Superficial lesions Flashcards

1
Q

Key points in a lump examination

SSSCCCCTTTTFPS

Completion: 3

A
  • S
    • site
    • size
    • shape
  • C
    • Colour
    • Consistency
    • Contour
    • Cough impulse
  • T
    • Tenderness
    • Temperature
    • Translumination
    • Tethering deep/superficial
      • is it intradermal or subcutaneous?
        • Intraderma: cannot draw skin over lump
          • sebaceous cyst, neurofibroma, dermatofibroma
        • Subcutaneous; can move lump independently from skin
          • lipoma, ganglion, LN
  • FPS
    • Fluctuance assess with prest test
    • Pulsatile assess for bruits/bowel sounds
    • Spreaaaaads (LN)

Completion:

  • examine draining LN!
  • Examine neurovascular function distral to lump!
  • Look for similar lumps elsewhere!
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Lump history Qs; 3 headings

A
  • Onset
    • When and why did you notice it?
    • Any predisposing event: e.g. trauma?
  • Continued Symptoms
    • What symptoms does it cause: e.g. pain?
    • How has it changed?
    • Have you noticed other lumps?
  • Treatments and Cause
    • What treatments have you tried?
    • What do you think the cause is?
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Lipoma

  • Pathology:
  • Features:
    • Inspection:
    • Palpation:
  • ‘Viva’-Syndromes: 4
  • Management: 2
A

Lipoma

  • Pathology: benign tumour of mature adipocystes. Sarcomatous change probably doesn’t occur.
    • Liposarcomas arive de novo in; older pt/deeper tissues of lower limbs
  • Features:
    • Inspection: occur anywhere where fat can expand ie. not scalp or palms incl spermatic cord and submucosa
    • Palpation: soft + subcutaneous + imprecise margins + fluctuant
  • ‘Viva’-Syndromes: 4
    • Dercum’s disease/ adiposis dolorosa:
      • multiple, painful lipomas
      • associated peripheral neuropathy
      • obese, postmenopausal women
    • familial multiple lipomatosis
    • madelung’s disease
    • Bannaya-Zonana Syndrome:
      • AD, multiple lipomas, macrocephaly, haemangiomas
  • Management:
    • non-surgical; leave
    • surgical; excise (but recur!)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Sebaceous cyst

  • Pathology: 2 types
  • Features:
    • Inspection:
    • Palpation:
  • ‘Viva’-Syndromes: 2 + Complications
  • Management: 2
A

Sebaceous cyst

  • Pathology: Epithelial-lined cyst containing keratin (Two histological subtypes:)
    • 1) Epidermal Cyst - Arise from hair follicle infundibulum
    • 2) Trichilemmal Cyst / Wen - Arise from hair follicle epithelium, Often multiple, May be AD
  • Features:
    • Inspection:Occur at sites of hair growth ie scalp, face, neck, chest, back NOT soles or palms, central punctum
    • Palpation: Firm + smooth + Intradermal
  • ‘Viva’
    • Complications: Infection (pus discharge) + ulceration + calcification
    • Syndromes:
      • Cock’s peculiar tumour: large ulcerating trichilemmal disease on scalp, resemble SCC
      • Gardener’s syndrome = FAP + Thyroid Tx + Osteomas + Dental abnormalities + Epidermal cysts (Garden TOAD)
  • Management:
    • non-surgical
    • Surgical
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Ganglion

  • Pathology:
  • Features:
    • Inspection:
    • Palpation:
  • ‘Viva’-Differential
  • Management: 2
A

Ganglion

  • Pathology: cystic swelling related to synovial-lined structures: joint, tendon. Myxoid degeneration of fibrous tissue. They contain thick gelatinous material
  • Features:
    • Inspection: can be found anywhere e.g. dorsum of hand or wrist. There may be a scar from recurrence. May weakly transilluminate
    • Palpation: soft + subcutaneous + teathered to tendon
  • ‘Viva’-Differential
    • Bursae
    • cystic protrusion from synovial cavity of arthritic joint
  • Management:
    • non-surgical: aspiration followed by 3 wks of immobilisation
    • surgical excision: 50% recurrence + risk neovasc damage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Seborrhoeic Keratosis

