Sarcoidosis Flashcards

1
Q

What is sarcoidosis?

A

Granulomatous inflammatory condition
Granulomas are nodules of inflammation full of macrophages

Usually associated with chest symptoms but also has multiple extra-pulmonary manifestations such as erythema nodosum and lymphadenopathy

Spikes in young adults and around 60

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Lung symptoms in Sarcoid

A

Mediastinal lymphadenopathy
Pulmonary fibrosis
Pulmonary nodules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Systemic symptoms in Sarcoid

A

Fever
Fatigue
Weight loss

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Liver symptoms in sarcoid

A

Liver nodules
Cirrhosis
Cholestasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Eye symptoms

A

Uveitis
Conjunctivitis
Optic neuritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Skin symptoms in sarcoid

A
Erythema nodosum (tender, red nodules on the shins caused by inflammation of the subcutaneous fat)
Lupus pernio (raised, purple skin lesions commonly on cheeks and nose)
Granulomas develop in scar tissue
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Heart symptoms

A

Bundle branch block
Heart block
Myocardial muscle involvement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Kidney symptoms

A

Kidney stones (due to hypercalcaemia)
Nephrocalcinosis
Interstitial nephritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

CNS Symptoms

A

Nodules
Pituitary involvement (diabetes insipidus)
Encephalopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

PNS Symptoms

A

Facial nerve palsy

Mononeuritis multiplex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Bone symtoms

A

Arthralgia
Arthritis
Myopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is Lofgren’s Syndrome?

A

Specific presentation of sarcoidosis. It is characteristic by a triad of:

Erythema nodosum
Bilateral hilar lymphadenopathy
Polyarthralgia (joint pain in multiple joints)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Differential diagnosis for sarcoid

A
Tuberculosis
Lymphoma
Hypersensitivity pneumonitis
HIV
Toxoplasmosis
Histoplasmosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Blood tests in sarcoid

A

Raised serum ACE. This is often used as a screening test.
Hypercalcaemia (rasied calcium) is a key finding.
Raised serum soluble interleukin-2 receptor
Raised CRP
Raised immunoglobulins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Imaging in sarcoid

A

Chest xray shows hilar lymphadenopathy
High-resolution CT thorax shows hilar lymphadenopathy and pulmonary nodules
MRI can show CNS involvement
PET scan can show active inflammation in affected areas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Gold standard for confirming sarcoid?

A

Histology from biopsy, usually from bronchoscopy with US guided biopsy of mediastinal lymph nodes

Shows characteristic non-caseating granulomas with epithelioid cells

17
Q

Test for other organ involvement in sarcoid (6)

A

U&Es for kidney involvement
Urine dipstick or urine albumin-creatinine ratio to look for proteinuria indicating nephritis
LFTs for liver involvement
Ophthalmology review for eye involvement
ECG and echocardiogram for heart involvement
Ultrasound abdomen for liver and kidney involvement

18
Q

Treatment for sarcoid

A

No treatment is considered as first line in patients with no or mild symptoms as the condition often resolves spontaneously

Oral steroids are usually first line where treatment is required
Given for between 6 and 24 months (bisphosphonates)

Second line options are methotrexate or azathioprine

Lung transplant is rarely required in severe pulmonary disease

19
Q

What is the prognosis for sarcoidosis?

A

spontaneously resolves within 6 months in around 60% of patients

Small number of patients it progresses with pulmonary fibrosis and pulmonary hypertension (lung transplant)

Death is usually due to heart or CNS involvement