This field shows a mixture of Gleason 3 and Gleason 4 cancer. Key features include:
- The presence of both well-formed glands separated by stroma (Gleason 3 pattern) and fused glands with absent intervening stroma (Gleason 4 pattern).
- It does not show the features of pure Gleason 5 cancer such as comedo-necrosis or single cells/cords without gland formation.
- Gleason 3 and 4 patterns are seen together, rather than one or the other, indicating a mixed rather than pure Gleason grade.
Therefore, the best description of this field is that it shows a mixture of Gleason 3 and Gleason 4 cancer.
Histopathological Grossing of Kidney Tumors with the common gross differentials encountered,
reference - TATA memorial grossing techniques , Rosai and ackerman surgical pathology , Fletcher , Springer histopathology Specimen
People with Lynch syndrome have a higher risk of certain types of cancer, including endometrial, colorectal, and ovarian cancers. Heather Hampel, MS, CGC, Associate Director of the Division of Genetics and Genetic Counseling at City of Hope, will discuss genetic testing, hereditary cancer risk, prevention, and the latest updates for Lynch syndrome care.
Histopathological Grossing of Kidney Tumors with the common gross differentials encountered,
reference - TATA memorial grossing techniques , Rosai and ackerman surgical pathology , Fletcher , Springer histopathology Specimen
People with Lynch syndrome have a higher risk of certain types of cancer, including endometrial, colorectal, and ovarian cancers. Heather Hampel, MS, CGC, Associate Director of the Division of Genetics and Genetic Counseling at City of Hope, will discuss genetic testing, hereditary cancer risk, prevention, and the latest updates for Lynch syndrome care.
Advances in risk assessment, differential diagnosis between aggressive and non-aggressive tumors, and the development of novel/optimized treatment for advanced disease are discussed.
This slide deck is made available for patients/caregivers. It is not a substitute for seeking medical help. Please check original sources listed in the deck and consult your physician for the latest information and advice.
Understanding Uterine Cancer Treatment Optionsbkling
Join Dr. Bhavana Pothuri, gynecologic oncologist at NYU Langone Medical Center, as she breaks down the different types of uterine cancer treatments available to patients based on their particular diagnosis. Learn about new research and treatment updates, options for when cancer recurs, side effects, and more.
EAU - Guidelines on Prostate Cancer dr. ali mujtabaDr Ali MUJTABA
EAU - Guidelines on Prostate Cancer Organ Confined by Dr. Ali Mujtaba, Sindh Institute of Urology and Transplantation (SIUT)
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- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
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Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
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Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
1. Gleason Grading of Prostate Cancer
Dr. Indranil Bhattacharya
Consultant Pathologist
Dept. of Pathology
Jagjivan Ram Hospital
Mumbai
2. Introduction:
• Tumour grade is the cornerstone of prostate cancer management.
• In 1978, the American Cancer Society organized a series of
workshops that compared several systems for grading prostate
cancer.
• The outcome was the recommendation that the Gleason grading
system should be adopted, because it was “definable, simple,
reproducible, and had compelling clinical relevance.”
• The Gleason system is now the globally utilized system for grading
prostate cancer and has proven to be a powerful predictor of
patient outcome, regardless of the treatment the patient receives
3. However, the Gleason grading system has undergone several modifications over the years.
The reporting rules have become increasingly complicated, which has resulted in reporting
variation, even amongst experts, and confusion for practicing pathologists.
The Gleason grading system is unusual in that it is based entirely on architectural features
of the tumour, rather than the cytological appearances, and is not based on the worst
pattern.
The Gleason score (GS) takes into account the two most common patterns that are present.
Thus, a tumour that is predominantly (95%) pattern 4 would be “down-graded” from GS 8
to 7 by the presence of a minor (5%) component of pattern 3.
Unlike other tumour grading systems, there are different rules for reporting the GS in
needle biopsy specimens and excision specimens, i.e. radical prostatectomies.
Finally, in contrast to other organs, a definitive grade based on the examination of the
entire tumour is available in only a minority of patients with organ confined prostate
cancer, because most of these patients do not have radical surgery.
4. The development of the Gleason grading system was initiated by an American urologist, George T Mellinger, Chair of Urology
at the Minneapolis Veteran’s Hospital.5 In 1960, he set up the Veterans Administration Cooperative Urological Research
Group (VACURG), which included urologists, statisticians and pathologists.
The VACURG organised large-scale, randomised, prospective clinical trials to compare treatments for prostate cancer and Dr
Mellinger suggested devising a grading system for prostate cancer. The Gleason grading system was a “bespoke” system
developed for a specific research project with a truly multidisciplinary approach.
