Fundamentals of

Pathology

Copyright Pathoma LLC. All Rights Reserved.

Purchase online at [Link]
mEDICAL COURSE AND STEP 1 REVIEW
first edition

Husain A. Sattar, MD
Assistant Professor of Pathology
Associate Director of Clinical Pathophysiology and Therapeutics
The University of Chicago
Pritzker School of Medicine
Chicago, Illinois

[Link]
Chicago 2011
 [Link]
Fundamentals of Pathology: Medical Course and Step 1 Review, First Edition
Copyright Pathoma LLC. All Rights Reserved.

ISBN 978-0-9832246-0-0
Purchase online at [Link]

Printed in the United States of America.

Copyright 2011 by Pathoma LLC.

All rights reserved. No part of this publication may be reproduced, distributed, or transmitted
in any form, or by any means, electronic or mechanical, including photocopying, recording,
or any information storage and retrieval system, without prior permission in writing from the
publisher (email: info@[Link]).

Disclaimer
Fundamentals of Pathology aims at providing general principles of pathology and its associated
disciplines and is not intended as a working guide to patient care, drug administration or
treatment. Medicine is a constantly evolving field and changes in practice regularly occur. It is
the responsibility of the treating practitioner, relying on independent expertise and knowledge
of the patient, to determine the best treatment and method of application for the patient.
Neither the publisher nor the author assume any liability for any injury and/or damage to
persons or property arising from or related to the material within this publication.

Furthermore, although care has been taken to ensure the accuracy of information present in
this publication, the authorand publisher make no representations or warranties whatsoever,
express or implied, with respect to the completeness, accuracy or currency of the contents of
this [Link] publication is not meant to be a substitute for the advice of a physician
or other licensed and qualified medical professional. Information presented in this publication
may refer to drugs, devices or techniques which are subject to government regulation, and it is
the responsibility of the treating practitioner to comply with all applicable laws.

This book is printed on acid-free paper.

Published by Pathoma LLC.

[Link]
info@[Link]

Cover and page design by Olaf Nelson, Chinook Design, Inc.

[Link]
 Contents
Chapter 1. Growth Adaptations, Cellular Injury, and Cell Death1

Chapter 2. Inflammation, Inflammatory Disorders, and Wound Healing 11

Chapter 3. Principles of Neoplasia 23

Copyright Pathoma LLC. All Rights Reserved.

Chapter 4. Hemostasis and Related Disorders 31

Chapter 5. Red Blood Cell Disorders 41

Purchase online at [Link]

Chapter 6. White Blood Cell Disorders 53

Chapter 7. Vascular Pathology 65

Chapter 8. Cardiac Pathology 73

Chapter 9. Respiratory Tract Pathology 85

Chapter 10. Gastrointestinal Pathology 99

Chapter 11. Exocrine Pancreas, Gallbladder, and Liver Pathology115

Chapter 12. Kidney and Urinary Tract Pathology125

Chapter 13. Female Genital System and Gestational Pathology137

Chapter 14. Male Genital System Pathology151

Chapter 15. Endocrine Pathology159

Chapter 16. Breast Pathology171

Chapter 17. Central Nervous System Pathology177

Chapter 18. Musculoskeletal Pathology191

Chapter 19. Skin Pathology201

Index 209
Copyright Pathoma LLC. All Rights Reserved.

Using this Book

This work is intended as a review for students during their preclinical years and while preparing
Purchase online at [Link]

for examinations, such as the USMLE. To this effect, the organization of this book follows that
of most primary texts in the field and parallels the syllabus used in pathophysiology courses in
medical schools throughout the United States. Ample space is provided for students to make
notes during course study and while viewing the online videos that cover each section of the
text ([Link]).
We recommend that students use Fundamentals of Pathology during their medical courses,
taking notes in the margin as pertinent topics are covered. When exam time comes around,
these notes will likely be invaluable.
For examination preparation, we suggest students read the material first, then listen to the
online lecture, and then reread the material to develop a solid grasp of each topic. One should
not become disheartened if they are not able to retain all the information contained herein.
This deceptively slim volume covers a tremendous amount of material, and repetition will be a
key aid as you progress in your studies.
An effort has been made to emphasize concepts and principles over random facts, the
forest rather than the trees. Attention to the same by the student will provide a deeper, more
meaningful understanding of human disease. We must always remind ourselves that ultimately
our goal is to learn, to share, and to serve. Fundamentals of Pathology was developed with this
goal in mind.
Husain A. Sattar, MD
Chicago, Illinois

Acknowledgments
This work would not have been possible without the support and encouragement of those
around me. To begin with, I would like to acknowledge Shaykh Zulfiqar Ahmad, whose clear
vision has guided me to horizons I would never have known. My family is to be acknowledged
for their limitless sacrifice, in particular the constant encouragement and support of my wife
Amina, who has proved through the years to be the wind under my wings. Thomas Krausz,
MD and Aliya Husain, MD (both Professors of Pathology at the University of Chicago) deserve
particular mention for their valuable advice and guiding vision, both in the development of
this book as well as my career. Special thanks to the multiple reviewers at medical centers
throughout the country for their critical comments, in particular Mir Basharath Alikhan, MD
(Pathology resident, University of Chicago) and Joshua T.B. Williams (Class of 2013, Pritzker
School of Medicine, University of Chicago) for their extensive review. Olaf Nelson (Chinook
Design, Inc.) is to be commended for his excellent layout and design. Finally, I would be remiss
without acknowledging my students, who give meaning to what I do.
 Growth Adaptations,
Cellular Injury, and Cell Death 1

GROWTH ADAPTATIONS
I. Basic Principles

Copyright Pathoma LLC. All Rights Reserved.

