NEET-PG 2012 - Pathology Practice Questions

Q: Nutmeg liver is associated with which condition?

Right sided heart failure. ***Right sided heart failure*** - **Nutmeg liver** is a classic finding associated with **congestion** in the liver due to **right-sided heart failure**, leading to the characteristic mottled appearance [1][2]. - **Impaired venous return** from the systemic circulation causes hepatic congestion, resulting in **enlargement and fibrosis** of the liver over time [2]. *Left sided heart failure* - Left-sided heart failure primarily affects the **lungs**, leading to pulmonary congestion rather than hepatic changes. - While it can cause secondary effects on the liver over time, it does not directly cause **nutmeg liver**. *Increased pulmonary pressure* - Increased pulmonary pressure is generally associated with conditions like **pulmonary hypertension**, affecting primarily the **lungs** rather than the liver directly. - It does not lead to the **congestive changes** observed in nutmeg liver [1], which is related to right heart function. *Decreased pulmonary pressure* - Decreased pulmonary pressure would typically improve pulmonary blood flow, therefore having no association with liver congestion. - It does not contribute to the **venous stasis** seen in right heart failure, which is pivotal for nutmeg liver. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Hemodynamic Disorders, Thromboembolic Disease, and Shock, p. 126. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Liver and Gallbladder, pp. 870-872.

Q: E-cadherin gene deficiency is associated with which type of cancer?

Gastric cancer. **Correct: Gastric cancer** - **E-cadherin** is a crucial cell adhesion molecule, and its deficiency is strongly linked to **diffuse-type gastric cancer**. - Mutations in the **CDH1 gene**, which encodes E-cadherin, predispose individuals to **hereditary diffuse gastric cancer (HDGC)** due to loss of cell-cell adhesion. - This is a classic tumor suppressor gene, and germline mutations lead to an autosomal dominant cancer syndrome. *Incorrect: Intestinal cancer* - While E-cadherin plays a role in various epithelial cancers, its deficiency is not the primary driver or defining feature of intestinal cancer (colorectal cancer). - **Colorectal cancer** is more commonly associated with mutations in genes like **APC**, **KRAS**, **TP53**, and mismatch repair genes. *Incorrect: Thyroid cancer* - E-cadherin expression can be altered in thyroid cancers, but its deficiency is not the hallmark genetic event. - **Thyroid cancer** (especially papillary and follicular types) is more frequently linked to gene rearrangements (e.g., **RET/PTC**, **PAX8/PPARγ**) or point mutations (e.g., **BRAF**, **RAS**). *Incorrect: Pancreatic cancer* - Although E-cadherin can be down-regulated in pancreatic cancer, it is not the principal genetic deficiency. - **Pancreatic ductal adenocarcinoma** typically involves mutations in **KRAS**, **TP53**, **SMAD4**, and **CDKN2A**.

Q: What is the chromosomal translocation associated with Acute Myeloid Leukemia M3?

t(15;17). ***T (15,17)*** [1][2][3] - This translocation pertains to **Acute Promyelocytic Leukemia (APL)**, associated with the fusion gene **PML-RARA** [1][3]. - APL is characterized by **promyelocytes** with heavy granulation and a clinical presentation that includes coagulopathy [2][3]. *T (8, 21)* - This translocation is associated with **AML M2**, involving the **RUNX1-RUNX1T1** fusion gene [3]. - It does not correlate with the classic features of AML M3, which is specifically characterized by T (15,17). *T (9,11)* - Primarily seen in **AML M5**, this translocation is not related to the pathophysiology of AML M3. - The fusion commonly observed here is **MLL-AFF1**, which affects different types of leukemias, not APL. *T (18,21)* - This translocation does not have a significant association with any specific type of acute myeloid leukemia. - Unlike T (15,17), it is not linked to the classic features or unique clinical presentation seen in AML M3. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of White Blood Cells, Lymph Nodes, Spleen, and Thymus, pp. 620-621. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of White Blood Cells, Lymph Nodes, Spleen, and Thymus, pp. 621-622. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of White Blood Cells, Lymph Nodes, Spleen, and Thymus, p. 620.

Q: What is the cell of origin of B-cell Acute Lymphoblastic Leukemia (B-ALL)?

Immature B cells. ***Immature B cells*** - B acute lymphoblastic leukemia (B ALL) is primarily derived from the **malignant transformation of precursor B lymphocytes** [1]. - The disease is characterized by the presence of **immature B cell blasts** in the bone marrow and peripheral blood [1]. *T cells* - T cells are involved in a different lineage of leukemia known as T-ALL, not B ALL [1]. - The pathophysiology of B ALL specifically relates to **B cell precursors**, not T cell involvement. *Both T & B cells* - This option is incorrect as B ALL specifically originates from **B cell lineage**, and T cells are unrelated to its pathogenesis [1]. - The presence of both T and B cells together characterizes mixed lineage leukemias, which is not the case here. *Immature T cells* - Immature T cells are precursors for **T acute lymphoblastic leukemia (T-ALL)**, not for B ALL [1]. - B ALL does not involve T cell precursors; the focus is solely on **immature B cells** [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of White Blood Cells, Lymph Nodes, Spleen, and Thymus, pp. 596-600.

