NEET-PG 2012 - Pathology Practice Questions

Q: In which condition is pannus formation typically observed?

RA. ***RA*** - **Pannus** is a characteristic feature of **rheumatoid arthritis**, representing an aggressive, hyperplastic synovial tissue that invades and destroys cartilage and bone [1], [2]. - This destructive granulation tissue primarily consists of fibroblasts, macrophages, and inflammatory cells, contributing to joint erosion [1]. *Osteoarthritis (OA)* - While **osteophytes** (bone spurs) and **cartilage degradation** are hallmarks of OA, **pannus formation** is not seen. - OA involves breakdown of articular cartilage due to mechanical stress and biochemical changes, not synovial invasion. *Gout (Gouty Arthritis)* - Gout is characterized by the deposition of **monosodium urate crystals** in joints, leading to acute inflammation [4]. - The formation of **tophi** (urate crystal deposits) is typical, but not **pannus** [4]. *Psoriatic Arthritis (PsA)* - PsA can cause joint inflammation and erosion similar to RA but does not typically involve the extensive **pannus formation** characteristic of RA [3]. - Specific features of PsA include **enthesitis**, dactylitis and involvement of **DIP joints** [3]. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Osteoarticular And Connective Tissue Disease, pp. 677-678. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Bones, Joints, and Soft Tissue Tumors, p. 1212. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Bones, Joints, and Soft Tissue Tumors, pp. 1214-1215. [4] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Bones, Joints, and Soft Tissue Tumors, p. 1218.

Q: Which of the following statements BEST characterizes the clinical significance of Barrett's esophagus?

Barrett's esophagus is a precancerous condition. ***Predisposes to SCC*** - Barrett's esophagus primarily predisposes individuals to **adenocarcinoma**, not squamous cell carcinoma (SCC) [2][3]. - SCC is associated with other conditions, such as **smoking** and **chronic irritation**, not Barrett's [3]. *Intestinal type is the most common type* - The intestinal type is indeed **common** in Barrett's esophagus, but it's not the only type present [2]. - Barrett's esophagus can also have a **gastric** type, but the intestinal type predominates in adenocarcinoma risk. *Metaplasia of cells* - This condition is defined by **intestinal metaplasia**, where squamous epithelium is replaced by columnar epithelium [2]. - Metaplasia is a **hallmark** of Barrett's esophagus and crucial for its diagnosis [2]. *Precancerous condition* - Barrett's esophagus is considered a **precancerous condition** because it increases the risk of transitioning to esophageal adenocarcinoma [1][2]. - The progression from Barrett's to cancer is well-documented in medical literature [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Gastrointestinal Tract, pp. 764-765. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Alimentary System Disease, pp. 348-349. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Gastrointestinal Tract, pp. 766-767.

Q: Which of the following is the most common type of tongue cancer?

Squamous cell carcinoma. ***Adenocarcinoma most common*** - The most common type of tongue cancer is **squamous cell carcinoma (SCC)**, not adenocarcinoma [1]. - Adenocarcinomas are less frequently associated with the tongue compared to SCC, which constitutes the majority of cases. *Tobacco is the cause* - Tobacco use is indeed a **significant risk factor** for various head and neck cancers, including tongue cancer [1]. - Smoking and smokeless tobacco are linked to increased incidence and severity of **squamous cell carcinoma** on the tongue [1]. *Deep cervical lymph nodes not involved* - Tongue cancers often metastasize to **deep cervical lymph nodes**, particularly in advanced stages. - Involvement of lymph nodes is a common feature that can affect prognosis and treatment strategies. *Lateral surface involved* - The **lateral surface** of the tongue is a common site for cancerous lesions, especially in cases related to tobacco use. - Tumors might also arise from other surfaces, but lateral involvement is characteristic of **squamous cell carcinoma**. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Lung, pp. 738-739.

Q: Which of the following diseases is NOT associated with Anti-Neutrophil Cytoplasmic Antibodies (ANCA)?