A. An organ is in homeostasis with the physiologic stress placed on it.
B. An increase, decrease, or change in stress on an organ can result in growth
adaptations.

Purchase online at [Link]

II. Hyperplasia and Hypertrophy
A. An increase in stress leads to an increase in organ size.
1. Occurs via an increase in the size (hypertrophy) and/or the number
(hyperplasia) of cells
B. Hypertrophy involves gene activation, protein synthesis, and production of
organelles.
C. Hyperplasia involves the production of new cells from stem cells.
D. Hyperplasia and hypertrophy generally occur together (e.g., uterus during
pregnancy).
1. Permanent tissues (e.g., cardiac muscle, skeletal muscle, and nerve), however,
cannot make new cells and undergo hypertrophy only.
2. For example, cardiac myocytes undergo hypertrophy, not hyperplasia, in
response to systemic hypertension (Fig. 1.1).
E. Pathologic hyperplasia (e.g., endometrial hyperplasia) can progress to dysplasia and,
eventually, cancer.
1. A notable exception is benign prostatic hyperplasia (BPH), which does not
increase the risk for prostate cancer.

III. Atrophy
A. A decrease in stress (e.g., decreased hormonal stimulation, disuse, or decreased
nutrients/blood supply) leads to a decrease in organ size (atrophy).
1. Occurs via a decrease in the size and number of cells
B. Decrease in cell number occurs via apoptosis.
C. Decrease in cell size occurs via ubiquitin-proteosome degradation of the
cytoskeleton and autophagy of cellular components.
1. In ubiquitin-proteosome degradation, intermediate filaments of the cytoskeleton
are tagged with ubiquitin and destroyed by proteosomes.
2. Autophagy of cellular components involves generation of autophagic vacuoles.
These vacuoles fuse with lysosomes whose hydrolytic enzymes breakdown
cellular components.

IV. Metaplasia
A. A change in stress on an organ leads to a change in cell type (metaplasia).
1. Most commonly involves change of one type of surface epithelium (squamous,
columnar, or urothelial) to another
2. Metaplastic cells are better able to handle the new stress.
B. Barrett esophagus is a classic example.

[Link] 1
 2 Fundamentals of pathology

1. Esophagus is normally lined by nonkeratinizing squamous epithelium (suited to

handle friction of a food bolus).
2. Acid reflux from the stomach causes metaplasia to nonciliated, mucin-producing
columnar cells (better able to handle the stress of acid, Fig. 1.2).
Copyright Pathoma LLC. All Rights Reserved.

C. Metaplasia occurs via reprogramming of stem cells, which then produce the new cell
type.
1. Metaplasia is reversible, in theory, with removal of the driving stressor.
Purchase online at [Link]

2. For example, treatment of gastroesophageal reflux may reverse Barrett

esophagus.
D. Under persistent stress, metaplasia can progress to dysplasia and eventually result in
cancer.
1. For example, Barrett esophagus may progress to adenocarcinoma of the
esophagus.
2. A notable exception is apocrine metaplasia of breast, which carries no increased
risk for cancer.
E. Vitamin A deficiency can also result in metaplasia.
1. Vitamin A is necessary for differentiation of specialized epithelial surfaces such
as the conjunctiva covering the eye.
2. In vitamin A deficiency, the thin squamous lining of the conjunctiva undergoes
metaplasia into stratified keratinizing squamous epithelium. This change is
called keratomalacia (Fig. 1.3).
F. Mesenchymal (connective) tissues can also undergo metaplasia.
1. A classic example is myositis ossificans in which muscle tissue changes to bone
during healing after trauma (Fig. 1.4).

V. Dysplasia
A. Disordered cellular growth
B. Most often refers to proliferation of precancerous cells
1. For example, cervical intraepithelial neoplasia (CIN) represents dysplasia and is
a precursor to cervical cancer.
C. Often arises from longstanding pathologic hyperplasia (e.g., endometrial
hyperplasia) or metaplasia (e.g., Barrett esophagus)
D. Dysplasia is reversible, in theory, with alleviation of inciting stress.
1. If stress persists, dysplasia progresses to carcinoma (irreversible).

VI. Aplasia and Hypoplasia

A. Aplasia is failure of cell production during embryogenesis (e.g., unilateral renal
agenesis).
B. Hypoplasia is a decrease in cell production during embryogenesis, resulting in a
relatively small organ (e.g., streak ovary in Turner syndrome).