The lead pathologist, Donald F Gleason, had, as a medical student, been involved in the development of the Minnesota
Multiphasic Personality index that sought to standardise the diagnosis of psychiatric conditions using a novel mathematical
scale.5 He also had a background in research and was a gifted artist. These diverse skills were critical in the development of
the Gleason grading system.
Dr Gleason opted to ignore all preconceptions of tumour grading and identified 9 distinct architectural patterns in prostate
cancer. He recognised the morphological heterogeneity of prostate cancer and recorded the two most common patterns for
each tumour. These patterns were subsequently correlated with patient survival data by statisticians at the National Cancer
Institute and the National Institute of Health, led by John C Baillar III. Some of the patterns that had similar biological
outcomes were merged, resulting in the five Gleason patterns that we recognise today.
The original Gleason grading system involved addition of scores for the primary pattern, the secondary pattern and the
clinical stage, resulting in a scale ranging from 3 to 15.
The clinical stage was subsequently dropped, resulting in the now familiar histological GS.
5. Definition:
• In 1966, Dr. Donald Gleason devised grades of 1 - 5 based on
glandular architecture and microscopic appearance using a 4x -
10x objective eyepiece that were shown to predict an outcome in
prostate cancer.
6. The modification of the Gleason grading system implemented by the International Society of Urological Pathology in
2005 and subsequent revision in 2014 has profoundly impacted how PCa is graded and managed.
7.
8.
9. Terminology
• Gleason score is the sum of the 2 most prevalent Gleason grades:
primary and secondary, designated according to separate rules for
biopsy and prostatectomy
• If only 1 pattern is present, the primary and secondary patterns are
given the same grade (ex: 3+3=6)
• Systematic needle biopsy sets contain cores from different
anatomically designated sites
• Gleason score should be assigned separately for each anatomically
designated site
• Highest score may serve as a basis to determine treatment
• Additional reporting of a global (case level) Gleason score is optional and
global scoring may show a marginal benefit over using highest score
according to Trpkov et al.
• Any glands showing perineural invasion must be excluded in assigning
Gleason grading because perineural invasion distorts gland morphology such
that Gleason 3 glands resemble Gleason 4
10. Grading rules:
• Recommendations are based on 3 International Society of
Urological Pathology (ISUP) grading consensus conferences:
• 2005
• 2014 and 2019 (Nice, France)
• Consensus of the GU Pathology Society that is nearly identical
• Minor variances are highlighted
• Some specimens may show a pattern that is the third most prevalent;
this is called a minor pattern
11. In radical prostatectomy
• Gleason score should be based on the primary and secondary
patterns; if a minor pattern constitutes < 5%, the pattern should
be mentioned as a minor (tertiary) pattern; any higher grade
minor pattern ≥ 5% should be incorporated into the Gleason
score and ISUP group as the secondary pattern (2019
consensus).
• Example: Gleason pattern 3=96% and pattern 4=4%, Gleason
score=3+3=6 with minor (tertiary) 4
• Example: Gleason pattern 3=95% and pattern 4=5%, Gleason
score=3+4=7
12. In needle biopsy
• Most prevalent pattern is graded as primary and any amount of
a worst pattern is graded as secondary
• Example: Gleason pattern 3=96% and pattern 4=4%, Gleason
score=3+4=7
• Example: Gleason pattern 3=95% and pattern 4=5%, Gleason
score=3+4=7
13. Epidemiology
• In 2014, the ISUP and World Health Organization adopted a simplified patient centric
grading system composed of 5 prognostic grade groups as proposed in 2013 based on
data and subsequently validated by biochemical recurrence hazard ratios on cases from 5
large academic centers
• Grade groups are as follows:
• Gleason score 3+3=6
• Gleason score 3+4=7
• Gleason score 4+3=7
• Gleason score 8 (4+4=8, 3+5=8, 5+3=8)
• Gleason score ≥ 9 (4+5=9, 5+4=9, 5+5=10)
• Note that Gleason grades 1 and 2 are no longer recommended for use, since those
patterns of cancer have an outcome no different from grade 3; moreover, pure grade 3
cancer almost never metastasizes and is reasonable to treat by active surveillance, which
has sparked speculation about whether it should even be labeled cancer.
• Divisions of Gleason score 3+4=7 from 4+3=7 and of 8 from 9-10, which had often been
bundled together for prognostic and research purposes, are supported by studies showing
significantly different outcomes.
• Percentage of grade 4 or 5, when heterogeneous grades are present, should be
mentioned in all specimens, although biopsy and prostatectomy have different rules for
scoring.
