ch 62 Flashcards
(107 cards)
1
Q
foregut
A
Pharynx Lower respiratory system Esophagus Stomach Part of the duodenum Liver and biliary apparatus Pancreas
2
Q
Esophageal atresia
A
Results from abnormal deviation of tracheoesophageal septum in posterior direction
3
Q
Stomach
A
Appears as fusiform dilation of caudal part of foregut During fifth and sixth weeks, dorsal border (greater curvature) grows faster than ventral border (lesser curvature)
4
Q
Duodenum
A
Develops from caudal part of foregut and cranial part of midgut Comes to lie primarily in retroperitoneum
5
Q
Liver and Biliary System
A
Liver, gallbladder, biliary ducts arise as bud from most caudal part of foregut in fourth week
6
Q
Hemopoiesis
A
(blood formation) begins during sixth week
7
Q
bile formation by hepatic cells begin when
A
12 wks
8
Q
Extrahepatic biliary atresia
A
Blockage of bile ducts results from failure to recanalize following solid stage of development
9
Q
Pancreas
A
Develops from dorsal and ventral pancreatic buds of endodermal cells that arise from caudal part of foregut
10
Q
Spleen
A
Lymphatic organ derived from mass of mesenchymal cells located between layers of dorsal mesogastrium
11
Q
The Midgut
A
Small intestines Cecum and cloaca exstrophy Ascending colon Most of transverse colon
12
Q
The Midgut
A
All structures supplied by superior mesenteric artery
13
Q
the midgut is suspended by
A
elongated dorsal mesentery
14
Q
The Midgut
A
Usually by 10th or 11th week, midgut herniation returns to abdomen
15
Q
Gastroschisis
A
Is usually located to right of umbilical cord
16
Q
Umbilical Hernia
A
Forms when: Intestines return normally to abdominal cavity Herniate either prenatally or postnatally through inadequately closed umbilicus
17
Q
Meckel’s Diverticulum
A
Is the most common malformation of midgut Remnant of proximal part of yolk stalk that fails to degenerate and disappear during early fetal period
18
Q
The Hindgut
A
Derivatives of hindgut: Left part of transverse colon Descending colon Sigmoid colon Rectum Superior portion of anal canal Epithelium of urinary bladder Most of urethra
19
Q
The Hindgut is supplied by
A
inferior mesenteric artery
20
Q
Stomach should be seen by
A
14 to 16 weeks
21
Q
if stomach is not seen RO
A
Central nervous system problem (swallowing disorders) Obstruction Oligohydramnios Atresia
22
Q
Echogenic debris may sometimes be seen along dependent wall of stomach
A
Vernix
23
Q
If stomach seen in right upper quadrant, condition is called
A
situs inversus
24
Q
If fetus is in vertex presentation with spine up, both aorta and stomach should be seen to left of spine
A
Stomach
25
can be visualized in thorax during second and third trimesters as two or more parallel echogenic lines (“multilayered” pattern)
Normal esophagus
26
Measured at level of portal sinus and umbilical portion of left portal vein (“hockey stick” appearance on sonogram)
Abdominal Circumference
27
Abdominal circumference should be round, not oval.
Abdominal Circumference
28
Joins umbilical portion of left portal vein at caudal margin of left intersegmental fissure of liver
Umbilical Cord Insertion
29
Visualization of insertion site must be made to rule out presence of omphalocele, gastroschisis, hernia, and mass formation.
