ORAL BIOPSY:
Introduction
Definition
History
Uses of Oral Biopsy
Indication for Oral Biopsy
Contraindication of Oral Biopsy
Precaution in Oral Biopsy
Armamentarium
Types of Oral Biopsy
Special consideration
Biopsy Arifact
Obtaining a Good Oral Biopsy
Complication of Oral Biopsy
Conclusion
Dr. Ahmed M. Adawy, Professor Emeritus, Dep. Oral & Maxillofacial Surgery. Former Dean, Faculty of Dental Medicine
Al-Azhar University. Oral biopsy; why, when, and how? Biopsy is the removal of the tissue from the living organism for the purpose of microscopic examination and diagnosis. Looking for a definitive diagnosis is the aim of biopsy. Types of Biopsy include incisional, excisional, drill, fine needle and frozen section biopsy.
Dr. Ahmed M. Adawy, Professor Emeritus, Dep. Oral & Maxillofacial Surgery. Former Dean, Faculty of Dental Medicine
Al-Azhar University. Oral biopsy; why, when, and how? Biopsy is the removal of the tissue from the living organism for the purpose of microscopic examination and diagnosis. Looking for a definitive diagnosis is the aim of biopsy. Types of Biopsy include incisional, excisional, drill, fine needle and frozen section biopsy.
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
Fibro-osseous lesions of the jaws
Fibrous dysplasia
Cemento-osseous dysplasia
Focal cemento-osseous dysplasia
Periapical cemento-osseous dysplasia
Florid cemento-osseous dysplasia
Ossifying fibroma
Juvenile aggressive ossifying fibroma
Cherubism
Fibro-osseous lesions (FOL) are characterized by replacement of normal bone architecture by collagen fibers and fibroblasts containing calcified tissue.
They include a wide variety of lesions of developmental, dysplastic and neoplastic origins with clinical and radiographic presentation and behavior.
Because of the histological similarities between diverse diseases, proper diagnosis requires correlation of history, clinical and radiographic findings.Fibrous Dysplasia
2. Reactive (dysplastic lesions arising in the tooth-bearing area (presumably of periodontal origin).
a. Periapical cemento-osseous dysplasia
b. Focal cemento-osseous dysplasia
c. Florid cemento-osseous dysplasia
3. Fibro-osseous neoplasms (widely designated as cementifying fibroma, ossifying fibroma or cemento-ossifying fibroma.Bone dysplasias
a. Fibrous dyspla i. Monostoticii. Polyostotic
iii. Polyostotic with endocrinopathy (McCune-Albright)
iv Osteofibrous dysplasia
b. Osteitis deformansc. Pagetoid heritable bone dysplasias of childhood
d. Segmental odontomaxillary dysplasia
2. Cemento-osseous dysplasias
a. Focal cemento-osseous dysplasia b. Florid cemento-osseous dysplasia
3.Inflammatory/reactive processes
a. Focal sclerosing osteomyelitisb. Diffuse sclerosing osteomyelitis
c. Proliferative periostitis
4. Metabolic Disease: hyperparathyroidism
5. Neoplastic lesions (Ossifying fibromas)
a. Ossifying fibromab. Hyperparathyroidism jaw lesion syndrome
c. Juvenile ossifying fibroma i. Trabecular typeii. Psammomatoid type
d. Gigantiform cementomas
Oral cancer is the world’s 6th most common malignancy and has one of the lowest survival rates, often due to late diagnosis. The most important determinant factor in cancer survival is diagnostic delay and it directly affects the survival rate.
Most oral cancers are preceded by precancerous lesions and early cancers that can be identified by visual inspection of the oral cavity. Conventional oral examination is useful in the discovery of some oral lesions, but it does not identify all potentially premalignant lesions, as some are not readily apparent to visual inspection alone.
Adjunctive techniques have emerged that may facilitate early detection of oral premalignant and malignant lesions. Thorough clinical examinations being one of the best modalities in suspecting the pathology, the biggest disadvantage in the diagnosis lies in detecting the site of biopsy and also whether biopsy is required or not in early lesions.
Nowadays various diagnostic aids have been established in detecting such lesions but easy chair-side techniques can be used if possible. And one such technique is by using vital staining with dyes which is used for early recognition of lesion and also can improve the patient survival rate.
Introduction
Development of Mast cell
Implication
Properties of Cell
Mediators of Mast cell
Types of Mast cell
Modes of degranulation
Ultra structure of mast cell
Role of mast cell in OLP,OSF, Wound healing, OSCC, pyogenic granuloma, periapical lesion, orofacial granulomatosis
Conclusion
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
Fibro-osseous lesions of the jaws
Fibrous dysplasia
Cemento-osseous dysplasia
Focal cemento-osseous dysplasia
Periapical cemento-osseous dysplasia
Florid cemento-osseous dysplasia
Ossifying fibroma
Juvenile aggressive ossifying fibroma
Cherubism
Fibro-osseous lesions (FOL) are characterized by replacement of normal bone architecture by collagen fibers and fibroblasts containing calcified tissue.