14. • Grade group 4 is heterogeneous as it includes 4+4=8, 3+5=8
and 5+3=8, with recent data showing no or minimal long term
outcome difference when present as the highest score in biopsy
sampling; instead, the presence or absence of cribriform growth
of cancer was a significant prognosticator
• If tumor is minimal on biopsy (≤ 1 mm), Gleason score does not
predict tumor stage and this can be noted on the report (ex: in a
minimal focus with pattern 4, rather than doubling to 4+4=8,
tumor can be designated on the report as too small for scoring)
• Targeted biopsies detect a higher percentage of pattern 4 than
systemic ones and are less likely to be upgraded on
prostatectomy
15. Evolution of grading of special prostate cancer patterns
Histologic pattern 2005 consensus 2014 consensus 2019 consensus
Branched / undulating glands Include as Gleason 3
Cribriform (under Gleason
scheme: mostly 3, sometimes 4)
4 but can be 3 if much larger than
benign gland, round and has
loose cells
Always 4
Always 4 and presence or absence
should be specified for 3+4, 4+3
or 4+4
Glomeruloid variant No consensus, 3 versus 4 Always 4 --
Mucinous variant No consensus, some favored 4
Depends on growth pattern
regardless of mucin; could be 3, 4
or 5
--
Small cell (pure) Do not grade -- --
Intraductal, pure form -- Do not grade Do not grade
Intraductal, associated with
invasive cancer
-- --
Include in estimating the
percentage of grade 4, instead of
keeping it separate
Ductal 4+4=8 -- --
Adenoid cystic / basal cell
carcinoma
-- Do not grade Do not grade
16. Microscopic (histologic) description
• Discontinued Gleason grades 1 and 2
• It was agreed at the 2014 consensus conference that Gleason grades
1 and 2 should be discontinued because grade 1 or 2 cancer in needle
biopsy does not predict better prostatectomy findings than grade 3 and
these grades show marked interpathologist variability
• Gleason score of 1+1=2 was originally described as single, separate,
closely packed, uniform round glands arranged in a circumscribed
nodule with pushing borders; many of such cases would, with the
benefit of today's immunostains, be referred to as atypical
adenomatous hyperplasia (AAH or adenosis)
17. Gleason grade 3
• Single, separate glands
• May be either minute or large and cyst-like; glands have an irregularly
separated, ragged, poorly defined edge, looser than a nodule and are
infiltrative
• Key feature is retention of at least a wisp of stroma intervening between
neighboring glands
• Tangentially cut glands may appear as if they are poorly formed but should not
get graded as a 4 unless poorly formed and fused glands persist on several
levels
• Patterns of Gleason grade 3 prostatic adenocarcinoma:
• Most common pattern is well formed, relatively uniform glands infiltrating between benign
glands; glands may be angulated or compressed, separated by > 1 gland diameter
• Small glands with pinpoint lumina, glands still separate
• Medium sized glands with undulating luminal contours or large glands or branching
• Large glands with a pseudo-atrophic appearance
• Cribriform cancer no longer qualifies as Gleason 3, even if the glands are
similar in size to normal glands
18. Gleason grade 4
• Key finding is coalescent or fused glands with > 1 lumen and
absence of intervening stroma between adjacent glands
• Patterns of Gleason grade 4 prostatic adenocarcinoma:
• Most common is small acinar structures, some with well formed lumina,
fusing into cords or chains; may be undergraded as Gleason 3
• Cribriform (often merging with papillary, see by consensus has a confluent
sheet of contiguous malignant epithelial cells with multiple glandular lumina
that are easily visible at low power (objective magnification 10x); there should
be no intervening stroma or mucin separating individual or fused glandular
structures.
• Nodule of a cribriform gland should be larger than normal prostate gland
• Large nodules of cribriform Gleason 4 lack supporting stroma and tend to fragment
• Thus, fragments of cribriform glands on needle biopsy represent Gleason 4
• Hypernephroid pattern, with nests of clear cells resembling renal cell
carcinoma; small, hyperchromatic nuclei; fusion of acini into more solid
sheets with the appearance of back to back glands without intervening
stroma
19. • Intraductal carcinoma, when admixed with invasive carcinoma, should be counted as
Gleason 4 and not counted separately for quantitation purposes.
• Its presence and significance should be mentioned
• This emphasizes the adverse influence which has a unique phenotype of certain driver mutations as
shown by Khani et al.
