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A Practical Guide to the
Differential Diagnosis
felice.d’arco@gosh.nhs.uk
Summary
o Essential Anatomy of The Neck
 Superficial Fascia (subcutaneous Tissue)
 Neck Spaces (3 layers of the deep cervical
fascia)
o Features of the Lesion: Where? Cystic?
Solid?
Anatomy of the Neck
 Superficial Cervical Fascia: thin layer of
subcutaneous connective tissue that lies between
the dermis of the skin and the deep cervical fascia
 Contents: platysma, nerves, blood / lymphatic
vessels, fat.
 Pathology (related to the content!!):
Teratoma, Vasc. Malformations/neoplasm, Cellulitis,
Plexiform Neurofibromas (NF1), Subcutaneous Fat
Fibrosis (neonates)
NB: It is considered by some to be a part of the Panniculus adiposus, and
not true fascia. Bailey, B.J. Ed: Head and Neck Surgery-Otolaryngology 2006.
Superficial Cervical Fascia (yellow)
From internet
Subcutaneous fat
tissue between
the skin and the
superficial layer of
the deep cervical
fascia (green)
Superficial layer DCF
Skin
Anatomy of the Neck
 Deep Cervical Fascia (DCF): 3 layers 
superficial (SL), middle (ML) and deep (DL)
 The layers divide neck in compartments (on
the axial plane).
 Neck is also divided in Suprahyoid neck
(SHN) Infrahyoid neck (IHN) (on the coronal
and sagittal plane)
Hyoid Bone
Superficial Layer DCF
SHN: Around Masticatory Sp. & Parotid Sp; part of
carotid space
www.statdx.com
Superficial layer
DCF
Superficial Layer DCF
IHN: surrounds strap, sternocleidomastoid
& trapezius muscles
www.statdx.com
Superficial layer
DCF
Middle Layer DCF
SHN: defines Pharyngeal Mucosal Space
deep margin; contributes to carotid space
www.statdx.com
ML - DCF
Middle Layer DCF
IHN: Surrounds Visceral Sp.; contributes of
carotid space
www.statdx.com
ML - DCF
Deep Layer DCF
www.statdx.com
SHN & IHN: Surrounds perivertebral space (paraspinal and pre-vertebral
components), Contributes to carotid space.
DL - DCF
Deep Layer DCF: Alar Fascia
Part of the DL-DCF which forms the lateral and posterior walls of the
Retropharyngeal space and separates this space from the Danger Space (virutal
space)
www.statdx.com
DS: from the skull base to the mediastinum;
Boundaries ANT: Retropharyngeal Sp. POST: pre-
vertebral component of periveterbal space
Neck Masses in Children: Solid
 Reactive/metastatic Lymph nodes
 Lymphoma
 Infantile Hemangioma
 Rhabdomyosarcoma
 Lipoma
 Matastatic Neuroblastoma (mostly osseous);
Primary Neck Neuroblastoma (posterior
carotid space)
 Fibromatosis Colli (neonate)
Neck Masses in Children: Cystic
 Thyreoglossal Duct Cyst
 Laryngocele
 Abscess
 Branchial Cleft Cyst
 Lymphatic Malformation
 Dermoid/Epidermoid
 Teratoma (mixed solid and cystic)
Space or Anatomic
region Differential Diagnosis
Superficial Fascia Teratoma, Vascular Malformations, lipoma, plexiform
Neurofibroma, fibromatosis colli of SCM (in neonates)
Danger Sp. Cellulitis/Abscess
Masticator Sp. Venous/lymphatic Malf., rhabdomyosarcoma, cellulitis/abscess
Parotid Sp. Infection, Lymphatic malf., RMV thrombosis
Carotid Sp. IJV thrombosis, lymphadenopathy, abscess, neuroblastoma
Retropharyngeal Sp. Cellulitis/Abscess, extension of tumours or goiter
Perivertebral Sp. Neuroenteric cyst, Cellulitis/Abscess, Spondylodiskitis
Posterior Cervical Sp. Lymphatic malf., lymphadenopathy, lymphoma
Submandibular/Subling
ual Sp.
Thyroglossal cyst, venous/lymphatic Malf, dermoid cyst, ranula,
sublingual gland disease
Pharyngeal and
Parapharyngeal Sp.
Lymphangioma, paraganglioma, rhabdomyosarcoma, abscess,
Lymphoma
Infantile Hemangioma : can occur in any space!
