Removal of the _______ would be more harmful to a one-year-old child than an adult.
Spleen
lymph node
thymus
appendix
palatine tonsil
The Correct Answer is C
A. Spleen: While splenectomy increases the risk of overwhelming post-splenectomy infection (OPSI) in both children and adults, it is not the primary organ of early immune development. The spleen functions largely in filtering blood and recycling erythrocytes. Its loss is significant but manageable through prophylactic antibiotics and vaccinations at any age.
B. lymph node: The human body contains hundreds of lymph nodes distributed throughout various regional chains. The surgical removal of a single node or even a small group does not compromise systemic immune competence. Their redundancy ensures that lymphatic filtration and antigen presentation continue effectively despite the loss of individual nodes.
C. thymus: In a one-year-old, the thymus is at its peak physiological activity, driving the maturation and selection of the entire T cell repertoire. Early childhood thymectomy leads to profound and permanent immunodeficiency due to the lack of newly educated T cells. In adults, the thymus has already undergone involution and its removal is far less detrimental.
D. appendix: This structure contains a small amount of mucosa-associated lymphoid tissue but is not essential for systemic immune development. Its removal, typically performed during an appendectomy, does not result in measurable immunocompromise in infants or adults. It serves as a secondary rather than primary lymphoid organ.
E. palatine tonsil: Tonsillectomy is a common pediatric procedure that generally has no significant long-term impact on systemic health or immune function. While these tonsils assist in local oral immunity, other lymphoid tissues in Waldeyer's ring compensate for their absence. Their removal is not considered harmful to the overall development of the child.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is E
No explanation
Correct Answer is C
Explanation
A. Pancreas: This gland regulates blood glucose levels by secreting the hormones insulin and glucagon from the islets of Langerhans. While it monitors glucose concentrations, it does not serve as a primary storage depot for glycogen. It facilitates glucose uptake in other tissues rather than sequestering it.
B. Stomach: The primary functions of this organ are mechanical churning and initial chemical proteolysis of the ingested bolus. It does not possess the metabolic pathways for glycogenesis or glycogenolysis. It serves as a temporary reservoir for food but not for systemic energy substrates.
C. Liver: Hepatocytes convert surplus blood glucose into glycogen through the process of glycogenesis for long-term storage. When blood sugar levels decline, the liver performs glycogenolysis to release glucose back into the systemic circulation. It acts as the central metabolic hub for glucose homeostasis.
D. Spleen: This lymphatic organ is primarily involved in filtering blood, recycling iron from senescent erythrocytes, and mounting immune responses. It serves as a reservoir for platelets and white blood cells rather than carbohydrates. It plays no significant role in the regulation of blood glucose levels.
E. small intestine: This is the principal site for the absorption of monosaccharides into the portal venous system following digestion. While it transports glucose across its epithelial lining, it does not store significant quantities of glycogen for systemic use. It functions as a gateway rather than a storage organ.
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