratory symptoms: coughing, coughing up blood,
wheezing or shortness of breath systemic symptoms: weight
loss, fever, clubbing of the fingernails, or fatigue symptoms
due to the cancer mass pressing on adjacent structures:
chest pain, bone pain, superior vena cava obstruction,
difficulty swallowing If the cancer grows in the airways, it
may obstruct airflow, causing breathing difficulties. The
obstruction can lead to accumulation of secretions behind
the blockage, and predispose to pneumonia.
T1a tumor.
Stage T2 tumors.
Stage T2 tumors.
Stage T3.—Tumors larger than 7 cm are now considered stage T3 tumors.
Stage T3 tumors. Chest CT scan shows a primary mass (arrow)
with satellite nodules (arrowheads) in the right lower lobe
Stage T4 tumors.
Chest CT scan shows
a primary lung
tumor in the right
upper lobe (long
arrow) with a
smaller separate
nodule in the right
lower lobe (short
arrow). In the 7th
edition, this is
considered stage T4
disease (stage M1
[metastatic] disease
in the 6th edition).
Stage T4 tumors. Chest CT
scan shows a right upper
lobe mass (arrow) with
mediastinal and carinal
invasion, ipsilateral
loculated pleural effusion,
and thickening and
enhancement of the pleura.
Note the tumor encasement
and resultant narrowing of
the right main-stem
bronchus (arrowhead). The
pleural thickening and
enhancement, although
nonspecific, are suggestive
of metastatic pleural
disease. In the 7th edition,
proved pleural
carcinomatosis is considered
stage M1a disease.
Stage N1 lymph nodes. (a) Chest CT scan obtained in a patient with right-sided lung cancer
shows an enlarged right hilar lymph node (level 10) (arrow) measuring 15 mm in the short
axis. (b) Chest CT scan obtained in a different patient shows a left lower lobe mass and an
ipsilateral enlarged interlobar lymph node (level 11) (arrow) measuring 11 mm.
Stage N2 lymph nodes. (a) Chest CT scan shows an enlarged (1.6-cm) right upper paratracheal
lymph node (level 2) (arrowhead). (b) Chest CT scan obtained in a different patient shows an
enlarged (1.5-cm) right lower paratracheal lymph node (level 4) (arrowhead). Like the lymph
node in a, it is clearly to the right of the new border proposed by the IASLC (ie, the left lateral
border of the trachea). (c) Chest CT scan obtained in a third patient shows a right lower lobe
mass (white arrow) with an enlarged (1.6-cm) subcarinal lymph node (level 7) (black arrow).
Stage N3 lymph nodes. (a) Axial PET/CT image of the chest shows a primary mass in the
left lung (arrow) and a right lower paratracheal lymph node (arrowhead), both of which
demonstrate intense radiotracer uptake. Metastatic involvement of the lymph node was
confirmed at mediastinoscopic resection. (b) Chest CT scan obtained at the lung apex in a
different patient shows enlarged bilateral supraclavicular lymph nodes (arrows).
Small cell lung cancer. Chest CT scan (a) and corresponding PET/CT image (b) show a mass in the
left lung (top arrow) with intense radiotracer uptake on the PET/CT image. The mass proved to be
small cell lung cancer at pathologic analysis. Note the confluent ipsilateral prevascular (bottom
arrow) and left paratracheal lymphadenopathy (N2), which shows intense uptake as well.
Chest wall and pleural invasion. Chest CT scans obtained with a soft-tissue window (a) and a
bone window (b) show a right upper lobe mass measuring 4.9 cm in diameter, with a chest wall
mass (arrow in a) and associated bone destruction of the adjacent posterior rib (arrow in b).
X-Ray and CT scan showing an intraparenchymal cavitating lung lesion
adjacent to the anterior thoracic wall. Histology confirmed a large-cell NHL.
Pulmonary parenchymal lymphoma in a 41-year-old HIV-positive man.
