Professional Documents
Culture Documents
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Khaled Mohammed Almaz
GIT specialty
Green Belt Lean Six Sigma , 6 sigma school , Cairo , Egypt 2019
= Sonography
= Sonar
= U/S (ultra-sound)
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Khaled Mohammed Almaz
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Khaled Mohammed Almaz
N or abnormal
L ¢ (liver)
Nephropathy (kidney)
Ascites
-------------------------------------------------
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Report (example)
Abd. U/S
Name :
Date:
Pancreas : Normal
Conclusion
Thx
Dr/
Density = genecity
Iso
Hypo
Hyper
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Khaled Mohammed Almaz
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Abdominal U/S
1) Site
2) Size
3) Border (capsule)
4) Echo pattern
5) Blood vessels
6) Biliary system “intra-hepatic dilatation” ,
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Khaled Mohammed Almaz
Findings
Benign hyper:
Mostly hemangioma
Adenoma
Malignant hyper:
Hepatic metastasis
Colorectal cancer
Breast cancer
Thyroid cancer
HCC (hepatoma)
Cholangio carcinoma
-------------------------------------------------
1) Focal lesion
• Hyper echo
• Hypo echo → metastasis
• Simple hepatic cyst
• Hepatic hemangioma
• Hepatic ademoma
• Hepatic metastasis
• Hepatic abscess
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Khaled Mohammed Almaz
2) Diffuse
• Acute hepatitis
• L¢
• Hyper-diffuse steatosis
3) Hepatic vasculature
• Normal hepatic vessel
• Portal HTN
• Portal vein thrombosis
4) Hepatic trauma
5) Biliary
• Choledocholithiasis
• Dilated intrahepatic bile ducts
• Bile duct wall thickening
• Cholangiocarcinoma
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Abdominal Sonar :
5. Showing edema
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• DD Hepato-SplenoMegaly
•
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• Common causes
•
• Infection:
• Acute viral hepatitis[1 ]2[]
• Infectious mononucleosis[1 ]2[]
• Cytomegalovirus[1 ]2[]
• Rubella]1[
• Brucella infection]3[
• Hyper active malaria syndrome]1[
• Leishmaniasis]1[
• Fasciolosis
• Typhoid fever]4[
• Schistosomiasis or filariasis importants
• Septicemic plague
• Hematologic diseases:
• Myeloproliferative disease[1 ]2[]
• Leukaemia[1 ]2[]
• Lymphoma[1]2[]
• Pernicious anaemia]2[
• Sickle cell anaemia]2[
• Thalassaemia]2[
• Myelofibrosis]1[
• Metabolic disease:
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Khaled Mohammed Almaz
• Rare disorders
•
• Lipoproteinlipase deficiency
• Multiple sulfatase deficiency
• Osteopetrosis
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Khaled Mohammed Almaz
HEPATOMEGALY
CAUSES
HEPATITIS/INFECTION
ACUTE
• Alcohol
• Viruses
• Bacteria
• Protozoans
• Parasites
CHRONIC
• Constrictive pericarditis
• Budd–Chiari syndrome
INFILTRATION
• Fatty liver
• Amyloid
BILIARY TRACT DISEASE
• Sclerosing cholangitis
• Metastases
• Hepatoma
• Myeloproliferative disorders
• Myelofibrosis
• Leukaemia
METABOLIC
• Haemochromatosis
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Khaled Mohammed Almaz
• Cryptogenic cirrhosis
• Riedel’s lobe
Liver ++
Symptoms
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Signs and symptoms of conditions that commonly cause liver enlargement include:
Causes
• Alcoholic liver disease, which includes alcoholic fatty liver disease, alcoholic
hepatitis and cirrhosis
• Nonalcoholic fatty liver disease, a lifestyle-related metabolic disease
• Viral hepatitis (hepatitis A, B, C, D or E )
• Liver cancer, or cancer that has spread to the liver from a different organ
Many less-common liver diseases may also cause liver enlargement, as do some
diseases that primarily affect other organs but involve the liver indirectly. A partial
list includes:
Cancers
Genetic diseases
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Khaled Mohammed Almaz
• Hemochromatosis
• Wilson's disease
• Glycogen storage diseases
• Gaucher's disease
Infections
• Amyloidosis
• Autoimmune hepatitis
• Primary biliary cirrhosis
• Primary sclerosing cholangitis
Causes
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Khaled Mohammed Almaz
• Alcohol use
• Cancer metastases (spread of cancer to the liver)
• Congestive heart failure
• Glycogen storage disease
• Hepatitis A
• Hepatitis B
• Hepatitis C
• Hepatocellular carcinoma
• Hereditary fructose intolerance
• Infectious mononucleosis
• Leukemia
• Niemann-Pick disease
• Primary biliary cirrhosis
• Reye syndrome
• Sarcoidosis
• Sclerosing cholangitis
• Steatosis (fat in the liver from metabolic problems such as diabetes,
obesity, and high triglycerides, also called nonalcoholic
steatohepatitis, or NASH)
Infective
Leptospirosis
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Malaria]2[
Amoeba infections]3[
Hydatid cyst]4[
Leptospirosis]5[
Actinomycosis]6[
Neoplastic
Metastatic tumours]1[
Hepatocellular carcinoma]1[
Myeloma]2[
Leukemia]1[
Lymphoma]2[
Biliary
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Metabolic
Haemochromatosis]2[
Porphyria]2[
Wilson's disease]2[
Alcohol abuse]1[
Drug-induced hepatitis]2[
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Congenital