  • Pathology: 3
  • Features: 3
  • Management: 2
A

Seborrhoeic Keratosis

  • Pathology: benign hyperplasia of basal cell layer
    • hyperkeratosis: coneum thickening
    • acathosis: spinosum thickening
    • hyperplasia of basal cells
  • Features:
    • stuck on appearance + dark brown + greasy
  • Management:
    • non-surgical
    • surgical: superficial shaving or cautery
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Neurofibroma

  • Pathology:
  • Features:
    • Inspection:
    • Palpation:
    • Extras:
  • Viva: syndrome
  • Management: 1
A

Neurofibroma

  • Pathology: benign nerve sheath tumour arising from schwann cells
  • Features: Numerous small violaceous nodules present on the back and forwarm in no particular distribution; neurofibromas​
    • Inspection: solitary or multiple, pedunculated nodules
    • Palpation: fleshy consistency + pressure can -> paraesthesia
    • Extras: examine:
      • skin: cafe au lait spots
      • eyes: lisch nodules
      • Acilla: freckles
      • CN: 8 (NF2 schwannoma)
      • BP: phaeochromocytoma/RAS
  • Viva: NF 1
    • AD Chr 17
    • cafe au lait spots >6 >15mm + freckling + neurofibromas + lisch nodules (iris)
  • Management:
    • surgical excision ONLY indicated is malignancy suspected
    • local regrowth = common!
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Papilloma

  • Pathology: 1
  • Features: 3
  • Management: 1
A

Papilloma

  • Pathology: overgrowth of all layers of the skin with a central vascular core
  • Features: Skin tage/fibroepithelial polyp, pedunculated, flesh coloures
  • Management: excision + diathermy to control bleeding
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Pyogenic granuloma

  • Pathology:
  • Features:
    • Inspection:
    • Palpation:
  • Viva: ?association
  • Management: 2
A

Pyogenic granuloma

  • Pathology: rapidly growing capillary haemangioma, neither pyogenic nor granuloma!
  • Features:
    • Inspection:
      • most commonly hands, face, gums, lips
      • bright red hemispherical nodule
      • may have seous/purulent discharge
    • Palpation: soft + bleed easily
  • Viva: ?association
    • previous trauma? more common in preg
  • Management:
    • non-surgical: regression is uncommon
    • surgical: curretage and diathermy of base
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Dermoid cyst

  • Pathology: congenital vs acquired
  • Features:
    • Inspection:
    • Palpation:
  • Viva: ?association
  • Management: 2 (C/A)
A

Dermoid cyst

  • Pathology: epidermal lined cyst deep to the skin
    • congenital/inclusion cyst: developmental inclusion of epidermis along lines of skin fusion e.g. midline of neck and nose, medial and lateral ends of eyebrows
    • aquired/implantation cyst: Implantation of epidermis in dermis. often secondary to trauma e.g. piercing
  • Features:
    • Inspection:
      • smooth spherical swelling
      • sites of embryological fusion
      • scar from recurrence
    • Palpation: soft, non-tender, subcutaneous
  • Viva: ?association
    • congenital: child/young adult
    • acquired: adult- ask re trauma
  • Management: 2 (C/A)
    • congenital; CT to establish extend and surgical excision
    • Aquired: surgical excision
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Dermatofibroma

  • Pathology:
  • Features:
    • Inspection:
    • Palpation:
  • Viva: differential
  • Management: 1
A

Dermatofibroma

  • Pathology: benign neoplasm of dermal fibroblasts
  • Features:
    • Inspection:
      • can occur anywhere, mostly on lower limbs of younf to middle aged women
      • small brown pigmented nodule
    • Palpation: Firm + woody feel = characteristic, Intradermal + mobile over deep tissue
  • Viva: differential: malignancy e.g. melanoma, BCC
  • Management: Excision and HISTOLOGY!
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Kerato-acanthoma

