Most Common Page 5 Flashcards

1
Q

MC childhood tumor to metastasize to the liver

A

neuroblastoma (followed by lymphoma, leukemua, and Wilm’s tumor)

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2
Q

MC causes of splenomegaly in the newborn and young infant

A

bacterial sepsis and infection

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3
Q

MC endocrine tumor

A

benign islet cell adenoma (insulinoma

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4
Q

MC malignant tumor of the small intestine

A

non-Hodgkin lymphoma

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5
Q

MC colon lesions

A

inflammatory polyps or polyps associated with one of the colonic polyposis syndromes

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6
Q

MCC of pneumoperitoneum in the NICU

A

necrotizing enterocolitis

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7
Q

MCC of secondary peritonitis in children

A

perforated appendix

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8
Q

m MC type of peritoneal TB

A

wet type

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9
Q

MCC of peritoneal calcification in the neonate

A

meconium peritonitis

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10
Q

MC type of vasculolymphatic malformation to affect the peritoneal cavity and mesentery

A

lymphatic malformations (formerly known as lymphangiomas)

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11
Q

MCC of pseydomyxoma peritonei

A

rupture of appendiceal mucinous adenoma

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12
Q

MC anterior abdominal wall defect

A

gastroschisis (2nd MC: omphalocele)

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13
Q

MC sites of primary malignant mesenchymoma

A

retroperitoneum or thigh

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14
Q

MC complication of a choledochal cyst

A

ascending cholangitis

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15
Q

MCC of neonatal cholestasis, primary indication for pediatric liver transplantation

A

biliary atresia

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16
Q

MCC of pancreatitis (in children)

A

idiopathic or posttraumatic

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17
Q

MCC of chronic liver disease in pediatric patients

A

hepatic steatosis

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18
Q

MC site of duplications after the ileum

A

esophagus

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19
Q

MC neurologic abnormality resulting to swallowing disorders in infants and children

A

cerebral palsy

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20
Q

MC location where coins typically lodge

A

thoracic inlet

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21
Q

MCC of food bolus impaction in children

A

eosinophilic esophagitis

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22
Q

MC finding of eosinophlic esophagitis

A

normal

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23
Q

2nd MC GI manifestation of CMV infection after colitis

A

esophagitis

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24
Q

Most commonly ingested foreign body

A

coins

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25
Q

MC location of congenital gastric diverticula

A

posterior wall

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26
Q

MC heterotopia in the GIT

A

ectopic pancreas

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27
Q

MC surgical entity affecting infants during the 1st 6 months of life

A

hypertrophic pyloric stenosis (HPS)

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28
Q

MC antropyloric abnormality mimicking HPS on an UGIS

A

pylorospasm

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29
Q

MC location of gastric perforations

A

high in the stomach along the greater curvature

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30
Q

3 MC bezoar types

A

trichobezoars, phytobezoars, lactobezoars

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31
Q

MC smooth muscle neoplasm arising in the GIT (but very rare outside of the esophagus

A

nd rectosigmoid) polypoid leiomyomas

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32
Q

MC gastric tumors in children

A

polyps

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33
Q

MC associated neoplasm in Meckel’s diverticulum

A

carcinoids

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34
Q

MC presentation of Meckel diverticulum

A

painless rectal bleeding

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35
Q

MC location of lymphatic malformations in the mesentery

A

ileal mesentery

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36
Q

MCC of duodenal injury

A

non-accidental trauma

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37
Q

MC finding in an acute duodenal ulcer

A

contrast within an ulcer crater

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38
Q

MCly associated systemic abnormality in patients w/ duodenal adenomatous polyps

A

FAP

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39
Q

MC abnormality on barium studies in patients with HIV enteropathy

A

nonspecific edema

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40
Q

MC extraintestinal condition of Crohn disease in the pediatric population

A

arthritis

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41
Q

MC abdominal radiograph finding in patients with IBD

A

absence of stool in the involved portions of the colon

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42
Q

Most commonly affected GI segment in patients with Behcet syndrome

A

ileocecal area

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43
Q

MCC of intestinal malabsorption in childhood

A

celiac disease (aka nontropical sprue / gluten enteropathy)

