Pediatric Surgery Practice Questions

Q: Most common congenital diaphragmatic hernia is:

Bochdalek hernia. ***Bochdalek hernia*** - This is the most common type of **congenital diaphragmatic hernia (CDH)**, accounting for approximately **95% of all CDH cases**. - It occurs due to a defect in the **posterolateral diaphragm** (pleuroperitoneal membrane), typically on the **left side**. - Presents in neonates with respiratory distress due to herniation of abdominal contents into the thorax. *Morgagni hernia* - This is a rare type of **congenital diaphragmatic hernia**, occurring through the **anterior retrosternal diaphragm** (foramen of Morgagni). - Accounts for only **2-5% of all CDH cases**, usually on the right side. - Often asymptomatic and diagnosed incidentally in adults. *Paraesophageal hernia* - This is an **acquired hiatal hernia** where part of the stomach herniates alongside the esophagus through the esophageal hiatus. - While **hiatal hernias are the most common diaphragmatic hernias overall**, they are **not congenital** and therefore not the answer to this question. - Seen commonly in older adults. *None of the options* - Incorrect, as **Bochdalek hernia** is definitively the most common congenital diaphragmatic hernia.

Q: Hirschsprung disease is confirmed by ?

Rectal biopsy. ***Rectal biopsy*** - A **rectal biopsy** is the most definitive diagnostic test for Hirschsprung disease, revealing the absence of **ganglion cells** in the submucosal and myenteric plexuses. - This procedure involves taking a small tissue sample from the rectum, which is then examined under a microscope for characteristic histological changes. *Per/Rectal examination* - A **per/rectal examination** may reveal an empty rectum followed by a gush of stool and gas upon withdrawal of the finger, which is suggestive but not diagnostic. - It is a **clinical finding** that prompts further investigation but does not provide histological confirmation of aganglionosis. *Rectal manometry* - **Rectal manometry** measures pressures within the rectum and can detect the absence of the **rectoanal inhibitory reflex** (RAIR), a hallmark of Hirschsprung disease. - While highly sensitive, it is a **physiological test** indicating functional abnormalities, but it does not provide the definitive histological diagnosis of aganglionosis. *X-ray abdomen* - An **X-ray of the abdomen** may show dilated loops of bowel proximal to a narrowed, aganglionic segment, indicating intestinal obstruction. - This imaging study is useful for **initial assessment** and identifying signs of obstruction, but it is not specific for Hirschsprung disease and cannot confirm the absence of ganglion cells.

Q: What is the primary condition treated by the Kasai operation?

Biliary atresia. ***Biliary atresia*** - The **Kasai operation**, or **hepatoportoenterostomy**, is the primary surgical treatment for **biliary atresia**, a condition where the bile ducts are blocked or absent. - The procedure aims to establish bile flow from the liver to the small intestine to prevent liver damage. *Choledochal cyst* - A **choledochal cyst** is a congenital dilation of the bile ducts and is typically treated by surgical excision of the cyst and a **Roux-en-Y hepaticojejunostomy**. - While it involves the biliary system, it is a distinct condition from biliary atresia and requires a different surgical approach. *Hepatocellular carcinoma* - **Hepatocellular carcinoma** is a primary liver cancer, and its treatment options range from **surgical resection** and **transplantation** to **chemotherapy** and **radiation**, which are distinctly different from the Kasai operation. - The Kasai operation is not used for malignant conditions of the liver or bile ducts. *Primary biliary cirrhosis* - **Primary biliary cirrhosis** is a chronic autoimmune disease affecting the small bile ducts within the liver, causing progressive cholestasis. - Its management is primarily medical, focusing on symptom control and preventing disease progression with drugs like **ursodeoxycholic acid**, and surgery is not a primary treatment.

Q: In Congenital Diaphragmatic Hernia (CDH), the most commonly associated anomaly affects the

Congenital heart defects. ***Congenital heart defects*** - **Congenital diaphragmatic hernia (CDH)** is frequently associated with other congenital anomalies. - **Cardiac malformations** are the most common co-occurring defects, affecting a significant proportion of CDH patients. *Anomalies of the urinary tract* - While **urogenital anomalies** can occur with CDH, they are less prevalent than congenital heart defects. - These typically include conditions like **renal agenesis** or **hydronephrosis**. *Anomalies of the skull* - **Skull anomalies** are not a primary or common association with congenital diaphragmatic hernia. - Genetic syndromes associated with both CDH and skull anomalies are relatively rare. *Craniofacial anomalies* - **Craniofacial anomalies**, such as **cleft lip/palate**, can occur with CDH but are less common than cardiac anomalies. - These are often seen within the context of specific genetic syndromes.

Q: What is the type of Intussusception that is most frequently observed?

