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64 Cards in this Set

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DDX gb wall thickness

hepatitis,
ascites,
cholecystitis,
hypoalbuminemia,
heart failure,
portal venous hypertension,
hypoproteinemia,
adenomyomatosis,
gallbladder tumor,
pericholecystic collections,
varices resulting from portal hypertension
obstructed lymphatics
contracted gallbladder in a non-fasting patient,
hyperplastic cholecystoses,
carcinoma of the gallbladder,
hepatic fluid overload with secondary gallbladder wall edema.

differential diagnosis of non-shadowing, non-dependent, echogenic intraluminal masses in the gall bladder
tumefactive sludge,
polypoid tumors,
organized hemorrhage in patients with hematobilia.
DDX conditions that predispose to echogenic bile or sludge formation include

hemolytic anemia,
prolonged fasting, hyperalimentation,
cholestasis with extrahepatic bile duct obstruction, and intrinsic disorders of the gallbladder such as abnormal mucoprotein production.
Cystic fibrosis is associated with gallbladder sludge and splenomegaly in a child

differential diagnosis of non-shadowing, non-moving focal echogenic areas within the gallbladder includes

small adherent gallstones, adenomyomatosis,
focal inflammatory disease, papillomas, and carcinoma.

What is the fatty meal challenge

used to separate those patients with large but unobstructed ducts from those patients with a partial or complete obstruction. Fat given orally releases cholecystokinin from the duodenum. Intravenous cholecystokinin could be used instead to elicit the same response.

Increased incidence of cholangiocarcinoma in patients with

chronic ulcerative colitis, cystic diseases of the liver biliary tract (such as Caroli's disease),
Clonorchis sinensis infestation (Oriental cholangiohepatitis)

Sonographic features that have been described as being suggestive of a hilar cholangiocarcinoma include:

1. Dilated intrahepatic bile ducts with normal-sized extrahepatic biliary tree and gallbladder.
2. Intraductal mass at the confluence of the left and right hepatic ducts.
3. Porta hepatis mass or enlarged portal lymph nodes.

Biliary atresia assoc.

Down syndrome,
polysplenia syndrome,
Alagille syndrome arteriohepatic dysplasia (characterized by intrahepatic biliary ductule hypoplasia, pulmonary artery hypoplasia, vertebral anomalies and typical facies), and
Byler's disease (familial intrahepatic cholestasis in the Amish).

DDX Pneumobilia
surgically created biliary-enteric anastomosis,
post sphincterotomy, incompetent sphincter of Oddi, wall erosion by a gallstone or ulcer into common bile duct.
DDX Fatty Pancreas
(1) elderly, (2) obese, (3) diabetes mellitus, (4) Cushing's disease, (5) lipomatosis, and (6) after steroid administration.
The double systolic peak is referred to as bisferiens or "twice beating" pulse and is seen in three clinical entities:
aortic regurgitation,
combined aortic stenosis and regurgitation,
obstructive hypertrophic cardiomyopathy.
main clinical indications for performing a duplex ultrasound examination include:
the evaluation of patients with confusing or nonhemispheric symptoms; patients with asymptomatic bruits; patients scheduled to undergo major cardiac or vascular surgery; and follow-up of patients postendarterectomy.
DDX vaginal bleeding in a postmenopausal woman

atrophic endometrium and exogenous estrogen. Other causes include endometrial hyperplasia, polyps, and submucosal fibroids. Endometrial carcinoma is less common.

ultrasound findings suggestive of an ectopic
adnexal ring,
complex mass
cyst
presence of free fluid
DDX Sac like pelvic structures

ectopic pregnancy
pyosalpinx
endometrioma
hemorrhagic corpus luteum.

differential diagnosis in postmenopausal women with endometrial fluid collection includes
carcinoma (endometrial and cervical),
endometrial polyp,
in patients who are status-post pelvic radiation therapy. However, probably the most common cause is exogenous estrogen administration in the presence of cervical stenosis.
DDX Medullary nephrocalcinosis

hypercalcuria and often with hypercalcemia.
Primary hyperparathyroidism and distal renal tubular acidosis account for over 60% of these cases.
hypercalciuria,
medullary sponge kidney,
milk-alkali syndrome, Cushing's syndrome,
bony metastases, hyperthyroidism, hypothyroidism,
sarcoidosis,
furosemide therapy,
vitamin D and phosphorus therapy in a case of hypophosphatemic rickets.
williams's syndrome

