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Title: NSG 530 Advanced Pathophysiology Exam 3 – Wilkes University – Complete Exam Questions with Answers and Explanations

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Description: This document contains the complete set of exam questions and answers for NSG 530 Advanced Pathophysiology (Exam 3) at Wilkes University. It features multiple-choice questions with correct answers and in-depth rationales, covering gastrointestinal disorders, liver and biliary diseases, pancreatic pathophysiology, urinary tract disorders, reproductive system conditions, and selected endocrine dysfunctions. The explanations are expert-verified, making this a comprehensive and reliable resource for exam preparation and clinical application.

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Subido en
27 de agosto de 2025
Número de páginas
64
Escrito en
2025/2026
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Examen
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NSG 530 / NSG 530
EXAM 2 STUDY GUIDE
Advanced Pathophysiology - Wilkes



THIS GUIDE CONTAINS:
 NSG 530 Exam 2 Study Guide

 key Terms and Definitions

 Review Course

 Expert-Verified




### Autoimmunity

,Autoimmunity refers to the inappropriate immune response where the body's immune
system targets and attacks its own tissues, mistaking them for foreign invaders. This aberrant
response can lead to the development of various autoimmune diseases that often involve
multiple organ systems. Understanding the mechanisms of autoimmunity is crucial for
targeting therapies and managing symptoms in affected patients.


### Tolerance
Tolerance is the physiological state where the immune system recognizes self-antigens and
refrains from mounting an immune response against them. It is essential for preventing
autoimmune diseases and is achieved through various mechanisms, including clonal
deletion of self-reactive lymphocytes and regulatory T cells' inhibition of these cells'
activation. A breakdown in tolerance can lead to autoimmunity.


### Systemic Lupus Erythematosus (SLE)
Systemic lupus erythematosus (SLE) is one of the most common autoimmune diseases,
predominantly affecting women. It is a chronic inflammatory disorder characterized by the
production of autoantibodies that can target multiple organs, leading to a wide range of
clinical manifestations, including arthritis, skin rashes, kidney disease, and cardiovascular
issues. The heterogeneity of SLE requires comprehensive management strategies tailored to
the individual's symptoms and organ involvement.


### Notable Autoimmune Diseases
Several autoimmune diseases exemplify the spectrum of this category, including Type 1
Diabetes Mellitus (an autoimmune destruction of insulin-producing pancreatic beta cells),
Multiple Sclerosis (where the immune system attacks the myelin sheath of neurons), and
Rheumatoid Arthritis (characterized by synovial inflammation and joint destruction).
Understanding these diseases helps tailor patient management and develop therapeutic
options.


### Clinical Manifestations of SLE

,The clinical manifestations of systemic lupus erythematosus encompass a wide range of
symptoms, including arthralgias or arthritis, vasculitis leading to distinct rashes, kidney
involvement manifesting as nephritis, hematologic changes (particularly anemia and
leukopenia), and increased cardiovascular risk. These symptoms reflect SLE's systemic
nature, making regular monitoring and management critical.


### SLE Positive Labs
A hallmark laboratory finding in diagnosing systemic lupus erythematosus is a positive
antinuclear antibody (ANA) screen. While a positive ANA test indicates the presence of
autoantibodies, it is not specific to SLE and can occur in several other conditions. Therefore,
it must be interpreted in conjunction with clinical findings and additional serological tests
for more definitive diagnosis.


### Alloimmunity
Alloimmunity describes an immune response directed against transfused blood, transplanted
organs, or fetal cells during pregnancy, where the immune system recognizes these as foreign
due to the genetic differences between individuals. Understanding alloimmunity is essential,
particularly in contexts like blood transfusions and organ transplants, to prevent adverse
reactions.


### Alloantigens
Alloantigens are nonself antigens that originate from members of the same species, often
leading to alloimmune responses. These antigens are critical in contexts such as blood
transfusions and organ transplants, where mismatches can trigger severe immune reactions,
making it imperative to match donor and recipient antigens as closely as possible.


### Transfusion Reactions
Transfusion reactions represent a serious and potentially fatal complication occurring when
the recipient's immune system mounts a vigorous response against incompatible donor
blood. Symptoms can include fever, chills, and hemolysis, which may lead to acute renal

, failure. Proper blood type matching and screening are fundamental in preventing such
reactions.


### Universal Donor and Recipient
Type O blood is often referred to as the universal donor type due to the absence of A and B
antigens, allowing it to be transfused to patients of any blood type without triggering an
immune response. Conversely, type AB blood is considered a universal recipient, as these
individuals possess no anti-A or anti-B antibodies, enabling them to receive any blood type.


### Rh Blood Type
The Rh blood type is determined by the presence or absence of the Rh factor (D antigen) on
the surface of erythrocytes. Individuals with the Rh antigen are classified as Rh-positive,
while those without it are termed Rh-negative. This classification is crucial for blood
transfusions and maternal-fetal compatibility.


### Hemolytic Disease of the Newborn
Hemolytic disease of the newborn (HDN) can occur when an Rh-negative mother carries an
Rh-positive fetus. During birth, exposure to Rh-positive blood can stimulate the mother’s
immune system to produce antibodies against the Rh factor, which may subsequently attack
the fetal red blood cells in subsequent pregnancies. Preventive measures, such as
administering Rh immunoglobulin (RhoGAM), are vital to avoid this condition.


### RhoGAM
RhoGAM is an immunoglobulin preparation that contains anti-D antibodies, used to
prevent Rh incompatibility in pregnant women who are Rh-negative. Administered during
pregnancy and after delivery, it effectively prevents the mother's immune system from
recognizing and attacking the red blood cells of an Rh-positive fetus, thereby minimizing the
risk of hemolytic disease of the newborn.


### Transplant Rejection
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