 TRIANGLES OF
NECK:-
Neck can be divided into
anterior & posterior
triangle by
STERNOCLIDOMASTOID
MUSCLE
 In pediatric age group - 90% benign.
 50% out of which may be congenital.
 In adult population – 80% non- thyroid
masses
 MID LINE ANTREIOR TRIANGLE POSTERIOR TRIANGLE
 CONGENITAL
 Thyroglossal cyst
 Dermoid cyst
 INFLAMMATORY
 Lymphadenitis
 TUMOUR
 Thyroid
 Lymphoma
 OTHERS
 Sternoclidomastoid
 Hematoma/fibroma
 CONGENITAL
 Brachial cyst
 Thymic cyst
 INFLAMMATORY
 Adenitis
 Sialadenitis
 TUMOUR
 Metastatic
 Lymphoma
 Vascular
CONGENITAL
Lymphangioma
INFLAMMATION
Adenitis
TUMOUR
Lymphoma
Metastaic
Supraclavicular
OTHERS
neuroma
 AGE:-
 < 20 yrs
20 – 40 yrs
> 40yrs
congenital
inflammatory
Inflammatory, salivary gland.
lymphoma
metastatic
 SEX :-
 Male preponderance- hodgkins lymphoma,
nasopharyngeal carcinoma, thyroid mass in
pediatric age group.
 Female preponderance – Thyroid swelling in
adult age group.
 DURATION:-
 Acute
 Chronic
Mode of onset?
 Progressive/non progressive?
 Site?
 Painful/painless?
 Associated systemic symptoms
 Personal habits
 Previous irradiation or surgery

SITE OF THE SWELLING:-
-tells about the organ of origin
-certain swellings are site specific
-dermoid cyst
-thyroid swelling
 *Size
 *Number :- .
 - solitary ( dermoid cyst & lipoma)
 - multiple ( NFM & hodgkin’s lymphoma)
*Shape:-
 -Spherical
 -irregular
*Surface:-
 - smooth ( cystic & benign)
 - irregular.
*Margins:-
 - Well defined
 - diffuse
*Colour
* Overlying skin
Special signs :-
- -Pulsation
- - movement with swallowing
- - movement with protusion of tounge
PALPATION:-
Temp
tenderness
Site
Size
Surface – smooth , irregular, lobulated
Margins – well defined, ill defined
Extension
Consistency – solid, soft , firm , hard , rubbery.
Mobility
Tense/fluctuation
Transillumination
Pulsation
Relation to surrounding structures
Draining lymph node
Fluctuation test
pulsation
Relation to muscle
BLOOD:-
CBC, ESR, TFT, CRP,
IMAGING:-
Xray, USG, CT scan, MRI , Radionuclitide scan, PET
Sialography
CYTOLOGY
TISSUE:-
Incisional/excisional biopsy
Standard for diagnosis.
Indications:-
- Any neck mass that is not an obvious abscess
- Persistent after 2 wks of antibiotics
Inexpensive
easily available
Non invasive
Not associated with radiation
Solid versus cystic masses
Congenital cyst from solid nodes/ Tm.
calcification
Extent & vascularity.
Guided FNAC
 Distinguish cystic from solid
 Extent of lesion
 Anatomical relations
 Vascularity with contrast
 Pathological node( lucent, > 1.5 cm, loss of
shape, rim
enhancement)
 Detection of unknown primary
 Similar information as CT

 Better soft tissue contrast
 Better for upper neck and skull base
 Uses flourine labelled deoxyglucose
 Valuable tool – evaluation of regional LN
 - detect distant metastasis
 - synchronous primary lesion
 - unknown primary
Any solid assymetric mass MUST be considered
a metastatic neoplastic lesion until proved
otherwise.
Asymptomatic cervical mass ~ 12% cancer
 80% are SCCS
 Asymptomatic neck swelling
 Associated symptoms – otalgia, dysphagia,
voice change, difficult breathing, weight loss,
loss of appetite, bone pain , chest pain.