• Glomeruloid pattern (2014 consensus), a rare small cribriform variant, contains a tuft of cells that is
mostly detached from its surrounding duct space except for a single point of attachment
• Hypernephroid pattern, with nests of clear cells resembling renal cell carcinoma; small,
hyperchromatic nuclei; fusion of acini into more solid sheets with the appearance of back to
back glands without intervening stroma
• Research and 2014 consensus support grading all cribriform cancer as Gleason
4 because the presence and amount of cribriform cancer carries a distinctly
adverse prognosis for recurrence and for death from cancer
• Its presence or absence in Gleason 4 cancer should be commented on
• Note: patients with Gleason 8 at biopsy may have Gleason 7 at prostatectomy due to
unsampled Gleason 3
• Note: basal cell markers are crucial in distinguishing cribriform high grade
prostatic intraepithelial neoplasia, cribriform intraductal carcinoma and invasive
cribriform carcinoma
• Rarely, pure intraductal carcinoma occurs in biopsy specimens
• Rare in totally embedded prostatectomies as shown by Robinson
• In its pure form it should not be graded
• Diagnosis of intraductal carcinoma has modest reproducibility
20. Gleason grade 5
• Grade 5 has 2 patterns:
• Comedo-necrosis: central necrosis with intraluminal necrotic cells or
karyorrhexis within papillary / cribriform spaces; caution should be exercised
since many such foci have demonstrable basal cells, making them intraductal
carcinoma instead; thus, immunostaining is recommended if this would alter
the grade group Single cells, possibly forming cords, possibly with vacuoles
(signet ring cells) but without glandular lumens; this pattern may mimic
lymphocytes at low power
• Gleason 5 pattern has moderately good reproducibility, although
certain patterns are more problematic
• Gleason 5 cancer is often missed or underdiagnosed on needle
biopsy
• Presence of Gleason grade 5 in prostate biopsy specimens predicts
higher rates of metastasis and death compared with Gleason 4+4=8
cancer and even the smallest amounts of 5 predict outcome after
prostatectomy
21. Sample pathology report
• Prostate, left lateral, prostate needle core biopsy:
• Prostatic adenocarcinoma, Gleason score 4+3=7 (Grade group 3)
involving 2 of 4 cores and 30% of the tissue (40%, 2 mm and 20%, 4
mm) (60% of the tumor is Gleason pattern 4, not cribriform)
• Prostate, radical prostatectomy:
• Prostatic adenocarcinoma, Gleason score 3+3=6 with tertiary 4 (Grade
group 1) (Gleason pattern 3=96% and pattern 4=4%)
22. Question # 1
Per the 2019 ISUP consensus conference, a prostate biopsy report
for high grade cancer must include:
a) A case level global Gleason score
b) A grade if the entire cancer focus consists of perineural invasion
c) Both a primary and secondary grade for tumor measuring less
than 1 mm
d) For Gleason grade 4, a mention of whether or not cribriform /
large gland pattern is present
e) Gleason grades 1 and 2, if present
23. Ans: D.
• For Gleason grade 4, a mention of whether or not cribriform / large
gland pattern is present. By consensus, the presence of cribriform
carcinoma should be reported.
• Gleason grades 1 and 2 are discontinued. Grading is not
recommended for perineural invasion because perineural invasion
distorts gland morphology (grade 3 looks like 4).
• For tumor that is 1 mm or less, only 1 grade needs to be assigned,
avoiding doubling Gleason 4 to 4+4=8, which would be misleading if
cancer in other cores is mostly Gleason 3. A case level global score
is optional.
24. This field from a prostate biopsy
shows:
1.Entirely Gleason 3 cancer
2.Entirely Gleason 4 cancer
3.Entirely Gleason 5 cancer
4.Mixture of Gleason 3 and
Gleason 4 cancer
5.Mixture of Gleason 4 and
Gleason 5 cancer
Question # 2
25. Ans: B.
• Entirely Gleason 4 cancer. The tumor consists entirely of
ragged and fused glands. Discrete, round to angulated gland
spaces, separated by stroma, diagnostic of Gleason 3 are not
present. Single cells without glandular lumen formation,
diagnostic of Gleason 5 are not present.
32. Conclusion:
The Gleason grading system that was initiated by a surgeon, created by a
pathologist and developed by a statistician predated serum PSA testing,
systematic 18-gauge needle biopsy protocols and immunohistochemistry.
It has undergone a series of modifications, initially by Veterans
Administration Cooperative Urological Research Group and later by the
International Society of Urological Pathologists following consensus
meetings in 2005 and 2014.
Precision of grading becomes less important if the pathologist uses
judgment to determine the Gleason score most suitable for that patient,
communicates this data effectively in the report and helps clinicians
interpret the information correctly