OB Final Images Flashcards

1
Q
A

Boy! “Turtle sign”

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2
Q
A

Long kidney. (c)=renal cortex, arrowhead=pelvis, (p)=pyramids, (r)=rib

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3
Q
A

kidneys

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4
Q

What are the markers measuring?

A

Anterior posterior diameter of the renal pelvis

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5
Q
A

keyhole bladder; enlarged bladder and urethra

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6
Q
A

Keyhole bladder; posterior urethral valve obstruction

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7
Q
A

Autosomal recessive polycystic kidney disease. A, Kidneys are enlarged with increased echogenicity

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7
Q
A

Unilateral multicystic kidney (arrows). Note the varying sizes of the cysts (c) and the normal contralateral kidney (k).

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8
Q
A

Unilateral dysplastic multicystic kidney (arrows). The contralateral kidney appear normal

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9
Q
A

Autosomal dominant polycystic kidney disease

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10
Q
A

Autosomal dominant polycystic kidney disease

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11
Q
A

Keyhole bladder, dilated ureters

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12
Q
A

Unilateral ureteropelvic junction obstruction showing collection of urine within the renal pelvis, communicating with the renal calyces

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13
Q
A

Measurement of the renal pelvic diameter is measured in the A-P direction (cursors).

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14
Q
A

Massively dilated renal pelvis (kidney) shown in a transverse plane

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15
Q
A

renal cyst ruptured, with only a small, upper-pole cyst (calipers) evident. A urinoma was suspected

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16
Q
A

Bilateral megaureters (hydroureters) (h) noted in an axial pelvic view. Partial blockage to the posterior urethra was found after birth

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17
Q
A

Posterior urethral valve syndrome, showing abnormally distended bladder with a keyhole urethra

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18
Q
A

thanatophoric dysplasia; right arm demonstrates micromelia

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19
Q
A

thanatophoric dysplasia; note the narrow thorax

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20
Q
A

Achondrogenesis

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21
Q
A

Achondrogenesis

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22
Q
A

Osteogenesis imperfecta (type II), small thoracic cavity (arrows) is shown. ABD=abdomen

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23
Q
A

Osteogenesis imperfecta; femoral fracture is shown (arrow)

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24
Q
A

Osteogenesis imperfecta; hypomineralization of the skull is evident.

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25
Q
A

Diastrophic Dysplasia; micromelia is demonstrated in this femur measurement

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26
Q
A

Camptomelic Dysplasia; bowing of the femur

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27
Q
A

Camptomelic Dysplasia; bowing of the tibia

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28
Q
A

Short-Rib Polydactyly Syndrome

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29
Q
A

Caudal Regression Syndrome/Sirenomelia

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30
Q
A

Postural Anomalies–Pena-Shokeir Syndrome

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31
Q
A

Limb anomaly–polydactyly

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32
Q
A

Polydactyly

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33
Q
A

Talipes

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34
Q
A

Omphalocele; arrows show the covering membrane projecting from the umbilical area

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35
Q
A

Gastroschisis

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36
Q
A

Abdominal ascites surrounding the small bowel (Sm); heart (h); liver (L); spine (S)

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37
Q
A

Gallbladder showing gallstones in the neonate

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38
Q
A

Meconium accumulates in the fetal bowel and is seen sonographically as echogenic reflections (notice shadowing) within the peristaltic small bowel

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39
Q
A

Fetal ascites (as) surrounds the umbilical vein (uv). Liver (l)

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40
Q
A

Ascites (as) completely surrounds the liver (L) and falciform ligament (FL). B, Bowel

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41
Q
A

Fetal heart and foramen ovale. The left atrial cavity is generally about the same size as the right atrial cavity. In utero the foramen opens toward the left atrium

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42
Q
A

Three of the four pulmonary veins (PV) enter the left atrial cavity

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43
Q
A

LVOT, aorta

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44
Q
A

LVOT

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45
Q
A

RVOT

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46
Q
A

Ductal Arch view

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47
Q
A

Umbilical cord as it exits placenta surface

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48
Q
A

Umbilical cord as it exits placenta surface

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49
Q
A

Omphalomesenteric Cyst

49
Q
A

Umbilical cord knots

50
Q
A

Nuchal Cord

51
Q
A

Single Umbilical Artery

52
Q
A

Amniotic Fluid mixed w/ partical matter or vernix

53
Q
A

Amniotic Fluid mixed w/ particla matter or vernix

54
Q
A

Premature rupture of membranes with oligohydramnios. s=spine

55
Q
A

Amniotic Band Syndrome. Entanglement of the bands around soft tissue is usually seen as an indentation of the soft tissue surrounded by edema

56
Q
A

Amniotic Sheets and Synechiae (arrow)

57
Q
A

Thanatophoric dysplasia with a clover-leaf skull or Kleeblattschädel

58
Q
A

Sagittal view of a fetus with premature closure of the metopic suture, which elongated and flattened the fetal forehead

