ENDOMYOCARDIAL
BIOPSY
Dr E Kiran Kumar
Professor of Pathology
MIMS, Vizianagaram,A.P
What is EMB ?
• Endomyocardial Biopsy(EMB) is a
technique by which heart tissue is
sampled from the pts with suspected
cardiac disorders for microscopic
diagnosis and evaluation of the lesions.
HISTORICAL ASPECTS
• Open surgical biopsies of heart-1950’s, followed
by needle bx using modified vim-silverman’s
needle through thoracotomy/trans-thoracic
approach- complications like pneumothorax/
cardiac tamponade. .
• The first trans-venous biopsy fx- KONNO-
SAKAKIBARA BIOPTOME- Japan-1962.
• Modified bioptome- CAVES-SCHULTZ-
STANFORD bioptome- Stanford-1972.
HISTORICAL ASPECTS (cont’d)
• Further modifications in catheter design-
sheathing and increased flexibility and easy
manouverability, e.g Modified Cordis Bioptome.
• Novel-shaped long-neck sheath for
endomyocardial biopsy through the internal
jugular approach- reduces trauma and provides
stability for the bioptome forceps,limits
radiation exposure.
• EMB –Initially performed via the “internal
jugular vein”, later- femoral venous approach is
used after the advent of long and flexible
bioptomes.
PREPARATION OF THE PATIENT
• Routine lab tests, an ECG and a chest x-
ray.
• Pt should have nothing to eat or drink, 6
hrs before the procedure, except the
medication.
• Done in Cardiac Catheterization lab.
• Anaesthetic medication used- novocaine.
TECHNIQUE
• Performed via the transvascular approach
and is done usually at the time of cardiac
catheterization.
• Right ventricle is preferred as it is easier
and safer to biopsy this chamber.
• Rt ventricle is the representative site in
diffuse diseases. Lt ventricle is preferred
in sarcoidosis and done via arterial
approach.
Technique (cont’d)
A flexible, plastic tube called a “sheath” is inserted into the
vein in the neck or groin, followed by insertion of
“pulmonary artery catheter” into the rt side of heart
( under fluoroscopic guidance), which measures the
pressures inside the heart. Then the catheter is removed.
• Then BIOPTOME is guided through the sheath into the
heart. Biopsy forceps can easily be taken upto the apical
portion of RVS.3-4 tissue samples of 2-3 mm size are
obtained.Then the bioptome and sheath are removed.
• Flexible, disposable bioptomes- presently available.
• Availability of catheters and bioptome forceps of
different sizes and designs - Apical curvature- for easy
sampling and grip on the tissue.
•Bioptome
forceps with
sheath
BIOPTOME FORCEPS
BIOPTOME FORCEPS WITH
SHEATH
Tissue Processing
• 4-5 biopsy fragments are processed
routinely and 1 fragment for EM exam.
• Transplant biopsies- if vascular rejection is
suspected, 1 fragment is frozen for
immunofluorescence.
• Anthracycline, Chloroquine and
Amiodarone toxicity- All fragments are
processed for EM.
INDICATIONS FOR EMB
Most common indications are-
1) To evaluate unexplained CCF
2) To diagnose myocarditis
3) Constrictive v/s Restrictive CMPs
4) To diagnose transplant rejection
5) To evaluate drug (anthracycline,herceptin,doxorubicin
) toxicity
6) To investigate effects of anabolic steroids, thalassemia
and HIV cardiomyopathy).
## “EMB is the most useful tool for the diagnosis and
monitoring of cardiac allograft rejection after cardiac
transplantation.” ##
INDICATIONS (cont’d)
• Less common indications are
1) To investigate idiopathic arrythmias
2) Biopsies of neoplasms .
One impt indication for Lt ventr bx-
“suspected cardiac sarcoidosis”- Involves
lt vent > rt vent – An arterial approach is
reqd for lt vent biopsy.
TISSUE EVALUATION
• Major limitation- SAMPLING
• Bioptome is guided towards the apex of the right
ventricle, yielding tissue from the ventricular
septum or right ventricular wall.
• FOCAL INVOLVEMENT -Inflamm and Infiltr
diseases like myocarditis, haemochromatosis,
sarcoidosis and amyloidosis . Hence easily
MISSED by biopsy.
• Hence SERIAL SECTIONING of multiple
sections through the block required.
PROBLEMS DURING
INTERPRETATION
• Sampling error-due to focal nature of disease
(e.g. myocarditis)
• Crush artifacts-mech trauma
• Contraction bands(AMI, Mech trauma)
• Focal interstitial fibrosis (non- specific finding)
• Interstitial mesenchymal cells closely resemble
lymphocytes.
• Endocardial thickening( non specific finding)
• Adipose tissue (normal in rt ventr biopsy)
COMPLICATIONS
PERFORATION – CLINICAL PERFORATION
(chest pain and pericardial effusion as judged by
transthoracic echocardiography or TEE) and
``NEAR PERFORATION'' (epicardial fat in
specimens.
• The risk of perforation can be reduced by using
a specially curved sheath to guide the biopsy
forceps toward the interventricular septum.
