Written by students who passed Immediately available after payment Read online or as PDF Wrong document? Swap it for free 4.6 TrustPilot
logo-home
Document preview thumbnail
Preview 3 out of 24 pages
Exam (elaborations)

WGU D236 PATHOPHYSIOLOGY COMPREHENSIVE ASSESSMENT QUESTIONS AND ANSWERS 2027

Document preview thumbnail
Preview 3 out of 24 pages

WGU D236 PATHOPHYSIOLOGY COMPREHENSIVE ASSESSMENT QUESTIONS AND ANSWERS 2027

Content preview

WGU D236 PATHOPHYSIOLOGY
COMPREHENSIVE ASSESSMENT
QUESTIONS AND ANSWERS 2027



1. A patient’s biopsy shows one adult cell type has been replaced by another adult cell type.

Which term describes this adaptation?

A. Metaplasia


B. Hyperplasia


C. Atrophy


D. Dysplasia


Answer: A


Conceptual Explanation: Metaplasia is the reversible replacement of one mature cell type

by another, often in response to chronic irritation.


2. Which electrolyte imbalance is most commonly associated with a positive Chvostek sign?

A. Hyponatremia


B. Hyperkalemia


C. Hypocalcemia


D. Hypomagnesemia

,Answer: C


Conceptual Explanation: Hypocalcemia increases neuromuscular excitability, leading to

the Chvostek sign (facial twitching when the facial nerve is tapped).


3. Which type of hypersensitivity reaction is characterized by an IgE-mediated response to an

allergen?

A. Type II


B. Type I


C. Type III


D. Type IV


Answer: B


Conceptual Explanation: Type I hypersensitivity is an immediate allergic reaction

mediated by IgE antibodies and mast cell degranulation.


4. In the TNM staging system for cancer, what does the ‘N’ represent?

A. Neoplasm size


B. Number of tumors


C. Necrosis level


D. Node involvement


Answer: D

, Conceptual Explanation: In TNM staging, T stands for Tumor size, N stands for regional

lymph Node involvement, and M stands for distant Metastasis.


5. Which condition is characterized by a 45,X karyotype and results in female phenotypic

features?

A. Down Syndrome


B. Klinefelter Syndrome


C. Edwards Syndrome


D. Turner Syndrome


Answer: D


Conceptual Explanation: Turner Syndrome occurs when a female is born with only one X

chromosome (45,X).


6. What is the primary pathophysiology behind Type 1 Diabetes Mellitus?

A. Insulin resistance in peripheral tissues


B. Excessive glucagon production by alpha cells


C. Autoimmune destruction of pancreatic beta cells


D. Decreased glucose absorption in the gut


Answer: C


Conceptual Explanation: Type 1 Diabetes is caused by an autoimmune-mediated

destruction of the insulin-producing beta cells in the pancreas.

Document information

Uploaded on
August 2, 2026
Number of pages
24
Written in
2026/2027
Type
Exam (elaborations)
Contains
Questions & answers
$15.99

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
Fyndlay
3.7
(75)
Sold
421
Followers
81
Items
20148
Last sold
1 week ago



Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions