NEET-PG 2023 - Internal Medicine Practice Questions

Q: A patient hailing from Delhi presents with fever, arthralgia, and extensive petechial rash for 3 days. Lab investigations revealed a hemoglobin of 9 g/ dL, a white blood cell count of 9000 cells/mm3, a platelet count of 20000 cells/mm3, and a prolonged bleeding time. The clotting time was normal. What is the most likely diagnosis?

Dengue. Dengue - The combination of **fever, arthralgia, extensive petechial rash**, and severe **thrombocytopenia** (platelet count 20,000/mm³) with **prolonged bleeding time** is highly characteristic of severe dengue infection, especially in an endemic area like Delhi [1]. - While leukocytosis (WBC 9000/mm³) is not typical for dengue (usually causes leukopenia), the other features strongly point to dengue hemorrhagic fever [1]. *Malaria* - Typically presents with **intermittent high fever**, chills, and sweats. While it can cause some thrombocytopenia and anemia, the **extensive petechial rash** is not a characteristic feature. - **Thrombocytopenia** in malaria is usually milder than observed here, and prolonged bleeding time is less common [2]. *Scrub typhus* - Caused by Orientia tsutsugamushi, it is characterized by **fever, headache, myalgia, and a characteristic eschar** (necrotic ulcer) at the bite site, which is not mentioned. - While it can cause rash and some thrombocytopenia, the **petechial rash** and such severe thrombocytopenia with prolonged bleeding time are less typical. *Typhoid* - Presents with **sustained high fever**, headache, bradycardia, and sometimes a **rose spot rash** (maculopapular), which is different from a petechial rash. - Typhoid typically causes **leukopenia** and can lead to gastrointestinal complications like intestinal bleeding, but severe thrombocytopenia and extensive petechiae are not common presenting features.

Q: A patient presents with polyuria following total hypophysectomy. Laboratory results show Na+ levels at 155 mEq/L and urine osmolarity at 200 mOsm/L. What is the definitive management for this patient?

Lifelong DDAVP supplementation. ### Lifelong DDAVP supplementation - The patient's **polyuria** after **total hypophysectomy**, coupled with **hypernatremia (Na+ 155 mEq/L)** and **low urine osmolarity (200 mOsm/L)**, strongly indicates **central diabetes insipidus (DI)** due to **ADH deficiency** [1]. - **Desmopressin (DDAVP)** is a synthetic analog of **ADH** and is the definitive treatment for central DI, replacing the missing hormone, and addressing the lifelong deficiency [1]. ### No treatment required as receptors are upset - This is incorrect as untreated **diabetes insipidus** can lead to severe **dehydration, hypernatremia, and neurological complications**, making intervention critical [2]. - The symptoms and lab findings indicate a clear deficiency, not merely "upset" receptors, which requires definitive management to prevent life-threatening complications. ### Thiazides for a limited duration of 2 weeks - **Thiazide diuretics** are used in **nephrogenic diabetes insipidus** to induce mild volume depletion, which can increase water reabsorption in the proximal tubule [1]. - However, they are not the definitive treatment for **central DI** where the primary problem is a lack of **ADH**, and using them for a *limited duration* would not address a lifelong condition. ### DDAVP for a limited duration of 2 weeks - While **DDAVP** is the correct treatment for **central DI**, the condition resulting from a total hypophysectomy is **permanent**. - Therefore, treatment for only a *limited duration* would lead to the recurrence of symptoms, and potentially life-threatening complications, making lifelong management essential.

Q: A young patient presents with a large retroperitoneal hemorrhage and a history of intermittent knee swelling after strenuous exercise. There is no history of mucosal bleeding. Which of the following clotting factors is primarily deficient in Hemophilia A?