  • Pathology:
  • Features: 3
  • Management:
A

Kerato-acanthoma

  • Pathology: benign overgrowth of hair follicle cells, cytologically similar to well-differentiated SCCs
  • Features:
    • fast growing
    • Dome shaped with keratin plug
    • Intraderma;
  • Management:
    • regress w/i 6 wks
    • excise to reduce scarring and obtain histology
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Thyroid examination

prep/gen inspection/hands/eyes/neck(IPA)/legs/complete

A
  • Preparation Ensure exposure down to the clavicles + Position pt. away from a wall
    • Qs:
      • Are you comfortable: not too hot or cold?
      • Hoarse voice: recurrent laryngeal nerve palsy
  • General Inspection
    • Nervous/agitated or slow/lethargic
    • Body habitus
    • Sweaty
    • Skin and hair condition
  • Hands
    • Thyroid acropachy
    • Palmar erythema
    • Temperature, sweating
    • Fine tremor: piece of paper on out-stretched hands
    • Pulse: rate and rhythm (AF in thyrotoxicosis)
  • Eyes
    • Sympathetic Overstimulation
      • Lid Retraction: sclera between iris and upper lid
      • Lid Lag
    • Graves:
      • Oedema: periorbital and chemosis
      • Exophthalmos: inspect from above and side
      • Ophthalmoplegia: esp. upgaze palsy
  • Neck
    • Inspect: from front and side.
      • Look for collar scars
      • Ask pt. stick out tongue and swallow water
      • Look in mouth for lingual thyroid
    • Palpate: from behind
      • Palpate masses: can you get under it?
      • Repeat the swallow and protrusion test
      • Lymphadenopathy
      • Check for tracheal deviation.
    • Percuss: for retrosternal extension
    • Auscultate: thyroid bruits (Graves’)
  • Legs
    • Pretibial myxoedema: brown swelling above lat. malleoli
    • Proximal myopathy: ask pt. to stand from chair (Graves)
    • Ankle reflexes: kneel on chair
      • Slow relaxing: hypothyroidism
      • Brisk: hyperthyroidism
  • Completion
    • Observation chart
    • History
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Exophthalmos differential:

A
  • Orbital cellulitis
  • Trauma
  • Masses: meningioma, glioma
  • Carotid cavernous fistula: pulsatile exophthalmos
  • Idiopathic orbital inflammatory disease
  • Graves
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Goitre differential

Diffuse: smooth/nodular

Solitary

A

Diffuse Enlargement

  • Smooth
    • Simple colloid goitre
    • Graves
    • Thyroiditis: Hashimoto’s, de Quervain’s, Riedel’s
  • Nodular
  • Multinodular goitre
  • Multiple adenomas

Solitary Nodule

  • Dominant nodule of a multinodular goitre
  • Adenoma
  • Malignant
    • 1O: papillary, follicular, medullary, anaplastic
    • 2O: breast
  • Cyst
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Commentest causes of

hyperthyroidism 2

hypothyroidism 3

A

Hyperthyroidism

  1. Graves’ (~2/3)
  2. Toxic Multinodular Goitre ( = Plummer’s)

Hypothyroidism

  1. Primary atrophic
  2. Hashimoto’s thyroiditis
  3. Iodine deficiency: commonest Worldwide
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Thyroid Qs 3

A
  1. Thyroid status
  2. Compression symptoms: dysphagia, difficulty breathing
  3. Previous thyroid medications or surgery
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Goitre investigations

Nlood/imaging/hisology/laryngoscopy

A

Bloods

  • TFTs: TSH, fT3, fT4
  • Other: FBC, Ca2+, calcitonin, ESR
  • Antibodies: anti-TPO, TSH

Imaging

  • CXR: goitre and mets
  • High resolution US
  • CT
  • Radionucleotide (Tc or I) scan: hot vs. cold

Histology or cytology

  • FNAC (can’t distinguish adenoma vs. follicular Ca)
  • Biopsy

Laryngoscopy: Important pre-op to assess vocal cords

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Features of multinodular diffuse goitre

A
  • Commonest goitre in UK
  • Progression of simple diffuse goitre to nodular enlargement.
  • Middle-aged women
  • Positive family Hx
  • Over-activity in parts may → mild thyrotoxicosis
    • Plummer’s Syndrome
  • Malignant change occurs in 5% of untreated MNGs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Management of multinodular diffuse goitre

n.b. most pts do not require intervention

nonsurg vs surg

A
  • Most pts. don’t require intervention*
  • *Non-Surgical**
  • Thyroxine → regression in 50-70% (Suppress TSH)
  • Toxic Multinodular Goitre
    • Propranolol + carbimazole
    • Radioiodine