Pleural metastasis. (a) Chest CT scan shows a right upper lobe mass
(arrow) abutting the mediastinum, along with pleural thickening and
effusion (arrowhead). (b) Axial FDG PET scan shows radiotracer uptake in
the right upper lobe mass (arrow) and ipsilateral pleura (arrowhead)
Anterior, Middle and posterior mediastinal enlarged lymph nodes.
Pleural tumours
solitary fibrous tumour of the pleura (pleural fibroma)
• mesothelioma
• localized mediastinal malignant mesothelioma
metastatic pleural disease, particularly from adenocarcinomas, e.g.
• bronchogenic adenocarcinoma
• breast cancer
• ovarian cancer
• prostate cancer
• gastrointestinal adenocarcinoma
• renal cell carcinoma
• lymphoma: pleural lymphoma
• invasive thymoma
Lipoma
loculated fluid (on plain film)
pleural effusion (pseudotumor)
empyema
hemothorax
mass related to ribs or chest wall, e.g. Ewing sarcoma of chest wall, Askin tumour
splenosis
infection including tuberculosis
Malignant mesothelioma: Axial contrast-enhanced CT scan showing
homogeneously enhancing nodular pleural thickening (arrows) involving the
mediastinal and costal pleura with volume loss changes in left hemithorax
Mesothelioma presenting as a pleural effusion: Axial contrast
enhanced CT scan showing moderate left pleural effusion as loculated
collection with thickening of pleura (arrows) in a case of mesothelioma
Benign solitary fibrous tumor: (A) Chest radiograph showing pleural-based
opacity (arrow) in right hemithorax with peripheral obtuse margins; (B)
axial contrast-enhanced CT scan showing heterogeneously enhancing
pleural-based mass (arrowhead) proved to be benign fibrous pleural tumor
Pleural fibroma: (A) Chest radiograph showing lobulated pleural-based opacity (arrow) in
right apical region; (B) axial contrast-enhanced CT scan showing heterogeneously enhancing
peripheral mass lesion (arrow) in a biopsy-proven case of benign pleural fibroma
Malignant solitary fibrous tumor of pleura: Plain axial CT scan showing pleural-based soft
tissue lesion with peripheral as well as internal calcification (arrow) abutting the liver
Pleural drop metastases in invasive thymoma: Axial contrast-enhanced CT image
showing heterogeneously enhancing anterior mediastinal mass (arrowhead)
with mild left pleural effusion and ipsilateral pleural implants (arrows)
Pleural metastases: Axial contrast-enhanced CT scan showing heterogeneously
enhancing pleural-based mass lesion (arrow) in left hemithorax with extrathoracic
extension in a case of metastatic adenocarcinoma
Pleural lymphoma: Axial contrast-enhanced CT scan showing heterogeneously
enhancing lobulated mass lesion involving the diaphragmatic pleura (arrow)
and invading the chest wall in a case of high-grade lymphoma
Spindle cell sarcoma of pleura: (A) Chest radiograph showing complete
opacification of right hemithorax (arrowhead) with mediastinal shift to the left;
(B) axial contrast-enhanced CT scan showing heterogeneously enhancing nodular
pleural-based lesions with pleural effusion displacing the heart to the left
Askin tumor: (A) Chest radiograph showing inhomogeneous opacity (arrow) right
hemithorax obscuring right hemidiaphragm without mediastinal shift; (B) axial
contrast-enhanced CT scan showing heterogeneously enhancing nodular pleural-based
lesions (arrows) involving the costal and mediastinal pleura with characteristic
involvement of the sympathetic chain (arrowhead) in right paraspinal region
Loculated empyema: (A) Chest radiograph showing pleural-based opacity (arrow) with
tapering obtuse margins in left hemithorax; (B) axial contrast-enhanced CT scan
showing loculated collection (arrowhead) with peripherally enhancing thick walls
Calcified empyema: (A) Chest radiograph showing volume loss right hemithorax
with veil-like calcified (arrow) pleural opacity; (B) axial contrast-enhanced CT scan
showing evidence of calcified chronic empyema (arrow) with proliferation of
extrapleural fat and crowding of ribs suggestive of volume loss in right hemithorax
Calcifying fibrous pseudotumor: (A) Chest radiograph showing pleural-based calcified
opacity (arrowhead) left hemithorax with incomplete border sign; (B) plain axial CT scan
image showing pleural-based calcified lesion (arrow) with no destruction of underlying ribs.
