NEET-PG 2012 - Pathology Practice Questions

Q: Tadpole cells, comma-shaped cells on histopathology are seen in -

Rhabdomyosarcoma. ***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.

Q: Which gene mutation is commonly associated with malignant melanoma?

CDKN2A. ***CDK2A*** - CDK2A mutations are implicated in malignant melanoma as they disrupt the **cell cycle regulation**, contributing to uncontrolled cell growth [1]. - Loss of CDK2A function leads to reduced **p16INK4A**, a crucial inhibitor of cyclin-dependent kinases involved in **G1/S phase transition** [1,3]. - Germline mutations of p16 (CDKN2A) are present in 25% of melanoma-prone kindreds [2], and germline mutations in CDKN2A are associated with familial forms of melanoma [3]. *RET* - RET mutations are primarily associated with **medullary thyroid carcinoma** and **multiple endocrine neoplasia type 2**, not melanoma. - It is involved in the signaling pathways but does not have a direct link to melanoma pathogenesis. *None* - Suggesting "none" misrepresents the reality that specific mutations do occur in malignant melanoma, including **CDK2A** and **BRAF**. - This option fails to recognize the importance of genetic alterations in cancer development and progression. *N-myc* - N-myc mutations are primarily associated with **neuroblastoma** and not typically linked to malignant melanoma. - In melanoma, mutations of this gene do not play a significant role in its pathophysiology compared to another tumor suppressor gene like **CDK2A**. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Skin, pp. 1150-1151. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Neoplasia, pp. 297-298. [3] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Neoplasia, pp. 305-306.

Q: ER positive status in carcinoma breast indicates?

Prognosis. ***Prognosis*** - **ER positive status** in breast cancer indicates a better prognosis, as these tumors often respond well to hormone therapy [1][2]. - Patients with **ER positive** breast cancer usually have a lower risk of metastasis compared to **ER negative** tumors, making the outcome more favorable [1]. *Site* - ER status does not provide information regarding the **anatomical location** of the breast cancer, as it can be present in different sites of the breast. - It primarily focuses on the **biologic characteristics** of the tumor rather than its site of occurrence [1]. *None* - Selecting 'None' suggests that ER positive status has no relevance, which is incorrect as it is significant for treatment and prognosis [1]. - It is a crucial indicator for deciding on **endocrine therapy**, impacting management strategies in breast cancer patients [1]. *Etiology* - ER positive status does not directly indicate the **cause** of breast cancer, as various genetic and environmental factors contribute to its development. - It mainly reflects tumor behavior and response to therapies, not the **underlying factors** that lead to the disease [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Breast, p. 1056. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Breast, pp. 1064-1066.

Q: Bollinger bodies are seen in ?

Fowlpox. **IMPORTANT NOTE:** In **human pathology**, the term "Bollinger bodies" classically refers to **sulfur granules** seen in **actinomycosis** (Actinomyces infection), which appear as basophilic masses with radiating eosinophilic clubs. However, this question uses the **veterinary pathology** definition, where Bollinger bodies refer to viral inclusions in avian diseases. ***Fowlpox*** - In **veterinary pathology**, **Bollinger bodies** are characteristic large, eosinophilic **intracytoplasmic inclusion bodies** found in cells infected with the **fowlpox virus** (avipoxvirus). - These inclusions are visible under light microscopy and are a diagnostic feature of **fowlpox**, a widespread avian disease. - Note: Fowlpox is **not a human disease** but affects birds. *Chickenpox* - Chickenpox, caused by the **varicella-zoster virus (VZV)**, is characterized by **intranuclear inclusion bodies** (Cowdry type A) [1]. - It does not form **Bollinger bodies**. *Cowpox* - Cowpox is caused by the **cowpox virus**, an **orthopoxvirus**, and produces **A-type cytoplasmic inclusion bodies** (A-type inclusions). - While these are cytoplasmic inclusions, they are not referred to as **Bollinger bodies**. *Smallpox* - Smallpox, caused by the **variola virus** (orthopoxvirus), is associated with **Guarnieri bodies**, which are **cytoplasmic inclusion bodies**. - These inclusions are distinct from **Bollinger bodies**. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Infectious Diseases, pp. 366-367.

Q: Glomus tumor is seen in -

Distal portion of digits. ***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.

Q: In which condition is retinal astrocytoma commonly seen?

Tuberous sclerosis. ***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.

Q: Sequestrum is best defined as

A piece of dead bone surrounded by infected tissue. ***A piece of dead bone surrounded by infected tissue*** * A sequestrum is a fragment of **necrotic (dead) bone** that has become separated from the surrounding living bone in the context of **chronic osteomyelitis**. * The dead bone is typically surrounded by **infected granulation tissue and pus**, making it the classic definition taught in the context of bone infections. * The sequestrum acts as a **nidus for persistent infection**, as antibiotics cannot penetrate the avascular dead bone, making surgical removal often necessary. *A piece of dead bone without surrounding infection* * While a sequestrum is fundamentally dead bone, in clinical practice and standard teaching, it is **intrinsically associated with infection** in osteomyelitis. * The phrase "without surrounding infection" makes this option incorrect, as the classic sequestrum occurs in the **inflammatory milieu of chronic osteomyelitis**. *A piece of bone with compromised blood supply* * This describes **ischemic or avascular bone**, which is the **initial pathological event** that leads to bone death. * However, this is not the definition of sequestrum itself—the sequestrum is the **end result** (dead bone fragment) rather than bone with compromised vascularity. * A sequestrum has **no blood supply** (completely avascular), not merely compromised supply. *None of the options* * This is incorrect because the first option accurately captures the **standard definition of sequestrum** as taught in the context of chronic osteomyelitis in medical education.