59
Q
A

Abnormalities of the facial profile–A fetus affected by familial midface hypoplasia

60
Q
A

Abnormalities of the facial profile–A fetus with trisomy 21 (Down syndrome )

61
Q
A

Abnormalities of the facial profile–mild frontal bossing

62
Q
A

Abnormalities of the facial profile–Absent nasal bone

63
Q
A

Beckwith-Weidemann syndrome

64
Q
A

Beckwith-Weidemann syndrome

65
Q
A

micrognathia

66
Q
A

Cyclopia with a small proboscis

67
Q
A

Cystic Hygroma

68
Q
A

Large cystic hygroma

69
Q
A

Anencephaly

70
Q
A

Anencephaly

71
Q
A

Acrania

72
Q
A

Cephalocele

73
Q
A

Spina bifida w/meningocele

74
Q
A

Spina bifida w/meningomyelocele

75
Q
A

Spina bifida w/myeloschisis

76
Q
A

Meningomyelocele with the spinal splaying appearing as a V

77
Q
A

Meningomyelocele identified in a fetus; note the neural elements protruding into the sac

78
Q
A

Spina bifida with a U-shaped configuration and an open cleft in the skin

79
Q
A

Abnormally shaped cerebellum “banana sign”
Note the lemon-shaped frontal bones consistent with frontal bossing

80
Q
A

Dandy-Walker cyst. Note the splayed cerebellar hemispheres

81
Q
A

Dandy-Walker malformation (A) and ventriculomegaly

82
Q
A

semilobar holoprosencephaly

83
Q
A

Facial features of holoprosencephaly

84
Q
A

Trisomy 18=Edwards Syndrome; note the bilateral choroid plexus cysts

85
Q
A

A porencephalic cyst identified communicating with the lateral ventricle

86
Q
A

Multiple arachnoid cysts

87
Q
A

Holoprosencephaly w/ massive collection of cerebrospinal fluid

88
Q
A

Ventriculomegaly

89
Q
A

Ventriculomegaly caused by spina bifida. The anterior choroid plexus “dangles” into the posterior ventricle

90
Q
A

Longitudinal scan of the diaphragm as it separates the thoracic from the abdominal cavities

91
Q
A

Fetal chest and abdomen shows the homogeneous, moderately echogenic texture of the lungs. Lu=lungs; L=liver; d=diaphragm; h=heart

92
Q
A

Bronchogenic cyst

93
Q
A

Bronchogenic cyst

94
Q
A

Hydrothorax

95
Q
A

Bilateral pleural effusion

96
Q
A

Bilateral pleural effusion

97
Q
A

Extralobar sequestration

98
Q
A

Extralobar/pulmonary sequestration

99
Q
A

Cystic adenomatoid malformation

100
Q
A

Type I cystic adenomatoid malformation: one or more large cysts

101
Q
A

Type II: multiple cystic areas under 1 cm in size.

102
Q
A

Cystic adenomatoid malformation type III: bulky large, noncystic lesions appear as echodense masses

103
Q
A

Diaphragmatic hernia

104
Q
A

Diaphragmatic left-sided hernia

105
Q
A

Longitudinal scan of the right-sided diaphragmatic hernia; the liver (L) is seen in the thoracic cavity

106
Q
A

Velamentous placenta; If the membranes cross the internal os it is known as vasa previa

107
Q
A

Subchorionic cyst w/ internal echoes, representative of blood flow (f); Amniotic fluid (A); placenta (p)

108
Q
A

Transverse image of the placenta as it lies along the anterior uterine wall. Sonolucencies are seen representing placental lakes (arrows).

109
Q
A

Vasa Previa–succenturiate lobe anterior (arrow) and main placenta posterior (currved arrow)

110
Q
A

Vasa Previa–Transvag image reveals fetal vessal (arrow) crossing the cervical os.

111
Q
A

Placenta accreta, increta and percreta–Sonographically, the hypoechoic myometrium will appear thinned or absent with adjacent, irregular sonolucencies in the placenta

112
Q
A

Placenta accreta, increta, and percreta–placenta and bladder. Arrows showing hypoechoic vascular lacunae; curved arrow is pointing at loss of subplacental hypoechoic zone

113
Q
A

Placenta accreta, increta, and percreta–color Doppler shows vessels in the thinned subplacental zone (curved arrow)

114
Q
A

Succenturiate placenta

115
Q
A

Circummarginate Placenta

116
Q
A

Ultrasound showing an abruption. Arrows point to the echolucent collection of blood lateral to the edge of the placenta. P, Placenta

117
Q
A

Retroplacenta abruption–Hematoma seen separating the placenta (arrow) from the uterine wall (curved arrow)

118
Q
A

Marginal Abruption; subchorionic bleed can be seen arising from the edge of the placenta (arrow)

119
Q
A

Hydatidiform mole

120
Q
A

Partial mole

121
Q
A

Chorioangioma

122
Q
A

Chorioangioma