Solid Neck Masses
Reactive Lymph Nodes
 Most frequent solid “masses” in children
 Benign, reversible enlargement of nodes in
response to antigen stimulus
 Acute/Chronic; Localized/Generalized
 IMAGING:
 Multiple well-defined, oval-shaped nodes that can be
enlarged (> 2 cm in children), typically oval-shaped
rather than round, mild homogeneous enhancement
CECT appearance Do not forget the levels of the Neck !
Drawing by F. Gaillard
Tonsils
LevelIIA
LevelIIA
Level V a
Differential Diagnosis
1) METASTATIC NODES
Rare in children
Bigger size (but in children this criterion
does not work as in adult!)
Round node shape rather than oval
Clustered nodes
Focal nodal defect/necrosis
Extracapsular spread
Primary Tumor! NB: DD between Meta Nodes and Suppurative Nodes is
often obvious clinically (Hot, tender, febrile patient)
Christine M. Glastonbury
Differential Diagnosis
2) Lymphoma (NHL and HL)
- SIZE ! BILATERAL non-symmetric!
-Posterior Cervical Space often involved
-Homogeneous lobulated nodal masses
-Single or multiple nodal chain
-Variable contrast enhancement
-Necrotic center may be present
Lymphoma Neck
Internal jugular chain
Spinal Accessory Chain
4 yo HL
Bilateral Internal jugular chain
Infantile Hemangioma
 Can be in different locations in the neck
(subcutaneous tissue)
 Is a benign neoplasm (not malformation)
 Proliferative phase: few weeks after birth to 1-2
years
 Involuting phase: gradual regression over next
several years (90% resolve by 9 years)
 Often single lesion.
 IMAGING Key Features:
 Well-defined enhancing mass, mildly hyper T2 to muscle
 Internal Vessels (Serpiginous Flow Voids)
 No Calcifications! (DD Venous Malformation)
 US: mean venous peaks not elevated (DD AVM)
 Involuting Phase: fatty replacement
Infantile Hemangioma
First
Diagnosi
s
After
Treatment
with
Propanolol
Differential Diagnosis
1) Venous Malformation
Large venous lakes
- T2 signal more hyperintense
- Variable enhancement (patchy,
heterogeneous)
- Phleboliths: Calcium within the
lesion
- No Flow voids
Differential Diagnosis
2) AVM
- High flow and tortuous feeding
arteries
- Large draining veins
- Nidus/AV shunting
- Ill defined mass
- US: elevated venous peaks
- Worsening overtime
- Clinical: arterial feeding is
evident
Differential Diagnosis
3) Rhabdomyosarcoma
- Different age : 2- 5 y; 15-19 y
- Aggressive behavior: bony erosion,
invasions surrounding tissues
- Non-Homogeneous appearance
(necrosis, hemorrhage) and contrast
- Diffusion restriction (Lope 2012)
Rhabdomyosarcoma Neck
Rhabdomyosarcoma Neck
T2 signal, hyper but not too much
statdx.com
 Fat signal/ density in all sequences, if associated
c.e. suspect liposcarcoma
Lipoma
CT: Low Density ( −100 to −50 HU)
Hyper in T1 Suppressed in Fat-Sat
 Metastatic : Typical Osseous Meta in Calvarium, Skull base, Orbits,
Temporal bones  DWI restriction, c.e.