Umbilical Cord Insertion
30
Movement of gastric musculature begins in
approximately fourth to fifth month of gestation
31
After 15th to 16th week, meconium begins to accumulate in distal part of small intestine
Bowel
32
Bowel
Distinction of large bowel from small bowel possible after 20 menstrual weeks
33
Appears as ill-defined area of increased echogenicity in mid to lower abdomen
Bowel
34
Hyperechoic appearance could be secondary to reflections from walls of collapsed loops of small bowel or from mesenteric fat between loops
Bowel
35
As pregnancy progresses: Hyperechoic area becomes less prominent Small bowel located more centrally in abdomen than colon
Bowel
36
peristalsis occurs
After 27 weeks
37
Normal diameter of small bowel lumen ≤5 mm, with length of 15 mm near term
bowel
38
Haustral folds of colon help to differentiate it from small bowel
Bowel
39
In early gestation, haustral folds appear as thin linear echoes within lumen of colon Later, colon diameter increases and folds become longer and thicker
Bowel
40
Colon seen near end of second trimester as long tubular hypoechoic structure with well-defined walls
Bowel
41
Normal measurements of colon diameter range from 3 to 5 mm at 20 weeks to 23 mm or larger at term
Bowel
42
does not have peristalsis like small bowel
Colon
43
more peripheral than small bowel
Colon
44
After 14 weeks of gestation, lipid absorbed from fetal colon and remaining contents collect in colon as meconium
Bowel
45
hypoechoic relative to fetal liver and in comparison with bowel wall
Meconium within lumen of colon
46
Liver
Relatively large compared with other intraabdominal organs Occupies most of upper abdomen in fetus
47
Accounts for 10% of total weight of fetus at 11 weeks and 5% of total weight at term
Liver
48
Liver
Hepatic veins and fissures formed by end of first trimester
49
Left lobe of liver larger than right in utero secondary to greater supply of oxygenated blood Reverses after birth
Liver
50
Gallbladder
May be seen sonographically after 20 weeks of gestation
51
Distinguished by location to right of portal-umbilical vein and as oblong, more oval structure than “tubular” intrahepatic umbilical vein
Gallbladder
52
Pancreas
Normal fetal pancreas has been seen in utero but is more difficult to routinely visualize because of the lack of fatty tissue within the gland
53
Lies in the retroperitoneal cavity anterior to the superior mesenteric vessels, aorta, and inferior vena cava (IVC)
Pancreas
54
Normal fetal pancreas has been seen in utero but is more difficult to routinely visualize because of the lack of fatty tissue within the gland
Pancreas
55
Homogeneous in texture Similar in echogenicity to kidney Slightly less echogenic than liver Increases in size during gestation Imaged on transverse plane posterior and to left of fetal stomach
Spleen
56
Is involved in several congenital anomalies but rarely affected by isolated hepatic lesions
Abnormalities of the Hepatobiliary System
57
Liver parenchymal cysts and hemangiomas of liver have been reported. Enlarges in fetuses with Rh-immune disease in response to increased hematopoiesis
Abnormalities of the Hepatobiliary System
58
Liver tumors, hamartoma, hepatoblastoma uncommon but may be seen
Liver
59
Hemangioendothelioma Most common symptomatic, vascular hepatic tumor of infancy (although rare) May cause nonimmune hydrops in fetus
Liver
60
Sonographic Findings of the liver
Most liver tumors appear as hypoechoic solid masses; cystic components have also been reported as mixed with solid masses
61
Partial situs inversus
Is more severe disorder May develop in two different combinations of organ reversals Thoracic viscera usually reversed Abdominal viscera may or may not be reversed
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Partial situs divided into asplenia and polysplenia
Situs Inversus
63
Situs Inversus
Polysplenia represented as transposition of liver, spleen, stomach, and absence of gallbladder
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Polysplenia
At least two spleens present along greater curvature of stomach Heart block common in polysplenia syndrome
65
Situs Inversus
Cardiac malformations common (99%) in asplenia syndrome; are seen with less frequency in polysplenia syndrome (90%)
66
Cardiac defects of situs inversus
Endocardial cushion defects Hypoplastic left heart Transposition of great vessels
67
total situs inversus
usually has normal outcome
68
Mortality rate for partial situs inversus
extremely high; death occurs in 90% to 95% with asplenia syndrome and 80% with polysplenia syndrome
69
Total situs inversus
right-sided heart axis and aorta; transposition of liver, stomach, spleen; left-sided gallbladder)
70
Partial situs inversus
(right-sided stomach, left-sided liver); dextrocardia with normal stomach position (see previous section)
71
Causes of Ascites
Genitourinary Gastrointestinal Liver Cardiac Infections Metabolic storage disorders Idiopathic
72
identified in fetus when calcifications are found within gallbladder.