Factor VIII. ***Factors VIII and IX*** - The symptoms indicate a **hemophilia**, where deficiencies in factors VIII or IX lead to a tendency for **retroperitoneal hemorrhage** and joint swelling, particularly after exercise [1]. - Intermittent swelling of the knees indicates **hemarthrosis**, a common manifestation in hemophilia, supporting the dysfunction of these factors [1]. *Factors XI and XII* - These factors are part of the **intrinsic pathway** but are not primarily associated with **joint bleeding** or sporadic retroperitoneal hemorrhage in young patients. - Deficiencies of these factors typically lead to a milder form of bleeding disorders and not the severe joint symptoms seen here. *Von Willebrand factor* - This factor is crucial for **platelet adhesion** and is associated with **mucosal bleeding**, which is not reported in this patient's history [2]. - The patient's **retroperitoneal hemorrhage** and knee swelling are not characteristic of von Willebrand disease, which typically involves more superficial bleeding [1,2]. *Lupus anticoagulant* - This is an **antiphospholipid antibody** associated with **thrombosis** rather than bleeding, and does not explain the joint swelling or hemorrhagic symptoms. - It leads to a false-positive on coagulation tests and can result in complications like recurrent **thromboembolic events**, rather than bleeding tendencies.

Q: A child presents with intermittent jaundice and splenomegaly. There is a history of similar complaints in the elder brother. Peripheral smear shows the following finding. What is the most appropriate investigation for this condition?

Osmotic fragility test. ***Osmotic fragility test*** - The image shows **spherocytes** (dense, small red cells lacking central pallor), a hallmark of **hereditary spherocytosis**. The clinical picture of intermittent jaundice, splenomegaly, and a family history further supports this diagnosis. - The **osmotic fragility test** measures the red blood cell's susceptibility to hemolysis in hypotonic solutions and is the most appropriate test to confirm hereditary spherocytosis. *Coombs test* - The Coombs test (direct antiglobulin test) detects **antibodies on the surface of red blood cells** or in the serum. It is primarily used to diagnose **autoimmune hemolytic anemia**. - Hereditary spherocytosis is a membrane defect, not an immune-mediated condition, so the Coombs test would typically be negative. *G6PD deficiency testing* - **Glucose-6-phosphate dehydrogenase (G6PD) deficiency** leads to episodic hemolytic anemia triggered by oxidative stress (e.g., fava beans, certain drugs, infections). - While it causes episodic hemolysis and jaundice, the peripheral smear typically shows **Heinz bodies** and **bite cells** during hemolytic episodes, not spherocytes, and without specific triggers, it doesn't fit the clinical picture as well as hereditary spherocytosis. *Flow cytometry for PNH* - **Flow cytometry** is used to diagnose **paroxysmal nocturnal hemoglobinuria (PNH)** by detecting the absence of GPI-anchored proteins (e.g., CD55, CD59) on blood cells. - PNH is characterized by dark urine (hemoglobinuria), thrombosis, and bone marrow failure, and its peripheral smear does not typically show spherocytes.

Q: A man presents with a history of dysuria and urethral discharge after having unprotected sexual intercourse. What is the treatment of choice for this infection?

Ceftriaxone. ***Ceftriaxone*** - The combination of **dysuria** and **urethral discharge** following unprotected sexual intercourse is highly suggestive of **gonorrhea**. - **Ceftriaxone** is the recommended first-line treatment for uncomplicated gonococcal infections due to increasing antibiotic resistance. *Erythromycin* - Erythromycin is primarily used for atypical bacterial infections, such as those caused by *Mycoplasma pneumoniae* or *Chlamydia trachomatis*. - While it can be used for chlamydia, it is not the preferred treatment for suspected gonorrhea. *Azithromycin* - Azithromycin is often used in combination with ceftriaxone for gonorrhea to cover potential co-infection with **Chlamydia trachomatis**. - However, **monotherapy with azithromycin is not recommended for gonorrhea** due to concerns about emerging resistance and suboptimal efficacy. *Penicillin G* - Penicillin G was historically used to treat gonorrhea, but this is no longer the case due to widespread **resistance** of *Neisseria gonorrhoeae* strains. - Its primary use now is for susceptible bacterial infections, such as syphilis and certain streptococcal infections.