 Radiologist need to suggest abdominal US
 MIGB uptake
 Rare Nodal Metastasis
Neuroblastoma
 Primary Neck NB : Posterior Carotid
Space
 1-5 % of NB
 Moderately enhancing mass
 Associated Lymphoadenopathy
 DD with Reactive Nodes and
Lymphoma very difficult (biopsy)
 Presence of Ca++ (extremely rare in
Lymphoma)
Neuroblastoma
 Sternocleidomastoid Enlargement of Infancy
 Appears within 2 weeks of delivery; regresses by 8 months
 Nontender (DD with myositis) , monolateral
 Enlargement of the muscle which enhances diffusely
 Surrounding tissues are normal (DD with
Rhabdomyosarcoma together with age)
 Diagnosis: Clinical + US
Fibromatosis Colli
Normal Fibromatosis Colli
Smiti et al.2010
Dr. B. Koch
Cystic Neck Masses
 Remnant of the TGD (Between foramen
cecum at tongue base → thyroid bed in
infrahyoid neck)
 Most common congenital neck
lesions
 Median cyst (could be also
paramedian in the infrahyoid neck)
 Thin rim of c.e. is possible (often
associated with infection)
 Embedded by strap muscles when
infrahyoid (“claw sign”)
Thyroglossal Duct Cyst
Harnsberger 2004
Differential Diagnosis
1) Lingual Thyroid
- Solid, enhancing mass
- Ectopic Thyroid Tissue in
the base of the tongue or
floor of the mouth
Differential Diagnosis
2) Laryngocele
- Traces back to the
Larynx
- Air and fluid
Differential Diagnosis
3) Median Sub-Lingual
Abscess
- Clinical: associated
Odontogenic or salivary
gland infection
- Thick enhancing wall, DWI
restriction in MRI
Harnsberger 2004
NB: most frequent location of an abscess in neck
is retropharyngeal space
 Congenital malformations during development of the
branchial apparatus
 4 types of branchial cleft anomalies: cysts, sinuses,
fistulas from the 1st , 2nd, 3rd and 4th branchial arches
 2nd branchial cleft anomaly is the most common:
95%
Branchial Cleft Anomalies
Head and neck region
at 4 weeks gestation
(Meuwly et al 2005)
 Unilocular cysts with thin wall
 Fluid content: CT hypodense, T1 hypohintense, T2
hyperintense
 No enhancement or subtle wall enhancement
 If infected: wall thickening/enhancement, increase
density of the fluid
 Neoplastic degeneration: enhancing nodules along
the wall
Branchial Cleft Anomalies
1st Branchial Cleft
Anomaly
 Benign, congenital cyst in or adjacent to parotid
gland, EAC, or pinna
 Several classifications related to embryology or
location
Postero-inferior to auricle Adjacent to parotid gl./mandible angle
B. Koch 2015
2nd Branchial Cleft
Anomaly
 Typical location: Antero-medially to the SCM
(superior 1/3), posteriorly to the submandibular
gland, laterally to the carotid space
B. Koch 2015
3rd Branchial Cleft Anomaly
-Medially to the middle 1/3 of the SCM
-Lower than 2nd BCC
-In the posterior cervical space
Carotid sp
3BCC
SCM
Post Cerv
Sp
4th Branchial Cleft Anomaly
It is a tract from the pyriform sinus to
the
Superior aspect of the thyroid
Thyroid
B. Koch 2015
 Uni- or multiloculated, non-enhancing, cystic neck
mass.
 Micro- and macro cystic
 Often trans-spatial, with fluid-fluid levels
(hemorrhage and high proteinaceous components)
 Venolymphatic Malf. : Combined elements of venous
malformation & lymphatic malformation (contrast
enhancement of the venous elements)
Lymphatic Malformation
 2nd BCC: unilocular cyst, typical location, no fluid-
fluid levels
 Abscess/suppurative nodes: clinical signs of
infection, peripheral enhancement and cellulitis
 Thyroglossal duct cyst: typical (midline) location,
single cyst
Differential Diagnosis
Dermoid/Epidermoid Cyst
 Definition: Cystic mass resulting from congenital
epithelial inclusion or rest
 Epidermoid: Epithelial elements only, fluid content
 Dermoid: Epithelial elements plus dermal
substructure, fluid, fatty or mixed content
 Location: oral cavity (DD with Ranula and TGDC),
midline anterior neck (DD with TGDC), orbit (DD
with abscess and lymphatic malf.), nasal with
associated nasal dermal sinus ± intracranial
extension
Imaging
Epidermoid: homogeneous T1
hypo and T2 hyper. Increase T1
signal if high protein fluid
Dermoid: heterogeneous
signal. Fatty elements are T1
hyper and low in fat sat T2.
Possible Ca++
Both can have DWI restriction
and thin rim enhancement
T1 T2 fat-sat
T1
Dermoid: tyipical “sac of marbles” appearance
due to area of fatty attentuation
Malik et al. 2012
Differential Diagnosis
 Ranula: salivary gland retention cyst in sublingual
space.
 Can be indistinguishable from epidermoid cyst
which doesn’t show restriction.
 Often is ruptured into the submandibular space
(diving ranula) which shows typical “comet shape”
(body in the SMS and tail in the SLS)
 No fat, no Ca++ and no DWI restriction
Malik et al. 2012
Tail
Body
Teratoma
 Anterior neck, midline mass containing all 3 germ
layers
 Mixed (cystic and solid) with fat and calcium
 DD: Lymphatic Malf (fluid with no fat, calcium or
solid components), Goiter (homogeneous, respects
limits of the thyroid gland)
Mixed solido-cystic mass with fat content
 Neck masses are common findings in children and
can be a diagnostic challenge
 Often trans-spatial
 No space-specificity
 Distinction in Solid or Cystic (or mixed) can help in
the differential diagnosis
Conclusion
Thank you

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Head and Neck Masses In Children

  • 1. A Practical Guide to the Differential Diagnosis felice.d’arco@gosh.nhs.uk
  • 2. Summary o Essential Anatomy of The Neck  Superficial Fascia (subcutaneous Tissue)  Neck Spaces (3 layers of the deep cervical fascia) o Features of the Lesion: Where? Cystic? Solid?
