Lymphatic Pathologies Flashcards

(31 cards)

1
Q

What is Lymphadenopathy?

A

the palpable enlargement (>1cm) of lymph nodes

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2
Q

How is a lymphadenopathy classified?

A

Localised: one body part

general: 2 or more areas = underline disease

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3
Q

What leads to splenomegaly?

A

INFECTIONS
e.g. glandular fever, TB, syphilis , HIV

PORTAL HYPERTENSION
e.g. cirrhosis, cardiac failure

LYMPHOID DISORDERS
e.g. leukaemia, lymphoma, multiple myeloma

RBC DISORDERS
e.g. thalassaemia (haemolytic anaemia)

INFLAMMATORY CONDITIONS

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4
Q

What is glandular fever?

A

Acute infection of B lymphocytes with Epstein-Barr Virus (EBV)

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5
Q

How is glandular fever transmitted?

A

Usually through close personal contact - most commonly saliva
Mucosal secretions of the respiratory tract, genital tract, blood

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6
Q

What is the pathophysiology of glandular fever?

A

EBV initially infects the oropharynx, nasopharynx and salivary epithelial cells

Later extends into lymphoid tissues and B cells

ADAPTIVE IMMUNE RESPONSE
Unaffected B cells produce antibodies against EBV

Cytotoxic T cells attack virus-infected B-cells directly

Enlargement of lymphoid tissue occurs due to:

Proliferation of lymphocytes
Removal of dead and damaged B cells

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7
Q

Clinical features of glandular fever?

A

Long incubation period: 30-50 days

Classical symptoms: fever, sore throat, cervical lymphadenopathy, fatigue

Progression of disease: generalised lymphadenopathy, splenomegaly, hepatomegaly

Rare complications (~5%): ocular, cardiac, CNS involvement

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8
Q

What is the management for glandular fever?

A

Rest
analgesics
antipyretics

treatment of secondary bacterial infection

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9
Q

What is leukaemia?

A

Proliferation of malignant leucocytes in the bone marrow

Overcrowding causes malignant cells to spill into blood

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10
Q

What is lymphoma?

A

Proliferation of malignant lymphocytes in lymphatic system

Formation of discrete tumours

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11
Q

What is multiple myeloma?

A

Proliferation of malignant plasma cells in the bone marrow

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12
Q

How is leukaemia classified?

A

Lymphoid leukaemia
Myeloid leukaemia

Acute leukaemia – rapid growth of immature cells (referred to as ‘blasts’)
Chronic leukaemia : slow growth

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13
Q

What are the 4 types of leukaemia?

A

Acute lymphoblastic leukaemia (ALL)

Acute myeloid leukaemia (AML)

Chronic lymphocytic leukaemia (CLL)

Chronic myeloid leukaemia (CML)

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14
Q

what is the Aetiology of leukaemia?

A

combination of genetics

environmental risk factors

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15
Q

What are the clinical features of leukaemia?

A

rapid onset of symptoms

  • Anaemia (↓ RBCs): fatigue, pallor, weakness
  • Decreased immunity (↓normal WBCs): fever, mouth ulcers, recurrent infections
  • Bleeding tendencies

OTHER:
bone pain

Splenomegaly, hepatomegaly, lymphadenopathy

Non-specific features

Nervous system infiltration

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16
Q

Management for acute Leukaemia?

A

blood marrow biopsy + combination of chemotherapy.

17
Q

What are the clinical features of chronic leukaemia?

A

splenomegaly, extreme fatigue, weight loss, night sweats, fever

18
Q

Management for chronic Leukaemia?

A

CLL - observation/ antibodies/ late chemo

CML - tyrosine kinase inhibitors

19
Q

How is lymphoma classified?

A

Hodgkin’s lymphoma

Non-Hodgkin’s lymphoma

20
Q

Risk factors for lymphoma?

A

Family history

Certain infections
Epstein-Barr Virus, HIV, HCV, HTLV, Herpes Virus-8, H. pylori

Obesity

Iatrogenic immunosuppression

Autoimmune conditions: RA, SLE

Exposure to ionizing radiation or mutagenic chemicals

21
Q

Clinical features of hotchkins lymphoma?

A

no spread

Lymphadenopathy

compresive features

B symptoms: fever, sweats, wt loss

Other: fatigue, anorexia, pruitis

22
Q

Clinical features of non-hotchkins lymphoma?

A

can spread to other organs

Lymphadenopathy

compresive features

B symptoms: fever, sweats, wt loss

23
Q

Management of non-hotchkins lymphoma?

A

Chemotherapy

Radiotherapy

Antibody therapy

Corticosteroids

Stem cell transplant
prognosis 75% cured

24
Q

Aetiology for multiple myeloma?

A

Chromosomal mutations play a key role
Exact aetiology unknown

Risk assoc. w/ radiation exposure

Familial predisposition?

25
Pathophysiology of multiple myeloma?
Myeloma cells: neoplastic plasma cells that produce excessive amounts of abnormal antibodies (M proteins) Result: decreased immunity, overcrowded marrow Antibody fragments (light-chains) are also produced and accumulate in tissues and organs Result: amyloidosis leads to renal failure Myeloma cells form discrete tumours (plasmacytomas) within bone Release of osteolytic cytokines destroys overlying cortical bone Result: radiographic ‘punched-out’ lesions (1-4cm in diameter)
26
Clinical features of multiple myeloma?
bone destruction marrow overcrowding extra-osseous plasmacytomas
27
What is HIV?
HIV is the pathogen responsible for acquired immunodeficiency syndrome (AIDS) It is a retrovirus and carries its genetic material as RNA (not DNA)
28
Modes of transmission of HIV?
- Exchange of body fluids - Children infected in placenta - occupational exposures
29
What is the pathophysiology | behind HIV?
Entry into cell Conversion of viral RNA Dormancy Activation Host cell death
30
Stages of HIV
STAGE 1: ACUTE INFECTION STAGE 2: CHRONIC INFECTION (CLINICAL LATENCY) STAGE 3: ACQUIRED IMMUNE DEFICIENCY SYNDROME
31
Management of HIV
MAINTAIN PHYSICAL & MENTAL HEALTH: POST-EXPOSURE PROPHYLAXIS PRE-EXPOSURE PROPHYLAXIS