 Fever & night sweats.
 Ipsilateral otalgia with normal otoscopy-
direct attention to tounge base, tonsil,
supraglottis & hypopharynx.
 U/L serous otitis media- direct attention to
nasopharynx.
Directed biopsy- primary is known.
 All suspicious mucosal lesions
 Areas of concern on CT/MRI
FNAC
Metastatic neck LAP withou the development of
primary lesion with a subsequent 5 yr period.
Head & neck cancer with unknown primary 3-
7% patients.
Most common – level LN II & III.
Supraclavicular nodal involement – below
clavicle
SCC thyroid, lung, breast, GI tract
 High risk nasopharynx, pyriform sinus &
base of tongue & tonsil.
 Full ENT examination.
 Level I – lip , anterior tongue, buccal mucosa.
Level II,III,V- tonsil or tounge base
nasopharyngeal examination,
tounge base biopsy from
concerned areas.
 Level IV,V – hypopharynx & larynx
 DL scopy, esophagoscopy, chest
abdomen CT, PET Scan.
 PET- CT negative & no primary on
endoscopy.
 -Tonsillectomy
 - tongue base biopsy & biopsies of postnasal
space & pyriform fossa
 -25% found at tonsil
 - clinical examination, panendoscopy, CT and
MRI with biopsy reveal primary in 40% cases.
 - definitive MND in all patients after FNAC
or biopsy.
Cystic remnant of the TGD between foramen
caecum of tounge base & thyroid bed in
infrahyoid neck.
 70% - congenital neck mass
 65% - between hyoid & thyroid
 50% - hyoid
 20% - suprahyoid
 1-2% - lingual
 1-2% - malignancy
A small, round, soft mass in
the midline of neck( 90%)
Infected cyst(5%) – enlarge
neck mass, fever, draining
sinus(15%) & dysphagia.
Moves with protrusion of
tounge.
Pre school age children or mid
adolescence.(5yr)
 History & examination
 Investigation -
 FNAC
 USG- location, cystic, normal thyroid.
 CT & MRI – large cyst, suspected malignancy,
lingual thyroid
 Surgical excision- T/t of
choice
 Sistrunk’s operation –
 Removal of cyst, the tract
, the central portion
of hyoid bone, as well
as core of tissue including
tissue tract or raphe
between mylohyoid
muscles, portion of
geinoglossus muscle and
up to foramen caecum
 4th- 6th week IUL.
 6 paired branchial
arches.
 Persistent cleft-
external sinus.
 Persistent pouch –
internal sinus
 Fistula.
 17% pediatric neck
masses.
5% of brachial cleft anamolies
M = F
Cyst ( adult> children),
fistula/sinus(children>
adult).
Line from tragus to hyoid
bone.
Left predominance.
2 types.
Type 1 Type 2
 Discharging ear with intact TM.
 Cyst or opening in preauricular area.
 May present as abscess.
 HISTOPATHOLOGY:-
 Lined by stratified squamous epithelium.
 Cyst may have lymphoid tissue with germinal
centers.
INVESTIGATION:-
Imaging usually not required.
Sinogram – extent & confirm the position of
upper end.
TREATMENT:-
Surgical excision.
Most common.
95% of the anomalies.
M =F
3RD n 4th decade
15% < 10yrs
Left predominance
Cysts> sinus/fistula
 Cysts > sinus/fistula
 Cyst- smooth , soft mass in the lateral neck &
located anterior and deep to SCM.
 Fistula/sinus- congenital opening on the
lower neck , ant to SCM.
 Recurrent neck infection
 Can present as pain , dyspnoea & dysphagia.
INVESTIGATION :-
 FNAC – epithelial elements & cholesterol
crystals.
 Radiological usually not required.
 Contrast sinogram to define track.
 USG.
Complete surgical excision.
Stepladder technique for sinus & fistula.
Delay until 2-3yrs of age.
Intraoral approach for isolated pharyngeal cysts.
 Rarely seen
 2 – 8 % all anomalies
 Left predominance.