Q: What is the most common type of degeneration observed in uterine fibroids?

Hyaline. ***Hyaline*** - **Hyaline degeneration** is the most frequent type of degeneration in uterine fibroids, occurring in about **60% of cases** [1]. - It involves the replacement of smooth muscle and connective tissue with **acellular, glassy, eosinophilic hyaline material** [1]. *Calcareous* - **Calcareous degeneration** (calcification) occurs when hyaline degeneration calcifies, typically seen in **postmenopausal women** or older fibroids. - While it can occur, it is a **secondary change** following hyaline degeneration rather than the primary and most common form. *Red* - **Red degeneration** (carneous degeneration) is acute, often occurring during **pregnancy** due to rapid growth and hemorrhagic infarction. - It presents with **acute pain** and is less common than hyaline degeneration. *Cystic* - **Cystic degeneration** is characterized by liquefaction within the fibroid, leading to the formation of **cysts**. - This typically results from advanced **hyaline degeneration** and is less common than hyaline degeneration itself. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Female Genital Tract, pp. 1024-1025.

Q: The immunoglobulin most commonly involved in Multiple Myeloma is:

IgG. ***IgG*** - In Multiple Myeloma, the most commonly involved immunoglobulin is **IgG**, which is often produced in excess by malignant plasma cells [1][2]. - The presence of **monoclonal IgG** in serum is a key indicator of this malignancy, evident in diagnostic tests like serum protein electrophoresis. *IgM* - While **elevated IgM** levels can occur in other conditions like Waldenström's macroglobulinemia, it is not typically associated with Multiple Myeloma [2]. - IgM is produced by a different type of plasma cell and does not reflect the classic presentation of Multiple Myeloma. *IgA* - Although **IgA** can be involved in some cases of Multiple Myeloma, it is much less common than IgG [1][2]. - Patients with predominately **IgA Multiple Myeloma** are relatively rare compared to those with IgG. *IgD* - **IgD** myeloma is a very rare type of Multiple Myeloma, accounting for less than 2% of cases [1][2]. - It is not typically associated with the classic symptoms and conditions that characterize the more common IgG or IgA forms. **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. 608-609. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Blood And Bone Marrow Disease, pp. 616-617.

Q: Most common CNS tumor associated with NF1

Optic glioma. ***Optic glioma*** - **Optic gliomas** (specifically **pilocytic astrocytomas**) are the most common CNS tumor found in association with **Neurofibromatosis type 1 (NF1)** [1]. - These tumors typically affect the **optic nerve** and can cause vision impairment. *Optic nerve schwannoma* - **Schwannomas** are tumors arising from Schwann cells, and while they can affect cranial nerves, an **optic nerve schwannoma** is very rare and not characteristic of NF1. - The most common schwannoma associated with neurofibromatosis is a **vestibular schwannoma** (acoustic neuroma) in NF2, not NF1 [2]. *Astrocytoma* - While optic gliomas are a type of astrocytoma, simply stating "astrocytoma" is too broad; the specific location (optic nerve) and type (pilocytic) are key in NF1 [1]. - Other types of astrocytomas (e.g., glioblastoma) are not typically associated with NF1 as the *most common* CNS tumor. *Bilateral acoustic neuroma* - **Bilateral acoustic neuromas** (vestibular schwannomas) are the hallmark CNS tumor of **Neurofibromatosis type 2 (NF2)**, not NF1 [2]. - This symptom strongly points to NF2, a distinct genetic disorder from NF1 [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Central Nervous System, pp. 1319-1320. [2] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Manifestations Of Central And Peripheral Nervous System Disease, pp. 727-728.

Question 1

Tadpole cells, comma-shaped cells on histopathology are seen in -

Accepted Answer

Rhabdomyosarcoma

Answer

Trichoepithelioma

Answer

Histiocytoma

Answer

Leiomyosarcoma

Question 2

Which gene mutation is commonly associated with malignant melanoma?

Accepted Answer

CDKN2A

Answer

MYCN

Answer

RET

Answer

BRAF

Question 3

ER positive status in carcinoma breast indicates?

Accepted Answer

Prognosis

Answer

Etiology

Answer

Site

Answer

None of the options

Question 4

Bollinger bodies are seen in ?

Accepted Answer

Fowlpox

Answer

Chickenpox

Answer

Cowpox

Answer

Smallpox

Question 5

Glomus tumor is seen in -

Accepted Answer

Distal portion of digits

Answer

Rare locations such as retroperitoneum

Answer

Long bones and vertebrae

Answer

Proximal portion of digits (less common site)

Question 6

In which condition is retinal astrocytoma commonly seen?

Accepted Answer

Tuberous sclerosis

Answer

Sturge weber syndrome

Answer

Von Hippel-Lindau syndrome

Answer

Neurofibromatosis

Question 7

Sequestrum is best defined as

Accepted Answer

A piece of dead bone surrounded by infected tissue

Answer

A piece of dead bone without surrounding infection

Answer

A piece of bone with compromised blood supply

Answer

None of the options

Question 8

What is the most common type of degeneration observed in uterine fibroids?

Accepted Answer

Hyaline

Answer

Calcareous

Answer

Red

Answer

Cystic

Question 9

The immunoglobulin most commonly involved in Multiple Myeloma is:

Accepted Answer

IgG

Answer

IgM

Answer

IgA

Answer

IgD

Question 10

Most common CNS tumor associated with NF1

Accepted Answer

Optic glioma

Answer

Astrocytoma

Answer

Bilateral acoustic neuroma

Answer

Optic nerve schwannoma

NEET-PG 2012 — Pathology