JC WCS 16: PLEURAL EFFUSION & BRONCHIAL CARCINOMA

Prof WK Lam

Medicine

Mon 11-11-02

PLEURAL EFFUSION

INTRODUCTION

  1. Usu. few mm fluid in pleural space ® lubricate visc + parietal layers
  2. Pro of pleural fluid = 15g/L
  3. Maintained by balance (disruption = abn pleural fluid)
    1. Hydrostatic press caps: force fluid fr BV ® pleural space (9cm H2O)
    2. Oncotic press: draw fluid into BV (10cm H2O)
    3. Pleural cap perm'y
    4. Pleural lymphatic drainage

AETIOLOGY

  1. ­ Hydrostatic press
  1. CHF
  2. Renal F (H2O reten'n)
  3. Other vol o'load
  1. ¯ Oncotic press (¯ albumin: ¯ product'n vs. ­ loss - usu kid, rarely GIT)
  1. Cirrhosis: ¯ product'n
  2. Nephrotic syndr: ­ ­ loss
  3. Severe malnutrit'n: ¯ product'n
  4. Other h-albuminaemia
  1. ­ Cap perm'y (inflamed pleura)
  1. Infect'n lung/pleura (incl. TB)
  2. Collagen vasc dis (vasculitis)
  3. Malig
  4. Intraab (pancreatitis, liver abscess)
  5. Pul embol'm
  1. ¯ Lymphatic drainage
  1. Malig infiltration lymphatics (mediast, pul, pleural)
  2. Necrotising/ granulomatous infect'n (HK = TB, Other = fungal)
  3. Pleural fibrosis

CLINICAL FEATURES (dep. effusion size)

  1. Hx
  1. Asympt to SOB
  2. Irritant cough
  3. Chest pain (pleural acutely inflam - "pleuritic")
  4. Other rel to u'lying dis
  1. P/E
  1. < 500ml - no sign
  2. Mod - dull percuss'n, ¯ breath sound/ fremitus
  3. >1500ml - as above + insp lag (¯ expansion), medias shift
  4. Atelectasis (lung collapse) above effusion (bronchial BS, aegophony - high-pitch nasal speech b/c low-freq sounds dispersed)
  5. Other: ankle oedema (CHF), lymphadenopathy (malig)

INVESTIGATIONS

  1. CXR
  1. PA - ³ 300ml, blunt costophrenic ang, fluid meniscus shadow
  2. Lat - fluid meniscus (free-flow) vs. pockets (loculated)
  3. Lat decubitus - sm effus'n, confirm free-flow
  4. Contralat mediast shift if ³ 1500ml (no shift if collapse)
  5. Other: pul congest'n, lung mass, rib erosion
  1. US pleura
  1. Non-Dx CXR
  2. Sm effus'n 10-15mm on lat decub CXR
  3. Loculated (cannot tap w/thoracentesis)
  1. Thoracentesis
  1. Unilat effus'n (bilat asymm)
  2. Pleuritic pain, F
  3. Pleural fluid ® LDH, pro, cell count, differential, mibi, cytol
    1. Light's criteria 4 exudate
    1. Appearance
    1. Biochem
    1. Cell count + differential
    1. Cytol
    1. Mibi
    1. Additional
  1. Biopsy (Percutaneous Pleural)
  1. Exduative pleural effus'n with no obvious aetiology (after above Ix)
  2. Usu TB, neoplasm
  1. Thoracoscopy
  1. Isolated exudative pleural eff (+ no obvious aetiology after above Ix)

MANAGEMENT

  1. Transudate
  1. Address systemic issue
  1. Parapneumonic effus'n + empyema
  1. Stages
    1. Pleuritis sicca: pneum ® extend to pleura ® pleuritis (± pleura eff)
    2. Exdudative: "UPE - uncomplicated parapneumonic effusion", inflam med ® ­ cap perm ® exudate (fluid: clear, sterile, ­ neutrophil, pH N, LDH < 1000U)
    3. Fibropurulent: "CPE - complicated…", no appropriate ABX ® inv pleura ® locul'n due to fibrin clot/membr (fluid: turbid, infective agent, pH < 7.2, LDH>1000)
    4. Organisation: fibroblasts ® pleura ® thick non-elastic pleural peel (trapped lung) = perm func disab'y
  1. Systemic ABX (earlier better)
  2. Chest tube drainage - not UPE, for CPE, empyema (loculation: US/CT guide)
  3. Intrapleural fibrinolytic agents - CPE with locul'n, empyema, can avoid (f)
  4. Therapeutic thorascopy (adhesionolysis, fibrinolysis) - failed Tx after ABX, tube, fibrinolytics
  5. Thoracotomy w/decortication (rare) - chronic post-pneumonic empyema w/no response to ABX/tube
  1. Other causes of exudate effus'n
  1. TB effus - TB meds
  2. Pul emb - anti-coag
  3. Collagen vasc dis - Tx
  4. Chylothorax - thoracic duct repair, med-chain TG diet if chronic
  5. Pseudochylothorax - u'lying cause
  6. Malig effus - observe, Tx ca, thoracentesis (<1.5L/time), if repeated chest tap ® chemical pleurodesis

