Theme 10 - SOFT TISSUE, BONE AND JOINTS Flashcards

1
Q

what is “soft tissue”?

A

supportive tissue of organs and lymphoid tissue e.g. fibrous, adipose, skeletal (bone) and PNS

mesodermal in origin

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2
Q

Soft tissue tumours names (benign)

A

Most of them are benign

Lipomas- fat tissue
Fibromas- fibrous tissue
Leiomyomas- smooth muscle
Heamangiomas- blood vessel
Lymphangiomas- lymphatics
Neuromas- Peripheral nerves
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3
Q

Nature of malignant soft tissue tumours

A

Sarcomas

Account for 1% of malignancies

Blood spread (haematogenous) to liver and lung but can spread via lymph system but this is less common

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4
Q

What syndromes are associated with soft tissue tumours?

A

Neurofibromatosis Type 1- Neurofibroma

Gardner syndrome-Fibromatosis

Carney syndrome-

Myxoma, melanotic schwannoma

Turner syndrome - cystic hygroma

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5
Q

How can soft tissue tumours be diagnosed?

A

Ultrasound guided core biopsy

Wide excision
(by musculoskeletal radiologist)

Genetically:

Cytogenetics- culture of fresh tissue and karyotypic analysis

Molecular genetics-
FISH and PCR and RT-PCR

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6
Q

Where do bone tumours arise and what are they called?

A

Arise from bone and cartilage

Osteoma if benign and osteosarcomas if malignant

benign cartilage tumours are chondromas

osteochondromas are mixec cartilage and bone tumours

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7
Q

osteosarcomas are most seen in what type of patients and which body parts?

A

young age group - teens

presents mainly in the knee (60% of cases)

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8
Q

other bone tumours

A

Ewing’s sarcoma

Giant cell tumours - can be benign or malignant

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9
Q

metastatic bone tumours - where are the primary sites?

A
thyroid
prostate
kidney
breast
GI tract
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10
Q

Systemic Lupus Eryth. symptoms and associated co morbidities

A

Cutaneous- Butterfly rash is typical affecting the bridge of nose and the cheeks

Cardiac- cardiomegaly,
endocarditis

CNS- important cause for morbidity and mortality- convulsions, hemiplegia

Renal- 45% of patients, Nephrotic syndrome and glomerulonephritis

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11
Q

What is systemic sclerosis?

A

Vessel damage and inflammatory response

causes diffuse widespread cutaneous lesions

Has renal, cardiorespiratory and GI tract implications

Artharlgia and arthritis involvement too

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12
Q

What is polymyalgia rheumatica symptoms?

A

Stiffness, weakness, aching and pain in the muscles of neck, limb girdles and upper limbs.

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13
Q

What is polymyalgia rheumatica associated with?

A

giant cell arteritis-
affects occipital or facial arteries- pyrexia, headache and severe scalp pain

granulomatous chronic inflammation

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14
Q

What are the 2 main categories of muscle diseases?

A

Myopathy-
Muscle disease unrelated to any disorder of innervation or neuromuscular junction

Myositis-
muscle fibres and overlying skin are inflamed and damaged resulting in muscle weakness

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15
Q

Muscular dystrophy pathogenesis & aetiology

A

inherited disorder (heterogenous)

causing progressively severe muscle weakness
and wasting

Begins in childhood

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16
Q

what are the signs of malignant hyperthermia? (why is it only discovered during surgery?)

A

fast rise in body temperature and severe muscle contraction when the patient gets general anaesthesia

MAIN SYMPTOMS:
bleeding
dark brown urine
muscle rigidity

17
Q

What is rhabdomyolysis?

A

The destruction of skeletal muscle that then causes the release of muscle fibre content into blood.

18
Q

Why do patients with rhabdomyolysis present with brown urine (myoglobinuria)?

A

Myoglobin is released into the blood stream due to muscle fibre being in the blood
Filtered through the kidney and enters urine- brown urine

19
Q

what causes rhabdomyolysis?

A

Trauma, crush injuries
cocaine, amphetamine

Extreme temperature

Severe exertion-marathon running

Lengthy surgery

Severe dehydration

Important complication- acute renal failure