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44
Q

MC vasculitis of childhood (2-6 yo)

A

Henoch-Schonlein purpura

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45
Q

Most commonly involved location of Peutz-Jeghers syndrome

A

small bowel (exception siya sa mga polyposis syndromes kasi in general, colon iyong primary site of involvement

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46
Q

MC location of Burkitt lymphoma

A

terminal ileum (high concentration of lymphatic nodal tissue)

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47
Q

MC subtye of non-Hodgkin lymphoma that occurs in children

A

Burkitt lymphoma

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48
Q

MC cardiovascular abnormalities in anorectal malformation

A

ASD and PDA, followed by TOF and VSD

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49
Q

Hirschsprung diease is most commonly associated with?

A

Down syndrome

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50
Q

MC newborn surgical emergency

A

NEC

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51
Q

MC underlying malignancies in pediatric patients with neutropenic colitis

A

ALL and AML

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52
Q

MC site of neutropenic colitis

A

cecum (hence, typhlitis)

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53
Q

MC area to twist in colonic volvulus in children

A

cecum (in adults, sigmoid colon)

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54
Q

MC neoplasm of the colon

A

juvenile polyps

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55
Q

MC intestinal tumors in childhood

A

isolated juvenile or hamartomatous polyp

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56
Q

MC location of juvenile or hamartomatous polyps

A

sigmoid colon and rectum

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57
Q

MC of the hamartomatous syndromes

A

juvenile polyposis syndrome

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58
Q

MC subtype in sporadic cases of pediatric colon cancer

A

mucinous ca

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59
Q

MC site of carcinoid tumor involving the GIT

A

appendix

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60
Q

MC type of interrupted aortic arch

A

type B (between the left common carotid and left subclavian arteries)

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61
Q

MC CHD in NF1

A

pulmonary stenosis

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62
Q

2nd MC genetic anomaly associated with CHD after Down syndrome

A

Noonan syndrome

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63
Q

Pneumopericardium is most often seen in?

A

premature infants who undergo positive pressure ventilation

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63
Q

MCC of cardiomegaly in an acyanotic patient with increased pulmonary vascularity

A

VSD

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63
Q

MC identifiable causes of pericardial effusion in children

A

infectious and iatrogenic

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64
Q

MC cardiac malformation in fetal alcohol exposure

A

VSD

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65
Q

MCC of congenital aortic stenosis

A

bicuspid aortic valve

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65
Q

MC risk factor for pulmonary embolism in children

A

catheter thrombosis

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66
Q

MC bacterial infection presenting as multiple bilateral alveolar opacities (same din sa adults)

A

adults) staphylococcal

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67
Q

MCC of lobar pneumonia throughout childhood (same sa adults)

A

Strep pneumoniae

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68
Q

MCC of acute peribronchial opacities

A

viral respiratory infections

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69
Q

MC associated CHD in the presence of congenital lung hypoplasia

A

TOF or persistent truncus arteriosus

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70
Q

MCC of bilateral pulmonary hypoplasia

A

compression of the lungs during fetal development

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71
Q

MCC of intrathoracic compression of the fetal lungs

A

congenital diaphragmatic hernia

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72
Q

MCC of extrathoracic compression of the fetal lungs

A

oligohydramnios

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73
Q

MCC of bilateral overaeration of the lungs

A

airway obstruction

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74
Q

MCC of widespread obstruction of the peripheral airway which is a common cause of obstructive emphysema

A

viral bronchitis and bronchiolitis or asthma

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75
Q

MCC of obstructive emphysema in older infants and children

A

endobronchial foreign body or mucous plug

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76
Q

Mucous plugs occur most commonly in

A

asthmatics and children with viral LRTI (see above, similar lang)