Cutaneous opening along anterior border of
SCM
Neck abscess, retropharyngeal abscess or
hypoglossal nerve palsy
INVESTIGATION:-
As for 2nd arch anomaly
Laryngoscopy-opening in pyriform sinus
TREATMENT:-
Surgical excision.
 Lymphangiomas & hemangiomas
 Usually 1st yr of life.
 Hemangiomas often resolve spontaneously,
while lymphangiomas unchanged.
 75% head & neck region
 Left predliction
 Posterior triangle of neck
 50- 65% at birth, 80- 90% by 2 yrs age.
 Karyotypic abnormality in 25-70% children.
 Macrocystic – cystic hygroma.
 Microcystic.
Location:-
 Microcystic- oral cavity as clusters of clear,
red or balck vesicles.
 Cystic hygroma – soft, painless , compressible
mass.
 Typically transilluminates.
 Airway compromise.
 INVESTIGATION:-
 FNAC- little or no value.
 Plain xray
 USG – cystic nature, relationship to
surrounding structures & differentiate btw
micro and macrocystic.
 CT & MRI.
Medical T/t :-
 Sclerosant agent- bleomycin, pure
ethanol,doxycycline, sodium tetradecyl
sulfate & OK -432( inactive group a
streptococcus pyogene).
Surgical excision- mainstay of T/t.
Laser- microcystic lesion.
20% in neck.
28% all midline cyst
M = F
TYPES:- Epidermoid cyst
true dermoid cyst
teratoid cysts
ETIOLOGY:- ectodermal differentiation of
mulitpotent cells trapped along the lines of
tissue fusion.
 2ND & 3RD decade.
 Cystic or solid painless mass .
 Submental region , above or below
mylohyoid muscle.
 Inflammatory swelling.
 INVESTIGATION:-
 Clinical diagnosis
 FNAC
 TREATMENT:-
 Complete surgical excision.
 Lymphadenopathy:-
 Most common clinical problem in children.
 38-45%
 90% are benign in children
 Cervical lymph nodes- infectious pathology.
 reactive.
 infection(most common)
 proliferation – lymphomas
 Infiltration- metastatic
 metabolic
 Newborn – any palpable mass
 Children – cervical LN size 2cm, axillary 1cm &
inguinal 1.5 cm is normal.
 Symptoms of URI.
 Fever, irritability, anorexia
 Poor dental health
 Contacts with animals
 Tender lymph node
 GRANULOMATOUS :- weeks to months
 Minimal systemic c/o
 Firm realtivly fixed node
empirical antibiotics for 2 weeks
Blood investigations – CBC, ESR, CRP
Serology
Chest xray
FNAC - no response
Progressively enlarging
Solitary & assymetric node
Supraclavicular mass
Firm, rubbery consistency
biopsy
 Expectant - <3cm , non tender, no skin
changes & present for 2 wks or less.
 Antimicrobial therapy- > 2-3 cm, overlying
erythema & tender.
 ATT
 Chemotherapy & radiotherapy.
LUDWIG’S ANGINA:-
 Rapidly progressive
cellulitis of soft tissue
of neck & floor of
mouth.
 Submandibular space –
sublingual

Submaxillary space
 Dental infection – 80%
cases
 Aerobes & anaerobes
95% cases have B/L submandibular swelling.
Brawny and tense with overlying erythema.
Neck pain, dysphagia, respiratory distress.
Elevated or protuded tounge.
Complications:-
airway obstruction
Retropharyngeal & parapharyngeal infection
Septicemia
Aspiration pneumonia
 Systemic antibiotics
 Incision & drainage :- intraoral
 external
 Tracheostomy
Base of skull to
bifurcation of
trachea.
Retropharyngeal lymph
nodes.
Parapharyngeal space
communicates.
 Common in children <3 yrs
 Suppuration of retropharyngeal LN – infection of
adenoid, nasopharynx, PNS or nasal cavity.
 Adults- injury to PPW, cevical esophagus.
