The document provides detailed information on the anatomy and physiology of the esophagus. It describes the extension, length, diameter and location of landmarks along the esophagus at different ages. It discusses the layers of the muscular coat, sphincters at the upper and lower ends, blood supply, lymphatic and nerve supply. Development, variations and imaging modalities for evaluating the esophagus are also summarized.
radiological anatomy of retroperitoneum powerpointDactarAdhikari
brief and concise on radiological anatomy of retroperitoneum
includes topic like pararenal space,perirenal space,fascial plane,retroperitoneum hematoma and sign of mass origin
radiological anatomy of retroperitoneum powerpointDactarAdhikari
brief and concise on radiological anatomy of retroperitoneum
includes topic like pararenal space,perirenal space,fascial plane,retroperitoneum hematoma and sign of mass origin
Anatomy and malignant diseases of esophagusDr Sajad Nazir
This presentation is for post graduate surgery residents. Anatomy with pictorial representation and management of carcinoma esophagus is being explained. Barretts esophagus, diagnosis and management is being explained. This presentation is subjected to errors and mistakes. I have consulted 2, 3 books to make this presentation.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
- 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
New Drug Discovery and Development .....NEHA GUPTA
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.
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
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New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
2. EXTENSION:
From lower border of cricoid at V C6 level
Passes through diaphragm at V T10 level
Ends at V T11 near cardiac orifice.
In the newborn:
Upper limit is at the level of-C4/C5 and
Lower at T9
Length:
At birth: 8-10 cm,
End of 1st yr: 12cm,
5th Yr.:16cm
15th yr: 19cm
DIAMETRE: 2.5-3cm
3. At cricopharyngeal
sphincter15cms from
incisors.
Where aortic arch
crosses22-25cms from
incisors.
Where it is crossed by left
bronchus27-28cms from
incisors.
Where it passes through
diaphragm38-40cms
from incisors.
4. CERVICAL OESOPHAGUS:
Extends from the
pharyngoesophageal
junction to the suprasternal
notch.
About 4 to 5 cm long.
At this level, the esophagus
is bordered
anteriorly by the trachea,
posteriorly by the vertebral
column
laterally by the carotid sheaths
and the thyroid gland.
5. THORACIC
OESOPHAGUS:
Extends from the
suprasternal
notchdiaphragma
tic hiatus.
Passes posterior to
the trachea, the
tracheal bifurcation,
and the left main
stem bronchus.
6. The esophagus lies
posterior and to the
right of the aortic
arch at the T4
vertebral level.
From the level of T8
until the
diaphragmatic hiatus
the esophagus lies
anteriorly to the aorta
8. The muscular coat consists
-external layerlongitudinal fibers
-internal layercircular fibers.
LONGITUDINAL FIBRES: form a uniform layer that covers
the outer surface of the esophagus.
CIRCULAR FIBRES: provides the sequential peristaltic
contraction that propels food toward the stomach.
The circular fibers are continuous with the inferior
constrictor muscle of the hypopharynx.
They run transversely in cranial & caudal regions.
obliquelybody of the esophagus.
9. The internal muscular layer is thicker than the
external muscular layer.
Below the diaphragm, the internal circular
musclethickens ,constituting the intrinsic
component of LES.
Muscular fibers in the cranial partconsist
chiefly striated muscle.
Intermediate partmixed.
Lower partcontains only smooth
muscle.
10. Two high-pressure
zones prevent the
backflow of food:
The upper and lower
oesophageal
sphincter.
Located at the upper
and lower ends of the
oesophagus.
11. Between pharynx and the
cervical oesophagus.
Located at C5-C6 level.
The UES is a
musculocartilaginous
structure.
Composed of mainly three
muscles: cricopharyngeus,
thyropharyngeus,cranial
cervical oesophagus.
12. The cricopharyngeus
muscle is a striated
muscle.
Produces maximum
tension in the A.P
direction and less
tension in lateral
direction.
Composed of a
mixture of fast- and
slow-twitch fibres.
This muscle forms the
main component of
UES.
13. Triangular area in the wall
of pharynx b/w
thyropharyngeus and
cricopharyngeus muscles.
14. The lower esophageal sphincter is a high-pressure zone
located where the esophagus merges with the stomach.
Mean pressure here is approx. 8mm Hg.
15. The LES is a functional unit
composed of an intrinsic and
an extrinsic component.
INTRINSICoesophageal
muscle fibers and is under
neurohormonal influence
EXTRINSICdiaphragm
muscle.
The endoscopic localization of
the LES is different from the
manometric localization.
The endoscopic
localizationdetermined by
changes in the esophageal
mucosal transition from
nonstratified squamous
esophageal epithelium to the
gastric mucosa “Z-line”or B
ring.
Functional location of LES is 3
cm distal to the Z-line.
16. The endoscopic localizationdetermined by changes in the esophageal
mucosal transition from nonstratified squamous esophageal epithelium to the
gastric mucosa “Z-line”or B ring.
17. The rich arterial supply of
the esophagus is segmental .
Branches of the inferior
thyroid arteryUES and
cervical esophagus.
Paired aortic esophageal
arteries or terminal branches
of bronchial
arteriesthoracic
esophagus.
