#4. Congenital Diseases Flashcards

1
Q

What are the Embryonic Stages of Kidney Development?

A

3 Phases:
1) Pre-Kidney = Pronephros
2) Primary Kidney = Mesonephros

3) Definitive Kidney = Metanephros (By 3rd Embryonal Month)

  • Kidney tubules are formed from it
  • Calcyces / Pelvis / Ureter are formed by UPWARD Movement of LOWER End of WOLF’S DUCT, which connects to the METANEPHROS
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2
Q

When and Where do the Testes from in Embryonic Development?

A
  • Occurs at a Later Stage due to MOST GONAD Structures belonging to OTHER Systems
  • By 3rd Month = Testes is located in Retroperitoneum and undergoes DESCENSUS where Testes moves towards Scrotum with help of FIBROMUSCLAR BOND (Gubernaculum)
  • Around 7th Month = Testes is at Abdominal Opening of Inguinal Canal
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3
Q

What are the Differences between Renal Agenesis, Aplasia, and Hypoplasia?

A

1) Renal Agenesis = Mother’s Kidneys purifies Foetal blood via Placenta and is manifested by Anuria

2) Renal Aplasia = Failure Development of Kidney, with Fibrous Mass occupying place of Kidney / Contralateral Kidney (Opposite Side) is Hypertrophied

3) Renal Hypoplasia = Smaller Kidneys, combined with other anomalies

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4
Q

What does the term “malrotation” mean?

A
  • Incomplete Intrauterine Rotation
  • Where Renal Pelvis lies VENTRALLY + EXTERNALLY to the Kidney
  • Normally = Renal Pelvis lies MEDIALLY to Kidney
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5
Q

What are the Forms of Dystopia?

A

{Dystopia = Kidney located to SAME Side, to where it normally should be)

  • Pelvic
  • Iliac
  • Lumbar
  • Thoracic
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6
Q

What Other Diseases is Horseshoe Kidney Associated with?

A

{Horseshoe Kidney = Kidney fused at their lower poles by Parenchymal / Fibrous Bridge)

  • Turner Syndrome
  • Trisomy 18
  • GU Anomalies
  • Duplication of Ureter
  • Vesicoureteral Reflux
  • Congenital Hydronephrosis
  • Wilms Tumour
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7
Q

Where are the Blood Vessels located in Nephroptosis?

A

{Nephroptosis = Weak Supporting Apparatus / Long Vessels; Standing px feel pain}

  • Blood Vessels are located in their NORMAL Position
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8
Q

After what does the Incidence of Simple Cysts Increase?

A

{Simple Cysts = Obstruction of Group of Nephrons}

  • AFTER AGE 50 the Incidence INCREASES to 50%
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9
Q

What is the Practical Use of Bosniak Classification?

A
  • Studied by Venous Contrast-Enhanced CT
  • Improves the degree of precision of malignant diseases
  • To reduce the frequency of unnecessary treatment of Benign Lesions

TYPES - Wall Thickness / Presence, Absence of Septa + Calcifications on Contrast / % of Malignancy
- Type 1
- Type 2, 2F
- Type 3
- Type 4

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10
Q

By What Mechanism of Polycystic Kidney Disease Inherited in Adults?

A
  • Autosomal DOMINANT Inheritance
  • 95% = Cystic Lesions affects BOTH Kidneys
  • 10 - 30% = Brain Aneurysms
  • 33% = Liver Cysts
  • 10% = Pancreatic Cysts
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11
Q

What is the Difference between a Duplicated and Bifid Ureter?

A

1) Duplicated Ureter = The LOWER Ostium drains the Ureter, which originates from PROXIMAL Part of Renal Pelvis

2) Bifid Ureter = The 2 Ureters JOIN at the Pelvis and END into 1 Ostium

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12
Q

What Imaging Method allows to Detect Vesicoureteral Reflux?

A

{Vesicoureteral Reflux = Functional Damage to the LOWER UT without Morphological Cause}

  • Ultrasound
  • CT
  • MRI
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13
Q

What are the Characteristics of Bladder Exstrophy?

A
  • Separation of Symphysis
  • Atrophy of Rectus Abdominis Muscles
  • Complete Absence of Anterior Bladder Wall / Anterior Part of Bladder Neck / Urethra
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14
Q

What are the 3 Characteristics of Hypospadias?

A

1) Displacement of Urethral Meatus along the Ventral Surface of the Penis / Scrotal / Perineal

2) Ventral Distortion DUE to Formation of CHORDAE

3) Absence of Ventral Part of the Foreskin

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15
Q

Which anomaly, hypospadias or epispadias can be seen in both sexes?

A

Epispadias are seen in BOTH Sexes

  • Boys = Glandular, Penile and Complete
  • Girls = Clitoric, Subsymphyseal and Complete
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16
Q

Which form of Hypospadias is only a cosmetic defect and does NOT affect the penis in terms of suction?

A

Types
1) Distal / Anterior = Glandular + Coronal = ONLY for Cosmetic Effect

2) Medium / Median = Corporal

3) Proximal / Posterior = Scrotal + Perineal

17
Q

What are the Options for Conservative Treatment of Primary Phimosis?

A
  • Corticosteroid Treatment = BETAMETHASONE
  • Applied for 4 - 6 Weeks
18
Q

What is the Incidence of Cryptorchidism?

A

{Cryptorchidism = Retained Testes / NO Descending into Scrotum}

  • 4% = Born with Undescended Testes
  • 1.5% = By the end of their 1st Year
19
Q

What are the Complications of Cryptorchidism?

A
  • 8x HIGHER Risk = Testicular Carcinoma
  • Reduced Fertility = IF Surgery is performed BEFORE 2 Years of Age, Fertility Potential INCREASES
  • Testicular Torsion
  • Indirect Inguinal Hernias
20
Q

At what age is the Surgical Treatment of Cryptorchidism most appropriate?

A

ORCHIDOPEXY = Fixing Testicle in the Scrotum

  • Recommended to do it at 12 - 18 months of age
21
Q

Do Retractile Testicles require treatment?

A

{Retractile Testes = INCREASED Cremasteric Reflex; Testes are found in Inguinal Canals}

  • NO, does NOT require treatment
22
Q

In a Communicating Hydrocele, which symptoms are most likely to be observed by Parents?

A
  • Retracts in SUPINE Position
  • Enlarges on Palpation in UPRIGHT Position / When Crying
23
Q

In Sex Chromosome Mosaicism, what changes can be found in the Genitals?

A

Multiple Variants = 45X, 45X/46XY, 47XXY

  • 1 Half of Scrotum contains Gonad / Testicle
  • Other Side of Scrotum is more of a Labia Majora