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Tower-Gilchrist
The below case study was pulled from WileyPlus. Please read the case carefully and answer the questions.
Presenting symptoms
Pain and swelling in hands and feet
Morning stiffness
Bilateral (both right and left) involvement of joint areas
Increasing hand and foot deformities
Difficulty in performing daily tasks
Weakness
Weight loss
Family history of similar complaints
Physical exam:
Metacarpo-phalangeal and proximal interphalangeal joints are
swollen, warm to the touch and tender
Ulnar deviation of fingers at metacarpo-phalangeal joints
Large subcutaneous nodule near the olecranon process of right
elbow
Vital signs:
Blood pressure 130/85; Heart rate 90 beats/min; and Temperature 99.7degrees F
Lab results:
Blood
White blood cells 13, 000/mm3
Test for rheumatoid factor:
positive
Erythrocyte sedimentation rate
(ESR) 35mm/hr
Hand X-ray:
Ulnar deviation at metacarpophalangeal joints, metacarpal dislocations, flexion of interphalangeal joints
We can begin with looking at the defects that were observed including chemical, cellular, and tissue defects.
Chemical Defects
In affected joints, cells of the immune secrete certain enzymes that
destroy the articular cartilage and underlying bone.
- Collagenase destroys collagen
- Protease destroy the components of the ground substance
Bone destruction and deformity reduces the joint’s range of motion.
Cellular Defects
In disease joints, articular cartilage is damaged by actions of cells:
T lymphocytes Plasma cells
Macrophages Neutrophils
Synociocytes Chondroblasts
Neutrophils migrate to the inflamed joint early in the disease process. Phagocytize RFs already formed in the joint.
Release collagenases and proteases that destroy joint cartilage and bone.
Let’s take a look at the structures that are found within a joint.
Synovial fluid- found within the joint cavity, this fluid lubricates
the joint and proves nutrients to cells of the articular cartilage
Matrix
-Collagen fibers form a structural frameworks that provides
strength and flexibility
-Gel-like ground substance contains proteoglycans and hyaluronic acid and provides resistance to compression
Tissue Defects
Mrs. Lewis suffers from a condition that affects distal joints.
The pathological hallmark of this condition which is a pannus, thickened layer of synovial membrane, that erodes
cartilage.
Normal joint (no pannus)
Pannus forms and begins to invade cartilage
Pannus continues to grows and reaches underlying bone
Pannus spans the entire join space, fusing and deforming bones
Rheumatoid nodules are common in severe cases and often appear as bony prominences under the skin in the hand,
elbow, forearm, and knee. They consist of fibrotic scar tissue surrounded by lymphocytes and plasma cells.
The inflammation and tissue changes symptomatic of this disease can be observed in many different organ systems
o Skin: Subcutaneous rheumatoid nodules
1. Which of the following conditions BEST describes Mrs. Lewis’ clinical signs and symptoms?
a. Gout
b. Tennis elbow
c. Osteoporosis
d. Cerebral palsy
e. Rheumatoid arthritis
2. Which of the following BEST explains Mrs. Lewis’ elevated white blood cell count
a. Viral osteomyelitis (infection of bone)
b. Bacterial joint infection
c. Autoimmune destruction of joints
d. Bacterial pneumonia
e. Normal
5. What is the role of this cell type in the synovial membrane of Mrs.
Lewis’ Joints?
a. Secretes collagenase and proteases
b. Protects lymphoid nodules
c. Secretes antibodies
d. Contributes to matrix repair
e. Ingests debris and dead cells