Thank You.

Presentation1.pptx, chest film reading. lecture 2

  • 1.
    Chest Film Reading,Lecture 11. Dr/ ABD ALLAH NAZEER. MD.
  • 2.
    Benign tumour ofthe lung. Benign lung tumour are a heterogenous group of neoplastic lesions originating from pulmonary structures. The term Benign may be misleading because these interface with lung function.(E. g.. Obstruction of a major bronchus may occur), depending upon tumour location. Benign tumours make up 2-5% of all primary lung tumours. The exact incidence is not known because these tumours are often asymptomatic and are only detected during autopathy. Reported series suggest that benign lung tumours affect men more frequently than women. The age range of patients affected is 17-77 years, with a mean age of 56 years for all types.
  • 4.
    Benign lung tumors: Arenot cancerous, so will not spread to other parts of the body , Grow slowly, or might even stop growing or shrink, Are usually not life-threatening , Usually do not need to be removed Can expand and push against nearby tissues but will not invade, destroy, or replace other tissues Hamartoma There are a number of different kinds of benign lung tumors, the most common being hamartomas. They account for about 55% of all benign lung tumors, and 8% of all lung tumors. Characteristics of lung hamartomas: About 80% are found in the peripheral, or outer, portion of the lung’s connective tissue. The remainder are found inside the bronchial tubes (the airways leading to the lungs). Deeper growths may be difficult to distinguish from cancerous nodules. Are made up of “normal” tissues such as cartilage, connective tissue, fat, and muscle but in abnormal amounts Are usually less than 4 centimeters in diameter Stay within a limited area and are not likely to press against nearby tissue Usually appear in chest X-rays as a coin-like round growth May look like fluffy wool or popcorn in about 15% of cases Are found more often in males than females, and between the ages of 50 and 70
  • 5.
    Papilloma Another type ofbenign lung tumor is called a papilloma. It grows in the bronchial tubes, sticking out from the surface area where it is attached. Papillomas are not very common and are divided into three types. Categories of pulmonary papillomas: Squamous Occur in both children and adults May appear as just one nodule or many Result from infection by human papilloma virus (HPV), the same virus that causes warts and certain sexually transmitted diseases Glandular No cause has been identified Are less common than squamous papillomas Develop in larger airways than squamous papillomas Can occur in all ages but mostly adults Almost always appear as one nodule, centrally located Mixed squamous and glandular Contain a mix of squamous and glandular papilloma tissue Only a small number of cases have been reported Has the potential to eventually turn cancerous because the squamous cells can change over time.
  • 6.
    Alveolar Adenoma Alveolaradenomas are unusual neoplasms that are typically identified in the periphery of the lung. Originally described in 1986 by Yousem and these tumors have been identified in adults ranging in age from 39 to 74 years, usually as an asymptomatic solitary pulmonary nodule. Alveolar adenomas are soft, multicystic, and lobulated. No definite gender predilection has been identified. Solitary Fibrous Tumor of the Lung. Solitary fibrous tumors are typically pleural-based tumors, but intrapulmonary examples have been described.50,51 Pulmonary SFTs are generally peripheral; they are sometimes on the pulmonary parenchymal side of the pleura but in some instances are completely separate from the pleura. They are firm and white with a whorled appearance. Solitary fibrous tumors may derive from submesothelial fibroblasts. Hemangiomas are a build-up of blood vessel cells in the skin or internal organs. Hemangiomas are a common type of birthmark, often occurring in the head, neck or trunk. They may appear red or bluish in colour. Most go away on their own. Those that interfere with vision, hearing or eating may require treatment.
