Non-malignant pathology Flashcards

1
Q

What are the symptoms of hashimotos thyroiditis?

A

hypothyroidism - weight gain, fatigue, constipation, depression, hair loss

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2
Q

What is seen histologically for hashimotos thyroiditis?

A

lymphocytic infiltrates and fibrosis

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3
Q

What is seen immediately in the blood post splenectomy?

A

granulocytosis - WBC - neuts/ eosin/ basophils

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4
Q

What is seen immediately in the blood in the first few days post splenectomy?

A

target cells, siderocytes, reticulocytes

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5
Q

Other blood cells seen in a splenectomy?

A

Howell- jolly bodies, pappenheimber bodies, target cells, Heinz bodies

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6
Q

What is seen in peutz jeghers syndrome?

A

Hamartomous polyps, muccocutaneous hyperpigmentation (lips, face, palms, soles)

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7
Q

what is the genetic pathway for peutz jeghers syndrome?

A

Autosomal dominant

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8
Q

What gene mutation is seen in familial adenomatous polyposis?

A

APC gene mutation

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9
Q

What gene mutation is seen in Cowden disease?

A

PTEN gene mutation

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10
Q

What is required for diagnosis of Kartageners syndrome?

A

Primarily immotile cilia combined with situs inverses

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11
Q

Primary TB - what is the lung and hilarious lymph nodes known as?

A

Ghon Complex

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12
Q

When does secondary TB occur?

A

If a host becomes immunocompromised - an initial infection can reactivate - lungs are common site

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13
Q

What histology will be seen in a granuloma in a TB patient?

A

epithelial histiocytes, caseous necrosis in the centre

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14
Q

What type of stain is used for TB?

A

Zeihl-Neelsen staining

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15
Q

What type of hypersensitivity reaction is TB?

A

T4 - stimulates specific T cell response of cell mediated immunity

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16
Q

What does amyloid look like under the microscope?

A

apple befringence with polarised light

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17
Q

What is Plummer Vinson syndrome?

A

oesophageal web associated with iron deficient anaemia

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18
Q

How do you investigate dysphagia?

A

upper GI endoscopy, fluoroscopic swallow, ambulatory ph

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19
Q

Which symptoms makeup antiphospholipid syndrome?

A

-foetal loss, venous/ arterial thrombus/ thrombocytopenia - APTT prolonged

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20
Q

blood tests for antiphospholipid syndrome?

A

lupus anticoagulant, anti-cardiolipin, anti beta 2

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21
Q

What is the most common causative organism for iliopsoas abscess

A

staph aureus

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22
Q

Which cell failures causes pernicious anaemia

A

lack of production of IF by the parietal cells

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23
Q

Where do you find dermoid cysts

A

at sites of embryonic developmental fusion

24
Q

What disease causes medial displacement of ureters?

A

retroperitoneal fibrosis

25
What is the genetic pathway of achondroplasia?
Autosomal dominant
26
What is a curling ulcer?
peptic stress ulceration
27
Which organism causes secondary infection in burns victims?
staph aureus
28
Which cell is needed for healing of a burn?
keratinocytes (needed from skin grafts in full thickness burns)
29
Which Ig is involved in T1 hypersensitivity reaction
IgE
30
Give an example of T1 hypersensitivity reaction
asthma/ hay fever
31
Give an example of a t2 hypersensitivity reaction
haemolytic anaemia/ autoimmune causes
32
What type of hypersensitivity reaction is aspergillosis ?
t3
33
Which is the delayed type of hypersensitivity reaction?
t4
34
Give an example of t4 hypersensitivity reaction
Graft vs host disease, contact dermatitis , granulomas
35
How soon is an acute blood transfusion reaction seen?
24 hours
36
How long after is a delayed transfusion reaction seen?
5-10 days afterwards
37
What causes a transfusion associated lung injury?
neutrophilic mediated allergic pulmonary oedema
38
What do you see in DIC?
prolonged pt, prolonged apt, prolonged bleeding time, low platelet count, fibrin degradation products raised
39
Which factors effect APTT
8,9,11,12
40
Which factors effect PT
2,7,9,10 - vit K dependent (think warfarin)
41
How is platelet function measured ?
Bleeding time
42
How is platelet function measured ?
Bleeding time
43
What will a liver cell adenoma look like on USS ?
mixed echogenicity and heterogenous texture
44
What is a hydatid cyst caused by ?
echinococcus infection - middle easter/ Mediterranean countries
45
neurofibromatosis t1 what are the signs?
schwannoma, axillary freckling, lisch nodules, optic glioma, meningiomas, glioma and >6 cafe au last spots
46
What is characteristic of neurofibromatosis T2?
bilateral acoustic neuromas and a FH of neurofibromatosis
47
What are the signs of tuberous sclerosis?
depigmented ash leaf spots, rough skin on lumbar spine, adenoma sebaceoum, care au lait spots
48
what is characteristic of dercums disease?
multiple lipomas
49
What causes graft vs host disease?
lymphocytic proliferation
50
What are the features of von hipple Lindau syndrome?
Cerebellar haemangiomas, retinal haemangionas, renal cysts, pheochromocytoma
51
What is coagulative necrosis?
Most common type of necrosis, early stage - little change, later stages loss of intracellular detail
52
What is colliquative necrosis?
in tissues with no supporting stroma seen in CNS
53
What is Caseous necrosis?
No definable structure seen - amorphous eosinophilic tissue seen histologically
54
What do dermoid cysts contain?
Multiple cell types, often hair is seen
55
What disease are asteroid bodies found in histologically?
Sarcoid
56
Which amino acid is present in all types of collagen?
Glycine