Q: Medial calcification is seen in -

Monckeberg's sclerosis. ***Monckeberg's sclerosis*** - This condition is characterized by **calcific deposits** within the **tunica media** of muscular arteries. - It typically does not occlude the vessel lumen and is often asymptomatic, though severe calcification can lead to vessel rigidity. *Atherosclerosis* - Involves the formation of **atheromatous plaques** in the **tunica intima** of large and medium-sized arteries. - These plaques consist of lipids, inflammatory cells, smooth muscle cells, and fibrous connective tissue, leading to luminal narrowing and hardening of arteries. *Arteriolosclerosis* - Refers to the thickening and hardening of the walls of **arterioles** (small arteries). - It is often associated with hypertension and diabetes, affecting resistance vessels but typically not involving extensive medial calcification. *Dissecting aneurysm* - This condition involves a **tear in the tunica intima** of an artery, allowing blood to enter and dissect between the layers of the arterial wall. - It is a life-threatening condition primarily affecting the aorta and is characterized by a false lumen, not medial calcification.

Q: Which condition is most commonly associated with systemic amyloidosis?

Chronic Kidney Disease. Type II DM - Amyloidosis is commonly associated with **chronic diseases** like type II diabetes mellitus due to insulin resistance leading to amyloid deposition [4]. - The presence of **amiloid in the pancreas** often correlates with the complications of this type of diabetes [3]. *Maturity onset DM* - While maturity-onset diabetes can lead to complications, it is often synonymous with **type II DM**, making this distinction inaccurate regarding amyloidosis. - This term is less commonly used and does not emphasize the direct link to amyloidosis seen in type II diabetes. *HTN* - Hypertension itself is not a direct cause of amyloidosis; it typically results from other underlying conditions. - The association of amyloidosis with hypertension is usually **secondary**, not a primary condition leading to amyloid deposits [2]. *Type I DM* - Type I diabetes is primarily **autoimmune**, resulting in insulin-deficient states and does not strongly associate with amyloidosis like type II [1]. - The amyloid deposits seen in type I are much less common compared to type II or associated chronic conditions.

Q: Creola bodies are seen in:

Bronchial asthma. ***Bronchial asthma*** - **Creola bodies** are clusters of **desquamated columnar epithelial cells** found in the sputum of patients with asthma. [1] - Their presence indicates ongoing **bronchial inflammation** and epithelial damage, characteristic of asthma exacerbations. *Chronic bronchitis* - Characterized by **mucus hypersecretion** and **chronic productive cough**, without the specific finding of Creola bodies. - Histologically, it involves **goblet cell hyperplasia** and **mucous gland enlargement**. *Emphysema* - Defined by irreversible enlargement of airspaces distal to the terminal bronchioles with **destruction of alveolar walls**, not specific cell aggregates. [1] - The primary defect is loss of **elastic recoil** and **airflow limitation**. *Bronchiectasis* - Involves **permanent abnormal dilation** of the bronchi due to destruction of the muscular and elastic components of the bronchial wall. [1] - Sputum typically contains inflammatory cells and bacteria, but Creola bodies are not a defining feature.

Q: Li–Fraumeni syndrome is associated with mutations in which of the following genes?

Gene TP53. ***Gene TP53*** - Li-Fraumeni syndrome is a rare, inherited cancer susceptibility syndrome associated with germline mutations in the **TP53 tumor suppressor gene**. - The **TP53 gene** encodes the p53 protein, which plays a critical role in cell cycle arrest, DNA repair, and initiation of apoptosis in response to cellular stress, thus preventing tumor formation. *Gene P21* - The **p21 gene** (CDKN1A) is a cyclin-dependent kinase inhibitor that acts downstream of p53, mediating p53-induced cell cycle arrest. - While p21 is involved in the p53 pathway, mutations in p21 itself are not the primary cause of Li-Fraumeni syndrome. *Gene RB1* - The **RB1 gene** encodes the retinoblastoma protein, a tumor suppressor involved in cell cycle regulation, particularly in controlling passage from G1 to S phase. - Mutations in **RB1** are primarily associated with hereditary retinoblastoma and osteosarcoma, not Li-Fraumeni syndrome. *Gene BRCA1* - The **BRCA1 gene** is a tumor suppressor gene involved in DNA repair, especially homologous recombination. - Germline mutations in **BRCA1** are strongly associated with hereditary breast and ovarian cancer syndrome, not Li-Fraumeni syndrome.

Q: Which of the following tumors is not derived from the meninges?