Surgical

  • Indications: 5 Ms
    • Mechanical obstruction
    • Malignancy
    • Marred beauty: cosmetic reasons
    • Medical Rx failure: thyrotoxicosis
    • Mediastinal extension: can’t monitor changes
  • Procedure
    • Total thyroidectomy
    • Removes risk of malignant change in thyroid remnant.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Plumbers Vs graves

  • age
  • Nod or diffuse?
  • extra?
  • AF?
  • AI features?
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Simple colloid goitre (smooth)

causes

Treatment

A

Hyperplasia of gland 2O to ↑TSH release
Causes

  • Iodine deficiency: commonest worldwide
  • ↑ physiological demand: pregnancy, puberty
  • Goitrogens: e.g. Li, uncooked cabbage

Rx

  • Not usually required
  • Thyroxine or ↑ dietary iodine
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Graves disease

epidemiology

  • Prevalence:
  • XX% of cases of thyrotoxicosis
  • Sex:
  • Age:
A
  • Prev: 0.5%
  • 60% of cases of thyrotoxicosis
  • Sex: F>>M=9:1
  • Age: 40-60yrs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Graves disease: features

A
  • Diffuse goitre c¯ bruit
  • Triggers: stress, infection, child-birth
  • Ophthalmopathy
    • Oedema: periorbital and chemosis
    • Exophthalmos → exposure keratopathy
    • Ophthalmoplegia: esp. upgaze palsy
    • Optic neuropathy: ↓ acuity and RAPD
  • Dermopathy: pre-tibial myxoedema
  • Acropachy: periosteal reaction (clubbing is soft tissue
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Pathology of grave’s eye disease:

exophthalmost

+

Lid-lag

A
  • Exophthalmos
    • Retro-orbital inflammation and lymphocytic infiltration → orbital oedema
    • 2O to anti-TSH abs
  • Lid-lag
    • Not Graves’ specific
    • Sympathetic overstimulation → restrictive myopathy of LPS
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Grave’s disease associations: (3)

A
  1. T1SM
  2. Vitiligo
  3. Pernicious anaemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Grave’s disease

treatment

A
  1. medical: propranolol + carbimaxole
  2. Radioiodine
  3. surgical: subtotal or total thyroidectomy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

Grave’s vs thyroiditis (and 4 example)

uptake?

A

Graves; high uptake

thyroiditis: low uptake e.g.

  1. hashimoto’s
  2. de Quervain’s
  3. Subacute lymphocytic: post-partum
  4. Riedel’s
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Follicular adenoma (benign solitary thyroid nodule)

Features

Management

A

Follicular adenoma (benign solitary thyroid nodule)

  • Features:
    • 2-4cm mass
    • +/- thyrotoxicosis
    • Indistinguishable from follicular Ca on FNAC- need excision histology to confirm Dx
  • Management
    • Hot:
      • <3cm: radioiodine
      • >3cm: surgical excision
    • COLD: excision!
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

thyroid cyst (benign solitary thyroid nodule)

Features

Management

A
  • Features:
    • true cysts= RARE
    • Mostly colloid degeneration, necrosis of H’gge wi benign or malignant tymours
    • Only benign if abolished by aspiration!
  • Management
    • cytology can be false negative in 30%!
    • <4cm: aspirate and reciw in 4/12
    • surgical excision if:
      • >4cm
      • blood stained aspirate
      • recurrence after aspiration
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Malignant solitary thyroid nodule

Papillary

Frequency:

Age:

Cell origin:

Spread:

Mx:

A
  • Frequency: 80%, associated with irradiation
  • Age: 20-40 yrs
  • Cell origin: follicular cells (thyroglobilin Tx marker)
  • Spread:
    • nodes and lung
    • JDG (JUGULODIAGASTRIC) node = lateral abberrant thyroid
    • may be multifocal
  • Mx:
    • total thyroidectomy
      • T4 to suppress TSH
    • +/- node excision
    • +/-radioiodine

