PaedsImagingQuizzesMZeba
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Dedicated for practice quizzes about Pediatric Imaging.
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Mesoblastic Nephroma

πŸŒ€Solid tumor of infancy, born with it
πŸŒ€Antenatal USG: ~Polyhydroamnios
πŸŒ€No invasion of;
βž–Collecting system
βž–Venous system
πŸŒ€Often involve renal sinus

MZeba
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Forwarded from MZeba
Crack2022
NAI#

🦴 LL#in non ambulantπŸ‘Ά
🦴 Metaphyseal corner/πŸͺ£ handle#
🦴Multiple#of Different age
🦴Scapula#
🦴Post rib#
🦴Sternal#
🦴Non parietalπŸ’€/#crossing suture

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IMAGING IN PEDIATRICS

Day1⃣ : Pedia MSK
πŸ“šCore(old): page 802-824
πŸ“šCrack: Section 13,14
πŸŽ₯ https://www.youtube.com/playlist?list=PLsYxTl3AgoMP02IMOdHsmuhoBdR90vOJG

Day2⃣ : Pedia GUT
πŸ“šCore(old): 791-801
πŸ“šCrack: Section 9,10,11&12
πŸŽ₯ https://www.youtube.com/playlist?list=PLsYxTl3AgoMMOE3DStypi7Jj_Cb8pHjrO

Day3⃣: Pedia GIT
πŸ“šCore(old): 770-790
πŸ“šCrack: Section 7,8
πŸŽ₯ https://www.youtube.com/playlist?list=PLsYxTl3AgoMPoNytJrmfegJBW80H1reIV

Day4⃣: Pedia Airway,πŸ’™& Chest
πŸ“šCore(old): page 742-769
πŸ“šCrack: Section 4,5,6
πŸŽ₯ https://www.youtube.com/playlist?list=PLsYxTl3AgoMN4Vkfr4K7AXoFqc4IbTpB3

Day5⃣: Pedia CNS
πŸ“šCore(old):825-835
πŸ“šCrack: Section 1,2 & 3
πŸŽ₯ https://www.youtube.com/playlist?list=PLsYxTl3AgoMP_rrHW10XCQoBYOHCRKaQ2



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#FRCR2B2024

Teaching files / Case Reviews
1️⃣ MZeba Playlist https://youtube.com/playlist?list=PLsYxTl3AgoMP0Zf3bmnhfSH-F8ABOGr8t

2️⃣ https://youtube.com/playlist?list=PLYcjsMRiuBVBcpJHZBSyKxbxhmS6Deugz

3️⃣

4️⃣

5️⃣
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Forwarded from FRCR 2B 2023/2024
TF#24
Pleuropulmonary Blastoma

πŸ’ŽBig chest mass 1-2Y, R>L, Pleural based
πŸ’ŽCystic type B9 younger kid
πŸ’ŽSolid type older kid, met to 🧠🦴
πŸ’ŽNo calcification, no rib erosion
πŸ’Ž 10% associated with MLCN

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OI
πŸ”ŽTotal lucent skull πŸ’€
πŸ”ŽMultiple fractures with hyperplastic callus
πŸ”ŽFibula longer than Tibia
πŸ”ŽWormian 🦴
πŸ”ŽBlue sclera
πŸ”ŽOtosclerosis
CTC#132
MZeba
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*Replogle tube*
🏎️ Used in esophageal atresia
🏎️ A double lumen tube which [in contrast to an NGT] has a number of side holes.
🏎️ The Replogle tube rests in the proximal oesophageal pouch to simultaneously irrigate and aspirate secretions/debris.

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Caffey Disease

πŸ’ŽSelf limiting within 6M of life
πŸ’ŽClassic:Hot mandible on bone scan
πŸ’ŽMandible,clavicle &Ulna
πŸ’ŽFever, irritability, periosteal rxn
πŸ’ŽCoarse,irregular,asymmetric periosteal rxnβž•soft tissue swelling over affected areas.

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ARPCKD Associations
1. Caroli disease
2. Congenital hepatic fibrosis: the degree of which is inversely proportional to the age of presentation
3. Multiple biliary hamartomas

(Radiopedia)
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PaedsImagingQuizzesMZeba pinned Β«PeadsπŸ‘¦ SBA Quizzes by MZeba --- MSK 🦴 1. http://t.me/QuizBot?start=7ZCBYEft 2. http://t.me/QuizBot?start=NYWP8qEz 3. http://t.me/QuizBot?start=7GHDWxhm --- 🧠 CNS 1. http://t.me/QuizBot?start=aPOzhCrg 2. http://t.me/QuizBot?start=k3VsR5Vu --- Chest 🫁 …»
HPS
βš€ Idiopathic, hypertrophy &hyperplasia= circular muscle pylorus
⚁ 1st borns, 2-12wk, projectile vomiting, olive shape mass β™‚>♀
βš‚ XR: πŸ›sign
βšƒ USG; ++gastric peristalsis, pyloric canal fail to open,
Pyloric canal leng➑14mm,
Pyloric canal  diameter➑11mm
Muscle wall thick➑4mm
βš„ Paradoxical aciduria.