Hemangioblastoma. ***Hemangioblastoma*** - This tumor is derived from **vascular endothelial cells and stromal cells**, not meningeal cells [1] - Typically found in the **cerebellum** and strongly associated with **von Hippel-Lindau disease** [1] - Has **no meningeal origin** and represents a distinct vascular neoplasm *Meningioma* - Derived from **arachnoidal cap cells** of the meninges [2] - Most common **benign primary intracranial tumor** arising from meningeal coverings [2] - Clearly of **meningeal origin** [3] *Schwannoma* - Originates from **Schwann cells** of peripheral nerve sheaths (neural crest origin) [4] - While not meningeal in origin, it commonly occurs **intracranially** affecting cranial nerves (especially CN VIII) [2] - Though also not meningeal, **hemangioblastoma is the better answer** as it's purely parenchymal/vascular, whereas schwannomas can have anatomic association with meninges [4] *Hemangiopericytoma* - Now classified as **solitary fibrous tumor/hemangiopericytoma** (WHO classification) - Arises from **meningeal pericytes** around blood vessels in the meninges - Despite mesenchymal origin, it is considered part of the **meningeal tumor spectrum** and has meningeal associations **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Manifestations Of Central And Peripheral Nervous System Disease, pp. 726-727. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Manifestations Of Central And Peripheral Nervous System Disease, pp. 727-728. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Central Nervous System, pp. 1316-1317. [4] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Peripheral Nerves and Skeletal Muscles, pp. 1248-1249.

Q: Which acquired condition is most commonly associated with spherocytes?

Autoimmune hemolytic anemia (AIHA). ***Autoimmune haemolytic anemia*** - This condition is characterized by the **production of antibodies** against the patient's own red blood cells, leading to **destruction** and the formation of spherocytes [1]. - The presence of ***maximum spherocytes*** in blood smears is a hallmark of this disorder due to **extravascular hemolysis** [1]. *Aplastic anemia* - Aplastic anemia is mainly due to **failure of hematopoiesis**, resulting in pancytopenia rather than spherocyte formation. - It typically presents with **normocytic** or **macrocytic anemia**, not spherocytes, as the bone marrow is not producing enough red blood cells [2]. *Vit B12 deficiency* - Vit B12 deficiency usually causes **macrocytic anemia** characterized by **megaloblastic changes** in the bone marrow and peripheral blood, not the formation of spherocytes. - The primary indicators would be **hypersegmented neutrophils** and large, ovalocytes rather than spherocytes. *None* - This option incorrectly implies that no condition causes maximum spherocytes, while autoimmune hemolytic anemia is the known condition for this finding. - Spherocytes are a specific sign in hemolytic processes and are definitely seen in conditions like **autoimmune hemolytic anemia**. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 602-603. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Red Blood Cell and Bleeding Disorders, pp. 662-663.

Question 1

Nutmeg liver is associated with which condition?

Accepted Answer

Right sided heart failure

Answer

Increased pulmonary pressure

Answer

Decreased pulmonary pressure

Answer

Left sided heart failure

Question 2

E-cadherin gene deficiency is associated with which type of cancer?

Accepted Answer

Gastric cancer

Answer

Intestinal cancer

Answer

Pancreatic cancer

Answer

Thyroid cancer

Question 3

What is the chromosomal translocation associated with Acute Myeloid Leukemia M3?

Accepted Answer

t(15;17)

Answer

t(18;21)

Answer

t(9;11)

Answer

t(8;21)

Question 4

What is the cell of origin of B-cell Acute Lymphoblastic Leukemia (B-ALL)?

Accepted Answer

Immature B cells

Answer

T cells

Answer

Immature T cells

Answer

Both T & B cells

Question 5

Medial calcification is seen in -

Accepted Answer

Monckeberg's sclerosis

Answer

Atherosclerosis

Answer

Arteriolosclerosis

Answer

Dissecting aneurysm

Question 6

Which condition is most commonly associated with systemic amyloidosis?

Accepted Answer

Chronic Kidney Disease

Answer

Multiple Myeloma

Answer

Rheumatoid Arthritis

Answer

Familial Mediterranean Fever

Question 7

Creola bodies are seen in:

Accepted Answer

Bronchial asthma

Answer

Emphysema

Answer

Chronic bronchitis

Answer

Bronchiectasis

Question 8

Li–Fraumeni syndrome is associated with mutations in which of the following genes?

Accepted Answer

Gene TP53

Answer

Gene RB1

Answer

Gene BRCA1

Answer

Gene P21

Question 9

Which of the following tumors is not derived from the meninges?

Accepted Answer

Hemangioblastoma

Answer

Meningioma

Answer

Hemangiopericytoma

Answer

Schwannoma

Question 10

Which acquired condition is most commonly associated with spherocytes?

Accepted Answer

Autoimmune hemolytic anemia (AIHA)

Answer

Vitamin B12 deficiency anemia

Answer

Aplastic anemia

Answer

None of the options

NEET-PG 2012 — Pathology