>95% 10 yrs

32
Q

Malignant solitary thyroid nodule

Follicular

Frequency:

Age:

Cell origin:

Spread:

Mx:

A
  • Frequency: 10%, F>M
  • Age: 40-60 yrs
  • Cell origin: follicular cells, thyroglobulin TMarker
  • Spread: Bone-> blood + lung
  • Mx:
    • total thyroidectomy
    • _ T4 syppresion
      • radioiodine

>95% 10yr

33
Q

Malignant solitary thyroid nodule

Medullary

Frequency:

Age:

Cell origin:

Mx:

A
  • Frequency: 5%, 30% = FAMILIAL! e.g. MEN2
  • Age:
    • sporadic = 40-50
    • MEN2 = young
  • Cell origin: parafollicular C cells - CEA + Calcitonin = Markers
  • Spread: //
  • Mx:
    • phaeo screen preop
    • thyroidectomy
    • node clearance
    • +/- radiotherapy
34
Q

Malignant solitary thyroid nodule

Anaplastic

Frequency:

Age:

Cell origin:

Spread:

Mx:

A
  • Frequency: rare, F>M 3:1
  • Age: >60
  • Cell origin: undifferentiaed follicular cells
  • Spread: rapid growth
    • aggressive: local + LN + blood
  • Mx:
    • usually palliative
    • may try thyroidectomy + radiotherapy
    • <1% 10 yrs
35
Q

Thyroid Nodule Facts
quick facts! (5)

A
  1. F>M = 4:1
  2. 4th and 5th decades
  3. 10% malignant in middle aged
  4. 50% malignant in young and elderly
  5. FNAC is most important Ix
36
Q

Investigation of thyroid nodule?

A

Ix: Triple Assessment

  1. Clinical examination
  2. US
  3. FNAC

Isotope scan: used if pt. is hyperthyroid

37
Q

MEN1: Wermer syndrome

A
  • Pituitary adenoma
  • Parathyroid hyperplasia or adenoma
  • Pituitary endocrine tumour
38
Q

MEN2 syndrome

A

Men 2

  • Medullary thyroid Ca
  • Phaeochromocytoma
  • A: hyperparathyroidism
  • B: marfanoid habitus
39
Q

Complications of thyroid surgery

early/late

A

Early

  • Reactionary haemorrhage → haematoma
  • Recurrent laryngeal nerve palsy
  • Hypocalcaemia
  • Thyroid storm

Late

  • Hypothyroidism and hypoparathyroidism
  • Recurrence of disease
  • Keloid scar
40
Q

Practicalities of Thyroid Surgery

A
  • Render euthyroid pre-op c¯ antithyroid drugs
  • Stop 10 days prior to surgery (they ↑ vascularity)
  • Alternatively just give propranolol
  • Check for phaeo pre-op in medullary carcinoma
  • Laryngoscopy: check vocal cords pre- and post-op
41
Q

Neck examination

(prep/inspect neck, mouth, eyes/palpate/percuss/ausc/other/complete)

A
  • *Preparation:** Ensure exposure down to the clavicles + Position pt. away from wall
  • *Inspect**: Scars, Sinuses, Masses
  • Neck
    • Look very carefully for scars: collar incision
    • Look for masses: which triangle?
    • Does mass move on swallowing or tongue protrusion?
  • Mouth
    • Lingual thyroid
    • Ranula (ruptured salivary gland → mucocele)
  • Eyes
    • Thyroid eye disease

Palpate

  • Best from behind the pt.
  • Palpate while pt. swallowing and protruding tongue
  • Assess for lymphadenopathy
  • Tracheal deviation
  • *Percuss** Retrosternal extension
  • *Auscultate**
  • Listen over lump for bruits.
  • Gurgle of pharyngeal pouch

If no obvious masses / skin lesions

  • Check neck pulses and listen for bruits
  • Test sensation and neck movements

Completion

  • If goitre → asses thyroid status
  • Lump history
42
Q

Quick differential for neck lumps

anywhere

midline: solid/cystic

ant triangl: solid/cystic

Post triangle: solic/cystic

A
43
Q

Investigation of neck lump; 3 special to think of

A
  • US: shows consistency
  • FNAC or core Bx
  • Consider CT/MRI to define relations
44
Q
A
45
Q

