Gastroenterology Practice Questions

Q: Which of the following is a characteristic feature of Crohn's disease?

Sinus & fistula. ***Sinus & fistula*** - **Transmural inflammation**, a hallmark of Crohn's disease, can extend through the bowel wall, leading to the formation of **sinus tracts** and **fistulae** (abnormal connections between organs or to the skin). [1] - These complications include enteroenteric, enterovesical, and perianal fistulae, which are highly characteristic of Crohn's. [1] *Continuous involvement* - Crohn's disease is characterized by **skip lesions**, meaning there are healthy segments of bowel interspersed with diseased segments, not continuous involvement. [1] - **Ulcerative colitis** typically presents with continuous inflammation, starting from the rectum and extending proximally. [1] *Mesenteric lymphadenitis* - While mesenteric lymph nodes can be involved in Crohn's disease due to inflammation, **mesenteric lymphadenitis** is more commonly associated with infectious etiologies or other inflammatory conditions, and not a primary defining characteristic. - It refers to inflammation of lymph nodes in the mesentery, which can cause abdominal pain but does not specifically differentiate Crohn's from other conditions. *Crypt abscesses* - **Crypt abscesses** are a characteristic histological feature of **ulcerative colitis**, where neutrophils infiltrate the glandular crypts. [1] - While they can occasionally be seen in Crohn's, they are much more common and prominent in ulcerative colitis and are not a defining feature of Crohn's.

Q: Best provocative test for diagnosis of Gastrinoma is:

Secretin injection test. ***Secretin injection test*** - The **secretin injection test** is the most reliable provocative test for gastrinoma, leading to a paradoxical increase in gastrin levels [1]. - In normal individuals, secretin suppresses gastrin release, but in gastrinoma, it stimulates **gastrin secretion** [1]. *Ca++ infusion test* - The **calcium infusion test** can also stimulate gastrin release in gastrinoma patients, but it is less specific and potentially more risky than the secretin test due to potential side effects like cardiac arrhythmias. - It involves infusing calcium gluconate to observe any uncharacteristic rise in gastrin. *ACTH stimulation test* - The **ACTH stimulation test** is used to evaluate adrenal gland function, particularly in suspected cases of adrenal insufficiency or hypercortisolism [2]. - It does not have any direct relevance to the diagnosis of **gastrinoma**. *Steroid assay* - **Steroid assays** measure levels of various steroid hormones (e.g., cortisol, aldosterone) in the body to assess adrenal or gonadal function. - This test is not used for diagnosing **gastrinoma**.

Q: Corkscrew esophagus is seen in which of the following conditions ?

Diffuse esophagus spasm. ***Diffuse esophagus spasm*** - **Corkscrew esophagus** is a classic radiographic finding in **diffuse esophageal spasm (DES)**, indicating multiple simultaneous, non-peristaltic contractions. [1] - This condition is characterized by **uncoordinated esophageal contractions** that can lead to chest pain and dysphagia. [1] *Scleroderma* - Scleroderma typically causes **hypomotility** or aperistalsis in the esophagus, especially in the distal two-thirds, rather than a corkscrew appearance. [1] - It results from progressive **fibrosis and atrophy of the smooth muscle**, leading to esophageal dilation and reflux symptoms. [1] *Achalasia cardia* - Achalasia is defined by the **failure of the lower esophageal sphincter (LES) to relax** and loss of peristalsis in the esophageal body, leading to a "bird-beak" appearance on barium swallow. [2] - It features a **dilated esophagus** proximally to the tight LES, not multiple indentations. [2] *Carcinoma esophagus* - Esophageal carcinoma usually presents as a **focal stricture**, mass, or irregular lumen on imaging, often causing dysphagia that is progressive. - It does not typically cause the diffuse, segmental contractions characteristic of a corkscrew esophagus.

Q: Secretory diarrhea is not typically associated with which of the following conditions?

Celiac disease. ***Celiac disease*** [1] - Characterized by **malabsorption** due to immune-mediated damage to the intestinal mucosa, leading to **osmotic diarrhea** rather than secretory diarrhea [1]. - Symptoms include **bloating**, **weight loss**, and **steatorrhea**, which are not consistent with secretory processes. *Cholera* - Caused by **Vibrio cholerae**, leading to **massive secretory diarrhea** due to the action of cholera toxin on intestinal epithelial cells. - Presents with **watery diarrhea**, potentially leading to **dehydration** and electrolyte imbalances. *Addison's Disease* - This condition may cause **diarrhea** but typically results in **non-secretory diarrhea**, often associated with adrenal insufficiency symptoms. - Presenting features include **fatigue**, **weight loss**, and **hyperpigmentation**, not primarily secretory processes. *Phenolphthalein* - A laxative that can induce **secretory diarrhea** through its stimulant effects on the bowel. - Its mechanism leads to increased fluid secretion in the intestines, thus contributing to secretory diarrhea.