Hemolytic anemia]2[
Others
Zellweger's syndrome]9[
Granulomatous: Sarcoidosis[
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Treatment
Treatment of hepatomegaly will vary depending on the cause of the liver enlargement
and hence accurate diagnosis is the primary concern. In the case of auto-immune liver
disease, prednisone and azathioprine may be used for treatment.[17]
In the case of lymphoma the treatment options include single-agent (or multi-agent)
chemotherapy and regional radiotherapy, also surgery may be an option in specific
situations.Meningococcal group C conjugate vaccine are also used in some cases.[18]
In primary biliary cirrhosis ursodeoxycholic acid helps the bloodstream remove bile
which may increase survival in some affected individuals.[19]
Abd. u/s
2) Size
3) Wall thickening
4) Stone
5) Posterior shadow
6) Pericholecystic collection if black with edematous wall thickening
so it is Cholecystitis
7) Mass (if present or not)
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Findings
Cholecystitis
Secondary thickening : LC
Hepatitis
Congestive Rt sided HF
Low Albumin
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Acute pancreatitis
Duodenal ulcer
GB tr : carcinoma (infiltrative)
GB tr : metastasis
GB tr : lymphoma
2- GB stones
3- GB polyp
7) DD focal lesion
• Cyst (an echo / jet black) [surface , shadow , echogenicity]
• Hypo-echo – Malignancy [lymphoma , metastasis]
• Inflammation (Abscess)
• Hyper echo → benign tr mostly Hemangioma
Calcification
• Bright echogenic
o Diffuse
TB
SLE
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Amyloidosis
o Focal lesion
Phlebitis
Hemangioma
Splenomegaly
INFECTIVE
BACTERIAL
• Typhoid
• Typhus
• TB
• Syphilis
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• Leptospirosis
• Septicaemia
• Abscess
PROTOZOAL
• Malaria
• (common in Africa)
Inflammatory
• Rheumatoid arthritis
• Sarcoidosis
• Lupus
• Amyloid
NEOPLASTIC
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• Metastases
• Primary tumours
• Leukaemia
• Lymphoma
• Polycythaemia vera
• Myelofibrosis
HAEMOLYTIC DISEASE
• Hereditary spherocytosis
• Thrombocytopenic purpura
STORAGE DISEASES
• Gaucher’s disease
DEFICIENCY DISEASES
• Pernicious anaemia
• Cirrhosis
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Khaled Mohammed Almaz
Spleen ++
Symptoms
See your doctor promptly if you have pain in your left upper abdomen, especially if
it's severe or the pain gets worse when you take a deep breath.
Causes
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A number of infections and diseases may cause an enlarged spleen. The enlargement
of the spleen may be temporary, depending on treatment. Contributing factors include:
The causes of splenomegaly vary widely and range from malignancy (cancers),
infections, congestion (increased blood flow), infiltration of the spleen from other
diseases, inflammatory conditions, and blood cell diseases.
Some of the most common causes of an enlarged spleen include the following:
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Causes
The possible causes of moderate splenomegaly (spleen <1000 g) are many, and
include:
Spherocytosis
Thalassemia
Hemoglobinopathies
Nutritional anemias
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Immune hyperplasia
Histoplasmosis
Ehrlichiosis ]6[
Disordered immunoregulation
serum sickness
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sarcoidosis
drug reactions
Extramedullary hematopoiesis
myelofibrosis
Organ Failure
cirrhosis
Vascular
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Budd–Chiari syndrome
Infections
hepatic schistosomiasis
hepatic echinococcosis
Metabolic diseases
Gaucher disease
Niemann–Pick disease
Alpha-mannosidosis
Amyloidosis
Tangier disease
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myeloproliferative disease
histiocytosis X
hemangioma, lymphangioma
splenic cysts
hamartomas
eosinophilic granuloma
The causes of massive splenomegaly (spleen >1000 g) are fewer, and include:
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myelofibrosis
malaria
Treatment
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AP diameter head : 34 mm
Body: 29mm
Tail: 32mm
Length: 12-20 cm
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Khaled Mohammed Almaz
Finding:
- Pancreatitis
- Necrosis
- Abscess
- Carcinoma
- Metastasis
- lymphoma
- trauma
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1- site
2- size : increase mass ( if mass + infiltration = lymphoma)
3- shape
4- parenchymal echogenicity
Nephropathy :
Grade II : chronic
Number : multi-cystic
Poly-cystic
Echogenicity
Type : are 4
8- mass : site
Size
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Shape
9- dromedary humps
Findings
Hydronephrosis
Renal stone
Polycystic kidney
Diffuse : pyelonephritis
Renal abscess
Renal trauma
Cortex
Medulla (pyramids)
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Sinus : Stone
> if there is obstruction سونار في وحدة غسيل الكلي او قسم المسالك (تنفع):
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KIDNEY SWELLINGS
Kidney swellings are not uncommon. They may present silently or may
be associated with haematuria, urinary tract infections and pyrexia.