  • 7.
    Leiomyomas. Primary solitarypulmonary leiomyomas can be endobronchial or parenchymal. Multiple smooth muscle tumors of the lung in women with history of uterine leiomyomas are more likely part of the entity of benign metastasizing leiomyoma. Chondromas. Chondromas are tumors composed of hyaline or myxohyaline cartilage without epithelial elements or other mesenchymal elements. Although these can represent isolated, sporadic tumors, such tumors with myxoid stroma in young women require examination for the Carney triad (gastric smooth muscle tumors, paraganglioma, chondromas). Lipomas. These can be intraparenchymal or endobronchial, the latter being more common.58 These tumors must be composed solely of adipose tissue; any component of lobulated cartilage or epithelial ingrowth on cleft like spaces raises the possibility of an adipose tissue–rich hamartoma. Granular Cell Tumors. Benign tumor classifications included granular cell myoblastoma (granular cell tumor), although these do not appear to be common benign lung tumors. In limited series of cases, these tumors occur in adults (average age, 40 years) with a male predominance. They are usually central tumors and therefore more likely to be symptomatic with cough, obstruction, or hemoptysis. They are often irregular and locally invasive and therefore can recur after conservative resection, but they do not metastasize.
  • 8.
    Pulmonary hamartoma with"popcorn calcifications."
  • 9.
    Pulmonary hamartoma with"popcorn calcifications."
  • 10.
    Pulmonary hamartoma with"popcorn calcifications."
  • 11.
    Respiratory papillomatosis. Endoluminal masses in respiratory papillomatosisseen on the axial computed tomography scan (black arrow) and on bronchoscopy (white arrow).
  • 12.
    Coronal multiplanar reconstruction andthe virtual bronchoscopic image showing extensive involvement of the distal trachea (arrow) and the right bronchus in a case of recurrent respiratory papillomatosis.
  • 13.
    Airway involvement in Wegner’sgranulomatosis. A: Axial computed tomography image shows cavitary lung nodules (large arrows); B: Coronal multiplanar reconstruction in lung window demonstrates irregular narrowing of the left main bronchus (small arrows).
  • 14.
  • 15.
  • 16.
    Alveolar adenoma atthe left inferior hilum.
  • 17.
  • 18.
    Bronchial mucous glandadenoma presenting as massive hemoptysis: A diagnostic dilemma.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
    benign localized fibrous tumor originatingfrom the mediastinal pleura.
  • 25.
    Pulmonary Leiomyoma, CTscan showing multiple well-defined rounded bilateral lung nodules with no 18F-FDG uptake.
  • 26.
    Pulmonary Leiomyoma, MRimages show multiple well-defined rounded bilateral lung nodules
  • 27.
  • 28.
  • 29.
  • 30.
    CT show mediastinallipoma compressing the lung.
  • 31.
    CT scan showinga mass of fatty content in the dorsal region of the left thorax.
  • 32.
    Mediastinal lipomatosis withcardiac intracavitary involvement.
  • 33.
    Lung cancer, alsoknown as carcinoma of the lung or pulmonary carcinoma, is a malignant lung tumor characterized by uncontrolled cell growth in tissues of the lung. Signs and symptoms which may suggest lung cancer include: respiratory symptoms: coughing, coughing up blood, wheezing or shortness of breath systemic symptoms: weight loss, fever, clubbing of the fingernails, or fatigue symptoms due to the cancer mass pressing on adjacent structures: chest pain, bone pain, superior vena cava obstruction, difficulty swallowing If the cancer grows in the airways, it may obstruct airflow, causing breathing difficulties. The obstruction can lead to accumulation of secretions behind the blockage, and predispose to pneumonia.
  • 42.
  • 44.
  • 45.
  • 46.
    Stage T3.—Tumors largerthan 7 cm are now considered stage T3 tumors.
  • 47.