They include a wide variety of lesions of developmental, dysplastic and neoplastic origins with clinical and radiographic presentation and behavior.
Because of the histological similarities between diverse diseases, proper diagnosis requires correlation of history, clinical and radiographic findings.Fibrous Dysplasia
2. Reactive (dysplastic lesions arising in the tooth-bearing area (presumably of periodontal origin).
a. Periapical cemento-osseous dysplasia
b. Focal cemento-osseous dysplasia
c. Florid cemento-osseous dysplasia
3. Fibro-osseous neoplasms (widely designated as cementifying fibroma, ossifying fibroma or cemento-ossifying fibroma.Bone dysplasias
a. Fibrous dyspla i. Monostoticii. Polyostotic
iii. Polyostotic with endocrinopathy (McCune-Albright)
iv Osteofibrous dysplasia
b. Osteitis deformansc. Pagetoid heritable bone dysplasias of childhood
d. Segmental odontomaxillary dysplasia
2. Cemento-osseous dysplasias
a. Focal cemento-osseous dysplasia b. Florid cemento-osseous dysplasia
3.Inflammatory/reactive processes
a. Focal sclerosing osteomyelitisb. Diffuse sclerosing osteomyelitis
c. Proliferative periostitis
4. Metabolic Disease: hyperparathyroidism
5. Neoplastic lesions (Ossifying fibromas)
a. Ossifying fibromab. Hyperparathyroidism jaw lesion syndrome
c. Juvenile ossifying fibroma i. Trabecular typeii. Psammomatoid type
d. Gigantiform cementomas
Oral cancer is the world’s 6th most common malignancy and has one of the lowest survival rates, often due to late diagnosis. The most important determinant factor in cancer survival is diagnostic delay and it directly affects the survival rate.
Most oral cancers are preceded by precancerous lesions and early cancers that can be identified by visual inspection of the oral cavity. Conventional oral examination is useful in the discovery of some oral lesions, but it does not identify all potentially premalignant lesions, as some are not readily apparent to visual inspection alone.
Adjunctive techniques have emerged that may facilitate early detection of oral premalignant and malignant lesions. Thorough clinical examinations being one of the best modalities in suspecting the pathology, the biggest disadvantage in the diagnosis lies in detecting the site of biopsy and also whether biopsy is required or not in early lesions.
Nowadays various diagnostic aids have been established in detecting such lesions but easy chair-side techniques can be used if possible. And one such technique is by using vital staining with dyes which is used for early recognition of lesion and also can improve the patient survival rate.
Introduction
Development of Mast cell
Implication
Properties of Cell
Mediators of Mast cell
Types of Mast cell
Modes of degranulation
Ultra structure of mast cell
Role of mast cell in OLP,OSF, Wound healing, OSCC, pyogenic granuloma, periapical lesion, orofacial granulomatosis
Conclusion
Chapter 2 of the ICD-10-CM contains the codes for most benign and all malignant neoplasms. Certain benign neoplasms, such as prostatic adenomas, may be found in the specific body system chapters.
BIOPSY AND HEALING OF THE BIOPSY WOUND / dental crown & bridge coursesIndian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
www.indiandentalacademy.com
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
2. CONTENT
• Introduction
• Definition
• History
• Uses of Oral Biopsy
• Indication for Oral Biopsy
• Contraindication of Oral Biopsy
• Precaution in Oral Biopsy
• Armamentarium
• Types of Oral Biopsy
• Special consideration
• Biopsy Arifact
• Obtaining a Good Oral Biopsy
• Complication of Oral Biopsy
• Conclusion Dr.Aldrin Jerry
3. INTRODUCTION
• The clinical presentation of any pathology can
be the mucosal surface change or it can be
submucosal structural alterations.
• The diagnosis of such pathology depends on
the history, examination, laboratory studies,
biopsy and other diagnostic techniques.
• GOLD STANDARD-Biopsy
Dr.Aldrin Jerry
4. Definition
• Biopsy (Greek terms) :bios (life) and opsis (vision):
vision of life
• Biopsy is the surgical removal of a tissue
specimen from a living organism for
microscopic examination and final diagnosis.