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77
Q

Unilateral pleural effusions are most commonly associated with

A

pneumonia

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78
Q

MCC of massive pleural effusion in the neonate / MCC of congenital hydrothorax

A

chylothorax

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79
Q

MC pulmonary “mass” in children

A

pseudomass caused by a spherical pnueumonia

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80
Q

MC true lung masses

A

postinflammatory granulomas (TB or fungal)

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81
Q

MC malignant neoplasm in the lung during childhood whether single or multiple

A

metastasis

82
Q

MC childhood tumors to metastasize to the lungs

A

Wilms tumor, Ewing sarcoma, osteosarc, rhabdomyosarc

83
Q

MC tumors with pulmonary metastasis in children

A

osteogenic sarcoma, Wilms tumor

84
Q

MC site of metastatic disease in children with Wilms tumor

A

lung

85
Q

MCC of an apparent anterior mediastinal mass

A

thymus gland

86
Q

MC middle mediastinal mass

A

lymphadenopathy

87
Q

MC malignancies to involve the chest wall in children

A

Ewing sarcoma and Askin tumor

88
Q

2nd MC primary malignancy that occurs in the chest wall in children

A

rhabdomyosarcoma

88
Q

MCC of symptomatic partial upper airway obstruction in INFANTS

A

laryngomalacia

89
Q

MCC of upper airway obstruction in children from 6 mo to 3 yrs of age

A

croup / laryngotracheobronchitis

90
Q

MC benign neoplasm to affect the larynx in children

A

recurrent respiratory papillomatosis

91
Q

MC primary neoplasm affecting the subglottic trachea

A

hemangioma

92
Q

MC type of tracheal agenesis

A

Type 2

93
Q

MC malignant lower large airway primary neoplasm

A

carcinoid tumor

94
Q

Most commonly affected segmental bronchus in bronchial atresia

A

apicoposterior segmental bronchus of the LUL

95
Q

MCC of pulmonary infections in infants and young children

A

RSV (2nd mcc: human metapneumovirus/HMV)

96
Q

MCC of bacterial pneumonia

A

Strep pneumoniae

97
Q

MC primary benign pulmonary neoplasm (although rare in children)

A

hamartoma

98
Q

MC tumorlike abnormality in the lungs of children

A

plasma cell granuloma

99
Q

MC primary lung malignancies in children

A

pleuropulmonary blastoma and carcinoid tumor

100
Q

MC bronchogenic ca in children

A

adenoca

101
Q

MC genetic disorder causing chronic pulmonary disease in children

A

cystic fibrosis

102
Q

MC findings in the chest in the case of collagen vascular diseases

A

pleural and pericardial effusions

103
Q

MCC of acquired extensive cystic lung disease in children

A

LCH

104
Q

MC drugs associated with pulmonary toxicity

A

chemotherapeutic agents

105
Q

MCC of accidental death in children

A

MVA then drowning

106
Q

Diffuse pulmonary calcifications are most commonly seen after

A

varicella infection

107
Q

MC location of chest masses in the pediatric population

A

mediastinum

108
Q

MC location of thymic cyst

A

lateral infrahyoid neck

109
Q

MC type of Non-Hodgkin lymphoma

A

lymphoblastic or T cell

110
Q

MC subtype of Hodgkin lymphoma

A

nodular sclerosing

111
Q

Least differentiated (hence most malignant) and MC of the tumors arising from the sympathetic chain

A

neuroblastoma

112
Q

Most commonly affected bone of the chest wall in TB infections

A

rib

113
Q

MC tumor of childhood

A

infantile hemangioma

114
Q

MC chromosomal abnormality that is associated with a Morgagni hernia

A

Down syndrome

115
Q

MC tumor found in the diaphragm

A

rhabdomyosarcoma

116
Q

MC neural tube defect

A

meningomyeloceles (associated with Chiari 2 malformation)

117
Q

MC MRS findings in neonates with neurologic and developmental abnormalities

A

elevated lactate and diminished NAA

118
Q

MC type of vein of Galen

A

choroidal type with innumerous connections

119
Q

MC imaging finding in persons with meningitis

A

ventricular enlargement (resulting from impaired CSF absorption by fibrinous inflammatory exudate)

