Which of the following statements about desmoid tumors is incorrect?
Vegetations in Libman-Sacks endocarditis are:
Which tumor marker is most commonly associated with lung and breast carcinoma?
Medial calcification is seen in -
What is the most common cause of nephritic syndrome in adults, excluding IgA nephropathy?
Glomus tumor is seen in -
In which condition is retinal astrocytoma commonly seen?
Orphan Annie nuclei are characteristic of which of the following?
Which of the following is the most likely proliferating breast mass?
Tadpole cells, comma-shaped cells on histopathology are seen in -
NEET-PG 2012 - Pathology NEET-PG Practice Questions and MCQs
Question 41: Which of the following statements about desmoid tumors is incorrect?
- A. Show infiltrative growth pattern
- B. Often seen below the umbilicus
- C. More common in women
- D. Highly radiosensitive (Correct Answer)
Explanation: ***Highly radiosensitive*** - This is the **INCORRECT** statement and hence the correct answer to this question. - Desmoid tumors are **radioresistant**, not radiosensitive, meaning they do not respond well to radiation therapy. - Radiation therapy is typically reserved for cases where surgery is not feasible or for local control after incomplete resection, but it is not highly effective as a standalone treatment. - The radioresistant nature is an important clinical characteristic that influences treatment planning. *Often seen below the umbilicus* - This statement is **correct** about desmoid tumors. - Desmoid tumors frequently arise from the **anterior abdominal wall**, with a common location being below the umbilicus, particularly in postpartum women. - Abdominal wall desmoids are strongly associated with **pregnancy** and trauma, and can be locally aggressive. *Show infiltrative growth pattern* - This statement is **correct** about desmoid tumors. [1] - Desmoid tumors are characterized by their **locally aggressive** and infiltrative growth pattern, often invading adjacent tissues like muscle, fascia, and neurovascular structures. [1] - This infiltrative nature makes complete surgical resection challenging and contributes to a high rate of **local recurrence** (up to 20-40% after surgery). - Despite their aggressive local behavior, desmoid tumors do not metastasize. *More common in women* - This statement is **correct** about desmoid tumors. - Desmoid tumors show a **female predominance**, particularly affecting women during their reproductive years (ages 25-40). - This gender predilection is linked to **hormonal influences**, with increased risk during **pregnancy** and the postpartum period. - The association with estrogen is further supported by occasional tumor regression after menopause. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Osteoarticular And Connective Tissue Disease, pp. 691-692.
Question 42: Vegetations in Libman-Sacks endocarditis are:
- A. Large and fragile
- B. Small warty along the line of closure of valve
- C. Small or medium sized on either or both sides of valve (Correct Answer)
- D. Small bland vegetations
Explanation: ***Small or medium sized on either or both sides of valve*** - **Libman-Sacks endocarditis** typically presents with vegetations that are **small to medium in size**, found on either aspect of the valve leaflets [1][2][3]. - These vegetations are **sterile**, non-infectious, and often associated with systemic lupus erythematosus (SLE) [2][3]. *Large and fragile* - Vegetations in Libman-Sacks endocarditis are not typically **large**; they are small or medium [1]. - The term **fragile** is misleading, as the vegetations are not characterized by fragility but by being sturdy yet non-infectious. *Small warty along the line of closure of valve* - While the vegetations are small, they are **not warty** and do not primarily form along the line of closure, which is common in infective endocarditis [1]. - Libman-Sacks vegetations can be found on either side of the valve, unlike warty vegetations [1]. *Small bland vegetations* - Vegetations in Libman-Sacks endocarditis are bland but not solely described as **small and bland**; their presence on either or both sides of the valve is critical [1]. - This option fails to capture the significance of their size and localization in the endocardial lesions associated with SLE. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Heart, p. 568. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of the Immune System, pp. 232-233. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Heart, p. 570.
Question 43: Which tumor marker is most commonly associated with lung and breast carcinoma?
- A. CEA (Correct Answer)
- B. hCG
- C. AFP
- D. CA-15-3
Explanation: ***CEA*** - **Carcinoembryonic antigen (CEA)** is a tumor marker commonly associated with **lung** and **breast cancers** [1]. - Elevated levels of CEA are often observed in **various malignancies**, making it useful for monitoring treatment response and recurrence. *CA-15-3* - While **CA-15-3** is a breast cancer marker, it is less specific than CEA and often used primarily for **monitoring** but not for initial diagnosis. - It is primarily elevated in **breast carcinoma**, not typically associated with **lung cancer**. *11CG* - This ppears to be incorrectly referenced and may not exist as a recognized tumor marker for lung or breast cancer. - There are no clinical associations with lung or breast cancer, making it irrelevant in this context. *AFP* - **Alpha-fetoprotein (AFP)** is primarily associated with **liver** and **germ cell tumors**, not commonly associated with lung or breast cancers [1]. - Elevated AFP levels do not correlate with lung or breast carcinomas, distinguishing it from CEA's relevance. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Neoplasia, p. 346.