Key neck Hx Qs

onset/continued Sx/Rx and causes

A
  • Onset
    • When and why did you notice it?
    • Any predisposing event: e.g. trauma?
  • Continued Symptoms
    • What symptoms does it cause: e.g. pain?
    • How has it changed?
    • Have you noticed other lumps?
  • Treatments and Cause
    • What treatments have you tried?
    • What do you think the cause is?
46
Q

Midline and anterior triangle: 3 key differentials

A
  1. Thyroglossal cyst
  2. Branchial cyst
  3. Chemodectoma
47
Q

Posterior triangle lumps: 3 key differential

A
  1. cystic hydroma
  2. pharyngeal pouch
  3. cervical rib
48
Q

Thyroglossal cyst

pathology

presentation

A

Pathology

  1. Persistence of any part of the thyroglossal duct which marks the developmental descent of the thyroid from the foramen caecum
  2. Ectopic thyroid tissue can be found anywhere along this path of descent.
  3. Cysts may contain thyroid tissue which can undergo malignant change → papillary Ca

Presentation:

  • Young pt.
  • Fluctuant midline neck lump
  • Usually subhyoid
  • Protrusion of tongue → elevation
  • Swallowing → elevation
  • May see opening of a thyroglossal sinus
  • Following removal there will be a transverse incision just above the thyroid cartilage.
49
Q

Thyroglossal cyst

differential

epidemiology

complications

A
  • *Differential**
  • Thyroid nodule and masses
  • Dermoid / epidermal cysts
  • Subhyoid bursa
  • *Epidemiology**
  • Rare
  • M=F
  • 40% in 1st decade
  • *Complications**
  • Infection
  • Sinus formation
  • Development of Ca
  • Recurrence post-op
50
Q

Surgical management of thyroglossal cyst

A
  • *Sistrunk’s Operation**
  • Inject patent tract c¯ dye at start
  • Excise cyst and patent tract
  • Need to resect central portion of hyoid as tract runs through it.
51
Q

Branchial cyst

pathology

presenation

A
  • Pathology:
    • Failed fusion of 2nd and 3rd branchial arches
    • Lined by squamous epithelium
    • Contain “glary” fluid c¯ cholesterol crystals
  • Presentation:
    • Young pt.
    • Ant. margin of SCM at junction of upper and middle thirds
    • Firm, fluctuant ovoid swelling
    • Opaque on transillumination
    • May be opening from branchial sinus
52
Q

Branchial cyst

COmplication

Management; surgical/medical

A
  • *Complications**
  • Infection
  • Sinus formation
  • Recurrence post-op
  • *Surgical Excision**
  • Bonney’s blue dye can be injected into fistula to allow more accurate excision
  • May be difficult due to proximity of carotids
  • *Medical**
  • Sclerotherapy is an option
53
Q

Chemodectoma

Pathology

presentation

A
  • Pathology:
    • Very rare
    • Tumour of the paraganglion cells of the carotid bodies: measure pH and PaO2 and PaCO2
    • Located @ the carotid bifurcation
    • Mostly benign (5% malignant)
  • Presentation:
    • Ant. triangle @ the angle of the jaw
    • Pulsatile
    • Moves laterally but not vertically
    • Pressure can → syncope
    • May be bilateral
54
Q

Chemodectoma

Investigations

Management: surgical/radiological

A
  • *Ix**
  • Duplex US
  • Angiography: splaying
  • CT / MRI
  • *Surgical Excision**
  • *Ultrasonic** surgical dissection
  • *Radiotherapy**
  • Large tumours
  • Unfit for surgery
55
Q

Cytic hydroma

pathology

presentation

complications

management

A

Pathology: Congenital multicystic lymphatic malformation

Presentation:

Usually paediatric
Lobulated cystic swelling
Soft and fluctuant
Compressible
Transilluminate brilliantly
↑s in size when infant coughs / cries
Look in the oropharynx- Cyst may extend intoretropharyngeal space