 Clinical features:-
 -Dysphagia
 - Difficult breathing
 - Stridor
 -Torticollis
 - Bulge in PPW
 INVESTIGATIONS:-
 Xray STN – lateral view
 TREATMENT:-
 Systemic antibiotics
 Incision & drainage
 Tracheostomy
 Infection :- pharynx( tonsil, adenoid,
peritonsillar abscess)
 Teeth(lower last molar)
 Ear( bezold abscess)
 Parotid, retropharyngeal & submaxillary
 External trauma
anterior compartment- triad( prolapse of tonsil &
tonsilar fossa, trismus & external swelling behind the
angle of jaw)
Odynophagia
Posterior compartment – bulge of pharynx, palsy of CN
9,10,11,12& sympathetic chain and swelling of parotid
area.
Complications:-
Respiratory obstruction
Septicimea
Retropharyngeal space infection
Mediastinum infection
Mycotic aneurysm of carotid
Systemic antibiotics
Drainage of abscess
tacheostomy
THYROID MASS :-
Leading cause of anterior neck masses.
CHILDREN- most common neoplastic condition
Male predominance
Higher incidence of malignancy
ADULTS –
Female predominance
Mainly benign
Goitre
Thyroid nodule
Cancer benign
Thyroid nodule
MNG
Simple cyst
Follicular adenoma
Hashimotos
thyroiditis
Malignant
Papillary Ca
Follicular Ca
Hurthel ce ll Ca
Medullary Ca
Anaplastic CA
 Thyroid mass
Associated symptoms of hyper/hypothyroidism
Associate compressive symptoms
Features suggestive of increase risk of malignancy:-
h/o irradiation
Family h/o MCT or men2
<20YRS > 70YRS
Male
Growing nodule
Firm & hard
Fixed
Cx adenopathy
Persistent hoarsness, dysphagia, dysphagia.
 TFT
 FNAC
 USG
 TREATMENT:- etiology
 Most common in children & young adult.
 Male predominance
 Hodgkin’s lymphoma & non- hogkin’s
lymphoma.
 80% children with hodgkin’s have neck mass.
 Lateral neck mass only – discrete , rubbery &
non tender
 Fever, night sweats & weight loss
 Hepatosplenomegaly
 Diffuse lymphadenopathy.
FNAC- first line diagnostic test.
If suggestive of lymphoma – open
biopsy.
Full work up- CT scan chest,
abdomen pelvis, head & neck &
bone marrow biopsy
PET scan
 Age
 Disease stage
 Potential T/t sequeale
 Chenotherapy- chemosensitive.(NHL)
 Radiotherapy- limited role (NHL)
 Advanced stage – combined
chemoradiotherapy.
 Arise from neural crest derivative
 Include schwannoma, neurofibroma,&
malignant pheripheral cell Tm.
 Increase incidence in NF syndrome
 Schwannoma most common in head & neck
region.
 Mostly sporadic cases
 25 – 45% neck when extracranial
 20 – 50yrs
 Benign < 1% malignant
 Signs & symptoms :-
Medial tonsillar enlargement
Hoarseness( vagus)
Horners syndrome
 INVESTIGATION:-
 Diagnosis- biopsy
 CT Scan & MRI
 TREATMENT :- surgical removal,
chemotherapy or radiotherapy.
Swelling :- reactive lesion
Infectious sialadenitis
Benign neoplasm
Malignant neoplasm
Rare lesion
Symptoms:- limited & non specific – swelling,
pain, xerostomia, foul taste & excessive
salivation.
 Signs :-
 Swelling of the gland
 Mucosal dryness
 Intraoral examination
 Facial nerve function.
INVESTIGATION :-
FNAC
Plain Xray ( occlusal view)
Sialography
sialendoscopy
USG
CT , MRI
 Acute infection – antibiotic .
 Stones-sumbandibular glad duct excision.
 - lithotrpsy
 Tumour- gland excision.
 Dealing with a mass in the neck may seem
daunting, but a systemic approach is all that is
needed.