CA BRONCHUS

EPIDEMIOLOGY

  1. Passive smoking: RR = 2 (cf. active = 10-20)
  2. Diet: ¯ fruit/ veg, Vit A
  3. Wok: oil emission at high T
  4. Other: kerosene stove, incense, radon, TB, HLA Ag, k-ras oncogene, p53 TSG

PATHOLOGY

 

M (%)

F(%)

SQ (squamous cell)

38

15

AD (adenocarcinoma)

32

60 *

LA (large cell)

15

10

SM (small cell)

15

15

Note: ­ AD in F, ­ 'ing AD in M (will o'take SQ)

CLINICAL FEATURES

1. CXR abn only (5%)

 

2. Constitutional symps

- Malaise, ¯ app/ BW

3. Primary lesion

 

a) Bronchial mucosa ulcer'n

- Cough, sputum, haemoptysis

b) Obstruct'n: partial (complete)

- Wheeze, pneum (dyspnoea)

4. Intrathoracic spread

 

a) Along lymph ® both lungs (lymphangitis carcinomatosis)

- Cough, dyspnoea

b) Pleura/ Pleural effusion

- Chest pain, dyspnoea

c) Pericardial (cardiac tamponade)

- Dyspnoea

d) SVCO

- Dyspnoea, stridor, dysphagia, facial swell

e) L recur laryngeal n

- Hoarse (hooks under aortic arch)

f) Brachial plexus (C8, T1,2) +

cervical symp ganglion (Horner)

- Pain: shoulder/ arm

- Sweat 1side/ face, ptosis, constrict pupil

g) Oeso

- Dysphagia

h) Chest wall/ rib

- Chest pain, swell

5. Distant metastases

 

a) Lymphatics

- Mass: neck, supraclav fossa

b) Blood

 

Skin

Bone

Liver

Brain

Adrenals - common, clinically silent

- Skin mass

- Bone pain (back, pelvis)

- Epigastric distending discomfort

- Hemiplegia, focal epilepsy

6. SNMS (Systemic Non-Metastatic Syn) *

 

a) CT: clubbing, HPOA

- Arthralgia, pain extremities

b) Ectopic H

 

ADH (¯ Na+)

- Confused, weak

ACTH (¯ K+)

- Weak

PCP (­ Ca++) - PT-like peptide

- Polyuria, thirst, confused

Bone metastases most common cause for ­ Ca++ in ca lung

 

c) NM

 

Encephalopathy

- Dementia, confusion

Cerebellar degeneration

- Ataxia, clumsiness

Peripheral neuropathy

- Paraesthesia, weakness

Myasthenia-like (Eaton-Lambert)

- Weakness

Dermatomyosis

Looks like sunburn, weakness, skin rash

* SNMS: 10% ca lung, 1st symp of occult tumour \ specific, effective Tx of symptoms

CELL TYPE CHARACTERISTICS

 

SQ

AD

LA

SM

Smoking

+++

+

+

+++

Sit

C

P

P

C

Pleural effusion

+

+++

+++

++

Growth

+

+

+

+++

Metastatic pot

+

++

++

+++

SNMS

+

+

+

+++

Chemo/ Rad

+

+

+

+++

INVESTIGATIONS

DIAGNOSIS

1. CXR

2. Cytology

 3. Histol

STAGING

MANAGEMENT

Surgery

Rad'n

  1. Radical/ cure: single tumour, if cannot do surg due to med reasons
  2. Palliative: metastasis (bone, cerebral, SC), SVCO

Chemo

  1. SC: 4-6 cse, 60-90% response (b/c fasting growing cf. NSC), eg. cisplatin + VP16, CAV, limited dis use chemo + rad (prophylactic cranial rad if complete response), survival 14-18m (vs. no Tx 3m)
  2. NSC: adv/ metastatic cases, 30-60% partial response (PR) (­ relapse), ­ survival 2-3m only, eg. MIP/ cisplatin + VP16 (PR 40%, cheaper), new: taxol/ taxotere/ gemcitabine (PR 60%, expensive)

Multimodal

Supportive

  1. Hospice
  2. Analgesic (opioid) - symptomatic: cough suppression, thoracentesis, pleurodesis
  3. Psychosocial

PROGNOSIS