  • *Complications:**
  • Obstruction of swallowing
  • Respiratory obstruction

Management:

  • Surgical excision
  • Hypertonic saline sclerosant
56
Q

Pharyngeal pouch

pathology

presentation

A

Herniation of pharyngeal mucosa through its muscular coat at its weakest point.
- Pulsion diverticulum

  • *Killian’s dehiscence**
    • Between thyro- and crico-pharyngeal muscles that form the inferior constrictor*

Presentation:

  • Elderly patient
  • Left sided cystic swelling
  • Palpation → gurgling
  • Hallitosis
57
Q

Pharyngeal pouch

symptoms

complications

Ix

Management: non surg/surg

A
  • *Symptoms**
  • Regurgitation
  • Dysphagia
  • *Complications**
  • Aspiration → pneumonia
  • Diverticular neoplasia (<1%)
  • *Ix**
  • Ba swallow

Management:

  • *Non-surgical**
  • If small and asymptomatic
  • *Surgical**: Dohlman’s Procedure
  • Minimally invasive endoscopic stapling
58
Q

Cervical rib

pathology

presentation (vasc/neuro)

management

A
  • Pathology:
    • Overdevelopment of transverse process of C7
    • Occur in 1:150

Presentation: Hard swelling: mostly asymmpto
Can → vascular symptoms
- Due to subclavian A. compression
- Subclavian steal
- Raynaud’s
Can → neurological symptoms
- Compress lower roots of brachial plexus, T1 or stellate ganglion
- Wasting of intrinsic hand muscles
- Paraesthesia along medial arm

management: Surgical excision

59
Q

Cervical lymphadenopathy

examination

Key features (5) + technique + additional examination!

A

Key Features

  1. Consistency
  2. Number
  3. Fixation
  4. Symmetry
  5. Tenderness

Technique

  • Ask pt. to drop chin to relax muscles
  • Chin backwards → pre-auricular
  • Down anterior cervical chain
  • Supra- and infra-clavicular nodes
  • Up posterior cervical chain
  • Mastoid → occipital nodes

Additional Examination

  • Face and scalp for infection or neoplasm
  • Chest exam: infection or neoplasm
  • Breast examination
  • Formal full ENT examination
  • Rest of reticuloendothelial system
60
Q

Lymphadenopathy

key history Qs

A
  • Symptoms from the lumps e.g. EtOH-induced pain
  • General symptoms; Fever, malaise, wt. loss
  • Systemic disease
  • PMH
  • Previous operations
  • Social history
  • Ethnic origin
  • HIV risk factors
61
Q

Causes of cervical lumphadenopathy: I LIST

A
  • Lymphoma and Leukaemia
  • Infection
  • Sarcoidosis
  • Tumours
    • ENT
    • Breast
    • Lung
    • Gastric

I= INFECTION

  • Bacterial
    • Tonsillitis, dental abscess
    • TB
    • Bartonella henselae (Cat scratch disease)
  • Viral
    • EBV
    • HIV
  • Protozoal
    • Toxoplasmosis
62
Q

Investigation of lymphadenopathy

blood/radiological/pathology

A

Blood

  • FBC, ESR, film (atypical lymphocytes)
  • TFTs, serum ACE
  • Monospot test, HIV test

Radiological

  • US
  • CT scan

Pathology

  • FNAC
  • Excision biopsy
63
Q

Salivary examination

inspect/palpate/complete

A

Inspection

  • Skin changes: swelling, scars, sinuses
  • Swelling / discrete lump
    • Parotid or submandibular?
    • Bilateral or unilateral?
  • Facial asymmetry
  • Inside the mouth c¯ a pen torch
    • Stenson’s duct opposite the 2nd maxillary molar
    • Wharton’s duct adjacent to the frenulum linguae
    • Inflammation, stone, pus

Palpation

  • Any tenderness?
  • Palpate from behind
  • Test muscle fixity: ask pt. to clench teeth
  • Palpate for cervical lymphadenopathy

Completion

  • Bimanual palpation of parotid and submandibular ducts for stones.
  • Bimanual palpation of submandibular gland
  • Test CN7
  • Perform full ENT examination
64
Q