PEDIATRIC AIRWAY EVALUATION & MANAGEMENT

  • 2.
     TRIANGLES OF NECK:- Neckcan be divided into anterior & posterior triangle by STERNOCLIDOMASTOID MUSCLE
  • 7.
     In pediatricage group - 90% benign.  50% out of which may be congenital.  In adult population – 80% non- thyroid masses
  • 9.
     MID LINEANTREIOR TRIANGLE POSTERIOR TRIANGLE  CONGENITAL  Thyroglossal cyst  Dermoid cyst  INFLAMMATORY  Lymphadenitis  TUMOUR  Thyroid  Lymphoma  OTHERS  Sternoclidomastoid  Hematoma/fibroma  CONGENITAL  Brachial cyst  Thymic cyst  INFLAMMATORY  Adenitis  Sialadenitis  TUMOUR  Metastatic  Lymphoma  Vascular CONGENITAL Lymphangioma INFLAMMATION Adenitis TUMOUR Lymphoma Metastaic Supraclavicular OTHERS neuroma
  • 10.
     AGE:-  <20 yrs 20 – 40 yrs > 40yrs congenital inflammatory Inflammatory, salivary gland. lymphoma metastatic
  • 11.
     SEX :- Male preponderance- hodgkins lymphoma, nasopharyngeal carcinoma, thyroid mass in pediatric age group.  Female preponderance – Thyroid swelling in adult age group.
  • 12.
     DURATION:-  Acute Chronic Mode of onset?  Progressive/non progressive?  Site?  Painful/painless?  Associated systemic symptoms  Personal habits  Previous irradiation or surgery 
  • 13.
    SITE OF THESWELLING:- -tells about the organ of origin -certain swellings are site specific -dermoid cyst -thyroid swelling
  • 14.
     *Size  *Number:- .  - solitary ( dermoid cyst & lipoma)  - multiple ( NFM & hodgkin’s lymphoma) *Shape:-  -Spherical  -irregular
  • 15.
    *Surface:-  - smooth( cystic & benign)  - irregular. *Margins:-  - Well defined  - diffuse
  • 16.
    *Colour * Overlying skin Specialsigns :- - -Pulsation - - movement with swallowing - - movement with protusion of tounge
  • 17.
    PALPATION:- Temp tenderness Site Size Surface – smooth, irregular, lobulated Margins – well defined, ill defined Extension Consistency – solid, soft , firm , hard , rubbery. Mobility Tense/fluctuation Transillumination Pulsation Relation to surrounding structures Draining lymph node
  • 18.
  • 19.
    BLOOD:- CBC, ESR, TFT,CRP, IMAGING:- Xray, USG, CT scan, MRI , Radionuclitide scan, PET Sialography CYTOLOGY TISSUE:- Incisional/excisional biopsy
  • 20.
    Standard for diagnosis. Indications:- -Any neck mass that is not an obvious abscess - Persistent after 2 wks of antibiotics
  • 22.
    Inexpensive easily available Non invasive Notassociated with radiation Solid versus cystic masses Congenital cyst from solid nodes/ Tm. calcification Extent & vascularity. Guided FNAC
  • 23.
     Distinguish cysticfrom solid  Extent of lesion  Anatomical relations  Vascularity with contrast  Pathological node( lucent, > 1.5 cm, loss of shape, rim enhancement)  Detection of unknown primary
  • 24.
     Similar informationas CT   Better soft tissue contrast  Better for upper neck and skull base
  • 25.
     Uses flourinelabelled deoxyglucose  Valuable tool – evaluation of regional LN  - detect distant metastasis  - synchronous primary lesion  - unknown primary
  • 26.
    Any solid assymetricmass MUST be considered a metastatic neoplastic lesion until proved otherwise. Asymptomatic cervical mass ~ 12% cancer  80% are SCCS
  • 27.
     Asymptomatic neckswelling  Associated symptoms – otalgia, dysphagia, voice change, difficult breathing, weight loss, loss of appetite, bone pain , chest pain.  Fever & night sweats.  Ipsilateral otalgia with normal otoscopy- direct attention to tounge base, tonsil, supraglottis & hypopharynx.  U/L serous otitis media- direct attention to nasopharynx.