Henoch schonlein purpura. ***Henoch schonlein purpura*** - **Henoch-Schönlein purpura (HSP)** is not associated with **ANCA**; it primarily involves IgA deposition [1]. - Commonly presents with **purpura**, **abdominal pain**, and **glomerulonephritis**, differentiating it from ANCA-associated vasculitides [1]. *Wegener's granulomatosis* - **Wegener's granulomatosis**, now known as **Granulomatosis with polyangiitis**, is strongly associated with **c-ANCA** and anti-PR3 antibodies. - It typically presents with **respiratory** and **renal symptoms** due to vasculitis [2]. *Microscopic PAN* - **Microscopic polyangiitis (PAN)** is associated with **p-ANCA** and myeloperoxidase (MPO) antibodies. - It leads to **glomerulonephritis** and **pulmonary hemorrhage**, indicating its vasculitic nature. *Churg Strauss syndrome* - **Churg-Strauss syndrome**, or **Eosinophilic Granulomatosis with Polyangiitis**, is associated with **p-ANCA** and perinuclear staining [1]. - Often presents with **asthma**, **eosinophilia**, and systemic vasculitis affecting multiple organs [1].

Q: Which of the following statements about hepatic adenoma is true?

Associated with OCP use. ***Associated with OCP use*** - Hepatic adenomas have a **strong association** with **oral contraceptive pill (OCP)** use, particularly in young women of childbearing age. - The risk increases with **prolonged OCP use** and higher estrogen doses, with lesions often regressing after discontinuation. *Common in older females* - Hepatic adenomas predominantly occur in **young women** aged 20-40 years, not older females. - The peak incidence coincides with **reproductive age** and OCP usage patterns. *Cold on isotope scan* - This statement is **correct** - hepatic adenomas appear **cold** on **99mTc-sulfur colloid scintigraphy** due to **absence of Kupffer cells**. - The cold appearance helps differentiate adenomas from **focal nodular hyperplasia (FNH)**, which appears hot. *Typically malignant tumor* - Hepatic adenomas are **benign lesions**, not malignant tumors. - While **malignant transformation** can occur rarely (<5%), they are classified as benign neoplasms. *Hot on isotope scan* - This is **incorrect** - hepatic adenomas appear **cold** on isotope scans due to lack of **reticuloendothelial cells**. - **Focal nodular hyperplasia (FNH)** appears hot, which helps in differential diagnosis.

Q: All of the following are features of juvenile CML except which of the following?

Philadelphia chromosome is positive. ***Philadelphia chromosome is positive*** - **Juvenile Chronic Myeloid Leukemia (JCML)**, now known as **Chronic Myelomonocytic Leukemia (CMML)** of childhood, is characterized by the **absence** of the **Philadelphia chromosome (Ph chromosome)**. - The Ph chromosome, a t(9;22)(q34;q11) translocation forming the **BCR-ABL1 fusion gene**, is the hallmark of adult Chronic Myeloid Leukemia (CML), but not JCML. *Thrombocytopenia* - **Thrombocytopenia** (low platelet count) is a common feature in JCML due to ineffective hematopoiesis and bone marrow infiltration. - This contrasts with adult CML, where **thrombocytosis** (high platelet count) is more characteristic of the chronic phase. *Fetal Hb is increased* - An **increased level of fetal hemoglobin (HbF)** is a characteristic laboratory finding in children with JCML. - This elevation is related to the dysregulated hematopoiesis and is a useful diagnostic marker. *Lymphadenopathy* - **Lymphadenopathy** (enlarged lymph nodes) is a frequent clinical manifestation in JCML, reflecting the widespread infiltration of monocytic cells. - This is part of the systemic involvement seen in this aggressive myeloproliferative disorder.

Q: Which of the following translocations is not associated with Down syndrome?

t(11;14). ***t (11: 14)*** - The **t(11;14) translocation** is commonly associated with **mantle cell lymphoma**, a B-cell non-Hodgkin lymphoma, and is not a cause of Down syndrome. - This translocation leads to the overexpression of the **cyclin D1 gene**, located on chromosome 11, which promotes cell growth and proliferation. *t (14; 21)* - This is a common **Robertsonian translocation** involving chromosomes 14 and 21, which results in an extra copy of chromosome 21 material [1]. - Individuals with this translocation can have **Down syndrome** because their cells end up with the equivalent of three copies of chromosome 21 [1]. *t (21; 21)* - This translocation is another type of **Robertsonian translocation** where two chromosome 21s fuse. - This specific translocation is rare and results in an extra copy of chromosome 21, leading to **Down syndrome** with a high recurrence risk in offspring. *t (15: 21)* - This is a **Robertsonian translocation** involving chromosomes 15 and 21, resulting in an extra copy of chromosome 21 material. - This translocation is a known cause of **Down syndrome** due to the dosage imbalance of genes on chromosome 21 [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Genetic Disorders, pp. 169-172.

