The Pathology of Neoplasia - Roswell Park Comprehensive ... · The Pathology of Neoplasia February...
Transcript of The Pathology of Neoplasia - Roswell Park Comprehensive ... · The Pathology of Neoplasia February...
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PAUL BOGNER, MD
A S S O C I A T E P R O F E S S O R O F O N C O L O G Y P A T H O L O G Y A N D D E R M A T O L O G Y
The Pathology of Neoplasia
February 2018
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Outline and Objectives
What is Pathology?
What is a Pathology Department?
The pathologist’s “tools”
Pathology Definitions and Concepts
How do we approach a pathology specimen?
A General Classification of Neoplasia.
The ugly histologic face of cancer (recognizing malignancy).
Grading and Staging Malignancy.
The Changing World of Pathology
Pathology and Research
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Clinical goals of cancer pathology
1. Identify presence of cancer
2. Classify cancer
3. Predict biology of cancer and prognosis
4. Identify optimal therapy
5. Evaluate success of treatment
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Pathology
“...branch of medicine which treats (studies) of the essential nature of disease, especially of the structural and functional changes in tissues and organs of the body which cause or are caused by disease.” Dorland’s Medical Dictionary 24th Ed.
“...something abnormal- the anatomic and physiologic deviations from the normal that constitute disease or characterize a particular disease.” Webster’s Seventh New Collegiate Dictionary
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A Department of Pathology
Patient Care
ANATOMIC PATHOLOGY
CLINICAL PATHOLOGY
Experimental (Research)
TISSUE PROCUREMENT
TRANSLATIONAL
BENCH
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Anatomic Pathology
Surgical Pathology
Frozen Section (Intra-operative consultations)
Biopsy and Resection specimens
Cytopathology
Pap smears (Gynecologic specimens)
Fine needle aspirates, washes, brushes
Autopsy
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Clinical Pathology
Hematology
Chemistry
Microbiology
Blood Bank (Transfusion Medicine)
Tissue Typing (Transplant Pathology)
Molecular Diagnostics
Flow Cytometry
Cytogenetics
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Anatomic Pathology in Cancer
Patient has signs or symptoms of cancer
Clinician/Radiologist performs biopsy
Pathologist diagnoses cancer on biopsy
Clinician performs resection/excision
Pathologist stages and evaluates cancer
Molecular Characteristics of Tumor Evaluated for use in “Personalized Medicine”
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The Pathologist’s Tools
The “Grossing Station”
Fixation (usually with Formalin- 37% formaldehyde) Preserve tissue, enhance detail for microscopy
Tissue Processing (usually overnight)
Remove tissue water gradually, replace with paraffin wax
Paraffin Embed and cut tissue sections
Hematoxylin and Eosin Stain
The Light Microscope
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Gross Examination
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Cassettes and Tissue Sections
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Tissue Processor
1. Dehydrate Tissue • Progressive series
of alcohols removes water
2. Clear Ethanol with xylene
3. Replace with paraffin
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Tissue Embedded in Liquid Paraffin
Pictures courtesy of www.protocolsonline.com
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Sections Cut (~ 5 μm) by microtome
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Hematoxylin and Eosin (the H&E)
The pink and purple foundation of pathology
Hematoxylin
Purple/blue stain (BASOPHILIC)
Stains acidic materials
Stains nuclear contents
Eosin
Pink stain (EOSINOPHILIC)
Stains most cytoplasmic contents
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Ancillary Studies
Flow cytometry
Immunohistochemical stains
Cytochemical stains
Cytogenetics
Electron microscopy
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Immunohistochemistry (IHC)
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IHC: what is it good for?
Identify or confirm the source of a tumor CK7, CK20, other markers “specific” to tumor type
Increase the sensitivity of tumor detection eg find individual metastatic melanoma cells in a lymph node
using Melan-A
Predict tumor behavior/prognosis proliferative index (Ki-67)
Identify potential therapeutic targets Estrogen receptor – Tamoxifen (breast cancer)
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Additional Markers Used as Suggested by Clinical Data (after a Preliminary
Workup with CK7 and CK20)
Tumor Marker
Urothelial carcinoma UROIII, THR, HMWCK
Breast carcinoma GCDFP-15, ER, PR
Lung (mainly adenocarcinoma) TTF-1, surfactant A and B
Medullary thyroid carcinoma TTF-1, Calcitonin
Merkel cell carcinoma CD117
Hepatocellular carcinoma Hep par-1
Prostate carcinoma PSA, PAP
Cholangiocarcinoma CK19
Mesothelioma Calretinin
from Varadhachary, GR. et al., Cancer 100(9):1776 (2004).
