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IKD8 - HRCT Lung Findings in Pulmonary Renal Syndromes

This document discusses pulmonary renal syndromes (PRS) and the findings on high-resolution CT (HRCT) of the lungs. PRS are rare medical syndromes characterized by respiratory failure from diffuse alveolar hemorrhage and renal failure from glomerulonephritis. On HRCT, PRS typically presents with a non-specific pattern of ground-glass opacities, consolidations, and nodules. Over time, recurrent bleeding can lead to organizing pneumonia and interstitial lung fibrosis. The HRCT findings are not pathognomonic, and diagnosis requires a multidisciplinary approach due to similarities with other diseases.
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0% found this document useful (0 votes)
432 views46 pages

IKD8 - HRCT Lung Findings in Pulmonary Renal Syndromes

This document discusses pulmonary renal syndromes (PRS) and the findings on high-resolution CT (HRCT) of the lungs. PRS are rare medical syndromes characterized by respiratory failure from diffuse alveolar hemorrhage and renal failure from glomerulonephritis. On HRCT, PRS typically presents with a non-specific pattern of ground-glass opacities, consolidations, and nodules. Over time, recurrent bleeding can lead to organizing pneumonia and interstitial lung fibrosis. The HRCT findings are not pathognomonic, and diagnosis requires a multidisciplinary approach due to similarities with other diseases.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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HRCT LUNGS FINDINGS IN

PULMONARY RENAL SYNDROMES

DR P A CHUI WAN CHEONG OSK


MB BCH BAO DMRD FRCR
• ANATOMY

• BASIC PATTERNS IN HRCT LUNGS

• PULMONARY RENAL SYNDROMES


HRCT LUNGS

• KNOWLEDGE OF LUNG ANATOMY IS ESSENTIAL


FOR UNDERSTANDING HRCT.
• THE SECONDARY LOBULE IS THE BASIC
ANATOMIC UNIT OF PULMONARY STRUCTURE
AND FUNCTION.
• THE INTERPRETATION OF INTERSTITIAL LUNG
DISEASES IS BASED ON THE TYPE OF
INVOLVEMENT OF THE SECONDARY PULMONARY
LOBULE.

• A PRIMARY PULMONARY LOBULE IS A MUCH


SMALLER LUNG UNIT WITH A SINGLE ALVEOLAR
DUCT BUT IS NOT IN COMMON USE.
Lung
Interstitium
PULMONARY LOBULE

- SMALLEST UNIT OF LUNG


STRUCTURE MARGINATED BY
CONNECTIVE TISSUE SEPTA.

- POLYHEDRAL IN SHAPE – UP
TO 2.5CMS IN DIAMETER.
- CLUSTER OF UP TO 30 ACINI

- SUPPLIED BY A DISTAL
PULMONARY ARTERY AND
BRONCHIOLE

- PULMONARY VEIN BRANCHES


AT THE EDGES OF THE UNIT
- LYMPHATICS AT THE EDGES
PULMONARY LOBULE

1. CENTRILOBULAR AREA IS THE


CENTRAL PART OF THE LOBULE

DISEASES COMING FROM AIRWAYS


• HYPERSENSITIVITY PNEUMONITIS
• RESP BRONCHIOLITIS ILD
• CENTRILOBULAR EMPHYSEMA.

2. PERI LYMPHATIC AREA


DISEASES COMING FROM
LYMPHATIC
• SARCOIDOSIS
• LYMPHANGITIC CA
• PULMONARY OEDEMA
HIGH RESOLUTION CT LUNGS
TECHNIQUE
• PLAIN STUDY / LUNG WINDOWS
• HRCT USES THIN SLICE IMAGES OF THE LUNG
PARENCHYMA.
• EXTREMELY HIGH DEFINITION IMAGES OF LUNG
ALVEOLI, AIRWAYS, INTERSTITIUM, AND PULMONARY
VASCULATURE.
• SUPINE POSITION. INSPIRATION IMAGES
• EXPIRATION IMAGES MAY ASSIST IN IDENTIFYING AIR-
TRAPPING IN PATIENTS WITH LUNG DISEASE.
• PRONE – TO DIFFERENTIATE BETWEEN EARLY LUNG
FIBROSIS AND PHYSIOLOGICAL DEPENDENT
ATELECTASIS AT THE LUNG BASES
NORMAL HRCT LUNGS
NORMAL HRCT LUNGS
NORMAL HRCT LUNGS
HRCT BASIC INTERPRETATION

WHAT IS THE DOMINANT


PATTERN ?
– 4 PATTERNS ANY ZONAL PREDOMINANCE?
• RETICULAR • UPPER VS LOWER

• NODULAR • CENTRAL VS PERIPHERAL

• HIGH DENSITY
ANY ANCILLARY FINDINGS?
• LOW DENSITY
• PLEURAL FLUID
WHERE IS IT LOCATED? • CARDIOMEGALY
• CENTRILOBULAR • PULMONARY ARTERIES
• PERILYMPHATIC • LYMPHADENOPATHY
• RANDOM • TRACTION BRONCHIECTASIS

MDTM essential for correct diagnosis.