Ileocolic type. ***Ileocolic type*** - This is the **most common form of intussusception**, accounting for approximately 75% to 90% of cases, especially in children. - It occurs when the **ileum telescopes into the colon** at the ileocecal valve. *Ileoileal type* - This type involves the **invagination of one part of the ileum into another part of the ileum**. - While it can occur, it is **less common than ileocolic intussusception** and is more often associated with a pathological lead point in older children and adults. *Colo-colic type* - This involves the **telescoping of one segment of the colon into another segment of the colon**. - It is **rare in children** and, when present, is almost always associated with a pathological lead point, such as a polyp or tumor, primarily in adults. *Caeco-colic type* - This type occurs when the **cecum telescopes into the ascending colon**. - It is also a **relatively uncommon form of intussusception** compared to the ileocolic type.

Q: The term 'raspberry tumor' is most commonly associated with which of the following conditions?

Umbilical granuloma. ***Umbilical granuloma*** - An **umbilical granuloma** is a common condition in newborns, presenting as a soft, red, moist growth at the umbilicus after the umbilical cord detaches. - Its characteristic appearance, resembling a small red berry, has led to the descriptive term "**raspberry tumor**." *Umbilical fistula* - An **umbilical fistula** is an abnormal connection that can occur between the intestine or bladder and the umbilicus, leading to the discharge of stool or urine from the umbilicus. - It does not present as a fleshy, raspberry-like growth, but rather as an opening with discharge. *Meckel’s diverticulum* - **Meckel's diverticulum** is a remnant of the **vitelline duct**, typically found on the anti-mesenteric border of the ileum, and is a congenital anomaly of the small intestine. - It is an internal structure and does not manifest externally at the umbilicus as a "raspberry tumor." *Umbilical adenoma* - An **umbilical adenoma** is a rare tumor of the umbilicus, often a remnant of the **vitelline duct** or **urachus**, which can present as a reddish mass. - While it can be a reddish mass, the specific term "raspberry tumor" is not commonly associated with umbilical adenoma but rather with umbilical granuloma due to its very distinct granular appearance.

Q: What is the optimal age range for performing surgery for hypospadias?

6 - 18 months. ***6 - 18 months*** - This age range balances favorable tissue response for **hypospadias repair** with minimizing psychological impact on the child. - At this age, the penile tissues are adequately developed for surgical reconstruction, anesthetic risks are lower than in the neonatal period, and the child has minimal **psychosexual awareness** of genital differences. - Performing surgery before toilet training (which typically begins after 18 months) avoids interference with this important developmental milestone. *0 - 4 months* - Performing surgery too early, particularly in the **neonatal period**, may lead to greater anesthetic risks and technical challenges due to smaller vessel size and less developed tissues. - The rapid growth and changes in infant anatomy during this period can also potentially affect the long-term results of the repair. *4 - 6 months* - While this period is past the immediate neonatal stage, it is still considered relatively early for optimal hypospadias repair. - The penile tissues may still be too small and delicate for complex reconstructions, increasing the operational difficulty and potential for **complications**. *> 2 years* - Delaying surgery beyond 2 years increases the risk of **psychological and psychosexual trauma** for the child, as they become more aware of their genital differences. - Older children may also be more difficult to manage post-operatively, and there is no significant surgical advantage to waiting this long compared to the 6-18 month window.

Q: A 5-year-old boy is brought to the pediatrician for a physical examination prior to beginning elementary school. On examination, the boy has only one palpable testis in the scrotum. Further examination reveals a palpable mass in the left inguinal region. What is this condition called?

Cryptorchidism. ***Cryptorchidism*** - The presence of only one palpable testis in the scrotum, with a palpable mass in the **left inguinal region**, indicates that the other testis is likely **undescended** and remains in the inguinal canal [2]. - This condition is common in young boys and is often discovered during routine physical examinations, as in this case [1]. *Varicocele* - Varicocele is characterized by **enlarged veins** in the scrotum, usually located above the testis, not as a palpable mass in the inguinal region. - It typically presents with a **bag of worms** feeling and may affect testicular function but does not explain the absence of a testis. *Hydrocele* - Hydrocele involves fluid accumulation around the testis, leading to **swelling** of the scrotum, but does not cause an inguinal mass or absence of a testis [2]. - The mass in hydrocele is usually **transilluminable** and does not correlate with undescended testis findings. *Orchitis* - Orchitis refers to inflammation of the testis, often due to infection; however, it would not result in the absence of a testis in the scrotum. - This condition typically presents with **pain and swelling** of the testes, which are both present in the scrotum, unlike the undescended testis described. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Lower Urinary Tract and Male Genital System, pp. 976-977. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Diseases Of The Urinary And Male Genital Tracts, pp. 508-509.

Q: A newborn male child presenting with severe respiratory distress, absent respiratory breath sounds, and a scaphoid abdomen is suffering from.