Q: Which of the following is a characteristic of Wilson's disease?

Increased copper in liver. ***Increased copper in liver*** - Wilson's disease is characterized by **accumulation of copper** in liver tissues due to defective copper transport [1]. - This excess leads to **hepatocellular damage**, resulting in liver dysfunction and potential cirrhosis [1]. *Decreased copper excretion in urine* - In Wilson's disease, there is actually **decreased excretion of copper**, which results in accumulation in the liver [1]. - **Urine copper levels** are typically low to normal in early stages because the liver fails to excrete excess copper effectively. *Autosomal dominant* - Wilson's disease is inherited in an **autosomal recessive** pattern, not dominant. - It is caused by mutations in the gene responsible for copper transport (ATP7B) [1]. *Increased serum ceruloplasmin* - Serum ceruloplasmin levels are often **decreased** in Wilson's disease due to impaired copper incorporation into this protein [1]. - Low ceruloplasmin is a key laboratory finding, contrasting the assertion of this option.

Q: What is the preferred test for confirming H. pylori eradication?

Urease breath test. ***Urease breath test*** - The **urea breath test** is highly sensitive and specific for detecting active *H. pylori* infection and its eradication by measuring radioactive or non-radioactive labeled carbon dioxide released from metabolizing urea. - It is a non-invasive test preferred after treatment to confirm eradication, as it directly detects bacterial urease activity. *Culture* - **Culture** requires an invasive endoscopic biopsy, is expensive, and takes several days to yield results; therefore, it is not the preferred method for routine eradication confirmation. - While it offers the advantage of **antibiotic susceptibility testing**, its invasiveness and turnaround time make it less practical for post-treatment assessment. *Serological test* - **Serological tests** (blood tests for antibodies) remain positive for **H. pylori antibodies** for extended periods even after successful eradication, rendering them unsuitable for confirming eradication. - These tests primarily indicate past exposure rather than current, active infection. *Biopsy urease test* - A **biopsy urease test** involves an invasive endoscopy to obtain a tissue sample, which is then tested for urease activity. - Although useful for initial diagnosis, its invasiveness makes it less preferred for confirming eradication compared to the non-invasive breath test.

Q: Which type of fatty acids should be included in the diet to manage chyluria?

Medium-chain fatty acids. ***Medium-chain fatty acids*** - **Medium-chain fatty acids (MCFAs)** are absorbed directly into the **portal circulation** without being re-esterified to triglycerides or incorporated into chylomicrons [1]. This helps bypass the compromised lymphatic system. - In **chyluria**, the lymphatic system's integrity is disrupted, leading to leakage of **chyle** (lymphatic fluid rich in chylomicrons) into the urinary tract. MCFAs provide a source of fat that does not rely on the lymphatic pathway for transport [1]. *Short-chain fatty acids* - **Short-chain fatty acids (SCFAs)** are primarily produced by bacterial fermentation in the colon and are absorbed directly into the portal circulation. - While they do not rely on the lymphatic system, their dietary contribution as a significant energy source is limited, and they are not the primary fat source for patients with chyluria. *Long-chain fatty acids* - **Long-chain fatty acids (LCFAs)** are absorbed with the help of bile salts, re-esterified into triglycerides, and packaged into **chylomicrons** within the intestinal cells [2]. - These chylomicrons then enter the **lymphatic system** and eventually the bloodstream, which is precisely the pathway that is compromised in chyluria, making them unsuitable [2]. *Omega-3 fatty acids* - **Omega-3 fatty acids** are a type of **long-chain polyunsaturated fatty acid** that also follow the chylomicron-lymphatic pathway for absorption [3]. - While beneficial for other health aspects, they are not suitable for managing chyluria due to their reliance on the **lymphatic system** for transport, which is dysfunctional in this condition.