1. RETICULAR PATTERN – NET LIKE
2. NODULAR PATTERN
LCH

SARCOID
3. HIGH DENSITY PATTERN

GROUND
GLASS

Consolidation

Mosaic

Crazy paving
4. LOW DENSITY PATTERN
PULMONARY RENAL SYNDROMES (PRS)

- RARE MEDICAL SYNDROME WITH A HIGH RATE


OF MORBIDITY AND DEATH

- RESPIRATORY FAILURE DUE TO DIFFUSE


ALVEOLAR HAEMORRHAGE (DAH)

- RENAL FAILURE – GLOMERULONEPHRITIS


PRS – COMMONLY CAUSED BY UNDERLYING AUTO IMMUNE DISEASES
1. PULMONARY VASCULITIDES – CAPILLARITIS
- ANCA ASSOCIATED PULMONARY VASCULITIDES
EG GPA - WEGENER’S, EGPA - CHURG STRAUSS, MICROSCOPIC PA
- NON ANCA PULMONARY VASCULITIDES EG. GOODPASTURE
2. OTHER CAUSES :
SLE
CONNECTIVE TISSUE DISORDERS EG. DERMATOMYOSITIS
POST STREP GN
RHEUMATOID ARTHRITIS
SYSTEMIC SCLEROSIS
3. TOXIC INJURY EG PARAQUAT
4. INFECTION – HANTA VIRUS LEPTOSPIROSIS LEGIONELLA
5. VASCULAR – NEPHROTIC SYNDROME WHERE RENAL VEIN THROMBOSIS
EMBOLISES TO THE LUNG
PRS CAUSES DAH

- CAPILLARITIS
- BLEEDING IS DIFFUSE AND
DIRECTLY INTO THE ALVEOLAR
SPACES
PULMONARY RENAL SYNDROMES (PRS)
HRCT LUNGS
• CXR – OFTEN NON
DIAGNOSTIC
• HEMOPTYSIS MAY BE
LACKING

• PULMONARY
HAEMORRHAGE
• - DIFFUSE INFILTRATIVE
PATTERN
• - MID ZONE PREDILECTION
• - APICAL SPARING
HRCT IN DAH
• CLINICAL CONTEXT IS CRUCIAL IN IMAGE
INTERPRETATION
• HRCT PATTERN CAN VARY WITH TIME OF ONSET OF
HAEMORRHAGE

MOST COMMON FINDINGS:


- PATCHY OR DIFFUSE GGO, CONSOLIDATION OR BOTH
- ILL DEFINED CENTRILOBULAR NODULES
- INTERLOBULAR SEPTAL THICKENING DEVELOPS OVER
DAYS
- GGO + RETICULAR = CRAZY PAVING PATTERN
CAUSES OF
GGO/CRAZY PAVING/CONSOLIDATION
 AIP / ARDS
• PULMONARY OEDEMA
• PULMONARY HAEMORRHAGE
• PNEUMONIA EG BACTERIAL MYCOPLASMA VIRAL - COVID 19
• ORGANIZING PNEUMONIA
• EOSINOPHILIC PNEUMONIA
• RADIATION PNEUMONITIS
• NSIP
• UIP/IPF
• RB-ILD / DIP (SMOKER’S LUNG DISEASE)
• HYPERSENSITIVITY PNEUMONITIS – ACUTE SUBACUTE CHRONIC
• BAC – LUNG ADENOCA
• SARCOIDOSIS
• LIPOID PNEUMONIA
• ALVEOLAR PROTEINOSIS
• LYMPHOMA - MALT
Stephano Palmucci et al, Diagnostics Dec 2021
PULMONARY HAEMORRHAGE – DIFFUSE ALVEOLAR
HAEMORRHAGE (DAH)