CAUSES
CONGENITAL
• Polycystic kidney
ACQUIRED
INFECTIVE
• Perinephric abscess
OBSTRUCTIVE
• Hydronephrosis
• Pyonephrosis
DEGENERATIVE
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• Solitary cyst
NEOPLASTIC
• Hypernephroma
• Nephroblastoma
HISTORY
Congenital
Acquired
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• Carcinoma
• Polycystic kidney
• Hydronephrosis
• Pyonephrosis
• Perinephric abscess
• TB
• Solitary cyst
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Kidneys ++
Hydronephrosis
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The following medical conditions are some of the possible causes of Kidney
enlargement. There are likely to be other possible causes, so ask your doctor about
your symptoms.
• Diabetes mellitus
• Lymphoma
• Bilateral hydronephrosis
• Amyloidosis
• Polycystic kidney disease
• HIV associated nephropathy
• Perinephric abscess
• Perinephric haematoma
• Wilms tumour
Other medical conditions listed in the Disease Database as possible causes of Kidney
enlargement as a symptom include:
• Amyloidosis
• Dioctophyma renale
• Hydronephrosis
• Polycystic kidney disease, adult (autosomal dominant)
• Renal adenocarcinoma
• Renal metastases
• Wiedemann-Beckwith syndrome
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This section shows a full list of all the diseases and conditions listed as a possible
cause of Kidney enlargement in our database from various sources.
• Amyloidosis
• Bilateral hydronephrosis
• Diabetes mellitus
• Dioctophyma renale
• HIV associated nephropathy
• Hydronephrosis
• Lymphoma
• Perinephric abscess
• Perinephric haematoma
• Polycystic kidney disease
• Polycystic kidney disease, adult (autosomal dominant)
• Renal adenocarcinoma
• Renal metastases
• Wiedemann-Beckwith syndrome
• Wilms tumour
Overview
Enlarged kidneys are uncommon and are usually related to a few specific disorders
that are caused by birth defects, structural abnormalities, infection, pregnancy,
blockage and injury. An enlarged kidney can only be felt occasionally during an
examination, usually when the patient is an infant, a child or a thin adult, according to
the Merck Manual Online Medical Library. Other symptoms of kidney disease are
usually identified first.
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Hydronephrosis
Pyelonephritis
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Causes
Sources of obstruction that can arise from other various causes include
kidney stones, blood clots, or retroperitoneal fibrosis.[8]
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Treatment
Acute obstruction of the upper urinary tract is usually treated by the insertion of a
nephrostomy tube. Chronic upper urinary tract obstruction is treated by the insertion
of a ureteric stent or a pyeloplasty.
Lower urinary tract obstruction (such as that caused by bladder outflow obstruction
secondary to prostatic hypertrophy) is usually treated by insertion of a urinary catheter
or a suprapubic catheter. Surgery is not required in all prenatally detected cases.[15]
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Nephropathy
Nephropathy is a broad medical term used to denote disease or damage of the kidney,
which can eventually result in kidney failure. The primary and most obvious functions
of the kidney are to excrete any waste products and to regulate the water and acid-
base balance of the body – therefore loss of kidney function is a potentially fatal
condition.
Diabetic nephropathy
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IgA nephropathy
Since its initial description in 1968, IgA nephropathy remains the most common form of
primary glomerulonephritis that can lead to chronic kidney disease. This condition is very
commonly observed in Southern Europe, Australia and Asia, whereas in Northern climates of
the Western World the incidence is approximately 5-10% of all biopsies for
glomerulonephritis.
The diagnostic hallmark of the disease is the deposition of IgA antibodies in the glomeruli,
alone or together with IgM or IgG antibodies. Activation of innate immune response and
complement, as well as the formation of immune complexes, play a significant role in clinical
presentation and severity of the IgA nephropathy.
Renal papillary necrosis (i.e. damage to the inner medulla caused by capillary
sclerosis) represents the characteristic feature of analgesic nephropathy, and most
often arises as a result of a long term use of phenacetin. Renal complications that can
ensue are acute or chronic pyelonephritis, calcification of necrotic papillae,
urolithiasis and uroepithelial tumors.
Acute uric acid nephropathy stems from the intratubular deposition of uric acid
crystals when a high serum uric acid concentration is present. This condition usually
occurs during induction chemotherapy for malignancies with high cell turnover.