MZeba

πŸ₯§ Ο€: 3.1415
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Imaging of Nephroblastomatosis:

πŸŒ€Nephrogenic Rests: May precede Wilms tumor.
πŸŒ€Age Factor: Rare after 7 years old.
πŸŒ€Symptoms: Usually asymptomatic or presents as a flank mass.
πŸŒ€Associated Syndromes:
πŸ”ΈHemihypertrophy,
πŸ”ΈBeckwith-Wiedemann syndrome,
πŸ”Έtrisomy 18,
πŸ”Έsporadic aniridia.
πŸŒ€Progression: Most regress spontaneously; up to 33% may develop Wilms tumor.
πŸŒ€Screening: Ultrasound (US) every 3 months until age 7.
πŸŒ€US Appearance: Hypoechoic or isoechoic to renal parenchyma.
πŸŒ€CT Appearance: Homogeneous, low attenuation; enhances less than normal renal tissue.

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Wormian Bones Causes:

P: yknodysostosis
O: osteogenesis imperfecta
R: rickets
K: kinky hair syndrome
C: cleidocranial dysostosis
H: hypothyroidism/hypophosphatasia
O: otopalatodigital syndrome
P: primary acroosteolysis (Hajdu-Cheney)/pachydermoperiostosis/progeria
S: syndrome of Downs

(Radiopedia)

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Multicystic Dysplastic Kidney (MCDK)

πŸŒ€Etiology: Often due to ureteral atresia or ureteropelvic junction obstruction in utero.
πŸŒ€Approximately 50% of cases show complete involution by age 7.
πŸŒ€Treatment: Resection is only necessary for complicated cases.
πŸŒ€Contralateral Kidney: Always check to rule out pathology; ~50% of cases have contralateral abnormalities: VUJ obstruction, VU reflux.

Imaging Findings:
πŸŒ€USG:
βž–Multiple non-communicating cysts of varying sizes with no intervening renal parenchyma.
βž–Normal renal cortex is not visualized.
πŸŒ€MAG 3
βž–No uptake or excretion in the affected kidney.


πŸŒ€DD:
βž–Distinguish from multilocular cystic nephroma, which typically does not involve the entire kidney
βž–Hydronephrosis: Communicating cysts with a larger cyst in the center.


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NEC

Stage I
πŸŒ€Intestinal dilatation
Treatment
.. Oral feeding cessation
.. Parenteral nutrition
.. NGT suction
.. Antibiotics
Stage II
πŸŒ€ Intestinal dilatation
πŸŒ€PV gas
πŸŒ€ Pneumatosis intestinalis

Treatment
βž•
Correction of metabolic acidosis

Stage IIIa:
πŸŒ€Shock
πŸŒ€Ascites

Treatment
Same as in stage II


Stage IIIb
πŸŒ€ Perforation
πŸŒ€ Pneumoperitoneum

Treatment: Surgery

(Radiopedia)

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Midgut Volvulus:

πŸŒ€Radiologic Emergency.
πŸŒ€Associated Conditions:
βž–Congenital diaphragmatic hernia,
βž–gastroschisis
βž–omphalocele.
πŸŒ€Cecum Position: Malrotation often involves an abnormal cecal position, but a normal enema does not rule out malrotation.
πŸŒ€Cross-Sectional Imaging:
βž–Abnormal SMA and SMV relationship; SMV should be anterior and to the right of SMA.
βž–Whirlpool sign of twisted mesentery
πŸŒ€On UGI study:
βž–corkscrew sign
βž–tapering or beaking of the bowel in complete obstruction
βž–malrotated bowel configuration


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Choanal Atresia:
πŸŒ€Two types: Bony (90%) and Membraneous (10%)
πŸŒ€It’s usually unilateral (65%)
πŸŒ€There is a known association with early
pregnancy use of anti thyroid drugs.
πŸŒ€There are multiple syndromes associated with this - the big one to know is CHARGE (Coloboma.
Heart Defects, Atresia - Choanal, Retardation.
Genital Issues, Ear Problems

(Source: CTC-CC)
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CPAM
πŸŒ€Best Imaging Modalities
βž–Prenatal: USG (first-line) – Cystic/hyperechoic lung lesion, MRI for better differentiation.
βž– Postnatal: Chest X-ray (cystic/solid lung mass), CT chest (Gold Standard) – Defines cystic vs. solid components, surgical planning.
πŸŒ€CPAM Types (Stocker Classification)
βž–Type 1 (Most common, 70%) – Large air-filled cysts (>2 cm).
βž–Type 2 (20%) – Small cysts (<2 cm), mixed solid-cystic.
βž–Type 3 (10%) – Solid, microcystic mass-like.
βž–Type 4 (Rare) – Large cystic, mimics pneumothorax.
πŸŒ€Differentiation on Imaging
βž–CPAM vs. BPS: CPAM lacks systemic arterial supply (confirm with CT angiography).
βž–CPAM vs. CDH: CPAM has no bowel loops in thorax (unlike diaphragmatic hernia).
πŸŒ€Complications
βž–Infection: Air-fluid levels in cysts.
βž–Malignancy Risk: Rare (e.g., pleuropulmonary blastoma).
βž–Hydrops Fetalis: Seen in large prenatal lesions.
πŸŒ€Management
βž–Small/asymptomatic: Follow-up imaging.
βž–Large/symptomatic: Surgical resection to prevent complications. MZeba
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