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Chapter 4 PART I: Essential Pathology - Mechanisms of Disease NeoplasiaCompanion site for Molecular Pathology Author: William B. Coleman and Gregory J. Tsongalis
FIGURE 4.1 Cancer incidence and mortality by site for both sexes (United States, 2008). The relative contributions of the major forms of cancer to overall cancer incidence and cancer-related mortality (both sexes combined) were calculated from data provided by Jemal et al. . Cancers of the reproductive organs include those affecting the prostate, uterine corpus, ovary, uterine cervix, vulva, vagina, testis, penis, and other organs of the male and female genital systems. Cancers of the digestive system include those affecting esophagus, stomach, small intestine, colon, rectum, anus, liver, gallbladder, pancreas, and other digestive organs. Cancers of the respiratory system include those affecting the lung, bronchus, larynx, and other respiratory organs. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
FIGURE 4.2 Age-specific incidence and mortality rates for selected sites, 1992–1996. The age-specific rates for breast cancer incidence and mortality are for females only. The age-specific rates for lung cancer and colorectal cancer are combined for both sexes. These data were adapted from the NCI SEER Statistics Database (http://seer.cancer.gov/index.html). Rates are per 100,000 population and are age-adjusted to the 1970 standard population of the United States. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
FIGURE 4.3 Progression of dysplasia in the cervix.(A) Normal squamous epithelium of the cervix. The basal (bottom) layer of cells appears dark, and there is cellular maturation as the squamous cells move to the surface. (B) Low-grade squamous dysplasia. The basal layer appears thicker with mild nuclear pleomorphism and mitotic figures involving the lower third of the epithelium. In this image, several HPV-infected cells, known as koilocytes, are present in the middle third of the epithelium. A koilocyte has a wrinkled nucleus with cytoplasmic clearing. (C) Moderate squamous dysplasia. The dysplastic squamous cells and mitotic figures involve the lower two-thirds of the epithelium. There is still some maturation toward the surface of the epithelium. (D) High-grade squamous dysplasia. Dysplastic squamous cells and mitotic figures involve the full thickness of the epithelium. There is no invasion into the underlying stroma. (E) Invasive squamous cell carcinoma. Dysplastic squamous cells invade into the underlying stroma in a haphazard fashion. There is prominent inflammation in the stroma in response to the invasive carcinoma. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Progression of neoplastic transformation in the colon. FIGURE 4.4 Progression of neoplastic transformation in the colon. (A) Low-grade glandular dysplasia. This image is of an adenomatous colon polyp, which is, by definition, polypoid low-grade dysplasia of the colonic glandular epithelium. The nuclei are hyperchromatic (dark) with pseudostratification (overlapping) and a higher nuclei to cytoplasmic ratio (the nucleus is occupying a larger percentage of cell volume than in a normal colon epithelial cell). (B) High-grade glandular dysplasia. Sometimes adenomatous polyps can harbor high-grade dysplasia. Features of high-grade dysplasia include both increased architectural complexity, including back-to-back glands without intervening stroma, and increased degree of nuclear pleomorphism. (C) Invasive adenocarcinoma. Glands, lined by dysplastic cells, are haphazardly invading through the musculars mucosa and into the underlying submucosa. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Courtesy of Kirsten Boland, MHS, PA(ASCP).FIGURE 4.5 Adrenal adenoma. The normal cortex of the adrenal gland is yellow-gold in appearance. The white arrow points to a well-delineated, round lesion arising in the adrenal cortex. It does not appear to invade into the adjacent tissue. Courtesy of Kirsten Boland, MHS, PA(ASCP). Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Pancreatic adenocarcinoma. FIGURE 4.6 Pancreatic adenocarcinoma. This is a cut section of a pancreatic tumor. It is poorly delineated (meaning it is difficult to identify the exact borders of the lesion) and appears to be infiltrating into adjacent adipose tissue (patchy bright yellow areas along the bottom of the specimen). Courtesy of Kirsten Boland, MHS, PA(ASCP). Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Neoplasms of mixed cell type. FIGURE 4.7 Neoplasms of mixed cell type. (A) Mature teratoma. This example demonstrates mature cartilage (right) and skin (left). (B) Immature teratoma. This type of teratoma contains areas of primitive-appearing hyperchromatic cells, known as blastema. There is focal rosette formation (white arrow). Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Metaplastic change in the stomach. FIGURE 4.8 Metaplastic change in the stomach. (A) Normal glandular epithelium of the stomach. (B) Intestinal metaplasia. This image displays glandular epithelium of the stomach with goblet cells (white arrows). Goblet cells contain a large, round intracytoplasmic vacuole of mucin and are normally found in the small and large intestine only. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Epithelial hyperplasia of the breast. FIGURE 4.9 Epithelial hyperplasia of the breast. Normal mammary ducts are lined by a single layer of cuboidal epithelial cells (as in the duct second from the center bottom). The lumens of the remaining ducts in this image are filled with bland appearing-epithelium cells, representing prominent ductal epithelial hyperplasia. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Nuclear pleomorphism and abnormal mitotic figures in neoplastic cells. (A) Pleomorphism. This is an example of leiomyosarcoma. Several of the malignant stromal cells are very large and different in shape from neighboring cells. (B) Mitotic figure (center). Malignant neoplasms often have an increased number of mitotic figures. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Progression of tumorigenesis in the breast. FIGURE 4.11 Progression of tumorigenesis in the breast. (A) Ductal carcinoma in situ (DCIS) of the breast. The lumen of this mammary duct is filled with pleomorphic cells with high nuclear to cytoplasmic ratios. Scattered mitotic figures are noted. This neoplastic process is in situ carcinoma because the dysplastic cells are confined to the lumen of the duct and have not invaded into the surrounding tissue. (B) Invasive adenocarcinoma of the breast. Glands lined by dysplastic cells haphazardly infiltrate into adipose tissue. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Childhood neuroblastoma. FIGURE 4.12 Childhood neuroblastoma. Neuroblastoma is considered one of the so-called small, round, blue cell tumors, as it is composed of small, hyperchromatic, monomorphic cells with scant cytoplasm. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
FIGURE 4.13 Lymphoma. This image of lymphoma demonstrates sheets of large cells with prominent nucleoli. Subclassification of the lymphoma depends on several additional laboratory tests. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Cellular pleomorphism. FIGURE 4.14 Cellular pleomorphism. The dysplastic cells in this adenocarcinoma demonstrate marked pleomorphism, meaning the cells vary widely in size and shape. The arrangement of the dysplastic cells is disordered, with only some residual gland formation. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
FIGURE 4.15 Tumor necrosis. Necrotic (dead tissue) debris is present within the center of the malignant glands in this adenocarcinoma. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Metastatic spread of malignant cells through the lymphatic system. FIGURE 4.16 Metastatic spread of malignant cells through the lymphatic system. (A) Metastatic adenocarcinoma to a lymph node, low power. Residual lymph node tissue is present along the upper portion of the image. Infiltrating glands of adenocarcinoma are noted at the lower aspect of the image. (B) Metastatic carcinoma to a lymph node, high power. Two nests of plump malignant epithelial cells are present within the sea of smaller lymphocytes of the lymph node. Companion site for Molecular Pathology Copyright © 2009 by Academic Press. All rights reserved.
Chapter 4 Essential Concepts in Molecular Pathology Companion site for Molecular Pathology Author: William B. Coleman and Gregory J. Tsongalis.
Dr. Manal Maher Hussein NEOPLASIA Thyroid, follicular adenoma Characteristics of benign tumors: 1. fibrous pseudocapsule separating –the adenoma.
Neoplasia p.1 SYLLABUS: RBP(Robbins Basic Pathology) Chapter: Neoplasia Definitions Nomenclature Characteristics of benign and malignant neoplasms Epidemiology.
NEOPLASIA (Malignant Tumors)
Precancerous lesion of FGT
Neoplasia II: Tumor Characteristics
Oral squamous cell carcinoma. A malignancy of epithelial cells Oral and oropharyngeal SCC represent about 3% of cancers in men and 2% of cancers in women.
Thyroid: Adenoma Lab 7, Case 1.
Female Genital Tract 1-Vulva 2-Vagina 3-Cervix 4-Uterine corpus
Female reproductive system 89Chronic cervicitis 302Naboth cysts 141Cervical squamous cell carcinoma 45Endometrial hyperplasia 129Endometrial carcinoma.