  • 3. Anatomy of the Neck  Superficial Cervical Fascia: thin layer of subcutaneous connective tissue that lies between the dermis of the skin and the deep cervical fascia  Contents: platysma, nerves, blood / lymphatic vessels, fat.  Pathology (related to the content!!): Teratoma, Vasc. Malformations/neoplasm, Cellulitis, Plexiform Neurofibromas (NF1), Subcutaneous Fat Fibrosis (neonates) NB: It is considered by some to be a part of the Panniculus adiposus, and not true fascia. Bailey, B.J. Ed: Head and Neck Surgery-Otolaryngology 2006.
  • 4. Superficial Cervical Fascia (yellow) From internet Subcutaneous fat tissue between the skin and the superficial layer of the deep cervical fascia (green) Superficial layer DCF Skin
  • 5. Anatomy of the Neck  Deep Cervical Fascia (DCF): 3 layers  superficial (SL), middle (ML) and deep (DL)  The layers divide neck in compartments (on the axial plane).  Neck is also divided in Suprahyoid neck (SHN) Infrahyoid neck (IHN) (on the coronal and sagittal plane)
  • 7. Superficial Layer DCF SHN: Around Masticatory Sp. & Parotid Sp; part of carotid space www.statdx.com Superficial layer DCF
  • 8. Superficial Layer DCF IHN: surrounds strap, sternocleidomastoid & trapezius muscles www.statdx.com Superficial layer DCF
  • 9. Middle Layer DCF SHN: defines Pharyngeal Mucosal Space deep margin; contributes to carotid space www.statdx.com ML - DCF
  • 10. Middle Layer DCF IHN: Surrounds Visceral Sp.; contributes of carotid space www.statdx.com ML - DCF
  • 11. Deep Layer DCF www.statdx.com SHN & IHN: Surrounds perivertebral space (paraspinal and pre-vertebral components), Contributes to carotid space. DL - DCF
  • 12. Deep Layer DCF: Alar Fascia Part of the DL-DCF which forms the lateral and posterior walls of the Retropharyngeal space and separates this space from the Danger Space (virutal space) www.statdx.com DS: from the skull base to the mediastinum; Boundaries ANT: Retropharyngeal Sp. POST: pre- vertebral component of periveterbal space
  • 13. Neck Masses in Children: Solid  Reactive/metastatic Lymph nodes  Lymphoma  Infantile Hemangioma  Rhabdomyosarcoma  Lipoma  Matastatic Neuroblastoma (mostly osseous); Primary Neck Neuroblastoma (posterior carotid space)  Fibromatosis Colli (neonate)
  • 14. Neck Masses in Children: Cystic  Thyreoglossal Duct Cyst  Laryngocele  Abscess  Branchial Cleft Cyst  Lymphatic Malformation  Dermoid/Epidermoid  Teratoma (mixed solid and cystic)
  • 15. Space or Anatomic region Differential Diagnosis Superficial Fascia Teratoma, Vascular Malformations, lipoma, plexiform Neurofibroma, fibromatosis colli of SCM (in neonates) Danger Sp. Cellulitis/Abscess Masticator Sp. Venous/lymphatic Malf., rhabdomyosarcoma, cellulitis/abscess Parotid Sp. Infection, Lymphatic malf., RMV thrombosis Carotid Sp. IJV thrombosis, lymphadenopathy, abscess, neuroblastoma Retropharyngeal Sp. Cellulitis/Abscess, extension of tumours or goiter Perivertebral Sp. Neuroenteric cyst, Cellulitis/Abscess, Spondylodiskitis Posterior Cervical Sp. Lymphatic malf., lymphadenopathy, lymphoma Submandibular/Subling ual Sp. Thyroglossal cyst, venous/lymphatic Malf, dermoid cyst, ranula, sublingual gland disease Pharyngeal and Parapharyngeal Sp. Lymphangioma, paraganglioma, rhabdomyosarcoma, abscess, Lymphoma Infantile Hemangioma : can occur in any space!