DDX Cortical Nephrocalcinosis
acute cortical necrosis
chronic glomerulonephritis, Alport's syndrome.
Primarily hyperoxaluria
renal vein thrombosis,
amyloidosis,
leukemic infiltration, and other causes of cortical nephrocalcinosis (chronic glomerulonephritis, Alport's syndrome, acute cortical necrosis). Other clinical manifestations include arthritis, cardiac conduction defects, localized ischemic skin lesions, and peripheral neuropathy.
DDX Dilated collecting systems in the absence of obstruction
prominent extrarenal pelves,
a distended bladder with delayed caliceal emptying, reflux, diuretic effect, congenital megacalices
differential diagnosis of a solitary small solid renal mass on ultrasound should include
renal cell carcinoma, oncocytoma, angiomyolipoma, and solitary metastasis.
Adrenal lesions that need to be included in the differential diagnosis
metastatic disease (especially if the patient has a primary lung or breast carcinoma), adenoma, lymphoma, hemorrhage (usually with obvious history of trauma or coagulopathy), and other less common primary adrenal neoplasms (pheochromocytoma, adrenal cortical carcinoma). Adrenal cysts and pseudocysts.
DDX Bladder Diverticula
1. Bladder ears, transitory bladder pouches projecting anteriorly into the inguinal rings in males under 6 months of age. Unlike congenital diverticula, they are anterior in position without an obvious neck connecting the pouch to the bladder.
2. Outpouching from the bladder, posterolateral to the ureteral orifices in girls. This area contains an anatomically thin muscle, so that the bladder normally bulges during voiding. Many regard this as a normal anatomical variation, although some feel that it is a true diverticulum.
3. Wide-mouthed lateral bladder pouches with a normal thickness of muscle. These contract when the bladder contracts and are considered a normal anatomical variation.
4. Extravasated urine that has become walled off after surgery or injury. This cavity, lined with granulation tissue, communicates with the bladder. The previous history is necessary to make the diagnosis.
DDX Bladder Tumors
normal bladder trabeculae, edema, mural folds, surgery scars, endometriosis, blood clot, and chronic cystitis.
the most common urachal remnant
cyst.
DDX Prostate mass
prastate ca,
focal prostatitis, prostatic intraepithelial neoplasia,
scarring,
atrophy
DDX Fatty infiltration of the liver
corticosteroid administration, chemotherapy,
diabetes mellitus,
small bowel bypass surgery, trauma,
obesity,
hyperalimentation.
DDX portal vein thrombosis
cirrhosis, intrahepatic malignancy, sepsis, pancreatitis, postoperatively or post-traumatically, and in hypercoagulable states, including blood dyscrasias, intra-abdominal malignancy, or even pregnancy
DDX hepatic cyst
simple cysts; pyogenic, amebic, and hydatid abscesses; polycystic liver disease; Caroli's disease; and traumatic hematomas.
DDX Benign primary liver neoplasms
capillary and cavernous hemangiomas, liver cell adenomas, focal nodular hyperplasia, and biliary cystadenomas.
DDX lg cystic liver mass
primary biliary cystadenoma/cystadenocarcinoma,
necrotic metastasis,
hydatid cyst.
differential diagnosis of a large solitary hepatic lesion includes
metastatic disease,
primary hepatocellular carcinoma, and benign hepatic lesions. In a patient with hepatic cirrhosis, hepatocellular carcinoma is likely.
Causes of hepatocellular carcinoma:
1. Hepatitis
2. Chronic liver disease
A. Alcoholic and postnecrotic cirrhosis
B. Alpha 1 antitrypsin deficiency
C. Hemochromatosis
D. Hereditary tyrosinosis
3. Mycotoxins (metabolites of Saprophytic fungi)
differential diagnosis of liver calcifications
primary or secondary malignancy.
primary mucinous carcinoma of the colon with secondary calcified liver metastases. Other common primary malignancies that have calcified metastases to the liver are the breast and ovary.
Causes for assymetric form of IUGR
\where the abdominal circumference is small in proportion to the head size and femur length. This is usually the result of placental insufficiency in patients with hypertension or diabetes mellitus. Less common causes include severe maternal malnutrition, heavy smoking, substance abuse, collagen vascular disease and anemia.
differential diagnosis of an encephalocele includes
cystic hygroma, scalp edema, branchial cleft cysts, hemangioma, and teratoma.
DDX masses in the sacrococcygeal region
chordoma, anterior sacral meningocele, neurenteric cyst, neuroblastoma, lipoma, rhabdomyosarcoma, hemangioma, malignant melanoma, and a meconium pseudocyst. A predominantly or entirely external cystic mass may resemble a myelomeningocele, which must be excluded by demonstrating intact posterior spinal elements
differential diagnosis for an entirely intra-abdominal sacrococcygeal teratoma includes
ovarian cyst, meconium pseudocyst, enteric duplication cyst, or anterior myelomeningocele
differential diagnosis of congenital diaphragmatic hernia includes
cystic adenomatoid malformation of the lung, bronchogenic and enteric cysts, mediastinal cystic teratoma, pulmonary sequestration, bronchial atresia, large chest wall or pleural-based masses, and unilateral agenesis of the lung.
causes for enlarged hyperechoic kidneys
include asphyxiating thoracic dysplasia and chromosomal disorders i.e. trisomy 13, 18, potter's, meckel gruber.
DDX fetal ovarian cyst
duplication cyst, mesenteric cyst, and urachal cyst.
Entities that cloverleaf skull occurs in
only in dysplasias that are either thanatophoric dysplasia, camptomelic dysplasia and homozygous achondroplasia

