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A comprehensive overview of abdominal pathology, focusing on the urinary system, hernias, and the appendix. It includes detailed descriptions of various conditions, their causes, symptoms, and diagnostic imaging findings. Particularly useful for students of medicine and healthcare professionals seeking to enhance their understanding of abdominal pathology.
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1.-retroperitoneal -measures 9-12cm (kidneys should be within 2cm of each other) -outer cortex is more hypoechoic -renal fascia=gerotas fascia -functioning unit of kidney=nephron: Kidney Anatomy 2.-obstruction -flank mass -renal abscess
2 / 17 13.Kidneys may be enlarged, having thinned cortex, and increased adipose tissue within the sinus that can have varied appearance (anechoic to densely echogenic) -can mimic infection, atrophy, hydronephrosis: Renal sinus lipomatosis (fi- brolipomatosis) on ultrasound 14.-separation of normal renal sinus by interconnected fluid filled calyces -often seen with urinary tract obstruction but they are not necessarily synony- mous (can also be seen in peds patients with vesicoureteral reflux) -can be deceiving(over hydration) check bladder: hydronephrosis 15.-flank pain
4 / 17 34.-renal stones -malignant solid or cystic masses often demonstrate calcifications -linear vascular calcifications may be seen with renal artery atherosclerosis and vascular malformation: Urinary tract calcifications 35.parenchymal calcifications, usually of the medulla, affecting both kidneys -can be metastatic -appears as increased echogenicity of the cortex and medullary pyramids -most commonly seen with: chronic glomerulonephritis, sickle cell disease: - Nephrocalcinosis 36.An abrupt decrease in renal function -potentially reversible: acute renal failure 37.-hypotension
5 / 17 45.-renal sinus cyst -doesn't communicate with the collecting system -many have irregular borders bc it may compress adjacent structures -can be misdiagnosed as hydronephrosis: Parapelvic cyst 46.autosomal dominant genetic disorder -abdominal cyst and tumors -renal and pancreatic cyst -abnormalities include: cerebellar hemangioblastomas: von Hippel-Lindau dis- ease 47.-an autosomal dominant genetic disorder -associated with renal lesions: multiple renal cyst , angiomyolipomas: Tuber- ous sclerosis Renal masses 48.Occurs in approximately 1-2% of simple renal cyst -usually due to hemorrhage or infection at some point -can be malignant -on US : layered, egg shell thin cyst wall is hyperechoic: Mural Calcification 49.-in a renal cyst or calyceal diverticulum is quite common -represents small calcium crystals, usually occurs after inflammatory process and urine flow stasis -on US: layering (mobile) linear band of hyperechoic echoes with reverb artifacts: Milk of calcium 50.autosomal dominant and autosomal recessive: 2 types of polycystic kidney disease 51.-also called infantile polycystic disease -fairly rare genetic disorder -causes renal failure -sonographic features: echogenic, enlarged kidneys due to multiple micro- scopic cysts: Autosomal recessive polycystic kidney disease 52.Fairly common genetic disorder -enlarged kidneys with multiple asymmetrical cysts varying in size and loca- tion -leads to end stage renal disease: Autosomal dominant polycystic kidney disease 53.-can be asymptomatic
7 / 17 -weight loss
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11 / 17 Rejection, acute tubular necrosis, obstruction, hemorrhage/ infarction, malig- nancy: renal transplant evaluation 88.-placed in iliopelvic region(RLQ) -baseline usually obtained with days after tx occurs evaluating for: renal size, fluid collections, echotexture, hydronephrosis: Renaltx 89.-hematomas: appearance depends on age, can appear solid
13 / 17 -fever, mass, dropping hematocrit -linear transducer can be of assistance in determining if hematoma is arising from sup abd wall: Bladder flap hematoma
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