Nearly all cervical carcinomas contain human papillomavirus (HPV). Which of the following types is never associated with such malignancy?

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Question 1 of 5

Nearly all cervical carcinomas contain human papillomavirus (HPV). Which of the following types is never associated with such malignancy?

Correct Answer: A

Rationale: The correct answer is A) type 6. The human papillomavirus (HPV) is a known risk factor for cervical carcinomas. Types 16 and 18 are the most common high-risk HPV types associated with cervical cancer. Type 31 is also considered a high-risk type. However, type 6 is classified as a low-risk HPV type and is not associated with cervical malignancy. Educational Context: Understanding the association between HPV types and cervical cancer is crucial for healthcare professionals, especially in pediatric care where prevention and early detection are key. By knowing which HPV types are high-risk for cervical cancer, healthcare providers can better inform and educate their patients about vaccination, screening, and early intervention strategies. This knowledge is essential for nurses, nurse practitioners, and physicians working in pediatric settings to provide comprehensive care and promote preventive health practices.

Question 2 of 5

Osteosarcoma is the most common primary malignant bone tumor in children and adolescents; it has multiple subtypes and requires different modalities of treatment including surgery and chemotherapy. Of the following, the subtype of osteosarcoma which is treated by surgery alone is

Correct Answer: D

Rationale: The correct answer is D) periosteal. Periosteal osteosarcoma is a subtype that is typically treated with surgery alone. Unlike other subtypes such as fibroblastic, chondroblastic, and parosteal osteosarcoma which often require a combination of surgery and chemotherapy, periosteal osteosarcoma is a low-grade tumor that can often be effectively treated through surgical resection alone. Fibroblastic and chondroblastic osteosarcomas are more aggressive subtypes that usually necessitate a multimodal approach involving surgery and chemotherapy to achieve the best outcomes. Parosteal osteosarcoma, although less common, also typically requires a combination of surgery and chemotherapy due to its location and characteristics. In an educational context, understanding the different subtypes of osteosarcoma and their respective treatment modalities is crucial for healthcare providers working with pediatric oncology patients. This knowledge helps in making informed decisions regarding treatment planning and providing optimal care to patients with osteosarcoma. By differentiating the subtypes and their treatment approaches, healthcare professionals can tailor interventions to individual patient needs, improving outcomes and quality of life.

Question 3 of 5

A 9-year-old boy develops acute myelogenous leukemia (AML) one year after completion of therapy for soft tissue sarcoma at his right thigh. Which of the following chemotherapeutic agents is MOST likely the cause of secondary acute myelogenous leukemia AML in this boy?

Correct Answer: C

Rationale: In understanding why etoposide is the most likely cause of secondary acute myelogenous leukemia (AML) in the 9-year-old boy, we need to consider the drug's mechanism of action. Etoposide is a topoisomerase II inhibitor, which can lead to DNA damage and chromosomal translocations associated with the development of secondary malignancies like AML. Regarding the other options: A) Cyclophosphamide is alkylating agent associated with secondary malignancies but less commonly linked to AML compared to etoposide. B) Vincristine is a microtubule inhibitor and is not typically associated with secondary AML. D) Doxorubicin is an anthracycline that can cause secondary leukemias, but etoposide has a stronger association with AML development. Educationally, this question highlights the importance of understanding the long-term effects of chemotherapy in pediatric oncology patients. Healthcare providers need to be aware of the potential risks associated with different chemotherapeutic agents to provide comprehensive care and long-term surveillance for these vulnerable patients.

Question 4 of 5

Which manifestation is more specific to occur in anaplastic large cell lymphoma (ALCL) than other types of non-Hodgkin lymphoma?

Correct Answer: D

Rationale: In anaplastic large cell lymphoma (ALCL), primary mediastinal involvement is more specific compared to other types of non-Hodgkin lymphoma. The characteristic presentation of ALCL often includes a mass in the mediastinum. This is due to the high expression of the CD30 antigen in ALCL cells, leading to a propensity for mediastinal lymph node involvement. This feature helps differentiate ALCL from other lymphomas. Option A, primary bone marrow involvement, is not specific to ALCL and can be seen in various lymphomas. Option B, intestinal involvement, is more typical of other types of lymphoma such as mucosa-associated lymphoid tissue (MALT) lymphoma. Option C, CNS involvement, is more commonly associated with lymphomas like Burkitt lymphoma or primary CNS lymphoma. Educationally, understanding the distinct clinical features of different types of lymphomas is crucial for accurate diagnosis and appropriate management. Recognizing specific manifestations like primary mediastinal involvement in ALCL can aid healthcare providers in providing targeted care and optimizing patient outcomes.

Question 5 of 5

A 2-year-old child is being evaluated for a right flank mass; radiological appearance is consistent with rupture of Wilms tumor. The BEST therapeutic approach for this child is

Correct Answer: B

Rationale: In this scenario, the BEST therapeutic approach for a 2-year-old child with a ruptured Wilms tumor is concomitant chemotherapy-radiotherapy (Option B). This approach is chosen because Wilms tumor is a type of kidney cancer that commonly affects children, and a multimodal treatment plan involving both chemotherapy and radiotherapy has been shown to be the most effective in improving survival rates and reducing the risk of recurrence. Option A, radiotherapy alone, is not the preferred treatment because Wilms tumor typically requires a combination of chemotherapy and radiotherapy for optimal outcomes. Option C, another surgery, is not the immediate course of action for a ruptured Wilms tumor as the primary treatment involves a combination of chemotherapy and radiotherapy. Option D, observation, is not suitable in this case as Wilms tumor is an aggressive cancer that requires prompt and aggressive treatment to improve outcomes. Educationally, it is crucial for healthcare providers, especially those specializing in pediatric oncology, to understand the importance of multimodal treatment approaches in managing pediatric cancers like Wilms tumor. This case emphasizes the significance of evidence-based practice and multidisciplinary collaboration in providing the best possible care for pediatric oncology patients.

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