differential diagnosis for a hypoechoic subchorionic hemorrhage beyond approximately 16 weeks includes a

myoma, area of uterine contraction, a succenturiate placenta, a marginal placental chorioangioma, and an amniotic sheet.
The differential diagnosis for solid hypoechoic masses in the pancreas include:
carcinoma, focal pancreatitis, lymphoma, metastases, islet cell tumors, thrombosed aneurysm and pancreatic phlegmon.
differential diagnosis of a low attenuation intrasplenic mass found on CT or a hypoechoic mass found on ultrasound
infarction, hematoma, splenic cyst, or a primary splenic neoplasm such as lymphoma.
differential diagnosis for low density areas noted in the spleen of patients with AIDS. These include:
disseminated Kaposi's sarcoma, lymphoma as well as other fungal and mycobacterial infections and pcp.
The most common site for a gastrointestinal duplication cyst is the
ileum.
DDX Retroperitoneal Lymphadenopathy
: lymphoma; metastases from pelvic malignancies, particularly cervical, uterine, bladder, or prostate carcinoma; other intra-abdominal malignancies such as colon, pancreas, or renal carcinoma; and extraabdominal malignancies such as lung or breast carcinoma. Sarcoidosis or retroperitoneal fibrosis, particularly in its inflammatory stage, may create a retroperitoneal mantle. Benign nodal hyperplasia is rare.
Types of Sacrococcygeal Teratomas
Type I: Predominantly external.

Type II: Dumbbell-shaped, predominantly external mass with significant intrapelvic component.

Type III: Predominantly intrapelvic lesion with small external mass.

Type IV: Totally intrapelvic presacral mass with no external component.
differential diagnosis of a presacral mass in children includes
neuroblastoma, chordoma, abscess, rectal duplication, and anterior sacral meningocele
mcc of hydrocephalus in a term infant
aqueductal stenosis
Benign appearing thyroid nodules
Benign
Solitary
Cystic
Eggshell or Peripheral Calcifications
DDX intra-testicular mass
neoplasm
infarction
abscess
Tumors of the epididymis in children include
rhabdomyosarcoma, hemangioma, lymphangioma, metastasis, and lymphoma (less likely leukemia).
Differential diagnosis of an adrenal cyst includes
adrenal abscess, hematoma, and cystic neoplasms (adenoma, carcinoma, pheochromocytoma, metastases
DDX adrenal tumor
adenomas (by far the most common), cysts, hematomas, myelolipomas, and rare lesions such as hemangiomas, lymphomas, nonhyperfunctioning pheochromocytomas, ganglioneuromas, and stromal tumors (fibromas, leiomyomas, etc.)
ACC may be seen in children with
Beckwith-Wiedemann syndrome or in association with hemihypertrophy
differential diagnosis of myelolipoma includes
lipoma and liposarcoma of the adrenal gland or retroperitoneum, or teratoma and angiomyolipoma arising from adjacent renal parenchyma. Recently a fat-containing adrenal adenoma was reported
Familial pheochromocytomas are most notable
in MEN syndrome, but can also occur with neurofibromatosis and von Hippel-Lindau disease
What 3 things can cause ring down artifact
gas
metal
crystals (cholesterol crystals in gallbladder adenomyomatosis)
dirty shadowing is usually caused by
gas

What is normal placental thickness?

2 to 4 cm

Risk factors for Placenta Accreta?

Risk factors for placenta accreta include:


placenta previa,


prior cesarean section,


prior uterine surgery breaching the endometrium, and


prior history of placenta accreta.

What are us and mri findings in placenta accreta?

Helpful ultrasound and MRI findings of placenta accreta include placental lacunae on ultrasound, hypervascularity on Doppler ultrasound or abnormal vessels on MRI, intraplacental dark bands on T2-weighted imaging, and focal uterine bulging.

What size adnexal cysts need to be followed and how often?

Cysts smaller than 3 cm do not need to be described in the imaging report. Cysts 3–5 cm in size should be described in the report but require no follow-up. Cysts 5–7 cm in size are to be followed with yearly US.