Maria received a diagnosis of this inflammatory bowel disease when she was 14 years old; the surface of her ascending colon resembles "cobblestones", known as skipped lesions, with thickened areas that resemble lead pipes. What type of inflammatory bowel disease does Maria have?
Diverticulitis
Crohn's Disease
Diverticulosis
Ulcerative Colitis
The Correct Answer is B
A. Diverticulitis: This condition involves inflammation or infection of diverticula (small pouches) in the colon wall, typically presenting with localized pain and not characterized by “cobblestone” appearance or skipped lesions seen on colonoscopy.
B. Crohn's Disease: The description of “cobblestone” mucosa, skipped lesions, and thickened bowel walls resembling “lead pipes” are classic features of Crohn’s disease. It can affect any part of the gastrointestinal tract and presents with patchy, transmural inflammation causing thickening and characteristic endoscopic findings.
C. Diverticulosis: This condition involves the presence of diverticula without inflammation. It does not cause the cobblestone or skipped lesion appearance seen in inflammatory bowel disease and is generally asymptomatic unless complicated by diverticulitis.
D. Ulcerative Colitis: This disease causes continuous inflammation usually starting in the rectum and extending proximally, leading to a loss of haustral markings but does not typically present with skipped lesions or a cobblestone appearance. The colon wall tends to be thin rather than thickened.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is ["A","G"]
Explanation
A. Transient Ischemic Attack (TIA): A TIA presents with stroke-like symptoms that resolve within minutes to hours without permanent damage. Ms. Lauren’s symptom resolution within 6 hours and return to baseline strongly suggests a TIA. Prompt recognition is essential, as TIAs are often precursors to future strokes and require further evaluation.
B. Hemorrhagic Stroke: Hemorrhagic strokes typically present with sudden, severe symptoms such as intense headache, vomiting, or rapid loss of consciousness. These symptoms usually do not resolve quickly. Ms. Lauren’s gradual symptom resolution and stable vital signs are not consistent with this type of stroke.
C. Severe vision loss in both eyes: While visual disturbances can occur during strokes, bilateral severe vision loss is less common and would typically be seen in strokes involving the occipital lobes or vertebrobasilar system. Ms. Lauren’s case does not provide evidence of this symptom, hence an unlikely feature here.
D. Sudden loss of consciousness: Loss of consciousness is more common in massive strokes, particularly hemorrhagic ones or those involving the brainstem. Ms. Lauren remained awake and was able to report symptoms and anxiety, which rules out this presentation.
E. Sudden severe headache with vomiting: This symptom combination is more typical of a hemorrhagic stroke or subarachnoid hemorrhage. Ms. Lauren did not report a headache or vomiting, which makes this an unlikely symptom in her current presentation.
F. Ischemic Stroke: Ischemic strokes result in prolonged neurological deficits lasting more than 24 hours. Since Ms. Lauren’s symptoms are resolving within a short window and she is returning to baseline, this is less likely than a TIA in her situation.
G. Sudden weakness or numbness, often on one side of the body: This is a hallmark sign of a TIA or stroke. Ms. Lauren’s initial symptoms were stroke-like and likely included unilateral weakness or numbness, which are classic indicators of a TIA.
Correct Answer is C
Explanation
A. Tubular necrosis: Tubular necrosis refers to the death of tubular epithelial cells in the kidneys, commonly due to ischemia or toxins. This is not the primary defect in Potter syndrome, which involves developmental abnormalities rather than acute tubular injury.
B. Renal hyperplasia: Hyperplasia means increased cell number leading to organ enlargement. Potter syndrome typically involves renal hypoplasia or agenesis rather than hyperplasia, so this is not consistent with the syndrome’s defect.
C. Renal failure: Potter syndrome primarily results from bilateral renal agenesis or severe renal dysplasia, leading to absent or nonfunctional kidneys and subsequent renal failure. The lack of functional kidneys leads to oligohydramnios and the characteristic features of Potter syndrome.
D. Renal metaplasia: Metaplasia refers to abnormal transformation of one differentiated tissue type into another. This process is not the main defect in Potter syndrome, which is related to kidney development failure rather than abnormal tissue differentiation.
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