Fig. 1.1 Left ventricular hypertrophy. (Courtesy of Fig. 1.2 Barrett esophagus.
Aliya Husain, MD)
 Growth Adaptations, Cellular Injury, and Cell Death 3

CELLULAR INJURY
I. Basic Principles
A. Cellular injury occurs when a stress exceeds the cells ability to adapt.
B. The likelihood of injury depends on the type of stress, its severity, and the type of
cell affected.
1. Neurons are highly susceptible to ischemic injury; whereas, skeletal muscle is
relatively more resistant.
2. Slowly developing ischemia (e.g., renal artery atherosclerosis) results in atrophy;
whereas, acute ischemia (e.g., renal artery embolus) results in injury.
C. Common causes of cellular injury include inflammation, nutritional deficiency or

Copyright Pathoma LLC. All Rights Reserved.

excess, hypoxia, trauma, and genetic mutations.

II. Hypoxia

Purchase online at [Link]

A. Low oxygen delivery to tissue; important cause of cellular injury
1. Oxygen is the final electron acceptor in the electron transport chain of oxidative
phosphorylation.
2. Decreased oxygen impairs oxidative phosphorylation, resulting in decreased
ATP production.
3. Lack of ATP (essential energy source) leads to cellular injury.
B. Causes of hypoxia include ischemia, hypoxemia, and decreased O2-carrying capacity
of blood.
C. Ischemia is decreased blood flow through an organ. Arises with
1. Decreased arterial perfusion (e.g., atherosclerosis)
2. Decreased venous drainage (e.g., Budd-Chiari syndrome)
3. Shockgeneralized hypotension resulting in poor tissue perfusion
D. Hypoxemia is a low partial pressure of oxygen in the blood (Pao2 < 60 mm Hg, Sao2
< 90%). Arises with
1. High altitudeDecreased barometric pressure results in decreased Pao2.
2. HypoventilationIncreased Paco2 results in decreased Pao2.
3. Diffusion defectPao2 not able to push as much O2 into the blood due to a
thicker diffusion barrier (e.g., interstitial pulmonary fibrosis)
4. V/Q mismatchBlood bypasses oxygenated lung (circulation problem, e.g.,
right-to-left shunt), or oxygenated air cannot reach blood (ventilation problem,
e.g., atelectasis).
E. Decreased O2-carrying capacity arises with hemoglobin (Hb) loss or dysfunction.
Examples include
1. Anemia (decrease in RBC mass)Pao2 normal; Sao2 normal
2. Carbon monoxide poisoning
i. CO binds hemoglobin more avidly than oxygenPao2 normal; Sao2 decreased

Fig. 1.3 Keratomalacia. (Courtesy of Fig. 1.4 Myositis Ossificans. (Reprinted with
[Link]) permission from [Link])
 4 Fundamentals of pathology

ii. Exposures include smoke from fires and exhaust from cars or gas heaters.
iii. Classic finding is cherry-red appearance of skin.
iv. Early sign of exposure is headache; significant exposure leads to coma and
death.
Copyright Pathoma LLC. All Rights Reserved.

3. Methemoglobinemia
i. Iron in heme is oxidized to Fe3+, which cannot bind oxygenPao2 normal;
Sao2 decreased
Purchase online at [Link]

ii. Seen with oxidant stress (e.g., sulfa and nitrate drugs) or in newborns
iii. Classic finding is cyanosis with chocolate-colored blood.
iv. Treatment is intravenous methylene blue, which helps reduce Fe3+ back to
Fe2+ state.

III. Reversible and Irreversible Cellular Injury

A. Hypoxia impairs oxidative phosphorylation resulting in decreased ATP.
B. Low ATP disrupts key cellular functions including
1. Na+-K+ pump, resulting in sodium and water buildup in the cell
2. Ca2+ pump, resulting in Ca2+ buildup in the cytosol of the cell
3. Aerobic glycolysis, resulting in a switch to anaerobic glycolysis. Lactic acid
buildup results in low pH, which denatures proteins and precipitates DNA.
C. The initial phase of injury is reversible. The hallmark of reversible injury is cellular
swelling.
1. Cytosol swelling results in loss of microvilli and membrane blebbing.
2. Swelling of the rough endoplasmic reticulum (RER) results in dissociation of
ribosomes and decreased protein synthesis.
D. Eventually, the damage becomes irreversible. The hallmark of irreversible injury is
membrane damage.
1. Plasma membrane damage results in
i. Cytosolic enzymes leaking into the serum (e.g., cardiac troponin)
ii. Additional calcium entering into the cell
2. Mitochondrial membrane damage results in
i. Loss of the electron transport chain (inner mitochondrial membrane)
ii. Cytochrome c leaking into cytosol (activates apoptosis)
3. Lysosome membrane damage results in hydrolytic enzymes leaking into the
cytosol, which, in turn, are activated by the high intracellular calcium.
E. The end result of irreversible injury is cell death.

A B C
Fig. 1.5 Coagulative necrosis of kidney. A, Gross appearance. B, Microscopic appearance. C, Normal kidney histology for comparison.
(A, Courtesy of Aliya Husain, MD)