You are discussing the risk of radiotherapy with the parents of a child with medulloblastoma; the mother has a concern about the late neurological complications post radiotherapy. The statement that should be included in the discussion that late neurological sequelae post radiotherapy is more severe with

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Question 1 of 5

You are discussing the risk of radiotherapy with the parents of a child with medulloblastoma; the mother has a concern about the late neurological complications post radiotherapy. The statement that should be included in the discussion that late neurological sequelae post radiotherapy is more severe with

Correct Answer: B

Rationale: In pediatric oncology, understanding the impact of radiotherapy on children with brain tumors is crucial. The correct answer, option B, stating that late neurological sequelae post radiotherapy are more severe in children less than 3 years old, aligns with the knowledge that younger children have developing brains that are more vulnerable to the effects of radiation. Option A is incorrect because craniospinal irradiation, while encompassing a larger area, is associated with more acute rather than late neurological complications. Option C, concomitant chemo-radiotherapy, may increase the overall toxicity but doesn't specifically correlate with increased late neurological sequelae. Option D is incorrect as the severity of late neurological sequelae is not determined by tumor grade. Educationally, this question underscores the importance of considering age as a factor in the risk assessment of late effects of radiotherapy in pediatric patients with medulloblastoma. It highlights the need for personalized treatment approaches based on age-related vulnerabilities in pediatric oncology. Understanding these nuances can help healthcare providers tailor discussions with parents to address concerns and make informed treatment decisions.

Question 2 of 5

In Langerhans cell histiocytosis (LCH), all the following manifestations are at high risk of mortality in patients EXCEPT

Correct Answer: C

Rationale: In Langerhans cell histiocytosis (LCH), manifestations in certain organs can pose a high risk of mortality due to potential complications. The correct answer, option C - lung, is not typically associated with high mortality risk in LCH patients. This is because lung involvement in LCH usually presents with pulmonary nodules or cysts, which are often manageable and do not directly lead to mortality. Options A, B, and D (liver, spleen, hematopoietic system) are at higher risk of mortality in LCH patients. Liver involvement can cause liver failure, spleen involvement can lead to severe cytopenias and hypersplenism, and hematopoietic system involvement can result in bone marrow dysfunction and subsequent complications. Educationally, understanding the specific organ manifestations and associated risks in Langerhans cell histiocytosis is crucial for healthcare providers managing these patients. Recognizing which organ involvement carries a higher mortality risk helps in timely intervention and appropriate management to improve patient outcomes.

Question 3 of 5

Poor prognostic factors in Hodgkin lymphoma include all the following EXCEPT

Correct Answer: A

Rationale: In Hodgkin lymphoma, poor prognostic factors are important to consider for treatment planning and patient outcomes. The correct answer is A) age of more than 15 years at the time of diagnosis. This is because pediatric patients with Hodgkin lymphoma generally have a better prognosis compared to older individuals. Younger age is associated with a more favorable response to treatment and overall survival. Option B) stage IV disease is a poor prognostic factor because it indicates widespread disease dissemination, making treatment more challenging and outcomes less favorable. Option C) manifested by PET scan positivity is also a poor prognostic factor as it suggests more aggressive disease behavior and resistance to treatment. Option D) poor response to therapy is an obvious poor prognostic factor as it indicates that the disease is not being controlled effectively. Educationally, understanding poor prognostic factors in Hodgkin lymphoma is crucial for healthcare providers involved in the care of pediatric patients with this condition. By recognizing these factors, clinicians can tailor treatment plans to optimize outcomes and provide appropriate support to patients and their families. It is essential to consider both clinical and biological factors when assessing prognosis in Hodgkin lymphoma to ensure the best possible care for patients.

Question 4 of 5

A 2-year-old male child has an asymptomatic right flank mass discovered incidentally by the mother while bathing. Suspicion of Wilms tumor is raised. Of the following, the LEAST likely investigation to be performed in this child is

Correct Answer: D

Rationale: The correct answer is D) biopsy of the mass. In the case of a suspected Wilms tumor in a pediatric patient, a biopsy of the mass is the least likely investigation to be performed initially. This is because biopsy carries the risk of causing tumor spillage and seeding, potentially complicating future surgical management. Option A) plain abdominal radiography is not the most useful imaging modality for evaluating a suspected Wilms tumor. Option B) and C) involve CT scans of the abdomen and chest, respectively, which are crucial in staging the tumor and evaluating any possible metastasis. In an educational context, it is important to emphasize the diagnostic approach in pediatric oncology. Understanding the appropriate sequence of investigations and their implications is vital for providing optimal care for pediatric patients suspected of having malignancies. Biopsy is often reserved for cases where imaging studies are inconclusive or for definitive diagnosis after surgical resection.

Question 5 of 5

Kasabach-Merritt syndrome is characterized by all the following EXCEPT

Correct Answer: D

Rationale: In Kasabach-Merritt syndrome, a rare and serious condition seen in pediatric patients, the correct answer is D) association with infantile hemangiomas. This is the exception among the listed characteristics. Infantile hemangiomas are not associated with this syndrome. Thrombocytopenia (low platelet count), microangiopathic hemolytic anemia (breakdown of red blood cells due to abnormal blood vessels), and coagulopathy (bleeding disorder) are all typical features of Kasabach-Merritt syndrome. These abnormalities result from the consumption of platelets and clotting factors within the abnormal blood vessels. Educationally, understanding the distinguishing features of Kasabach-Merritt syndrome is crucial for healthcare providers caring for pediatric patients. Recognizing the syndrome's typical presentation can lead to prompt diagnosis and appropriate management to prevent potentially life-threatening complications. Identifying the absence of infantile hemangiomas in this context is vital for accurate clinical assessment and decision-making.

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