  • 28.
    Directed biopsy- primaryis known.  All suspicious mucosal lesions  Areas of concern on CT/MRI FNAC
  • 29.
    Metastatic neck LAPwithou the development of primary lesion with a subsequent 5 yr period. Head & neck cancer with unknown primary 3- 7% patients. Most common – level LN II & III. Supraclavicular nodal involement – below clavicle SCC thyroid, lung, breast, GI tract
  • 30.
     High risknasopharynx, pyriform sinus & base of tongue & tonsil.  Full ENT examination.  Level I – lip , anterior tongue, buccal mucosa.
  • 31.
    Level II,III,V- tonsilor tounge base nasopharyngeal examination, tounge base biopsy from concerned areas.  Level IV,V – hypopharynx & larynx  DL scopy, esophagoscopy, chest abdomen CT, PET Scan.
  • 32.
     PET- CTnegative & no primary on endoscopy.  -Tonsillectomy  - tongue base biopsy & biopsies of postnasal space & pyriform fossa  -25% found at tonsil  - clinical examination, panendoscopy, CT and MRI with biopsy reveal primary in 40% cases.  - definitive MND in all patients after FNAC or biopsy.
  • 33.
    Cystic remnant ofthe TGD between foramen caecum of tounge base & thyroid bed in infrahyoid neck.
  • 34.
     70% -congenital neck mass  65% - between hyoid & thyroid  50% - hyoid  20% - suprahyoid  1-2% - lingual  1-2% - malignancy
  • 35.
    A small, round,soft mass in the midline of neck( 90%) Infected cyst(5%) – enlarge neck mass, fever, draining sinus(15%) & dysphagia. Moves with protrusion of tounge. Pre school age children or mid adolescence.(5yr)
  • 36.
     History &examination  Investigation -  FNAC  USG- location, cystic, normal thyroid.  CT & MRI – large cyst, suspected malignancy, lingual thyroid
  • 37.
     Surgical excision-T/t of choice  Sistrunk’s operation –  Removal of cyst, the tract , the central portion of hyoid bone, as well as core of tissue including tissue tract or raphe between mylohyoid muscles, portion of geinoglossus muscle and up to foramen caecum
  • 38.
     4th- 6thweek IUL.  6 paired branchial arches.  Persistent cleft- external sinus.  Persistent pouch – internal sinus  Fistula.  17% pediatric neck masses.
  • 39.
    5% of brachialcleft anamolies M = F Cyst ( adult> children), fistula/sinus(children> adult). Line from tragus to hyoid bone. Left predominance. 2 types.
  • 40.
  • 41.
     Discharging earwith intact TM.  Cyst or opening in preauricular area.  May present as abscess.  HISTOPATHOLOGY:-  Lined by stratified squamous epithelium.  Cyst may have lymphoid tissue with germinal centers.
  • 42.
    INVESTIGATION:- Imaging usually notrequired. Sinogram – extent & confirm the position of upper end. TREATMENT:- Surgical excision.
  • 43.
    Most common. 95% ofthe anomalies. M =F 3RD n 4th decade 15% < 10yrs Left predominance Cysts> sinus/fistula
  • 45.
     Cysts >sinus/fistula  Cyst- smooth , soft mass in the lateral neck & located anterior and deep to SCM.  Fistula/sinus- congenital opening on the lower neck , ant to SCM.  Recurrent neck infection  Can present as pain , dyspnoea & dysphagia.
  • 46.
    INVESTIGATION :-  FNAC– epithelial elements & cholesterol crystals.  Radiological usually not required.  Contrast sinogram to define track.  USG.
  • 47.
    Complete surgical excision. Stepladdertechnique for sinus & fistula. Delay until 2-3yrs of age. Intraoral approach for isolated pharyngeal cysts.
  • 48.