• Others- mostly in pediatric age group-
Arrythmias(AF/VF), Pneumothorax and
Haemopericardium.
TRANSPLANT REJECTION-
GRADING
TRANSPLANT REJECTION-GR 3B
TRANSPLANT REJECTION- GR3B
TRANSPLANT REJECTION GR 3A
TRANSPLANT REJECTION GR- 4
CMV INFECTION IN
ALLOGRAFT
PREVIOUS BIOPSY SITE AND
QUILTY EFFECT
MYOCARDITIS
HEMOCHROMATOSIS
DRUG TOXICITY
DOXORUBICIN TOXICITY
DILATED CMP
DILATED CMP
DILATED CMP- HP VIEW
DILATED CMP- MASSON’S
TRICHROME STAIN
Figure 1 (A) Biopsy from a 45 year old woman with dilated cardiomyopathy. Note the
endocardial fibrosis, myocyte hypertrophy, myocyte nuclei, and moderate interstitial
fibrosis (haematoxylin and eosin staining; original magnification, x10). (B) Elastic
trichrome stain of the same case showing thickened fibrous endocardium with
considerable interstitial fibrosis (original magnification, x10).
MYOCARDITIS
MYOCARDITIS- HP VIEW
GIANT CELL MYOCARDITIS
GIANT CELL MYOCARDITIS-HP
VIEW
EOSINOPHILIC MYOCARDITIS
CARDIAC AMYLOIDOSIS
CARDIAC AMYLOIDOSIS-
CRYSTAL VIOLET STAIN
CARDIAC AMYLOIDOSIS-
THIOFLAVIN T STAINING
CARDIAC AMYLOIDOSIS-
BLOOD VESSELS
RESTRICTIVE CMP
RESTRICTIVE CMP- MASSON’S
TRICHROME STAIN
SARCOIDOSIS OF HEART- NON
CASEATING GRANULOMA
TUBERCULOMA HEART-
CASEOUS NECROSIS
GLYCOGEN STORAGE DISEASE
##TAKE HOME MESSAGE ##
• Endomyocardial biopsy is an inevitable and an efficient
investigative tool for assesment of rejection grading of
the allograft after CARDIAC TRANSPLANTAION.
• There is a significant REDUCTION in the incidence of
complications of the procedure, due to the NEWER
MODIFICATIONS in the DESIGNING of the sheath and
bioptome forceps.
• Done in CARDIAC CATHETERISATION LAB, in the
presence of interventional cardiologist, and under
FLUOROSCOPIC guidance.
• Sampled heart tissue can be subjected to ROUTINE
TISSUE PROCESSING for HPE, ANCILLIARY
techniques like IHC, Enzyme Histochemistry, Special
Stains, ,EM, Molecular Phenotyping ,RT- PCR techniques
for detection of viral nuclei acids,etc.
RESOURCE MATERIAL
1)Silverberg’s –principles and practice of surgical
pathology and cytopathology.
2)Chopra’s-Text book of cardiovascular pathology.
3)Sternberg’s –Diagnostic surgical pathology.
4)Weidner’s – Modern Surgical Pathology
5) Anderson’s - Pathology
6) Internet -Cardiology and pathology journal
websites.

Endomyocardial biopsy

  • 1.
    ENDOMYOCARDIAL BIOPSY Dr E KiranKumar Professor of Pathology MIMS, Vizianagaram,A.P
  • 2.
    What is EMB? • Endomyocardial Biopsy(EMB) is a technique by which heart tissue is sampled from the pts with suspected cardiac disorders for microscopic diagnosis and evaluation of the lesions.
  • 3.
    HISTORICAL ASPECTS • Opensurgical biopsies of heart-1950’s, followed by needle bx using modified vim-silverman’s needle through thoracotomy/trans-thoracic approach- complications like pneumothorax/ cardiac tamponade. . • The first trans-venous biopsy fx- KONNO- SAKAKIBARA BIOPTOME- Japan-1962. • Modified bioptome- CAVES-SCHULTZ- STANFORD bioptome- Stanford-1972.
  • 4.
    HISTORICAL ASPECTS (cont’d) •Further modifications in catheter design- sheathing and increased flexibility and easy manouverability, e.g Modified Cordis Bioptome. • Novel-shaped long-neck sheath for endomyocardial biopsy through the internal jugular approach- reduces trauma and provides stability for the bioptome forceps,limits radiation exposure. • EMB –Initially performed via the “internal jugular vein”, later- femoral venous approach is used after the advent of long and flexible bioptomes.
  • 5.
    PREPARATION OF THEPATIENT • Routine lab tests, an ECG and a chest x- ray. • Pt should have nothing to eat or drink, 6 hrs before the procedure, except the medication. • Done in Cardiac Catheterization lab. • Anaesthetic medication used- novocaine.
  • 6.
    TECHNIQUE • Performed viathe transvascular approach and is done usually at the time of cardiac catheterization. • Right ventricle is preferred as it is easier and safer to biopsy this chamber. • Rt ventricle is the representative site in diffuse diseases. Lt ventricle is preferred in sarcoidosis and done via arterial approach.
  • 7.