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Breast Cancer Metastatic to Uterus MAMMAGLOBIN IHC STAIN
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Immunohistochemistry
DISADVANTAGES
FALSE Negative
Antigen- not present in tissue, degraded
Antibody- too dilute, expired, wrong antibody
FALSE Positive
Cross reactive or non-specific antibody binding
Endogenous peroxidase or avidin/biotin binding
Entrapped normal cells
Tumor uptake of normal cell antigens
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Definitions and Concepts
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Definitions
TUMOR
Swelling.
CANCER
“crab”, tumor with fatal course and association with formation of secondary tumors (metastasis)
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Definitions
EPITHELIUM (epithelial) when malignant it is called CARCINOMA
Derived from ectoderm or endoderm: the protective, absorptive and secretory lining of the body both
externally (e.g. skin), and internally (e.g. lining of colon, pancreatic glands)
Common types of epithelium are: squamous and columnar/glandular
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Epithelium and Basement Membrane
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Definitions
MESENCHYME (mesenchymal) when malignant it is called SARCOMA
Largely derived from mesoderm: structural and functional elements of the body- “connective tissue” (cartilage, bone, collagen, nerve, blood vessels, etc...)
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Definitions
NEOPLASIA
Any new or abnormal growth (typically implies a clonal population of cells).
NEOPLASM
Mass of new tissue which persists and grows independently of its surrounding structures and
which has no physiologic use
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Definitions
METAPLASIA
A change in tissue cells to a form not normal for that tissue, usually reversible and protective
HYPERPLASIA
An increase in the NUMBER of cells, while maintaining normal tissue architecture
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Normal esophagus Barrett’s metaplasia
Images taken from WWW: “The GastroLab Endoscopy Archive”
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Metaplasia (Barrett’s Esophagus)
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Definitions
INVASION
The penetration of neoplastic epithelial cells through the basement membrane.
Also used less specifically to refer to cells (epithelial or mesenchymal) penetrating any adjacent existing
structure.
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Invasion (Squamous Cell Carcinoma)
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Definitions
DIFFERENTIATION
Degree to which a neoplasm recapitulates normal tissue in all its characteristics (often assessed as a
GRADE)
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Well Differentiated Lung Adenocarcinoma (Bronchioloalveolar Carcinoma 200x)
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Poorly differentiated lung adenocarcinoma (200x)
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Definitions
ATYPIA
The condition of being irregular, refers generally to abnormalities of histologic appearance- not always neoplastic in nature (can be “reactive”, as in setting
of radiation therapy or inflammation)
ANAPLASIA
A loss of normal differentiation and form.
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Definitions
DYSPLASIA
Abnormality of maturation and development, manifesting as architectural, organizational and
cytologic atypia
MILD MODERATE SEVERE
(SEVERE usually is Carcinoma in-situ)
DYSPLASIA IS ALWAYS ATYPICAL, ATYPIA IS NOT ALWAYS DYSPLASTIC!
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Colonoscopy
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Colonic Adenoma (Dysplasia 100x)
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Colonic Adenoma (Dysplasia 200x)
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Definitions
PLEOMORPHISM
Variation in cellular size and shape
MALIGNANT
A neoplasm with invasive and metastatic capacity.
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Pulmonary Neuroendocrine Carcinoma
Carcinoid (400x) Small Cell Carcinoma (400x)
LOW GRADE, MINIMAL TO NO ATYPIA HIGH GRADE, SEVERE ATYPIA
MONOMORPHIC PLEOMORPHIC
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NEC: Small Cell Carcinoma (400x)
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A P P R O A C H I N G A P A T H O L O G I C S P E C I M E N .
Beware: gross photos ahead
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Approaching a pathologic specimen
GROSS APPEARANCE
“dissect” and describe the specimen
Take carefully selected portions of tissue for subsequent examination under the microscope
MICROSCOPIC APPEARANCE
Routine Hematoxylin and Eosin stained slides
Special histologic techniques (stains, immunohistochemistry)
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Gross Specimen...
Hepatocellular Carcinoma
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Another Gross Specimen
Adenocarcinoma
of colon
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Approaching a pathologic specimen
Is there pathology present?
What is the general nature of the pathology?
Infectious, neoplastic, inflammatory/autoimmune
If it IS neoplastic, what parameters must be collected?
Benign or malignant?