     Rarely seen 2 – 8 % all anomalies  Left predominance.
  • 51.
    Cutaneous opening alonganterior border of SCM Neck abscess, retropharyngeal abscess or hypoglossal nerve palsy
  • 52.
    INVESTIGATION:- As for 2ndarch anomaly Laryngoscopy-opening in pyriform sinus TREATMENT:- Surgical excision.
  • 53.
     Lymphangiomas &hemangiomas  Usually 1st yr of life.  Hemangiomas often resolve spontaneously, while lymphangiomas unchanged.
  • 54.
     75% head& neck region  Left predliction  Posterior triangle of neck  50- 65% at birth, 80- 90% by 2 yrs age.  Karyotypic abnormality in 25-70% children.  Macrocystic – cystic hygroma.  Microcystic.
  • 55.
    Location:-  Microcystic- oralcavity as clusters of clear, red or balck vesicles.  Cystic hygroma – soft, painless , compressible mass.  Typically transilluminates.  Airway compromise.
  • 56.
     INVESTIGATION:-  FNAC-little or no value.  Plain xray  USG – cystic nature, relationship to surrounding structures & differentiate btw micro and macrocystic.  CT & MRI.
  • 57.
    Medical T/t :- Sclerosant agent- bleomycin, pure ethanol,doxycycline, sodium tetradecyl sulfate & OK -432( inactive group a streptococcus pyogene). Surgical excision- mainstay of T/t. Laser- microcystic lesion.
  • 58.
    20% in neck. 28%all midline cyst M = F TYPES:- Epidermoid cyst true dermoid cyst teratoid cysts ETIOLOGY:- ectodermal differentiation of mulitpotent cells trapped along the lines of tissue fusion.
  • 59.
     2ND &3RD decade.  Cystic or solid painless mass .  Submental region , above or below mylohyoid muscle.  Inflammatory swelling.
  • 60.
     INVESTIGATION:-  Clinicaldiagnosis  FNAC  TREATMENT:-  Complete surgical excision.
  • 61.
     Lymphadenopathy:-  Mostcommon clinical problem in children.  38-45%  90% are benign in children  Cervical lymph nodes- infectious pathology.  reactive.  infection(most common)  proliferation – lymphomas  Infiltration- metastatic  metabolic
  • 62.
     Newborn –any palpable mass  Children – cervical LN size 2cm, axillary 1cm & inguinal 1.5 cm is normal.  Symptoms of URI.  Fever, irritability, anorexia  Poor dental health  Contacts with animals  Tender lymph node  GRANULOMATOUS :- weeks to months  Minimal systemic c/o  Firm realtivly fixed node
  • 63.
    empirical antibiotics for2 weeks Blood investigations – CBC, ESR, CRP Serology Chest xray FNAC - no response Progressively enlarging Solitary & assymetric node Supraclavicular mass Firm, rubbery consistency biopsy
  • 64.
     Expectant -<3cm , non tender, no skin changes & present for 2 wks or less.  Antimicrobial therapy- > 2-3 cm, overlying erythema & tender.  ATT  Chemotherapy & radiotherapy.
  • 65.
    LUDWIG’S ANGINA:-  Rapidlyprogressive cellulitis of soft tissue of neck & floor of mouth.  Submandibular space – sublingual  Submaxillary space  Dental infection – 80% cases  Aerobes & anaerobes
  • 66.
    95% cases haveB/L submandibular swelling. Brawny and tense with overlying erythema. Neck pain, dysphagia, respiratory distress. Elevated or protuded tounge. Complications:- airway obstruction Retropharyngeal & parapharyngeal infection Septicemia Aspiration pneumonia
  • 67.
     Systemic antibiotics Incision & drainage :- intraoral  external  Tracheostomy
  • 68.
    Base of skullto bifurcation of trachea. Retropharyngeal lymph nodes. Parapharyngeal space communicates.
  • 69.