The left gastric artery and a
branch of the left phrenic
arteryLES and the most
distal segment of the
esophagus.
18. The venous supply is also
segmental.
From the dense
submucosal plexus the
venous blood drains into
the superior vena cava.
Veins of proximal and
distal esophagus
azygous system.
Veins of mid
oesophaguscollaterals of
left gastric vein.
19. The lymphatics from
the proximal 1/3rd
drain into the deep
cervical LNs
subsequently into
the thoracic duct.
Middle 1/3rd into
superior and
posterior mediastinal
nodes.
Distal 1/3rd
gastric and celiac
lymph nodes.
20. Parasympathetic nerve
supply
(SENSORY,MOTOR,SECRE
TOMOTOR)
Upper ½rec.laryngeal
nerve.
Lower ½oesophageal
plexus formed by the 2
vagus plexus.
The sympathetic nerve
supply(VASOMOTOR)
Upper ½by fibres from
mid cervical ganglion.
Lower ½directly from
upper four thoracic ganglia.
21. The ganglia that lie between
the longitudinal and the
circular layersmyenteric
or Auerbach's plexus.
That lie in the submucosa
form the submucous or
Meissner's plexus.
Auerbach's
plexusregulates
contraction of the outer
muscle layers.
Meissner's
plexusregulates secretion
and the peristaltic
contractions of the
muscularis mucosae.
22. At a very early period the stomach is
separated from pharynx by a mere
constriction from primitive pharynx.
This constriction is future esophagus.
Previous to this elongation the
trachea and oesophagus form a single
structure.
This becomes divided into two by the
in growth of two lateral septa, which
fuse giving rise to trachea in front
and oesophagus behind.
At this stage the oesophagus becomes
converted into a solid rod of cells,
losing its tubular nature.
This eventually becomes canalised to
form a tube
23. The stratified squamous epithelium of the
oesophagus together with its associated
submucosal glands, is derived from the
endoderm of the foregut.
The striated muscle of the upper oesophagus is
derived from branchial arches 4 and 6, whereas
the smooth muscle of the lower oesophagus is
derived from somite mesenchyme.
The myenteric plexus is derived from neural
crest cells.
25. In most circumstances, plain radiographs reveal
little useful information regarding the oesophagus,
except in the context of foreign body ingestion.
Foreign bodies tend to lodge at one of the
oesophageal constriction points:
• cricopharyngeus;
• aortic arch;
• left main bronchus; or
• diaphragmatic hiatus.
26. Barium suspensions are
preferred for most
indications; a density of 100%
w/v is often used to provide
a balance between good
mucosal coating and not
being too dense.
Water-soluble contrast
medium is used initially
when a tear, perforation or
anastomotic leak is suspected.
Low osmolar agents such as
iopamidol should always be
used to prevent pulmonary
oedema, which can occur
following aspiration of high
osmolar agents such as
meglumine diatrizoate.
27. Oesophagogastroduodenoscopy or
‘endoscopy’
It is the initial investigation of choice for most
oesophageal indications, particularly dysphagia. It
permits the direct visualisation of the mucosa and,
crucially, biopsies can be taken.
A wide variety of therapeutic manoeuvres may be
carried out endoscopically. The most common of
these is the treatment of upper GI haemorrhage.
Elective procedures include balloon dilatation
and/or stenting of strictures, radiofrequency
ablation (RFA) of dysplastic or malignant
epithelium and injection of botulinum toxin for
motility disorders..
28. This technique uses a high-frequency (7–12 MHz)
ultrasound probe mounted at the end of an
endoscope (an ‘echoendoscope’).
Used for oesophageal cancer staging.
Used for EUS-guided fine needle aspiration (EUS-
FNA). EUS-FNA allows sampling of structures
deep to the oesophageal mucosa, particularly
thoracic and upper abdominal lymph nodes. This
can be particularly useful in the staging of
oesophageal and lung malignancy, and in the
diagnosis of tuberculosis.
29. Ultrasound
The majority of the oesophagus is inaccessible to conventional
ultrasound examination. The short cervical and abdominal
segments are amenable to imaging in this way, but this is
rarely used in clinical practice.
CT
It is most widely used in the staging of oesophageal cancer.
Intravenous contrast medium should be used whenever
possible, with the upper abdomen imaged in both the arterial
and portal venous phases.
For the investigation of patients with suspected oesophageal
trauma (including Boerhaave’s syndrome) and in the
postoperative setting, positive oral contrast medium is
required.
MRI
In current clinical practice, magnetic resonance imaging (MRI)
is not used for imaging the oesophagus.
30. For patients with oesophageal
cancer, F18- fluorodeoxyglucose
(FDG) PET-CT is now the
standard of care.
Technetium-based radionuclide
imaging of the oesophagus can be
used for the identification of
oesophageal motility disorders
and gastro-oesophageal reflux
disease (GORD).
Patients can be imaged
swallowing both liquid and solid
material (usually 99mTc-labelled
sulphur colloid and scrambled
egg, respectively)
Coronal PET-CT image of an FDG-avid
left supraclavicular
lymph node (arrow) metastasis in a
patient with a
distal oesophageal adenocarcinoma.