Question 44: Medial calcification is seen in -
- A. Atherosclerosis
- B. Arteriolosclerosis
- C. Dissecting aneurysm
- D. Monckeberg's sclerosis (Correct Answer)
Explanation: ***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.
Question 45: What is the most common cause of nephritic syndrome in adults, excluding IgA nephropathy?
- A. FSGS
- B. Membranous glomerulonephritis
- C. Membranoproliferative glomerulonephritis (Correct Answer)
- D. Post-infectious glomerulonephritis
Explanation: ***None*** - Nephritic syndrome in adults is often caused by various conditions, but there is **no single most common cause** that universally applies. - The true prevalence can vary by population, but conditions like **IgA nephropathy** or **post-infectious glomerulonephritis** [1] are frequently encountered rather than one specific disease. *Membranoproliferative glomerulonephritis* - This condition can cause a **nephritic syndrome** [1], but it is not the most common cause in adults, often seen in association with **hepatitis C** or other infections. - In practice, **IgA nephropathy** or **post-streptococcal glomerulonephritis** [1] are more frequently recognized causes of nephritic syndrome in adults. *Membranous glomerulonephritis* - Primarily presents with **nephrotic syndrome** rather than nephritic features [1], making it less likely to be cited as a common cause of nephritic syndrome. - It is associated with **anti-phospholipase A2 receptor antibodies** but lacks the inflammatory features of nephritis [1]. *FSGN* - **Focal Segmental Glomerulosclerosis** is associated with nephrotic syndrome and doesn't typically lead to classic nephritic features, such as hematuria and hypertension [1]. - Its primary presentation is with **proteinuria** and possible renal failure but not with the typical characteristics of nephritic syndrome [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Kidney, pp. 915-919.
Question 46: Glomus tumor is seen in -
- A. Rare locations such as retroperitoneum
- B. Long bones and vertebrae
- C. Proximal portion of digits (less common site)
- D. Distal portion of digits (Correct Answer)
Explanation: ***Distal portion of digits*** - **Glomus tumors** are most commonly found in the **distal extremities**, especially the **subungual region** (under the nail) of the fingers and toes. - This location accounts for over 75% of all glomus tumors, where they originate from specialized **neuromyoarterial glomus bodies** involved in thermoregulation. - The classic clinical triad includes **paroxysmal pain, point tenderness, and cold sensitivity**. *Rare locations such as retroperitoneum* - While glomus tumors can occur in unusual sites, the **retroperitoneum** is an exceptionally rare location for primary glomus tumors. - Extradigital glomus tumors account for approximately 25% of cases and can occur in various soft tissue sites. *Long bones and vertebrae* - Glomus tumors do not typically arise in **bone tissue** as they originate from glomus bodies in soft tissue. - Bone involvement, when present, is usually secondary due to pressure erosion from an adjacent soft tissue tumor rather than primary bone origin. *Proximal portion of digits (less common site)* - While glomus tumors can occasionally be found in less common digital locations, the **proximal portion of digits** is significantly less frequent than the distal, and particularly the subungual, region. - Their primary association remains with the **distal phalanx** and nail bed.
Question 47: In which condition is retinal astrocytoma commonly seen?
- A. Tuberous sclerosis (Correct Answer)
- B. Sturge weber syndrome
- C. Von Hippel-Lindau syndrome
- D. Neurofibromatosis
Explanation: ***Tuberous sclerosis*** - **Retinal astrocytoma**, also known as **retinal astrocytic hamartoma**, is a common ocular manifestation of **tuberous sclerosis complex (TSC)** [1]. - These lesions can appear as **mulberry-like nodules** or flat, whitish patches on the retina. - Found in approximately **40-50% of patients** with tuberous sclerosis. *Sturge weber syndrome* - Characterized by a **port-wine stain (facial nevus flammeus)**, **leptomeningeal angioma**, and **glaucoma**. - Ocular manifestations include **choroidal hemangiomas** and increased episcleral venous pressure. - Does not typically involve **retinal astrocytomas**. *Von Hippel-Lindau syndrome* - Associated with **retinal capillary hemangioblastomas** (vascular tumors) and various tumors in other organs like the kidneys, pancreas, and brain. - This condition involves **vascular tumors** in the retina, not astrocytic tumors. - Important differential as it also presents with retinal lesions. *Neurofibromatosis* - A neurocutaneous syndrome characterized by **café-au-lait spots**, **neurofibromas**, and **Lisch nodules** (iris hamartomas). - Ocular manifestations include **optic nerve gliomas** and iris hamartomas, but **not retinal astrocytomas**. - NF-1 is the most common neurocutaneous syndrome but has different retinal pathology. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Central Nervous System, pp. 1318-1319.