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Recommended treatment options for this condition are alkalization of the urine and a
drug known as rasburicase (a recombinant urate oxidase).
Reflux nephropathy
Contrast nephropathy : DM Pt – MM Pt
Malarial nephropathy
Ischemic nephropathy
Diagnostic Considerations
Diabetic nephropathy must be differentiated from cholesterol embolization, amyloidosis, and other
glomerulopathies affecting patients with diabetes.
Differential Diagnoses
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Pre-renal
Renal
Postrenal
As 1- aspirin
2- paracetamol
3- NSAID
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Special nephropathy
Also
1- Pyelonephritis
2- Urological stones
3- Iatrogenic due to ttt by drugs :
NSAID
Vancomycin
Aminoglycosides : Garamycin / Amikacin
4- GN
5- Hereditary : Alport`s $
Buerger`s $
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ألم شديد أسفل الظهر أو فى الجنب & قد يكون األلم فى جانب واحد أو فى الجانبين من الخلف
**ألم فى البطن,فىgroin
*Fever
==============================
**أنواع الحصوات حسب مكانها فى الجسم؟؟
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A cyst is a sac-like pocket of membranous tissue that contains fluid, air, or other
substances. Cysts can grow almost anywhere in your body or under your skin.
There are many different types of cysts. Most cysts are benign, or noncancerous.
Site
Shape round
Ovoid
Lobulated
Well marginated
Few septa
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Simple cyst:
• abnormal
• fluid-filled sac
• not cause harm to kidney (organ)
• not genetic as polycystic kidney (organ)
• not enlarge kidney (organ) : not reduce organ function
• not replace N structures
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Report on cyst
Simple cyst
• thin wall
• regular thin wall (same thickness)
• Jet black
• No calcification (hyper echo)
• No soft tissue components
• No septation (septum)
• Posterior Acoustic enhancement
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Report on
Hydatid cyst
1) Large cyst
2) Turbidity
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Types of cysts
There are hundreds of different types of cysts. They can grow almost anywhere in
your body. Some cysts occur as part of another condition, such as PCOS or PKD.
Some of the more common types of cysts include the following:
Epidermoid cyst
These are small, benign bumps filled with keratin protein. If you have trauma around
a hair follicle within the skin, an epidermoid cyst may occur. If part of the top layer of
your skin, called the epidermis, grows deeper instead of moving outward toward the
surface to eventually be shed off, an epidermoid cyst will have a chance to form.
Sebaceous cyst
Sebaceous cysts often form within sebaceous glands. These glands are part of the skin
and hair follicles. Ruptured or blocked sebaceous glands can lead to sebaceous cysts.
Sebaceous glands make oil for your skin and hair. Sebaceous cysts fill with sebum
and are less common than epidermoid cysts.
Ganglion cyst
These benign cysts usually form near the joint areas of your wrist or hand. However,
they can also develop in your feet or ankle areas. The reason they form isn’t known.
Ganglion cysts tend to occur along a tendon sheath near a joint. They’re more
common in women than in men.
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Ovarian cyst
Ovarian cysts often form when the follicle that normally releases an egg doesn’t open.
This causes fluid to build up and form a cyst.
Another common type of ovarian cyst occurs after the follicle releases the egg and
improperly recloses and collects fluid. Ovarian cysts occur most often in women of
menstrual age. They’re usually found during pelvic exams.
Ovarian cysts are associated with an increased risk of cancer when they occur after
menopause.
Breast cyst
Benign cysts can develop in your breasts when fluid collects near your breast glands.
They commonly occur in women in their 30s and 40s. They can cause pain or
tenderness in the affected area.
Chalazia
Chalazia are benign cysts that occur on your eyelids when the oil gland duct is
blocked. These cysts can cause tenderness, blurred vision, and painful swelling. If
they get too big, they can cause vision problems.
Pilonidal cyst
These cysts form near the top, middle part of the buttocks. They’re usually filled with
skin debris, body oils, hair, and other matter.
Pilonidal cysts occur more often in men than in women. They can develop when loose
hairs become embedded in your skin. According to the Mayo Clinic, chronic
infections in these cysts might increase your risk of a type of skin cancer called
squamous cell carcinoma. Know the signs for different types of skin cancer to treat it
early.
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Baker’s cyst
A Baker’s cyst, also known as a popliteal cyst, is a fluid-filled cyst that forms at the
back of the knee. These cysts are usually due to problems with the knee, like knee
injury or arthritis. Mobility can be limited and painful with a Baker’s cyst.
Physical therapy, fluid draining, and medication can all be used to help treat a Baker’s
cyst.
Cystic acne
Cystic acne results from a combination of bacteria, oil, and dead skin clogging the
pores. It’s the most severe type of acne in young adults, but usually improves with
age. Cystic acne can look like large, pus-filled boils on the skin. It can also be painful
to the touch.
If you believe you may have cystic acne, your dermatologist can prescribe
medications to help treat it.