    Stage T3 tumors.Chest CT scan shows a primary mass (arrow) with satellite nodules (arrowheads) in the right lower lobe
  • 48.
    Stage T4 tumors. ChestCT scan shows a primary lung tumor in the right upper lobe (long arrow) with a smaller separate nodule in the right lower lobe (short arrow). In the 7th edition, this is considered stage T4 disease (stage M1 [metastatic] disease in the 6th edition).
  • 49.
    Stage T4 tumors.Chest CT scan shows a right upper lobe mass (arrow) with mediastinal and carinal invasion, ipsilateral loculated pleural effusion, and thickening and enhancement of the pleura. Note the tumor encasement and resultant narrowing of the right main-stem bronchus (arrowhead). The pleural thickening and enhancement, although nonspecific, are suggestive of metastatic pleural disease. In the 7th edition, proved pleural carcinomatosis is considered stage M1a disease.
  • 50.
    Stage N1 lymphnodes. (a) Chest CT scan obtained in a patient with right-sided lung cancer shows an enlarged right hilar lymph node (level 10) (arrow) measuring 15 mm in the short axis. (b) Chest CT scan obtained in a different patient shows a left lower lobe mass and an ipsilateral enlarged interlobar lymph node (level 11) (arrow) measuring 11 mm.
  • 51.
    Stage N2 lymphnodes. (a) Chest CT scan shows an enlarged (1.6-cm) right upper paratracheal lymph node (level 2) (arrowhead). (b) Chest CT scan obtained in a different patient shows an enlarged (1.5-cm) right lower paratracheal lymph node (level 4) (arrowhead). Like the lymph node in a, it is clearly to the right of the new border proposed by the IASLC (ie, the left lateral border of the trachea). (c) Chest CT scan obtained in a third patient shows a right lower lobe mass (white arrow) with an enlarged (1.6-cm) subcarinal lymph node (level 7) (black arrow).
  • 52.
    Stage N3 lymphnodes. (a) Axial PET/CT image of the chest shows a primary mass in the left lung (arrow) and a right lower paratracheal lymph node (arrowhead), both of which demonstrate intense radiotracer uptake. Metastatic involvement of the lymph node was confirmed at mediastinoscopic resection. (b) Chest CT scan obtained at the lung apex in a different patient shows enlarged bilateral supraclavicular lymph nodes (arrows).
  • 53.
    Small cell lungcancer. Chest CT scan (a) and corresponding PET/CT image (b) show a mass in the left lung (top arrow) with intense radiotracer uptake on the PET/CT image. The mass proved to be small cell lung cancer at pathologic analysis. Note the confluent ipsilateral prevascular (bottom arrow) and left paratracheal lymphadenopathy (N2), which shows intense uptake as well.
  • 61.
    Chest wall andpleural invasion. Chest CT scans obtained with a soft-tissue window (a) and a bone window (b) show a right upper lobe mass measuring 4.9 cm in diameter, with a chest wall mass (arrow in a) and associated bone destruction of the adjacent posterior rib (arrow in b).
  • 62.
    X-Ray and CTscan showing an intraparenchymal cavitating lung lesion adjacent to the anterior thoracic wall. Histology confirmed a large-cell NHL.
  • 63.
    Pulmonary parenchymal lymphomain a 41-year-old HIV-positive man.
  • 65.
    Pleural metastasis. (a)Chest CT scan shows a right upper lobe mass (arrow) abutting the mediastinum, along with pleural thickening and effusion (arrowhead). (b) Axial FDG PET scan shows radiotracer uptake in the right upper lobe mass (arrow) and ipsilateral pleura (arrowhead)
  • 75.
    Anterior, Middle andposterior mediastinal enlarged lymph nodes.
  • 88.