Cholelithiasis (gallstones)
73
Choledochal cyst (dilation of CBD) may be diagnosed when
cystic mass identified adjacent to fetal stomach and gallbladder
74
Agenesis of gallbladder occurs in approximately
20% of patients with biliary atresia
75
Absence of gallbladder can occur in association with
polysplenia and rare multiple anomaly syndromes
76
Atresias
Develop when portion of bowel grows and infarcts Occurs anywhere in gastrointestinal tract Polyhydramnios evident on ultrasound
77
Blockage results in
back-up of amniotic fluid and hydramnios
78
Esophageal Atresia
Most common form occurs in conjunction with a fistula, communicating between trachea and esophagus (tracheoesophageal fistula). allows passage of amniotic fluid into stomach
79
Esophageal Atresia
Gastric secretions may contribute to stomach fluid
80
Combination of polyhydramnios and absent stomach over repeated studies may be suggestive of
esophageal atresia
81
In \>50% of cases, stomach present because fistula usually present that leads to fluid filling stomach
Esophageal Atresia
82
Esophageal Atresia
Hydramnios may exist from impaired reabsorption of swallowed fluid and be associated with esophageal atresia; usually does not develop until third trimester
83
Esophageal Atresia
Growth restriction present in 40% of cases Chromosomal trisomies (18 and 21) reported Coexisting anomalies common in 50% to 70% of fetuses with esophageal atresia
84
Duodenal Atresia
Blockage of duodenal lumen by membrane that prohibits passage of swallowed amniotic fluid
85
Duodenal Atresia Sonographic Findings
Two echo-free communicating structures (stomach and duodenum) found in upper fetal abdomen Sonographic appearance termed “double bubble sign” Hydramnios almost always seen with duodenal atresias later in pregnancy
86
Causes of Double Bubble
Duodenal atresia Duodenal stenosis Annular pancreas Ladd’s bands Proximal jejunal atresia Malrotation Diaphragmatic hernia
87
About 30% of fetuses with duodenal atresia have
trisomy 21 (Down syndrome)
88
Anomalies occur in approximately with duodenal atresia
50%
89
Occurs in 1 in 3000 to 5000 live births; thought to be secondary to vascular accident, volvulus or gastroschisis or be sporadic
Bowel Intestinal Obstructions
90
Bowel Intestinal Obstructions
Atresia or stenosis of jejunum or ileum, or both, and small bowel atresia slightly more common than duodenal atresia
91
Blockage of jejunum and ileal bowel segments
(jejunoileal atresia or stenosis) appears as multiple cystic structures (more than two) proximal to site of atresia within fetal abdomen
92
Bowel Intestinal Obstructions
General rule: The more distal the obstruction, the less severe the hydramnios, and the later it will develop.
93
Causes of fetal small-bowel obstruction include:
Malrotation Atresias Volvulus Peritoneal bands Cystic fibrosis Dilated bowel loops isolated or associated with other anomalies, ascites, or meconium peritonitis
94
Sonographic Findings
Intestinal obstructions appear as cystic bowel loops discontinuous with stomach Fetal intestinal obstruction should be suspected when clear cystic structures found in pelvis Vascular restriction may lead to obstruction secondary to gastroschisis
95
Meconium Ileus
Is a small-bowel disorder marked by presence of thick meconium in distal ileum
96
Earliest manifestation of cystic fibrosis occurring (%)
10% to 15% of patients; is third most common form of neonatal bowel obstruction after atresia and malrotation
97
Meconium begins to accumulate in the fetal bowel in the second trimester, at which time it can be seen sonographically as tiny echogenic reflections within the peristaltic small bowel.
Meconium Ileus
98
Meconium Ileus
The anal sphincter prevents the passage of meconium (meconium plug) into the amniotic fluid, unless the fetus is stressed or traumatized.
99
Meconium Ileus Sonographic Findings
Ileum dilates because of impacted meconium (which appears echogenic) Increased production of mucus by GI organs and electrolyte imbalance explains overproduction of meconium (characteristic of cystic fibrosis)
100
Anorectal Atresia
Presents as complex disorder of bowel and genitourinary tract Imperforate anus is disorder that occurs when membrane covers anus, prohibiting expulsion of meconium
101
Hirschsprung’s Disease
Megacolon is congenital disorder in which there is abnormal innervation of large intestine
102
Meconium Peritonitis
Condition that may arise when fetus has sterile chemical peritonitis secondary to in utero bowel perforation Hydramnios present in 65% of fetuses
103
Sonographic FindingsMeconium Peritonitis
Calcifications seen on peritoneal surfaces or in scrotum via processus vaginalis Ascitic fluid may be echogenic. Is unusual to see calcification in meconium ileus in fetus with cystic fibrosis
104
Hyperechoic Bowel
Grade 1: Mildly echogenic and typically diffuse Grade 2: Moderately echogenic and typically focal Grade 3: Very echogenic; similar to that of bone structures
105
True ascites in fetal abdomen always
abnormal
106
Prognosis is
poor in nonimmune hydrops
107
Other conditions that may cause ascites to develop include bowel perforation or urinary ascites secondary to bladder rupture.
Ascites