Q: A patient comes with abdominal pain, jaundice, and portal hypertension. Anastomosis between which of the following veins is seen?

Esophageal veins and left gastric veins. ***Esophageal veins and left gastric veins*** - This anastomosis is crucial in **portal hypertension**, as increased pressure in the **portal venous system** (e.g., due to liver cirrhosis) causes blood to back up into the **systemic venous circulation** through these collateral vessels. - This shunting creates **esophageal varices**, which can rupture and lead to life-threatening **upper gastrointestinal bleeding**, commonly presenting with **jaundice** and **abdominal pain** in liver disease. *Left colic vein and middle colic veins* - Both the left colic and middle colic veins are tributaries of the **inferior mesenteric vein** and **superior mesenteric vein**, respectively, and are part of the **portal system**. - While they form an anastomosis (via the **marginal artery of Drummond**), this connection is within the portal system and does not typically serve as a portosystemic shunt to decompress portal hypertension in the way esophageal varices do. *Superior rectal and phrenic veins* - The **superior rectal vein** drains into the **inferior mesenteric vein** (part of the portal system), and the **phrenic veins** drain into the **inferior vena cava** (part of the systemic system). - There is no direct significant portosystemic anastomosis between these two veins that would be clinically relevant in portal hypertension. *Sigmoid and superior rectal veins* - Both the **sigmoid veins** and the **superior rectal vein** are part of the **inferior mesenteric venous system**, which drains into the **portal circulation**. - While there are anastomoses between these veins within the mesenteric circulation, they are not a direct portosystemic shunt used to relieve pressure in portal hypertension causing the described symptoms.

Q: A young male came to the hospital with a clean-cut wound without any bleeding. The patient received a full course of tetanus vaccination 10 years ago. What is the best management for this patient?

Single-dose tetanus toxoid. ***Single-dose tetanus toxoid*** - For a **clean-cut wound** in a patient who completed a **primary tetanus vaccination series** and received their last dose more than 5 years ago but less than 10 years ago, a **single booster dose** of tetanus toxoid is recommended. [1] - A booster ensures continued protection, as vaccine-induced immunity wanes over time, but the prior full course provides a robust anamnestic response with a single dose. *Human tetanus immunoglobulin and a full course of vaccine* - This regimen (tetanus immunoglobulin + vaccine) is typically reserved for patients with **unvaccinated status**, an **unknown vaccination history**, or a **severely contaminated wound** (e.g., rusty nail, soil contamination) who have not been fully vaccinated. - The patient had a **clean-cut wound** and completed a full course of vaccination 10 years ago, making immunoglobulin unnecessary and a full course of vaccine excessive. *Human tetanus immunoglobulin only* - Administering **tetanus immunoglobulin alone** is appropriate for immediate, passive immunity in situations where a patient is unvaccinated or has an unknown vaccination status and has a significant risk of tetanus from a contaminated wound. [2] - This patient has a clean wound and a history of full vaccination, so a booster is sufficient to stimulate active immunity. *No treatment required* - While the patient was fully vaccinated 10 years ago, the protection from tetanus vaccination can **wane over time**, especially after 5-10 years. - A **booster dose** is crucial to maintain adequate protection against tetanus, even for a clean wound, given the 10-year interval since the last dose.

Q: In a patient presented with a fever and a positive filarial antigen test, what is the next appropriate method of management?