Q: Which of the following is a feature not typically associated with Hereditary Spherocytosis?

Direct Coombs Positive. ***Direct Coomb's Positive*** - In Hereditary Spherocytosis, the **Coomb's test** is typically **negative**, indicating that hemolysis is not due to autoimmune factors. - Presence of **spherocytes** on the blood smear and increased fragility are hallmark findings, not antibodies against red cells [1]. *Splenomegaly* - **Splenomegaly** is common in Hereditary Spherocytosis as the spleen actively removes abnormal spherocytes from circulation [1]. - It can lead to **hypersplenism**, with resultant anemia and thrombocytopenia. *Increased Osmotic Fragility* - Increased osmotic fragility is a key feature of Hereditary Spherocytosis, as red blood cells are less able to withstand hypotonic solutions [1]. - This results from a defect in the red cell membrane, causing spherocyte shape and fragility. *Gall stones* - Patients may develop **gallstones** due to increased bilirubin from the breakdown of spherocytes, leading to **bilirubin stones** [1]. - Gallstones are a common complication due to chronic hemolysis. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 597-598.

Question 1

What is the most common cerebellar tumor in children?

Accepted Answer

Medulloblastoma

Answer

Ependymoma

Answer

PNET

Answer

Astrocytoma

Question 2

In which condition is pannus formation typically observed?

Accepted Answer

RA

Answer

Osteoarthritis (OA)

Answer

Gout (Gouty Arthritis)

Answer

Psoriatic Arthritis (PsA)

Question 3

Which of the following statements BEST characterizes the clinical significance of Barrett's esophagus?

Accepted Answer

Barrett's esophagus is a precancerous condition

Answer

Barrett's esophagus involves metaplasia of esophageal cells

Answer

Intestinal type is the most common type

Answer

It does not predispose to SCC but to adenocarcinoma

Question 4

Which of the following is the most common type of tongue cancer?

Accepted Answer

Squamous cell carcinoma

Answer

Lymphoma

Answer

Adenocarcinoma

Answer

Basal cell carcinoma

Question 5

All the following are true about multiple myeloma except for which of the following?

Accepted Answer

Chromosomal translocation t(8;14), commonly seen in Burkitt's lymphoma

Answer

Hypercalcemia

Answer

Presence of Bence-Jones proteins in urine

Answer

Osteolytic bone disease

Question 6

Which of the following diseases is NOT associated with Anti-Neutrophil Cytoplasmic Antibodies (ANCA)?

Accepted Answer

Henoch schonlein purpura

Answer

Wegener's granulomatosis

Answer

Microscopic PAN

Answer

Churg Strauss syndrome

Question 7

Which of the following statements about hepatic adenoma is true?

Accepted Answer

Associated with OCP use

Answer

Common in older females

Answer

Cold on isotope scan

Answer

Typically malignant tumor

Answer

Hot on isotope scan

Question 8

All of the following are features of juvenile CML except which of the following?

Accepted Answer

Philadelphia chromosome is positive

Answer

Fetal Hb is increased

Answer

Lymphadenopathy

Answer

Thrombocytopenia

Question 9

Which of the following translocations is not associated with Down syndrome?

Accepted Answer

t(11;14)

Answer

t(21;21)

Answer

t(14;21)

Answer

t(15;21)

Question 10

Which of the following is a feature not typically associated with Hereditary Spherocytosis?

Accepted Answer

Direct Coombs Positive

Answer

Gall stones

Answer

Splenomegaly

Answer

Increased Osmotic Fragility

NEET-PG 2012 — Pathology