    Technique (cont’d) A flexible,plastic tube called a “sheath” is inserted into the vein in the neck or groin, followed by insertion of “pulmonary artery catheter” into the rt side of heart ( under fluoroscopic guidance), which measures the pressures inside the heart. Then the catheter is removed. • Then BIOPTOME is guided through the sheath into the heart. Biopsy forceps can easily be taken upto the apical portion of RVS.3-4 tissue samples of 2-3 mm size are obtained.Then the bioptome and sheath are removed. • Flexible, disposable bioptomes- presently available. • Availability of catheters and bioptome forceps of different sizes and designs - Apical curvature- for easy sampling and grip on the tissue.
  • 8.
  • 10.
  • 11.
  • 12.
    Tissue Processing • 4-5biopsy fragments are processed routinely and 1 fragment for EM exam. • Transplant biopsies- if vascular rejection is suspected, 1 fragment is frozen for immunofluorescence. • Anthracycline, Chloroquine and Amiodarone toxicity- All fragments are processed for EM.
  • 13.
    INDICATIONS FOR EMB Mostcommon indications are- 1) To evaluate unexplained CCF 2) To diagnose myocarditis 3) Constrictive v/s Restrictive CMPs 4) To diagnose transplant rejection 5) To evaluate drug (anthracycline,herceptin,doxorubicin ) toxicity 6) To investigate effects of anabolic steroids, thalassemia and HIV cardiomyopathy). ## “EMB is the most useful tool for the diagnosis and monitoring of cardiac allograft rejection after cardiac transplantation.” ##
  • 14.
    INDICATIONS (cont’d) • Lesscommon indications are 1) To investigate idiopathic arrythmias 2) Biopsies of neoplasms . One impt indication for Lt ventr bx- “suspected cardiac sarcoidosis”- Involves lt vent > rt vent – An arterial approach is reqd for lt vent biopsy.
  • 15.
    TISSUE EVALUATION • Majorlimitation- SAMPLING • Bioptome is guided towards the apex of the right ventricle, yielding tissue from the ventricular septum or right ventricular wall. • FOCAL INVOLVEMENT -Inflamm and Infiltr diseases like myocarditis, haemochromatosis, sarcoidosis and amyloidosis . Hence easily MISSED by biopsy. • Hence SERIAL SECTIONING of multiple sections through the block required.
  • 16.
    PROBLEMS DURING INTERPRETATION • Samplingerror-due to focal nature of disease (e.g. myocarditis) • Crush artifacts-mech trauma • Contraction bands(AMI, Mech trauma) • Focal interstitial fibrosis (non- specific finding) • Interstitial mesenchymal cells closely resemble lymphocytes. • Endocardial thickening( non specific finding) • Adipose tissue (normal in rt ventr biopsy)
  • 17.
    COMPLICATIONS PERFORATION – CLINICALPERFORATION (chest pain and pericardial effusion as judged by transthoracic echocardiography or TEE) and ``NEAR PERFORATION'' (epicardial fat in specimens. • The risk of perforation can be reduced by using a specially curved sheath to guide the biopsy forceps toward the interventricular septum. • Others- mostly in pediatric age group- Arrythmias(AF/VF), Pneumothorax and Haemopericardium.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
    PREVIOUS BIOPSY SITEAND QUILTY EFFECT
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
    Figure 1 (A)Biopsy from a 45 year old woman with dilated cardiomyopathy. Note the endocardial fibrosis, myocyte hypertrophy, myocyte nuclei, and moderate interstitial fibrosis (haematoxylin and eosin staining; original magnification, x10). (B) Elastic trichrome stain of the same case showing thickened fibrous endocardium with considerable interstitial fibrosis (original magnification, x10).
  • 34.
  • 35.
  • 36.
  • 37.
  • 38.
  • 39.
  • 40.
  • 41.
  • 42.
  • 43.
  • 44.
  • 45.
    SARCOIDOSIS OF HEART-NON CASEATING GRANULOMA
  • 46.
  • 47.
  • 48.
    ##TAKE HOME MESSAGE## • Endomyocardial biopsy is an inevitable and an efficient investigative tool for assesment of rejection grading of the allograft after CARDIAC TRANSPLANTAION. • There is a significant REDUCTION in the incidence of complications of the procedure, due to the NEWER MODIFICATIONS in the DESIGNING of the sheath and bioptome forceps. • Done in CARDIAC CATHETERISATION LAB, in the presence of interventional cardiologist, and under FLUOROSCOPIC guidance. • Sampled heart tissue can be subjected to ROUTINE TISSUE PROCESSING for HPE, ANCILLIARY techniques like IHC, Enzyme Histochemistry, Special Stains, ,EM, Molecular Phenotyping ,RT- PCR techniques for detection of viral nuclei acids,etc.
  • 49.
    RESOURCE MATERIAL 1)Silverberg’s –principlesand practice of surgical pathology and cytopathology. 2)Chopra’s-Text book of cardiovascular pathology. 3)Sternberg’s –Diagnostic surgical pathology. 4)Weidner’s – Modern Surgical Pathology 5) Anderson’s - Pathology 6) Internet -Cardiology and pathology journal websites.