An ingrown hair cyst forms when a hair grows into the skin and a cyst forms beneath
it. These cysts are more common in people who shave or wax to remove hair.
Most of the time, professional medical care isn’t needed to treat ingrown hair cysts.
However, see a healthcare professional if you suspect it’s infected.
Pilar cyst
Pilar cysts are flesh-colored, benign lumps that form on the surface of the skin. Since
they’re benign, they’re typically not cancerous. However, they can grow to a size that
can be uncomfortable.
Removal is typically not necessary, but they can be removed for cosmetic preference.
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Mucous cyst
A mucous cyst is a fluid-filled lump that forms on the lip or around the mouth when
the salivary glands become plugged with mucous. The most common causes of
mucous cysts include:
Often, mucous cysts will go away on their own. However, if you have recurring or
frequent mucous cysts, medical treatment may be required.
Branchial cleft cysts are a type of birth defect that forms a lump on an infant’s neck or
below the collarbone. This cyst can look like a large skin tag.
Schedule an appointment with your healthcare provider if your cyst becomes very
painful or red. This could be a sign of a rupture or an infection.
A healthcare provider should check your cyst even if it isn’t causing any pain or other
problems. Abnormal growths can be a sign of cancer. Your healthcare provider may
want to remove a tissue sample for testing.
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3- Wall thickness:
Diffuse
Hematuria
Focal lesion
5- Cystitis
D.D. : UB stone
Back pressure of ureter then kidneys
8- Stone
9- Lower obstructive uropathy : prostate – valve – urethra
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Finding
- Carcinoma
- Neurogenic bladder
- Bladder outlet obstruction
- Cystitis (follow : Chemotherapy , radiotherapy))
- Bladder diverticulum
o (out pouch from bladder wall)
- Bladder stones (calculi)
o Mobile
o Echo genic
o Black shadow
o Associated with bladder wall thickening
▪ Due to inflammation
- Bilharziasis schistosomiasis
o Nodular bladder wall thickening
o Contracted bladder
o Fibrosis of thick wall of UB
o Calcification
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1) LN “lymph node”
o Hypo echo
o Multiplicity
o Soft tissue
o lymphoma
o kidneys
o Spleen
o Para-aortic LN
o Related to retroperitoneal structures
o Liver
o IVC
o Aorta
o Helium of spleen
2) Supra renal glands
3) Stomach:
o If mass presence (gas at fundus)
o Pyloric stenosis
o Gastritis (by patient history 5 inflammation)
o Gastric ulcer by pt history 5 criteria of inflammation
o Gastric ulcer
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7 sites
o Trauma → hematoma
o Blood clots
o Rupture Aorta (due to Aortic Aneurysm)
D → Aspiration
• Sites of hematoma
o Pancreas
o Kidneys
o Aorta
o Posterior wall of UB
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1) Stomach
Embolus are
as in portal vein
D → Air Embolism
Question:
Answer:
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2) C/P
1- Vomiting
2- Abdominal distension
3- BP is Fluctuating
70/50 or 80/60
4- O2 saturation
< 90%
Normal: >92%
Nearly up to 97%
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Sites of
Fluid collection
Trauma (collection)
Ascites
Blood clots
7- Pelvic region
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HF
LC
Nephrotic $
Respiratory Failure
T.B. Peritonitis
Mesothelioma
Psoas abscess
Distended colon
TB peritonitis
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DD of Ascites
-Gastric carcinoma.
-Atrophic gastritis.
-Intestinal lymphangiectasia.
-Whipple's disease.
-Inflammatory bowel disease.
-Celiac and tropical sprue.
-TB enteritis.
-Cancer colon.
-Congestive heart failure.
-Constrictive pericarditis.
- Esophageal carcinoma.