Detection of microfilariae in the blood smear. ***Detection of microfilariae in the blood smear*** - A positive **filarial antigen test** indicates the presence of adult worms, and the next step is to confirm active infection by identifying **microfilariae**. [1] - **Nocturnal blood samples** are crucial because microfilariae of *Wuchereria bancrofti* and *Brugia malayi* exhibit **nocturnal periodicity**, meaning they are most abundant in peripheral blood between 10 PM and 2 AM. [1] *Bone marrow biopsy* - This procedure is typically used to diagnose **hematological disorders**, such as leukemia or lymphoma, or investigate causes of unexplained fever, but it is not indicated for filariasis. - While filariasis can rarely lead to **eosinophilia**, a bone marrow biopsy is not a diagnostic tool for filarial infection itself. *DEC provocation test* - The **diethylcarbamazine (DEC) provocation test** is used to bring out microfilariae into the peripheral blood during the daytime for species that exhibit nocturnal periodicity. [1] - However, it carries a risk of severe adverse reactions due to rapid killing of microfilariae, especially in cases of heavy infection, and is generally avoided when antigen tests are positive. [1] *Ultrasound of the scrotum* - Scrotal ultrasound can detect the characteristic "filarial dance sign" (motile adult worms) in the **lymphatic vessels of the scrotum and epididymis**, confirming lymphatic filariasis. [2] - While useful for assessing advanced disease manifestations like **hydrocele**, it does not quantify microfilaremia or replace the need for microscopic confirmation of circulating microfilariae to guide treatment.

Q: A bronchial asthma patient on inhalational steroids presented with white patchy lesions on the tongue and buccal mucosa. What condition is likely to be present in this patient?

Oral candidiasis. **Oral candidiasis** - **Inhaled corticosteroids** can suppress the local immune response in the oral cavity, creating an environment conducive to the overgrowth of *Candida albicans*. - The classic presentation includes **white patchy lesions** on the tongue and buccal mucosa, which can often be scraped off. *Oral lichen planus* - Characterized by **reticular (Wickham's striae)**, papular, or erosive lesions, which are often bilateral and symmetric [1]. - While it can present with white lesions, they are typically not easily scraped off and are not primarily associated with inhaled corticosteroid use [1]. *Aphthous ulcers* - These are typically **painful, solitary, or multiple ulcers** with a red halo and a yellowish-gray center [2]. - They are distinct from widespread white patchy lesions and are not directly caused by inhaled corticosteroid use [2]. *Oral leukoplakia* - Defined as a **white patch or plaque** on the oral mucosa that cannot be characterized clinically or pathologically as any other disease, and which is not removable by scraping. - It is often associated with tobacco use and alcohol consumption, and carries a risk of malignancy; it does not typically appear as a direct side effect of inhaled corticosteroids.

Q: A male patient presents with sensory loss and weakness of limbs for 3 months. He also has angular stomatitis. On examination, there is loss of proprioception, vibration sensations, UMN type of lower limb weakness, and absent ankle reflex. What is the most probable diagnosis?

Subacute combined degeneration of cord. ***Subacute combined degeneration of cord*** - The combination of **sensory loss (proprioception, vibration)**, **UMN weakness**, **absent ankle reflex** (suggesting LMN involvement or peripheral neuropathy), and **angular stomatitis** (a sign of nutritional deficiency) is highly characteristic of **vitamin B12 deficiency**, leading to subacute combined degeneration. - This condition affects the **posterior and lateral columns of the spinal cord**, explaining the broad neurological symptoms. *Extradural compression of the spinal cord* - While it can cause sensory loss and weakness, **extradural compression** typically presents with a more localized deficit and would not explain the **angular stomatitis** or the specific pattern of combined UMN/LMN signs without a clear lesion level. - Would primarily cause symptoms related to the compressed spinal cord segments, often with **radicular pain** or a **sensory level**, which are not explicitly described. *Progressive muscular atrophy* - This is a form of **motor neuron disease** characterized by **pure lower motor neuron (LMN) degeneration**, leading to **muscle weakness, atrophy, and fasciculations**. - It would not typically present with **UMN signs** (like UMN type weakness) or **sensory loss** (proprioception, vibration), nor angular stomatitis. *Cervical spondylotic myelopathy* - This condition involves **compression of the cervical spinal cord** due to degenerative changes, leading to **UMN signs below the level of compression** and sometimes LMN signs at the level of compression. - It would not typically cause widespread **proprioception and vibration loss** in a diffuse pattern or **angular stomatitis**, and the absent ankle reflex without other LMN signs is less typical for isolated cervical involvement.