Q: Obstruction of the hepatic vein by thrombosis or a membranous web is known as

Budd-Chiari syndrome. ***Budd-Chiari syndrome*** - **Budd-Chiari syndrome** is specifically defined as the obstruction of outflow from the liver due to occlusion of the **hepatic veins** or the suprahepatic inferior vena cava [1]. - This obstruction can be caused by **thrombosis** or a **membranous web**, leading to hepatomegaly, ascites, and abdominal pain [1]. *Schatzki's ring (esophageal narrowing)* - A **Schatzki's ring** is a benign circumferential stenosis of the distal esophagus, typically at the **squamocolumnar junction**. - It primarily causes **dysphagia** (difficulty swallowing) for solids and has no relation to hepatic vein obstruction. *Plummer Vinson Syndrome* - **Plummer-Vinson syndrome** is a rare condition characterized by the triad of **iron deficiency anemia**, **dysphagia** (due to esophageal webs), and **glossitis**. - It involves the **upper gastrointestinal tract** and is unrelated to liver or hepatic venous outflow obstruction. *Caroli's disease* - **Caroli's disease** is a rare congenital disorder characterized by multifocal, segmental dilatation of the **intrahepatic bile ducts**. - It is associated with recurrent **cholangitis** and an increased risk of cholangiocarcinoma, but does not involve hepatic vein obstruction.

Q: Anti-transglutaminase antibody is seen in?

Celiac disease. ***Celiac disease*** - Anti-transglutaminase antibodies are **highly specific and sensitive** for celiac disease, indicating an autoimmune response to gluten [1]. - This antibody is associated with **intestinal damage** and the clinical features of malabsorption in affected individuals. *Collagenous colitis* - This condition typically involves **chronic diarrhea** without the elevation of anti-transglutaminase antibodies. - The main feature is a **thickened collagen layer** in the intestinal wall, not directly related to gluten intolerance. *SLE* - Systemic lupus erythematosus (SLE) is associated with multiple autoantibodies, but **not specifically** anti-transglutaminase antibodies [1]. - Key features include **butterfly rash** and **renal involvement**, which are not relevant to gluten sensitivity. *Tropical sprue* - Characterized by **malabsorption**, often in travelers to tropical areas, but does not involve the presence of anti-transglutaminase antibodies [1]. - It is linked to deficiencies in **vitamin B12** and **folate**, rather than gluten-related disorders.

Question 1

Which of the following is a characteristic feature of Crohn's disease?

Accepted Answer

Sinus & fistula

Answer

Mesenteric lymphadenitis

Answer

Continuous involvement

Answer

Crypt abscesses

Question 2

What is a feature of short bowel syndrome?

Accepted Answer

Malabsorption leading to diarrhea, dehydration, and malnutrition.

Answer

Hypergastrinemia & high gastric secretion is seen

Answer

Diarrhea, dehydration and malnutrition

Answer

Chronic TPN dependence

Question 3

Best provocative test for diagnosis of Gastrinoma is:

Accepted Answer

Secretin injection test

Answer

Ca++ infusion test

Answer

ACTH stimulation test

Answer

Steroid assay

Question 4

Corkscrew esophagus is seen in which of the following conditions ?

Accepted Answer

Diffuse esophagus spasm

Answer

Scleroderma

Answer

Achalasia cardia

Answer

Carcinoma esophagus

Question 5

Secretory diarrhea is not typically associated with which of the following conditions?

Accepted Answer

Celiac disease

Answer

Phenolphthalein

Answer

Cholera

Answer

VIPoma

Question 6

Which of the following is a characteristic of Wilson's disease?

Accepted Answer

Increased copper in liver

Answer

Autosomal dominant

Answer

Increased serum ceruloplasmin

Answer

Decreased copper excretion in urine

Question 7

What is the preferred test for confirming H. pylori eradication?

Accepted Answer

Urease breath test

Answer

Culture

Answer

Serological test

Answer

Biopsy urease test

Question 8

Which type of fatty acids should be included in the diet to manage chyluria?

Accepted Answer

Medium-chain fatty acids

Answer

Short-chain fatty acids

Answer

Long-chain fatty acids

Answer

Omega-3 fatty acids

Question 9

Obstruction of the hepatic vein by thrombosis or a membranous web is known as

Accepted Answer

Budd-Chiari syndrome

Answer

Plummer Vinson Syndrome

Answer

Caroli's disease

Answer

Schatzki's ring (esophageal narrowing)

Question 10

Anti-transglutaminase antibody is seen in?

Accepted Answer

Celiac disease

Answer

Systemic lupus erythematosus (SLE)

Answer

Collagenous colitis (CC)

Answer

Tropical sprue (TS)

Gastroenterology — MCQs

Gastroenterology — MCQs

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