120
Q

MC imaging findings in the neonate with candida

A

multiple microabscesses within the subcortical and periventricular regions and basal ganglia

121
Q

MC commisural malformation

A

callosohippocampal agenesis

122
Q

MCC of macrocephaly in infants

A

benign extraaxial collections of infancy / BESS / benign external hydrocephalus / benign macrocrania / benign subdural effusion of infancy

123
Q

Most commonly involved locations in MELAS syndrome

A

basal ganglia and parietal and occipital lobes

124
Q

MC form of pediatric CNS infection

A

bacterial meningitis

125
Q

MC causative organisms of bacterial meningitis in infants older than 1 mo

A

HIB, Strep pneumonia

126
Q

MC solid pediatric tumors

A

brain tumors

127
Q

Most commonly used parameter in evaluation of brain tumors

A

CBV

128
Q

Most commonly involved vessels in sickle cell disease

A

proximal MCA or distal ICA branches

129
Q

2 MCC of intractable focal epilepsy

A

malformations of cortical development and brain tumors (hippocampal sclerosis is
less common in children compared with adults)

130
Q

Most commonly involved bones in skull fractures

A

parietal and occipital bones (followed by frontal and temporal bones)

131
Q

Most commonly involved bone in basilar fractures

A

temporal bone

132
Q

MC location of traumatic SAH

A

posterior interhemispheric fissure and along the tentorium

133
Q

MCC of extracranial carotid artery injury in children

A

intraoral trauma

134
Q

MC vertebral anomalies seen with OEIS (omphalocele-exstrophy-imperforate anus- spinal defects) and VACTERL

A

spinal defects) and VACTERL hemivertebrae or butterfly vertebrae

135
Q

MC site of intradural lipomas

A

cervicothoracic or thoracic

136
Q

MC site of transverse myelitis

A

midthoracic spine

137
Q

MC site of simple posterior meningocele

A

thoracic spine

138
Q

MC site of neurenteric cyst

A

thoracic

139
Q

MC site of discitis and osteomyelitis

A

midlumbar spine

139
Q

MC site of split cord malformation

A

lumbar

139
Q

MC reason for newborn spinal US imaging

A

simple coccygeal pimples

139
Q

Perhaps the MC entity within the caudal cell mass dysplasia spectrum

A

tethered cord syndrome

139
Q

MC parasitic infection within the spinal cord

A

cysticercosis

139
Q

MC etiologic organism in discitis and osteomyelitis

A

Staphylococcal aureus

140
Q

Most commonly affected bones in chronic recurrent multifocal osteomyelitis

A

metaphyses of long bones and the medial clavicles

140
Q

MCC of acute motor paralysis in children

A

GBS or acute inflammatory demyelinating polyradiculoneuropathy

140
Q

What segment of the spinal cord is spinal MS predominant?

A

cervical

140
Q

MC location of intramedullary tumors

A

cervicothoracic

140
Q

MC site of CSF mets

A

distal thecal sac (most dependent?)

141
Q

MC AVM in the pediatric population

A

glomus spinal cord fast-flow AVM

141
Q

MC locations of gangliogliomas

A

temporomesial (50%) or temporolateral (29%)

141
Q

Physiologic periosteal new bone (infants 1-4 mos) is MC in the?

A

tibia, femur, and humeral diaphysis

141
Q

MC site of local cortical thickening

A

deltoid insertion at the lateral aspect of the humeral diaphysis

141
Q

MC spinal anomaly in the fetus

A

dysraphism of posterior elements in a neural tube defect

141
Q

MC fetal MSK tumor

A

sacral teratoma

141
Q

MC tumor in the newborn infant

A

sacrococcygeal teratoma

141
Q

MC hemimelia / MC congenital anomaly of the fibula

A

fibular hemimelia

141
Q

MC fusions in tarsal coalition

A

talocalcaneal and calcaneonavicular

141
Q

MC carpal fusion

A

lunate and triquetrum

141
Q

Most commonly identified congenital abnormality of the elbow

A

congenital radial head dislocation (posterior - MC)