Question 1

A patient hailing from Delhi presents with fever, arthralgia, and extensive petechial rash for 3    days. Lab investigations revealed a hemoglobin of 9 g/ dL, a white blood cell count of 9000    cells/mm3, a platelet count of 20000 cells/mm3, and a prolonged bleeding time. The clotting    time was normal. What is the most likely diagnosis?

Accepted Answer

Dengue

Answer

Malaria

Answer

Scrub typhus

Answer

Typhoid

Question 2

A patient presents with polyuria following total hypophysectomy. Laboratory results show Na+ levels at 155 mEq/L and urine osmolarity at 200 mOsm/L. What is the definitive management for this patient?

Accepted Answer

Lifelong DDAVP supplementation

Answer

No treatment required as receptors are upset

Answer

Thiazides for a limited duration of 2 weeks

Answer

DDAVP for a limited duration of 2 weeks

Question 3

A young patient presents with a large retroperitoneal hemorrhage and a history of intermittent knee swelling after strenuous exercise. There is no history of mucosal bleeding. Which of the following clotting factors is primarily deficient in Hemophilia A?

Accepted Answer

Factor VIII

Answer

Von Willebrand factor

Answer

Lupus anticoagulant

Answer

Factor IX

Question 4

A child presents with intermittent jaundice and splenomegaly. There is a history of similar complaints in the elder brother. Peripheral smear shows the following finding. What is the most appropriate investigation for this condition?

Accepted Answer

Osmotic fragility test

Answer

Coombs test

Answer

G6PD deficiency testing

Answer

Flow cytometry for PNH

Question 5

A man presents with a history of dysuria and urethral discharge after having unprotected sexual intercourse. What is the treatment of choice for this infection?

Accepted Answer

Ceftriaxone

Answer

Erythromycin

Answer

Azithromycin

Answer

Penicillin G

Question 6

A patient comes with abdominal pain, jaundice, and portal hypertension. Anastomosis    between which of the following veins is seen?

Accepted Answer

Esophageal veins and left gastric veins

Answer

Left colic vein and middle colic veins

Answer

Superior rectal and phrenic veins

Answer

Sigmoid and superior rectal veins

Question 7

A young male came to the hospital with a clean-cut wound without any bleeding. The patient    received a full course of tetanus vaccination 10 years ago. What is the best management for    this patient?

Accepted Answer

Single-dose tetanus toxoid

Answer

Human tetanus immunoglobulin only

Answer

Human tetanus immunoglobulin and a full course of vaccine

Answer

No treatment required

Question 8

In a patient presented with a fever and a positive filarial antigen test, what is the next appropriate method of management?

Accepted Answer

Detection of microfilariae in the blood smear

Answer

Bone marrow biopsy

Answer

DEC provocation test

Answer

Ultrasound of the scrotum

Question 9

A bronchial asthma patient on inhalational steroids presented with white patchy lesions on the tongue and buccal mucosa. What condition is likely to be present in this patient?

Accepted Answer

Oral candidiasis

Answer

Oral lichen planus

Answer

Aphthous ulcers

Answer

Oral leukoplakia

Question 10

A male patient presents with sensory loss and weakness of limbs for 3 months. He also has    angular stomatitis. On examination, there is loss of proprioception, vibration sensations, UMN    type of lower limb weakness, and absent ankle reflex. What is the most probable diagnosis?

Accepted Answer

Subacute combined degeneration of cord

Answer

Extradural compression of the spinal cord

Answer

Progressive muscular atrophy

Answer

Cervical spondylotic myelopathy

NEET-PG 2023 — Internal Medicine