ACUTE PHASE:
LOBULAR OR LOBAR AREAS OF
GROUND GLASS OPACITIES TO
PREDOMINANT CONSOLIDATION.
Stephano Palmucci et al, Diagnostics Dec 2021
PULMONARY HAEMORRHAGE – DIFFUSE ALVEOLAR
HAEMORRHAGE (DAH)

• SUB ACUTE : 2-3 DAYS


• RETICULAR SHADOWS :
INTRALOBULAR AND
INTERLOBULAR SEPTAL
THICKENING
SUPERIMPOSED ON AREAS
OF GGO.
• CRAZY PAVING PATTERN
• THESE CAN OFTEN
RESOLVE

CHURG STRAUSS
PULMONARY HAEMORRHAGE – DIFFUSE ALVEOLAR
HAEMORRHAGE (DAH)

BETWEEN CHRONIC
RECURRENT BLEEDING
EVENTS:

- ILL DEFINED CENTRILOBULAR


NODULES
- REFLECTING AN INTRA ALVEOLAR
ACCUMULATION OF PULMONARY
MACROPHAGES
- NODULES ARE USUALLY UNIFORM
IN SIZE (1-3 MM)
- MAY CAVITATE
- DIFFUSELY DISTRIBUTED GPA – WEGENER’S
- NO ZONAL PREDOMINANCE
PULMONARY HAEMORRHAGE – DIFFUSE
ALVEOLAR HAEMORRHAGE (DAH)

• WITH SEVERE REPEATED


HAEMORRHAGE CAN LEAD TO
ORGANIZING PNEUMONIA
ORGANIZING PNEUMONIA

• REPRESENTS AN INFLAMMATORY
PROCESS IN WHICH THE HEALING
PROCESS IS CHARACTERIZED BY
ORGANIZATION AND
CICATRIZATION OF THE EXUDATE
RATHER THAN BY RESOLUTION
AND RESORPTION.

• IT IS ALSO DESCRIBED AS
'UNRESOLVED PNEUMONIA'.
• GRANULOMATOUS TISSUE IN THE
AIR SPACES
• FORM MASSON BODIES -
FIBROBLASTS, INFLAMMATORY
CELLS, FIBRIN.
OP : CAUSES

• CRYPTOGENIC – COP - 50%


• PNEUMONIA
• ASPIRATION
• TOXIC FUME INHALATION
• DRUGS
• RADIATION
• CHEMOTHERAPY
• CONNECTIVE TISSUE DISEASE - DAH
• GRAFT VS HOST DISEASE
OP – HRCT PATTERN

MANY TYPES OF APPEARANCES -

• ATOLL SIGN OR REVERSE HALO SIGN


• CENTRAL PERI-BRONCHIAL OR PERIPHERAL
CONSOLIDATION
• PERILOBULAR INTERSTITIAL THICKENING OR
CONSOLIDATION
• LINEAR OR BAND LIKE OPACITIES
• NODULES
Peri broncho vascular consolidation
PERIPHERAL PERI LOBULAR
CONSOLIDATION INTERSTITIAL THICKENING

Post Covid 19 OP
DDay 10
Day 5

OP - Toxic NH3 inhalation


Linear / band like opacities

Day 10
COP – NODULAR PATTERN

? COP
OP – ATOLL SIGN / REVERSE HALO SIGN
OP – ATOLL SIGN / REVERSE HALO SIGN

Mass like consolidation


DIFFUSE ALVEOLAR HAEMORRHAGE (DAH)

• WITH SEVERE REPEATED HAEMORRHAGE:


ORGANIZING PNEUMONIA MAY PROGRESS
TO INTERSTITIAL LUNG FIBROSIS.
VOLUME LOSS
UIP/IPF : TRACTION BRONCHIECTASIS
- CORRUGATED APPEARANCE
HONEYCOMBING – END STAGE LUNG FIBROSIS

Small cystic spaces with irregularly thickened


walls composed of fibrous tissue.
Stephano Palmucci et al, Diagnostics Dec 2021
SUMMARY – PRS
• THE HRCT LUNG PATTERN IN PRS NON
SPECIFIC – MAINLY GGO, CONSOLIDATIONS
AND NODULES.
• THE DIAGNOSIS IS OFTEN DELAYED— AS
OTHER DISEASE COULD HAVE SIMILAR
CLINICAL AND RADIOLOGICAL
MANIFESTATIONS.
• FIBROTIC CHANGES CAN OCCUR AND
OFTEN NOT PATHOGNOMONIC.
• A MULTIDISCIPLINARY APPROACH IS
STRONGLY RECOMMENDED FOR
DIAGNOSIS.
THANK YOU

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