Malignant Epithelial Tumors. Fig.9.1.Histological features of differentiation of the neoplasms Behavior Benign tumor Malignant tumor Rate of growth Progressive,
The tumor appears as a fairly well circumscribed, pale, fleshy, homogeneous mass Seminoma of the testis.
Cytopathology-7 DR. MAHA AL-SEDIK.
Thanaa Helal Professor of Pathology Faculty of Medicine – Ain Shams University.
Gastrointestinal system SYLLABUS: RBP(Robbins Basic Pathology) Chapter: The Oral Cavity and the Gastrointestinal Tract.
Cytopathology. 7 Dr. Maha Al-Sedik 2015 CLS Neoplasm. 2- Stages of carcinoma. 3- Differences between benign and malignant neoplasm. 4- Dysplasia.
Module 6: Clinical Stage and Grade. Introduction Stage and grade determine prognosis Staging reflects the clinical extent of the tumor Grading a tumor.
Neoplasia Lecture 1 Dr. Maha Arafah. Neoplasia Upon completion of these lectures, the student should: Define a neoplasm. Contrast neoplastic growth with.
Pathology Practical: Female Genital Tract.
Neoplasia Lecture 2 Dr. Maha Arafah.
Introduction to Neoplasia
Adenoma of the ampulla of vater There is exophytic tumor at the ampullary orifice.
Pathology Lap Pictures and Explanation POD II BLOCK Abdullah Al Garni.
Male genital pathology
Neoplasia 1: Introduction. terminology oncology: the study of tumors neoplasia: new growth (indicates autonomy with a loss of response to growth controls)
Microscopically Yours: A Glimpse at our Cells, in Sickness and in Health Nina C. Zanetti Siena College Department of Biology.
Neoplasia I Introduction Husni Maqboul, M.D. Terminology Tumor : Pathologic disturbance of growth, characterized by excessive and unnecessary proliferation.
Neoplasia Lecture 2 Maha Arafah,MD,KSFP Abdulmalik Alsheikh, MD, FRCPC CHARACTERISTICS OF BENIGN AND MALIGNANT NEOPLASMS EPIDEMIOLOGY CHARACTERISTICS OF.
Neoplasia Dr. Raid Jastania. Neoplasia: Terminology Cancer is the 2 nd cause of death in the US Neoplasia is “new growth” Neoplasm is an abnormal mass.
Cellular Responses To Stress
CIN and mimics Dr Michael Coutts Consultant Gynaecological Pathologist
* For those free of cancer at beginning of age interval. Source: DevCan: Probability of Developing or Dying of Cancer Software, Version Statistical.
Human Biology Sylvia S. Mader Michael Windelspecht
CANCER HCT !. OBJECTIVES Define and understand the difference between benign and malignant tumors Students will be able to identify the classifications.
VULVA. NORMAL HISTOLOGY Keratinizing stratified squamous epithelium (epidermis) Adnexal structures may be present- pilosebaceous units, and sweat glands.
Pathology of Neoplasia
SMALL INTESTINE Practical II Pathology Dept, KSU GIT Block.
Revision respiratory practical block. A closer view of the lobar pneumonia demonstrates the distinct difference between the upper lobe and the consolidated.
RENAL TUMORS Renal BlockPathology Dept, KSU Renal Practical III.
Epidemiology 242: Pathology Basis of Caner Jian-Yu Rao, MD Professor of Pathology and Epidemiology Fall, 2009.
Abdulmalik Alsheikh, M.D, FRCPC Dr. Maha Arafah, MBBS, KSFP
Abdulmalik Alsheikh, MD, FRCPC Maha Arafah, MBBS, KSFP
WE WILL ALL DIE OF CANCER If something else doesn’t kill us first HYPOTHESIS:
Neoplasia Lecture 2 Abdulmalik Alsheikh, MD, FRCPC Maha Arafah, MBBS, KSFP Abdulmalik Alsheikh, MD, FRCPC Maha Arafah, MBBS, KSFP CHARACTERISTICS OF BENIGN.
Neoplasia Lecture 1 Abdulmalik Alsheikh, M.D, FRCPC Dr. Maha Arafah, MBBS, KSFP Foundation block 2013 Pathology Foundation block 2013 Pathology Definition.
Evolution of Neoplasia The Uterine Cervix As a Model Raj C. Dash, MD Duke University Medical Center Durham, North Carolina.
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