Liver Cirrhosis
Nephrotic Syndrome
Mal-Nutrition
PLE ( Protein Losing Entropathy )
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DD leg swelling
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5) Aorta
2. Pulsation of aorta
• Shock
• Internal bleeding
• Smoker
• Atherosclerosis
• Risky in the elderly
• Abd. pain & referred to the back
• Bruit → auscultation examination
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Intestine:
1) Appendicitis
2) Intestinal obstruction (Air fluid level)
3) Inguinal hernia
4) Hyper echo bowel
• Genetic as Turner $
Intestinal obstruction:
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Blood Vessels
1) Portal vein
= clear wall
= > 13mm → Liver Cirrhosis
= DD of L¢
DD
1) congested hepatopathy
2) Veno-Occlusive disease
3) Congested Rt sided heart Failure
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3) IVC
= > 20 mm or (2.5cm)
DD
1. Congested Liver
2. Budd Chiari
≡ volume overload
TR & PR
Rt sided HF
Trauma
---------------------------------------
----------------------------------------------
5) Splenic vein
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Hypo echo
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Prostate
1) Size: DD of enlargement
2) Volume / capacity (3 diameters)
→ = 25mg
→ weight
Not fluid as UB
Zone
Central 5% → adenoma
3) Homogenecity or heterogenicity
4) Calcification → chronic prostatitis
5) Fluid → clear or not clear
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Findings
** cyst :
Lymphoma
Metastasis
Abscess
Cyst
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Uterus site
Shape
Wall thickening
Echogenicity
Fallopian tube
UB
Ovary : site
Size
Shape
Cervix : length
Wall thickening
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Findings
Pelvic pain
Carcinoma
Polyp
Fluid
Endometritis
Myometrium fibroid
Ovary : cyst
Carcinoma
Polycystic ovary
Cervix : stenosis
Polyp
Cancer
Fibroid
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2-long axis of GB : 12 cm
4-CBD = 8 mm
Echo pattern
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معلومات
** بدون تصنيف و لكن وصف الورم :كبد – بنكرياس – كليتين – الم اررة
االستخدام indications
)5تحديد وجود و تضخم الغدد الليمفاوية وذلك سيكون البدء في الشك في
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االماكن في الجسم
كبد
طحال
ررة GB
كيس الم ا
الكليتين
البنكرياس
المثانة البولية
الرحم في النساء
المبيض في النساء
البروستاتا
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الحجم
الشكل
انسجة العضو
وجود cyst
وجود حصوات
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##مثل :الكبد
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Blood vessels :
Aorta : aneurysm
Hepatic vein : hepatic congestion
Portal vein : portal HTN
IVC: hepatic congestion then Rt sided HF
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9th rib
Pylorus of stomach
Fundus GB
Celiac trunk
Renal vessels
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Q&A
Difference between :
Focal lesion
1- Cyst
2- A- metastasis as lymphoma
B- hematoma
2- infarction as spleen
3- abscess
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Cancer
Malignant >> metastasis (M & M )
in kidney : lipoma
Colouration
Focal fat tissue : bright >> fatty liver
1- Isoechoic
2- Hyperechoic
3- Hypoechoic
4- Echo free – jet black – anechoic
5- Bright
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Colouration in details
Anechoic اسود
Hyperechoic ابيض
Examples :-
Hyper = white
Gas
Bone
Fat
Omentum in abdomen
Aorta and PV
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Black = anechoic
Fluid
Bright = echogenic
Fatty liver
Lymphoma
Malignant Tr
LN
Intestine
Liver
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2nd ry : metastasis
HCV
Ascites
LC
Cholangiocarcinoma
Focal lesion
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1- LC with ascites
2- Hemangioma with associated risky disease
HCV
Ascites
LC
Primary cancer
3- Focal fatty sparing (fat out)
All liver is fatty except focal lesion
4- Diffuse hepatic pathology
a- Dark than normal
b- Not reach criteria of LC
c- No clear irregular multiple focal lesions
Multiple nodules
N.B. : if polyp in GB
tr in body
cystitis or mass in UB
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Pain
Redness
Swelling
Vomiting
Asymptomatic
> 5 mm if emptied UB
> 3 mm if distended UB
Irregular surface of UB
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Burning sensation
difficulty urination
bloody urine
frequency
nocturia
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LN in ileocecal valve
Rebound tenderness
Abdominal pain
Vomiting
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Cholecystitis
Other cause : Obstruction of bile duct from : tumor – scar of the duct
Trauma
Surgery
Infection
Cyst
Parasite
Stricture
Inflammation
Fertile = pregnant
DM
Fair Caucasian
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Acute cholecystitis :
GB stone >>> block of bile flow >>> bile stasis >>> enlarged GB
Chronic cholecystitis :
Causes: GB stones
** GB stone types :-
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Difference
Stone = calculi
Sludge = biliary sand , increase mucous + crystals in bile
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C/P
Acute cholecystitis :-
Radiate to Rt shoulder
Pain > 6 hrs
Vomiting
Fever
U/S : edematous thick GB wall > 3 mm (fluid of edema : black)
Peri cholecystic fluid >>> black
+ ve sonographic Murphy`s sign
i.e. : abd. Tender from probe compression
chronic cholecystitis :-
risk factors 9 F or 6 F
asymptomatic
recurrent history
biliary colic
U/S : bright echo
Cholesterol stone : movable
Ca stone : not movable
Posterior shadow of stone
White thick wall
Chronic fibrosis
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Pancreatitis
Acute case : right pleural effusion (mostly right lung) ask for CXR
Severe epigastric pain
High lipase & amylase enzymes … increase 3 times
Fever
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An ultrasound may be performed for a variety of reasons, but looking at a baby in the
womb is the most common reason. If you have recently had an ultrasound and you
want to know how to interpret the images on your ultrasound, then you may benefit
from learning about some of the basics of ultrasound imaging. You may also want to
know how to pick out specific features of your pregnancy ultrasound, such as the
baby’s head, arms, or sex. Just keep in mind that ultrasounds can be difficult to
interpret, so it is best to do so with the help of your doctor.