Question 48: Orphan Annie nuclei are characteristic of which of the following?
- A. Paraganglioma with Zellballen pattern
- B. Meningioma with psammoma bodies
- C. Pituitary adenoma with atypical nuclei
- D. Papillary thyroid carcinoma (Correct Answer)
Explanation: ***Papillary carcinoma thyroid***[1][2] - Characterized by **Orphan Annie nuclei**[1], which are large and round with a clear or empty appearance due to the presence of intranuclear cytoplasmic inclusions[1]. - Often associated with **thyroid follicular structures** and is the most common type of thyroid cancer[2]. *Meningioma* - Typically presents with **dural-based tumors** and does not exhibit Orphan Annie nuclei. - Histologically, it may demonstrate **whorled patterns** or calcifications instead. *Carcinoma pituitary* - Involves **adenomatous changes** in the pituitary gland but does not demonstrate the characteristic Orphan Annie nuclei. - More commonly shows **varied cellular morphology** depending on the type of secretory cells (e.g., prolactin, ACTH). *Paraganglioma* - Derived from **neuroendocrine cells**, and presents with **zellballen pattern** rather than Orphan Annie nuclei. - Often shows **chromaffin cells** and is typically associated with catecholamine secretion. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Endocrine System, p. 1099. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Liver And Biliary System Disease, pp. 429-430.
Question 49: Which of the following is the most likely proliferating breast mass?
- A. Duct ectasia
- B. Adenosis
- C. Papilloma
- D. Fibroadenoma (Correct Answer)
Explanation: **Fibroadenoma** - A **fibroadenoma** is a benign **biphasic breast tumor** composed of both glandular and stromal tissue, making it a common proliferating mass [3]. - It is often seen in **young women** and typically presents as a firm, movable, non-tender lump [3]. *Duct ectasia* - **Duct ectasia** is a non-proliferative condition characterized by dilation of the **subareolar ducts**, often with inflammation and fibrosis. - It is more commonly associated with **nipple discharge** and **periductal inflammation** rather than being a primary proliferating mass. *Adenosis* - **Adenosis** refers to an increase in the number of **glands or lobules** within the breast parenchyma, which can be sclerosing or florid [2]. - While it involves increased glandular elements, it is generally considered a **benign proliferative change** and less likely to form a distinct, palpable mass compared to a fibroadenoma [1], [4]. *Papilloma* - A **papilloma** is a benign epithelial proliferation within a **duct**, characterized by a central fibrovascular core [2]. - It commonly presents with **nipple discharge**, often bloody, and is typically a smaller lesion within the ductal system rather than a large, palpable proliferating mass [2]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Breast, pp. 1052-1054. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Liver And Biliary System Disease, pp. 446-447. [3] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Liver And Biliary System Disease, pp. 448-449. [4] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Breast, p. 1052.
Question 50: Tadpole cells, comma-shaped cells on histopathology are seen in -
- A. Trichoepithelioma
- B. Rhabdomyosarcoma (Correct Answer)
- C. Histiocytoma
- D. Leiomyosarcoma
Explanation: ***Rhabdomyosarcoma*** - **Tadpole cells** and **comma-shaped cells** are characteristic histological features of **rhabdomyosarcoma**, representing primitive mesenchymal cells differentiating towards skeletal muscle. - These cells are often pleomorphic, with eccentric nuclei and fibrillar eosinophilic cytoplasm, giving them their distinctive shapes. *Trichoepithelioma* - This is a benign adnexal tumor of follicular differentiation, characterized by nests of **basaloid cells**, **horn cysts**, and rudimentary hair structures. - It does not typically feature tadpole or comma-shaped cells. *Histiocytoma* - A **benign fibrous histiocytoma** (dermatofibroma) is composed of fibroblasts and histiocytes forming storiform patterns. - **Malignant fibrous histiocytoma** (now often reclassified as undifferentiated pleomorphic sarcoma) features pleomorphic spindle cells and giant cells, but not specifically tadpole or comma-shaped cells. *Leiomyosarcoma* - This is a malignant tumor of **smooth muscle origin**, characterized by spindle cells with blunt-ended nuclei, arranged in fascicles. - It lacks the tadpole or comma-shaped cells seen in rhabdomyosarcoma.