Tumor type, grade, stage, resection margin status
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General Types of Neoplasia
EPITHELIAL (eg. Carcinoma) Generally derived from ectoderm or endoderm
MESENCHYMAL (eg. Sarcoma) Generally derived from mesoderm (neural tissue is an
exception it’s ectodermal)
HEMATOPOEITIC (eg. Lymphoma) Generally derived from mesoderm
MIXED (eg. Carcinosarcoma)
OTHER (eg. Germ cell tumor)
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adenoma papilloma carcinoma
etc
Epithelial Tumors
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Carcinoma
Malignant tumor of epithelium
Comes in different types depending on origin:
Squamous cell carcinoma
Adenocarcinoma (glandular)
Neuroendocrine carcinoma
Sometimes preceded by a pre-invasive lesion: severe dysplasia (carcinoma in-situ)
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Adenocarcinoma of Lung
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Normal Bronchial
Epithelium (400x) Bronchial Squamous
Metaplasia (200x)
Severe Bronchial
Squamous
Dysplasia/Carcinoma
in-situ (200x)
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Invasive Squamous Cell Carcinoma (400x)
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Carcinoma
One hallmark of an epithelial neoplasm is cellular expression of cytokeratin (CK) intermediate filaments
Cytokeratin expression profile can also help identify the primary site/source of a carcinoma (immunohistochemistry)
CK 7, CK 20, CK 5/6
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- OMA - SARCOMA
Mesenchymal tumors
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Mesenchymal tumors
Tumors of connective/mesenchymal tissue
Named according to their putative origin and differentiation:
Tissue Type Malignant Benign Smooth muscle leiomyosarcoma leiomyoma Skeletal muscle rhabdomyosarcoma rhabdomyoma Blood vessels angiosarcoma angioma Cartilage chondrosarcoma chondroma Bone osteosarcoma osteoma Adipose (fat) liposarcoma lipoma
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Chondrosarcoma (Humerus)
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Mesenchymal Tumors
Usually express the intermediate filament vimentin, and NOT cytokeratins
May also express markers of differentiation:
Smooth Muscle smooth muscle actin
Nerve S100
Vascular Cluster of Differentiation 31
(CD31)
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leukemia lymphoma
Hematopoetic Neoplasia
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Hematopoetic Neoplasia
Derived from bone marrow cells (red, white)
Lymphoma (cells usually involve lymph node or other lymphoid tissue like spleen)
T-cell (CD3+, CD20-)
B-cell (CD20+, CD3-)
NK cell (CD56+)
Leukemia (cells circulate in blood) Myeloid (acute or chronic)
Lymphoid (acute or chronic)
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MALT Lymphoma of Lung (40x)
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MALT Lymphoma (400x)
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Origin of B-cell lymphoma
Figure from: Lymphoma: Methods and Protocols,
Methods in Molecular Biology. Volume 971. R. Kuppers (ed.),
Springer 2013
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Simplified IHC small B-cell lymphoma
CD20+
Bcl-6+ Bcl-6-
Follicular CD5+ CD5-
CD23+ CD23- Marginal Zone
SLL Bcl-1+
Mantle Cell
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So how do we know if a bunch of cells is benign or malignant?
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Recognizing Malignancy
1. Architecture and Behavior
2. Proliferation (mitotic rate, antigenic markers)
3. Necrosis
4. Cytology (nuclear and cytoplasmic)
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Recognizing Malignancy
Architecture and behavior
How closely does tumor resemble normal tissue?
What is the contour of the tumor?
Is there invasion of adjacent tissue?
Is there invasion of blood vessels or nerves?
Does it have a capsule?
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Mammogram of Ductal Carcinoma
Copyright © 1999 by W. B. Saunders
Company
All rights reserved.
Produced in the United States of
America
ISBN: 0-7216-8462-9
Image from: medic.med.uth.tmc.edu
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BENIGN
- Organized
- Well
circumscribed
- No infiltration
of adjacent
tissue.
- Normal stroma
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MALIGNANT
-Disorganized.
- Poorly
circumscribed.
- Infiltrates
adjacent fat.
- Desmoplastic
stroma.
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Recognizing Malignancy
Proliferative Rate
What is the mitotic count? (number of mitoses per 10 high-power 400x microscopic fields)
Are mitoses normal in form?
What is the percentage of cells expressing markers of proliferation? (Ki-67/Mib-1)
Necrosis
Is there tumor necrosis? (function of rapid uncontrolled
proliferation, loss of cell cycle control)
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Hepatocellular Carcinoma with Necrosis
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Hepatocellular Carcinoma with Mitosis
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Recognizing Malignancy
Cytology (a function of rapid proliferative rate and abnormal, active cellular “machinery”)
What is the character of the nuclear chromatin?
Are there abnormal nucleoli present?
What is the contour of the nuclear membrane?
What is the nucleus:cytoplasmic ratio? (N:C ratio)
Is the cytoplasm mature?
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Benign or malignant nuclei (400x)?
MALIGNANT BENIGN
#1 #2
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END OF LECTURE ONE