     Common inchildren <3 yrs  Suppuration of retropharyngeal LN – infection of adenoid, nasopharynx, PNS or nasal cavity.  Adults- injury to PPW, cevical esophagus.  Clinical features:-  -Dysphagia  - Difficult breathing  - Stridor  -Torticollis  - Bulge in PPW
  • 70.
     INVESTIGATIONS:-  XraySTN – lateral view  TREATMENT:-  Systemic antibiotics  Incision & drainage  Tracheostomy
  • 72.
     Infection :-pharynx( tonsil, adenoid, peritonsillar abscess)  Teeth(lower last molar)  Ear( bezold abscess)  Parotid, retropharyngeal & submaxillary  External trauma
  • 73.
    anterior compartment- triad(prolapse of tonsil & tonsilar fossa, trismus & external swelling behind the angle of jaw) Odynophagia Posterior compartment – bulge of pharynx, palsy of CN 9,10,11,12& sympathetic chain and swelling of parotid area. Complications:- Respiratory obstruction Septicimea Retropharyngeal space infection Mediastinum infection Mycotic aneurysm of carotid
  • 74.
  • 75.
    THYROID MASS :- Leadingcause of anterior neck masses. CHILDREN- most common neoplastic condition Male predominance Higher incidence of malignancy ADULTS – Female predominance Mainly benign
  • 76.
    Goitre Thyroid nodule Cancer benign Thyroidnodule MNG Simple cyst Follicular adenoma Hashimotos thyroiditis Malignant Papillary Ca Follicular Ca Hurthel ce ll Ca Medullary Ca Anaplastic CA
  • 77.
     Thyroid mass Associatedsymptoms of hyper/hypothyroidism Associate compressive symptoms Features suggestive of increase risk of malignancy:- h/o irradiation Family h/o MCT or men2 <20YRS > 70YRS Male Growing nodule Firm & hard Fixed Cx adenopathy Persistent hoarsness, dysphagia, dysphagia.
  • 78.
     TFT  FNAC USG  TREATMENT:- etiology
  • 79.
     Most commonin children & young adult.  Male predominance  Hodgkin’s lymphoma & non- hogkin’s lymphoma.  80% children with hodgkin’s have neck mass.
  • 80.
     Lateral neckmass only – discrete , rubbery & non tender  Fever, night sweats & weight loss  Hepatosplenomegaly  Diffuse lymphadenopathy.
  • 81.
    FNAC- first linediagnostic test. If suggestive of lymphoma – open biopsy. Full work up- CT scan chest, abdomen pelvis, head & neck & bone marrow biopsy PET scan
  • 82.
     Age  Diseasestage  Potential T/t sequeale  Chenotherapy- chemosensitive.(NHL)  Radiotherapy- limited role (NHL)  Advanced stage – combined chemoradiotherapy.
  • 83.
     Arise fromneural crest derivative  Include schwannoma, neurofibroma,& malignant pheripheral cell Tm.  Increase incidence in NF syndrome  Schwannoma most common in head & neck region.
  • 84.
     Mostly sporadiccases  25 – 45% neck when extracranial  20 – 50yrs  Benign < 1% malignant  Signs & symptoms :- Medial tonsillar enlargement Hoarseness( vagus) Horners syndrome
  • 85.
     INVESTIGATION:-  Diagnosis-biopsy  CT Scan & MRI  TREATMENT :- surgical removal, chemotherapy or radiotherapy.
  • 86.
    Swelling :- reactivelesion Infectious sialadenitis Benign neoplasm Malignant neoplasm Rare lesion Symptoms:- limited & non specific – swelling, pain, xerostomia, foul taste & excessive salivation.
  • 87.
     Signs :- Swelling of the gland  Mucosal dryness  Intraoral examination  Facial nerve function. INVESTIGATION :- FNAC Plain Xray ( occlusal view) Sialography sialendoscopy USG CT , MRI
  • 88.
     Acute infection– antibiotic .  Stones-sumbandibular glad duct excision.  - lithotrpsy  Tumour- gland excision.
  • 89.
     Dealing witha mass in the neck may seem daunting, but a systemic approach is all that is needed.