141
Q

MC direction of radial head dislocation (in general)

A

anterior

141
Q

MC serious complication of hip reduction

A

epiphyseal osteonecrosis

142
Q

MCC chronic MSK pain in youths / MC chronic musculoskeletal disease of childhood

A

juvenile idiopathic arthritis (JIA)

142
Q

Most frequently affected joint in JIA

A

knee > ankle

142
Q

MCC of childhood pain

A

transient synovitis

142
Q

Most frequently affected in juvenile dermatomyositis

A

muscles of the scapular and pelvic girdles

142
Q

MC location for hematogenous osteomyelitis

A

about the knee - distal femur, proximal tibia

142
Q

MC location for direct inoculation osteomyelitis

A

foot / calcaneus

142
Q

MC fibrous tumor of infancy

A

infantile myofibromatosis

142
Q

MC locations of rhabdomyosarcoma

A

H&N and GUT

142
Q

MC malignancy associated with NF1

A

malignant peripheral nerve sheath tumor

142
Q

MC pediatric bone tumor

A

osteochondroma

142
Q

MCC of insufficient bone matrix (osteoid) formation

A

osteogenesis imperfecta

143
Q

MC and most well-recognized finding of hypervitaminosis A

A

long bone hyperostosis

143
Q

MC form of heavy metal poisoning

A

lead poisoning

143
Q

Most prevalent heritable lysosomal storage disorder

A

Gaucher disease

143
Q

MC radiographic abnormality of Gaucher disease

A

Erlenmeyer flask deformity

143
Q

MC finding in leukemia

A

osteopenia

143
Q

MC site of buckle fractures in children

A

distal radius

143
Q

MC Salter Harris fracture type

A

type II

143
Q

Most frequently fractured carpal bone

A

scaphoid > triquetrum

143
Q

MC metacarpal fracture in adolescents

A

fifth metacarpal (boxer’s fracture)

144
Q

MC hip disorder affecting the adolescent population

A

slipped capital femoral epiphysis (Salter Harris I)

144
Q

MC sites for apophyseal avulsion injuries

A

pelvis and knee

144
Q

MC location of osteochondritis dissecans

A

knee (lateral aspect of the medial femoral condyle - MC)

144
Q

MC location of osteochondritis dissecans in the elbow

A

capitellum

144
Q

MC site of symphalangism

A

5th ray of the hand and foot

144
Q

MC pathologic cause of amenorrhea

A

PCOS

144
Q

MC epithelial cell ovarian neoplasm

A

cystadenoma

144
Q

MC stromal/mesenchymal origin ovarian tumor

A

granulosa/theca cell tumor

144
Q

MC group of malignant ovarian tumours

A

GCTs

145
Q

MC malignant ovarian tumours / 2nd MC pediatric ovarian neoplasm

A

dysgerminoma

145
Q

MCC of abnormal sex differentiation in females

A

congenital adrenal hyperplasia

145
Q

MC benign cystic lesion in the phalanges

A

enchondroma

145
Q

Probably the mc bone lesion encountered by radiologists

A

non-ossiying fibroma, aka fibroxanthoma, fibrous cortical defect

145
Q

s MC primary malignant bone tumor

A

Osteosarcoma

145
Q

MC fracture that is associated with a perilunate dislocation

A

transscaphoid fracture

145
Q

MC carpal bone with avascular necrosis

A

lunate

145
Q

Spondylolisthesis associated with bilateral defects of the pars interarticularis occurs most frequently at this level

A

L5-S1

145
Q

Degenerative spondylolisthesis secondary to facet OA occurs at __ in 90% of cases

A

L4-L5

145
Q

Most common site of dislocation in children

A

Elbow joint

145
Q

Most commonly fractured of all the long tubular bones

A

Tibia

145
Q

MC locations of chondrocalcinosis in CPPD

A

medial and lateral compartments of the knee, TFCC, symphysis pubis

145
Q

MC locations of osteochondritis dissecans

A

medial epicondyle of the knee > dome of the talus > capitellum of the elbow