NEET-PG 2012 - Pathology Practice Questions

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: 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: 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: 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.

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: 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: 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.

Q: Lendrum's stain is done for:

Amniotic fluid embolism. ***Amniotic fluid embolism*** - **Lendrum's stain** (MSB - Martius Scarlet Blue) is specifically used to identify **fibrin**, **mucin**, and **squamous cells** in the pulmonary vasculature, which are characteristic findings in amniotic fluid embolism. [1] - This stain excellently demonstrates **fibrin** (stains red) and helps visualize components of amniotic fluid that embolize to the mother's lungs, leading to a severe, often fatal, obstetric emergency. [1] - Lendrum's method is particularly valuable in forensic pathology and autopsy diagnosis of this condition. *Air embolism* - Air embolism diagnosis relies on identifying **air bubbles** in the cardiovascular system, often confirmed by imaging studies or direct visualization during autopsy. [1] - Special stains are not typically used for direct detection of air in tissue sections. *Pulmonary embolism* - Pulmonary embolism, typically caused by a **blood clot**, is diagnosed by identifying **fibrin** and **red blood cells** within pulmonary arteries, often with stains like hematoxylin and eosin (H&E). [1] - While Lendrum's stain can demonstrate fibrin, it is specifically employed when amniotic fluid embolism is suspected, not for routine thromboembolic disease. *Fat embolism* - **Fat embolism** is diagnosed by demonstrating **fat globules** in the pulmonary microvasculature using **fat stains** like **Oil Red O** or **Sudan Black**, usually on frozen sections. - Lendrum's stain does not specifically highlight fat emboli. **References:** [1] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Respiratory Tract Disease, pp. 322-324.

Q: Rokitansky protuberances are seen in -

Teratoma. ***Teratoma*** - **Rokitansky protuberance** (mural nodule or dermoid plug) is a raised solid area found within a **mature cystic teratoma**, particularly in the ovary [1]. - It often contains various tissues derived from the three germ layers such as **hair**, **sebaceous glands**, bone, and teeth [3]. *Papillary carcinoma* - Characterized by **papillary projections** formed by tumor cells, often seen in thyroid, kidney, or ovary. - While it can have protuberances, these are **composed of malignant cells** and lack the diverse tissue components of a Rokitansky protuberance. *Epidermoid cyst* - A benign cyst lined by **stratified squamous epithelium** and filled with keratin debris, typically located in the skin or skull. - These cysts do not form internal protuberances with heterogeneous tissue types like those seen in teratomas. *Mucinous carcinoma* - A malignant tumor characterized by the production of **mucin**, often affecting the ovary, colon, or breast [2]. - Lesions are typically filled with mucinous material or present as mucinous masses, and do not contain the specific solid Rokitansky protuberance. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Female Genital Tract, p. 1034. [2] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. The Female Genital Tract, pp. 1033-1034. [3] Cross SS. Underwood's Pathology: A Clinical Approach. 6th ed. Common Clinical Problems From Female Genital Tract Disease, pp. 480-481.

Question 1

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 2

The immunoglobulin most commonly involved in Multiple Myeloma is:

Accepted Answer

IgG

Answer

IgM

Answer

IgA

Answer

IgD

Question 3

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 4

Most common CNS tumor associated with NF1

Accepted Answer

Optic glioma

Answer

Astrocytoma

Answer

Bilateral acoustic neuroma

Answer

Optic nerve schwannoma

Question 5

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

Accepted Answer

Hyaline

Answer

Calcareous

Answer

Red

Answer

Cystic

Question 6

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 7

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

Question 8

Lendrum's stain is done for:

Accepted Answer

Amniotic fluid embolism

Answer

Air embolism

Answer

Pulmonary embolism

Answer

Fat embolism

Question 9

Rokitansky protuberances are seen in -

Accepted Answer

Teratoma

Answer

Papillary carcinoma

Answer

Epidermoid cyst

Answer

Mucinous carcinoma

NEET-PG 2012 — Pathology