Differential for swelling of salivary gland

diffus/localised

A

Diffuse Swelling of Whole Gland

  • Infection: Parotitis
  • Autoimmune: Sjogren’s
  • Infiltration: Sarcoid
  • Systemic: Chronic liver disease, DM, anorexia, bulimia

Localised Swelling

  • Calculus
  • Lipoma
  • Salivary gland neoplasm
  • Leukaemia: ALL
65
Q

Salivary gland: key history Qs

A

Hx

  • Pain or swelling related to food: calculi
  • Fever / malaise: mumps
  • Dry eyes / mouth: Sjogren’s
  • SOB: sarcoid
66
Q

Salivary gland neoplasm

common types

A

Common Types

  • Benign
    • Pleiomorphic adenoma: 80%
      • <50yrs
    • Adenolymphoma: Warthin’s tumour
      • >50yrs
      • Smoking is important risk factor
  • Malignant
    • 1st: Mucoepidermoid
    • 2nd: Adenoid cystic
67
Q

Salivary Gland Neoplasms
Features

A

80% in the parotid gland
80% benign: 80% are pleiomorphic adenomas
Only 60% of submandibular gland tumours are benign

Malignant Features

  • Facial nerve palsy
  • Rapid growth and pain
  • Hyperaemic, hot skin
  • Hard consistency
  • Fixity to skin or underlying muscle
68
Q

Investigation of salivary gland mass

A

FNA

MRI: determine deep lobe involvement

69
Q

Salivary gland mass management

benign/malignant

A
  • Benign
    • Superficial: superficial parotidectomy
    • Deep: total parotidectomy
  • Malignant
    • Total parotidectomy ± adjuvant radiotherapy
70
Q

Complications of parotidectomy

(immediate/early/late)

A
  • Immediate
    • Facial nerve injury
    • Reactionary haemorrhage
  • Early
    • Temporary facial weakness: neuropraxia
    • Salivary fistula
    • Loss of pinna sensation: greater auricular nerve damage.
  • Late: Frey’s Syndrome (gustatory sweating)
    • Facial sweating while eating
    • Re-innervation of divided sympathetic nerves by fibres from the secretomotor branch of auriculotemporal branch of CNV3
71
Q

Hypertrophic scar

A
  • Scar confined to wound margins
  • Across flexor surfaces and skin creases
  • Appear soon after injury and regress spontaneously
  • Any age: commonly 8-20yrs
  • M=F
  • All races
72
Q

Keloid scar

A
  • Scar extends beyond wound margins
  • Earlobes, chin, neck, shoulder, chest
  • Appear months after injury and continue to grow
  • Puberty to 30yrs
  • F>M
  • Black and Hispanic
73
Q

Hypertrophic and keloid scar Wound type Associations

A
  • Infection
  • Trauma
  • Burns
  • Tension
  • Certain body areas
74
Q

Hypertrophic and Keloid Scars management

non-surge and surg

A

Non-surgical

  • Mechanical pressure therapy
  • Topical silicone gel sheets
  • Intralesional steroid and LA injections

Surgical: Revision of scar c¯ closure by direct suturing

75
Q

Causes of digital clubbing

A

Gastrointestinal
 CLD: esp. PBC
 IBD: esp. Crohn’s
 Coeliac disease
 GI lymphoma
Respiratory
 Chronic suppurative lung disease
 CF / bronchiectasis
 Abscess
 Empyema
 Malignancy: adenocarcinoma or mesothelioma
 Pulmonary fibrosis
Cardiac
 Infective endocarditis
 Congenital cyanotic heart disease
 Fallot’s
 Transposition
 Atrial myxoma: e.g. in Carney Complex
Miscellaneous
 Familial
 Thyroid acropachy
 Axillary artery aneurysms and brachial AVMs

76
Q

Pathophysiology of digital clubbing

A

Exact aetiology unknown
Platelet clumps and megakaryocytes bypass the lungs and impact in digital capillaries.
They release growth factors such as PDGF → clubbing

77
Q

Stages of digital clubbing

A

1: bogginess of the nail bed
2: loss of the nail angle
3: ↑ curvature
4: expansion of the distal phalanx