Diaphragmatic hernia. ***Diaphragmatic hernia*** * The classic triad of **respiratory distress**, the absence of **breath sounds** on the affected side, and a **scaphoid abdomen** is highly indicative of a **congenital diaphragmatic hernia (CDH)**. * In CDH, abdominal contents herniate into the chest cavity, compressing the lungs and causing **pulmonary hypoplasia**, leading to severe respiratory compromise. *Congenital pyloric stenosis* * Pyloric stenosis typically presents with **non-bilious projectile vomiting** and an **olive-shaped mass** in the epigastrium, usually in infants between 3-6 weeks of age, not in a newborn with respiratory distress. * It does not cause absent breath sounds or a scaphoid abdomen, as it is a gastrointestinal obstruction without thoracic involvement. *Intussusception* * Intussusception involves the telescoping of one part of the intestine into another, presenting with **colicky abdominal pain**, **vomiting**, and **"currant jelly" stools**. * This condition primarily affects older infants and young children, is an acute abdominal emergency, and does not directly cause severe respiratory distress or absent breath sounds unless there is significant abdominal distension compromising respiration. *Meconium ileus* * Meconium ileus is an obstruction of the small intestine by abnormally thick meconium, often associated with **cystic fibrosis**. * It presents with **abdominal distension**, **vomiting**, and **failure to pass meconium**, but not typically with severe respiratory distress unrelated to abdominal distension.

Q: Anorectal anomalies are commonly associated with which of the following congenital anomalies?

Cardiac anomalies. ***Cardiac anomalies*** - **Cardiac anomalies** occur in approximately 30-50% of patients with **anorectal malformations**, making them the most commonly associated congenital anomaly. - These can range from simple septal defects to complex **congenital heart diseases**, often requiring surgical intervention. *Duodenal atresia* - **Duodenal atresia** is a common gastrointestinal anomaly but is less frequently associated with **anorectal malformations** compared to cardiac anomalies. - It typically presents with **bilious vomiting** and a "double bubble" sign on X-ray, which is not directly linked to the embryological development of the anorectum. *CNS malformations* - **CNS malformations**, such as **spinal dysraphism** (e.g., tethered cord, myelomeningocele), are certainly associated with **anorectal malformations**, particularly in the context of **VACTERL association**. - While significant, their incidence is generally lower than that of **cardiac anomalies** in this group. *Abdominal wall defects* - **Abdominal wall defects** like **omphalocele** or **gastroschisis** are distinct congenital anomalies with different embryological origins than **anorectal malformations**. - They are not considered a primary or most common associated anomaly with **anorectal malformations**.

Question 1

Most common congenital diaphragmatic hernia is:

Accepted Answer

Bochdalek hernia

Answer

Morgagni hernia

Answer

None of the options

Answer

Paraesophageal hernia

Question 2

Hirschsprung disease is confirmed by ?

Accepted Answer

Rectal biopsy

Answer

Per/Rectal examination

Answer

Rectal manometry

Answer

X-ray abdomen

Question 3

What is the primary condition treated by the Kasai operation?

Accepted Answer

Biliary atresia

Answer

Choledochal cyst

Answer

Hepatocellular carcinoma

Answer

Primary biliary cirrhosis

Question 4

In Congenital Diaphragmatic Hernia (CDH), the most commonly associated anomaly affects the

Accepted Answer

Congenital heart defects

Answer

Anomalies of the urinary tract

Answer

Anomalies of the skull

Answer

Craniofacial anomalies

Question 5

What is the type of Intussusception that is most frequently observed?

Accepted Answer

Ileocolic type

Answer

Ileoileal type

Answer

Colo-colic type

Answer

Caeco-colic type

Question 6

The term 'raspberry tumor' is most commonly associated with which of the following conditions?

Accepted Answer

Umbilical granuloma

Answer

Umbilical fistula

Answer

Meckel’s diverticulum

Answer

Umbilical adenoma

Question 7

What is the optimal age range for performing surgery for hypospadias?

Accepted Answer

6 - 18 months

Answer

4 - 6 months

Answer

> 2 years

Answer

0 - 4 months

Question 8

A 5-year-old boy is brought to the pediatrician for a physical examination prior to beginning elementary school. On examination, the boy has only one palpable testis in the scrotum. Further examination reveals a palpable mass in the left inguinal region. What is this condition called?

Accepted Answer

Cryptorchidism

Answer

Hydrocele

Answer

Orchitis

Answer

Varicocele

Question 9

A newborn male child presenting with severe respiratory distress, absent respiratory breath sounds, and a scaphoid abdomen is suffering from.

Accepted Answer

Diaphragmatic hernia

Answer

Congenital pyloric stenosis

Answer

Intussusception

Answer

Meconium ileus

Question 10

Anorectal anomalies are commonly associated with which of the following congenital anomalies?

Accepted Answer

Cardiac anomalies

Answer

Duodenal atresia

Answer

CNS malformations

Answer

Abdominal wall defects

Pediatric Surgery — MCQs

Pediatric Surgery — MCQs

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