    Pleural tumours solitary fibroustumour of the pleura (pleural fibroma) • mesothelioma • localized mediastinal malignant mesothelioma metastatic pleural disease, particularly from adenocarcinomas, e.g. • bronchogenic adenocarcinoma • breast cancer • ovarian cancer • prostate cancer • gastrointestinal adenocarcinoma • renal cell carcinoma • lymphoma: pleural lymphoma • invasive thymoma Lipoma loculated fluid (on plain film) pleural effusion (pseudotumor) empyema hemothorax mass related to ribs or chest wall, e.g. Ewing sarcoma of chest wall, Askin tumour splenosis infection including tuberculosis
  • 92.
    Malignant mesothelioma: Axialcontrast-enhanced CT scan showing homogeneously enhancing nodular pleural thickening (arrows) involving the mediastinal and costal pleura with volume loss changes in left hemithorax
  • 93.
    Mesothelioma presenting asa pleural effusion: Axial contrast enhanced CT scan showing moderate left pleural effusion as loculated collection with thickening of pleura (arrows) in a case of mesothelioma
  • 94.
    Benign solitary fibroustumor: (A) Chest radiograph showing pleural-based opacity (arrow) in right hemithorax with peripheral obtuse margins; (B) axial contrast-enhanced CT scan showing heterogeneously enhancing pleural-based mass (arrowhead) proved to be benign fibrous pleural tumor
  • 95.
    Pleural fibroma: (A)Chest radiograph showing lobulated pleural-based opacity (arrow) in right apical region; (B) axial contrast-enhanced CT scan showing heterogeneously enhancing peripheral mass lesion (arrow) in a biopsy-proven case of benign pleural fibroma
  • 98.
    Malignant solitary fibroustumor of pleura: Plain axial CT scan showing pleural-based soft tissue lesion with peripheral as well as internal calcification (arrow) abutting the liver
  • 101.
    Pleural drop metastasesin invasive thymoma: Axial contrast-enhanced CT image showing heterogeneously enhancing anterior mediastinal mass (arrowhead) with mild left pleural effusion and ipsilateral pleural implants (arrows)
  • 102.
    Pleural metastases: Axialcontrast-enhanced CT scan showing heterogeneously enhancing pleural-based mass lesion (arrow) in left hemithorax with extrathoracic extension in a case of metastatic adenocarcinoma
  • 104.
    Pleural lymphoma: Axialcontrast-enhanced CT scan showing heterogeneously enhancing lobulated mass lesion involving the diaphragmatic pleura (arrow) and invading the chest wall in a case of high-grade lymphoma
  • 105.
    Spindle cell sarcomaof pleura: (A) Chest radiograph showing complete opacification of right hemithorax (arrowhead) with mediastinal shift to the left; (B) axial contrast-enhanced CT scan showing heterogeneously enhancing nodular pleural-based lesions with pleural effusion displacing the heart to the left
  • 106.
    Askin tumor: (A)Chest radiograph showing inhomogeneous opacity (arrow) right hemithorax obscuring right hemidiaphragm without mediastinal shift; (B) axial contrast-enhanced CT scan showing heterogeneously enhancing nodular pleural-based lesions (arrows) involving the costal and mediastinal pleura with characteristic involvement of the sympathetic chain (arrowhead) in right paraspinal region
  • 107.
    Loculated empyema: (A)Chest radiograph showing pleural-based opacity (arrow) with tapering obtuse margins in left hemithorax; (B) axial contrast-enhanced CT scan showing loculated collection (arrowhead) with peripherally enhancing thick walls
  • 108.
    Calcified empyema: (A)Chest radiograph showing volume loss right hemithorax with veil-like calcified (arrow) pleural opacity; (B) axial contrast-enhanced CT scan showing evidence of calcified chronic empyema (arrow) with proliferation of extrapleural fat and crowding of ribs suggestive of volume loss in right hemithorax
  • 109.
    Calcifying fibrous pseudotumor:(A) Chest radiograph showing pleural-based calcified opacity (arrowhead) left hemithorax with incomplete border sign; (B) plain axial CT scan image showing pleural-based calcified lesion (arrow) with no destruction of underlying ribs.
  • 110.