Method 1
1.
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Disregard the text and numbers at the top of your scan. Most hospitals and
ultrasound centers use this space to include details like your name, hospital
reference number, or ultrasound machine settings. Since this information does
not have anything to do with what you see on the ultrasound image, you can
ignore this information.[1]
2.
Start from the top of the image. The top of the screen or printed image is
where the ultrasound probe was placed. In other words, the image you see
shows what the organ or tissues look like from the side rather than from the
top.[2]
o For example, if you are having an ultrasound of your uterus, then what
you see at the top of the screen or printed ultrasound would be the
outline of the tissues above your uterus. As you look further down the
screen, you will see deeper tissues, such as the lining of your uterus,
the inside of your uterus, and the back of your uterus.
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3.
Consider the differences in colors. Most ultrasound images are in black and
white, but you can see differences in the shades of black and white in your
ultrasound scan. The color differences come from the differences in the
densities of the materials that the sound passes through.
o Solid tissues, like bone, will appear white because the outer surface
reflects more sound.
o Tissues that are filled with liquid, like the uterus, will appear dark.
o Ultrasound imaging does not work well for gas, so organs that are
filled with air, like the lungs, are generally not examined with
ultrasound.
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4.
Watch for common visual effects. Since ultrasound uses sound to create
images of the inner structures of your body, the images are not crystal clear.
There are many different visual effects that can happen as a result of the
ultrasound’s settings, angle, or of the density of the tissues being examined.
Some of the most common visual effects to watch for include:[3]
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Method 2
1.
Identify your womb. You can identify the outline of your uterus by finding
the white or light grey line around the edges of the ultrasound image. Just
inside of this area, there should be a black area. This is the amniotic fluid.[4][5]
o Keep in mind that the edge of the womb may not go around the entire
image. The technician may have positioned the probe in a way that
centered the image on your baby. Even if you only see white or grey
lines along one or two sides of the image, this is probably the outline of
your womb.
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2.
Spot the baby. Your baby will also look grey or whitish and will be located
within the amniotic fluid (the dark area inside of the womb). Look at the area
within your amniotic fluid to try to make out the outline and features of your
baby.
o The details that you see in the image will depend on the stage of your
pregnancy. For example, at 12 weeks, you may only be able to identify
the head of your baby, while at 20 weeks, you may be able to see the
spine, eyes, feet, and heart.[6]
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3.
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4.
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Q & A in U/S
Liver
DD of Lt lobe ++ : Focal
1-HCC
2-Hemangioma
3-Hydatid cyst
4-abscess
Echoic degree
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Hemangioma
Tr in blood vessels : vein
Artery
Not lymphatic vessels
Tumour = Tumor
Primary cancer: HCC = Hepatoma = Malignant tr
Cholangiocarcinoma
Focal lesions
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3 places in sonar
Between IVC & porta hepatis
Midline : sagittal
Subcostal : 9th rib oblique
Subcostal : 9th rib sagittal
IVC
Intra-hepatic part of IVC : Lt & Rt hepatic veins
Dilated IVC : congested liver – Budd Chiari $
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Portal vein : come from : splenic vein – SMV " superior mesenteric V "
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Nodular regeneration
Fibrosis
Coarse = heterogenous
++ PV > 13 mm
But the wrong name is peri-portal hepatitis ال يوجد هذا االسم
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Colouration in liver
An echo : hemangioma
hydatid cyst
hypoechoic
stage before LC
septum = septation
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Pleural effusion
Right side in the lung = Pancreatitis
ال يوجد كتم نفس بعد لما ياخذ المريض نفسه في حاالت فحص الكبد
بالسونار
لكن ينام علي الجانب اليسار لكي تكون الرئة اليمين عالية
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Porta hepatis
Mission is : diameter of PV
** خطأ ال يوجد قياس او مدي محدد والقياس غير مطلوب مع اطباء امراض
الباطنة
hepatic artery ** غير مطلوب كامراض باطنة اني ابحث و اعلق علي
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Notes in Hepatology
Size
Lt lobe > 10 cm
Examples : normal
Focal lesion
Hypoechoic surface
Irregular outline
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2- Hydatid cyst
3- Tumour = tumor
Hyperechoic
So hypoechoic
Hepatoma
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Q & A sonar
GB
GB mud
In MCL
Mucocele
Mass
L.N.
