Haematology + oncology Flashcards

1
Q

Beta Thallassaemia
- electrophoresis
-FBC

A

Absent B bands on electrophoresis
Microcytic anaemia
Low HCT
Appropriate reticulocyte count
Normal iron studies

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2
Q

SSD - diagnosis

A

Sickle cells on peripheral blood film
HbS on electrophoresis

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3
Q

Alpha Thalassaemia

A

alpha bands on electrophoresis

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4
Q

Carcinoid tumour vitamin deficiency

A

Nician B3 deficiency (Pellagra)
Increased tryptophan metabolism to serotonin
B3 is derived from tryptophan

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5
Q

Carcinoid tumour diagnosis

A

urine 5-OH-indoleacetic acid levels
(Increased)

Cromogranin A increased often in liver metastasis

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6
Q

Managing bowel colic in colorectal cancer

A

Buscopan

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7
Q

N+V from functional bowel obstruction in renal cancer

A

Metoclopramide

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8
Q

N+V due to mechanical bowel obstruction

A

Cyclizine

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9
Q

N+V from hypercalcaemia

A

Haloperidol

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10
Q

Haemophilia
- inheritance
- cause
- diagnosis

A

X-linked recessive

A = Factor VIII deficiency
B = Factor IX deficiency

Raised aPTT
Factor VIII/IX assay to confirm

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11
Q

Haemochromatosis features

A

Diabetes mellitus
Arthralgia
Hepatomegaly
Hypogonadism
Skin pigmentation

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12
Q

Paroxysmal nocturnal haemoglobinaemia
- Triad
- blood Ix
- treatment

A

Chronic compliment mediated haemolysis

  1. Acquired haemolytic anaemia
  2. Large vessel thrombosis
  3. Insufficient haematopoiesis

Raised LDH and reticulocytes indicates intravascular haemolysis

eculizumab, anticoagulation, steroids, bone marrow transplant

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13
Q

eculizumab

A

Inhibits compliment C5 activation and formation of cytolytic attack complex

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14
Q

Henoch-schonlein purpura
- cause/mechanism
- features
- management

A
  • IgA complex deposition in the skin and kidneys
  • Purpuric rash, arthritis, nephritis, abdominal pain, GI bleeding, orchitis
  • Self-limiting in most cases, monitor, supportive treatment for nephritis
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15
Q

Asbestos cancers

A

Lung adenocarcinoma
Mesothelioma
Renal adenocarcinoma
Gastrointestinal lymphoma

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16
Q

G6PD deficiency
- Inheritance
- Mechanism of disease

A

X-linked recessive
Cannot tolerate oxidative stress -> haemolytic anaemia triggered by infection, drugs, broad beans

17
Q

Hereditary spherocytosis
- Inheritance
- Presentation
- Complications

A

Autosomal dominant - abnormal RBC membrane

Mild intermittent jaundice, anaemia

Blood film: spherocytes, raised reticulocyte count

Aplastic crisis (parvovirus B19)
Megaloblastic crisis (Folate deficiency)

18
Q

ITP management

A
  1. Oral prednisolone
  2. Pooled normal IVIG (if bleeding or requires urgent invasive procedure)
19
Q

Bowel colic from cancer
- treatment

A

Hyoscine butylbromide

20
Q

Vitamin deficiency in carcinoid syndrome

A

Niacin B3 deficiency
B3 derived from tryptophan. Increased tryptophan metabolism to produce large amounts of serotonin -> decreased B3 production

21
Q

CAs most a/w hypercalcaemia

A

Breast + lung SCC, MM (via PTHrP secretion)