(Oral Surgery,Fragiskos D Fragiskos)
Dr.Aldrin Jerry
5. History
• early 16th century, Sir Marcello
Malphigi, "Father of microscopical anatomy,
histology, physiology and embryology"
• First, 1875 by M. M. Rudnev
• Term, 1879 by Ernest Besnier
• Late 19th century
Dr.Aldrin Jerry
6. Uses of Oral Biopsy
• Diagnostic
• Planning proper treatment
• Checking progression
• Checking the extension
• Evaluating end results
• Research
Dr.Aldrin Jerry
7. INDICATION
• ulcerated lesion
• growth
• White or red patches
• Intra-osseous arid
• Inflammatory lesion
• Persistent keratotic changes
• Persistent tumescence
• characteristics of malignancy
Dr.Aldrin Jerry
8. Contraindication of Oral Biopsy
• Normal structures
• Anatomical variation
• Responding lesion
• Compromised/ill patient
• Systemic disorder/therapy
• Difficult access
• Vascular lesion
• Intrabony radiolucent lesions without initial
aspiration
• pulsatile
Dr.Aldrin Jerry
9. Precaution in Oral Biopsy
• Avoid dyes/coloured antiseptic
• Planned incision
• Avoid crush
• Encapsulated lesion remove toto/ remove entire
mass
• Avoid tumor spilling
• Deep penetration but not to periosteam
• Surgeon should not section specimen
• Avoid drying of specimen
Dr.Aldrin Jerry
11. Types of Oral Biopsy
Tissue piece:
a) Incisional biopsy (including geographical
biopsies and vital staining)
b) Punch biopsy
c) Excisional biopsy
d) Electro-surgery biopsy
e) Curetting
Dr.Aldrin Jerry
12. Tissue core Biopsy:
a. Tru-cut needle biopsy.
b. Vin Silverman needle biopsy.
Cell aspirate:
Fine needle aspirate biopsy.
Scrapings:
Exfoliative cytology.
Dr.Aldrin Jerry
13. INCISIONAL BIOPSY
• Gold standard
• Removal of only a portion of a relatively more
extensive lesion
• Larger than 1 or 2 cm
• Multiple biopsy-Diagram
Dr.Aldrin Jerry
14. Principle:
• Representative areas should be biopsied in
wedge fashion from the edge of the lesion
including some of the normal tissue.
• Deep narrow biopsy
• Necrotic areas should be avoided
Dr.Aldrin Jerry
15. Demerits:
• Tumor spillage & leaking of residual disease
• Spread of malignant cells
• Scar
Dr.Aldrin Jerry
21. Advantages :
• Ease of technique
• Sutures may not be required if small diameter punch
• May produce a more satisfactory specimen in bound
down tissues (e.g. hard palate)
Drawbacks:
• May not be adequate for biopsy of deeper pathology
• May be difficult to biopsy freely movable tissues (e.g.
soft palate, floor of mouth)
Dr.Aldrin Jerry
23. Excisional Biopsy
Entire lesion/tumor is excised
Indication:
clinically benign lesions, be they superficial or
deep, soft or hard tissue
Dr.Aldrin Jerry
24. Principle
• The entire lesion with 2 to 3mm of normal
appearing tissue surrounding the lesion is
excised if benign
Surface-elliptical approach Base-V
cut
Dr.Aldrin Jerry
28. ELECTRO-SURGERY BIOPSY
• Cutting and coagulation of tissue using very
high-frequency, low-voltage electrical
currents.
• Bloodless operative field.
• Demerit: heat artifact in histology
Dr.Aldrin Jerry
29. The lesion is grasped
with forceps through
the loop electrode.
The electrode is
activated going under
the lesion, removing
the growth.
Dr.Aldrin Jerry
31. CURRETTAGE BIOPSY
• CURRETTE is a French word ‘Curer’- meaning to clean.
• It is indicated for intraosseous lesions and cystic lesions within the jaws.
• Also used in very friable cellular lesions like sinuses and fistulae within the
soft tissues when only small amounts of surface material are necessary for
evaluation.
• Although the sample produced is usually soft tissue but it may include
bone fragment as well.
• These extremely small segments of tissue after fixation are centrifuged
and then the sediment is placed in medium such as agar, they are then
sectioned as a cellblock.
Dr.Aldrin Jerry
32. TISSUE CORE/TREPHINE BIOPSY
• Core biopsy specimen is larger in size and
suitable for conventional histopathological
analysis than the cytologic material obtained
from FNB.
• Simpler, easier and faster
• It also eliminates the possibility of inadvertent
suction of specimen & fragments
• Demerit: spread of tumor cells along the
large-bore needle track
Dr.Aldrin Jerry
36. In large lesions
Accessible area
Characteristic portion.
For multiple lesions
Most representative site.
Material curetted from interior of the lesion .
SPECIAL CONSIDERATIONS
Dr.Aldrin Jerry
37. For red & white lesions include both red & white
area Dr.Aldrin Jerry
38. ULCERS
Include margin,
deep part of
ulcer and site of
maximal clinical
activity.
AVOID
Superficial
ulcers &
necrotic tissue
Dr.Aldrin Jerry
53. Obtaining a Good Oral Biopsy
• Selection of the area of biopsy
• Preparation of the surgical field
• Local anaesthesia
• The incision
• Tissue handling
• Suture
Dr.Aldrin Jerry
55. COMPLICATION OF ORAL BIOPSY
•Haemorrahage
•Infection
•Poor wound Healing
•Spread of tumor cells
•Injury to adjacent organs
•Others: post op pain, parasthesia, swelling,
recurrence, duct damage
Dr.Aldrin Jerry
56. CONCLUSION
•It is not easy to procure a good biopsy specimen, nor is it very intricate
• But the procedure must be carefully premeditated and expeditiously
carried out, and the provisional diagnosis must be borne in mind prior
to biopsy.
Dr.Aldrin Jerry