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Difference :
Cholesterol stone & Adhesions >> Movable >> ask for Dopplar
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By wall thickening
** cholesterol stone in GB
If post-cholecystectomy > 10 mm
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Dilatation
Intrahepatic
Cholangiocarcinoma
Cholangitis
Choledocholithiasis
Extrahepatic
Pregnancy
Choledocholithiasis
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Sonar : Hypoechoic
Pancreatitis
Stone > 2 – 20 mm
Cholangitis : inflammation
1- Ascending : infectious
Charcot triad
Fever
Jaundice
2- Sclerosing : idiopathic
Stricture of biliary ducts
Cirrhosis of biliary ducts
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Notes of GB
Patient fasting 6 -8 hrs
Except - small amount of diet
- juices & water
Findings :
** If chronic cholecystitis
& peri cholecystic edema collection " jet black around GB"
Mud = no fluid
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Acute or chronic
Mucocele
So = obstruction of GB neck
Q & A sonar
Pancreas
Hypoechoic
2- pancreatic duct
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Cause : as GB stones
calcification
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Notes in pancreas
Disease D by U/S :-
1- Pancreatitis inflammation
Dilated in CBD
Epigastric pain
Fever
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Pig tail
So ask for CT
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Q & A sonar
Spleen
Hemangioma
Lipoma
Plasmacytosis
Malignant tr
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DD of Hematoma
** hemangioma = benign tr
In internal organs
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Q & A Sonar
Kidney
Spleen
Pyelonephritis
Surgically removed
DD : Nephrotic $
DM
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Q & A Sonar
Retroperitoneal structures
Mesenteric artery
Renal artery
Branches of Aorta
1. inferior phrenic a.
2. celiac a.
1. left gastric a.
2. splenic a.
1. short gastric arteries (6)
2. splenic arteries (6)
3. left gastroepiploic a.
4. pancreatic arteries
3. common hepatic a.
1. right gastric a.
2. gastroduodenal a.
1. right gastroepiploic a.
2. superior pancreaticoduodenal a.
3. right hepatic a.
1. cystic a.
4. left hepatic a.
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3. superior mesenteric a.
1. inferior pancreaticoduodenal a.
2. jejunal and ileal arteries
3. middle colic a.
4. right colic a.
5. ileocolic a
1. anterior cecal a.
2. posterior cecal a. – appendicular a.
3. ileal a.
4. colic a.
4. middle suprarenal a.
5. renal a.
6. testicular or ovarian a.
7. four lumbar arteries
8. inferior mesenteric a.
1. left colic a.
2. sigmoid arteries (2 or 3)
3. superior rectal a.
9. median sacral a.
10. common iliac a.
1. external iliac a.
2. internal iliac a.
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Artery
Vertebra Type Paired? A/P Description
Branch
Originates above the celiac trunk, below the
diaphragm. Passes upward and medially to
inferior the suprarenal gland, and crosses crus of
T12 Parietal yes post.
phrenic diaphragm of corresponding side. Supplies
diaphragm and gives superior suprarenal
arteries.
celiac T12 Visceral no ant. Large anterior branch
superior Large anterior branch, arises just below
L1 Visceral no ant.
mesenteric celiac trunk.
middle Crosses crus of diaphragm laterally on each
L1 Visceral yes post.
suprarenal side; supplies the suprarenal gland.
Arises just below the superior mesenteric
artery. Right renal artery passes deep to the
In inferior vena cava to right kidney; here it
renal between Visceral yes post. divides into branches. Left renal artery
L1 and L2 passes deep to the left renal vein. Divides in
hilum of kidney. Both arteries give inferior
suprarenal arteries and ureteral branches.
Ovarian artery in females; testicular artery in
gonadal L2 Visceral yes ant.
males
Four on each side that supply the abdominal
wall and spinal cord. The fifth pair is the
lumbar branches of the iliolumbar arteries.
They pass deep to the crura on side of
vertebral bodies and pass deep to the psoas
lumbar L1-L4 Parietal yes post.
major and quadratus lumborum to enter the
space between the internal oblique and
transversus abdominis muscles. Each artery
gives off a small dorsal branch, which gives
a spinal branch to the vertebral canal and
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Lymphoma : renal
Spleen
Para aortic LN
Stomach report
Mass presence
Exclusion by sonar
Pyloric stenosis
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related to lesions
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Orientation in U/S
Mid line
Axillary
Angel of probe
Depth (zoom)
Gentle compression
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Ratio
Freeze
Gean
Caliber
Set
Track ball
Set
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غير مهم قيام طبيب امراض الباطنة بعمل معادالت حسابية علي لوحة المفاتيح في
جهاز السونار
Increase in size
1- by diameter
liver ( Rt & Lt lobes )
kidney ( Rt & Lt )
spleen
2- capacity (volume) 3 diameters
GB
UB
Prostate
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Sonar screen
Anterior – Posterior : the same in : saggital & coronal – axial
Tissue
Lt lobe of liver
Pancreas
Aorta
Shadow spine
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Q & A sonar
Measurements
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RUSH Examination
• Rapid Ultrasound for Shock and Hypotension – the RUSH Exam.
The RUSH Exam: Rapid Ultrasound for Shock and Hypotension.
.نوعها
➢ 6 Types of Shock
➢ Obstructive Shock :
*Example:
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Fast examination
❑ It is now the standard of care to perform focused assessment
using sonography for trauma (FAST).
و تقرير سونار في هذه حاالت بيتجاهل كتابة تفاصيل غير هامة في
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