  • 17. Reactive Lymph Nodes  Most frequent solid “masses” in children  Benign, reversible enlargement of nodes in response to antigen stimulus  Acute/Chronic; Localized/Generalized  IMAGING:  Multiple well-defined, oval-shaped nodes that can be enlarged (> 2 cm in children), typically oval-shaped rather than round, mild homogeneous enhancement
  • 18. CECT appearance Do not forget the levels of the Neck ! Drawing by F. Gaillard Tonsils LevelIIA LevelIIA Level V a
  • 19. Differential Diagnosis 1) METASTATIC NODES Rare in children Bigger size (but in children this criterion does not work as in adult!) Round node shape rather than oval Clustered nodes Focal nodal defect/necrosis Extracapsular spread Primary Tumor! NB: DD between Meta Nodes and Suppurative Nodes is often obvious clinically (Hot, tender, febrile patient) Christine M. Glastonbury
  • 20. Differential Diagnosis 2) Lymphoma (NHL and HL) - SIZE ! BILATERAL non-symmetric! -Posterior Cervical Space often involved -Homogeneous lobulated nodal masses -Single or multiple nodal chain -Variable contrast enhancement -Necrotic center may be present
  • 21. Lymphoma Neck Internal jugular chain Spinal Accessory Chain 4 yo HL Bilateral Internal jugular chain
  • 22. Infantile Hemangioma  Can be in different locations in the neck (subcutaneous tissue)  Is a benign neoplasm (not malformation)  Proliferative phase: few weeks after birth to 1-2 years  Involuting phase: gradual regression over next several years (90% resolve by 9 years)  Often single lesion.
  • 23.  IMAGING Key Features:  Well-defined enhancing mass, mildly hyper T2 to muscle  Internal Vessels (Serpiginous Flow Voids)  No Calcifications! (DD Venous Malformation)  US: mean venous peaks not elevated (DD AVM)  Involuting Phase: fatty replacement Infantile Hemangioma
  • 25.
  • 26. Differential Diagnosis 1) Venous Malformation Large venous lakes - T2 signal more hyperintense - Variable enhancement (patchy, heterogeneous) - Phleboliths: Calcium within the lesion - No Flow voids
  • 27. Differential Diagnosis 2) AVM - High flow and tortuous feeding arteries - Large draining veins - Nidus/AV shunting - Ill defined mass - US: elevated venous peaks - Worsening overtime - Clinical: arterial feeding is evident
  • 28. Differential Diagnosis 3) Rhabdomyosarcoma - Different age : 2- 5 y; 15-19 y - Aggressive behavior: bony erosion, invasions surrounding tissues - Non-Homogeneous appearance (necrosis, hemorrhage) and contrast - Diffusion restriction (Lope 2012)
  • 30. Rhabdomyosarcoma Neck T2 signal, hyper but not too much statdx.com
  • 31.  Fat signal/ density in all sequences, if associated c.e. suspect liposcarcoma Lipoma CT: Low Density ( −100 to −50 HU) Hyper in T1 Suppressed in Fat-Sat
  • 32.  Metastatic : Typical Osseous Meta in Calvarium, Skull base, Orbits, Temporal bones  DWI restriction, c.e.  Radiologist need to suggest abdominal US  MIGB uptake  Rare Nodal Metastasis Neuroblastoma
  • 33.
  • 34.
  • 35.  Primary Neck NB : Posterior Carotid Space  1-5 % of NB  Moderately enhancing mass  Associated Lymphoadenopathy  DD with Reactive Nodes and Lymphoma very difficult (biopsy)  Presence of Ca++ (extremely rare in Lymphoma) Neuroblastoma
  • 36.  Sternocleidomastoid Enlargement of Infancy  Appears within 2 weeks of delivery; regresses by 8 months  Nontender (DD with myositis) , monolateral  Enlargement of the muscle which enhances diffusely  Surrounding tissues are normal (DD with Rhabdomyosarcoma together with age)  Diagnosis: Clinical + US Fibromatosis Colli
  • 37. Normal Fibromatosis Colli Smiti et al.2010 Dr. B. Koch
  • 39.  Remnant of the TGD (Between foramen cecum at tongue base → thyroid bed in infrahyoid neck)  Most common congenital neck lesions  Median cyst (could be also paramedian in the infrahyoid neck)  Thin rim of c.e. is possible (often associated with infection)  Embedded by strap muscles when infrahyoid (“claw sign”) Thyroglossal Duct Cyst Harnsberger 2004
  • 40.
  • 41. Differential Diagnosis 1) Lingual Thyroid - Solid, enhancing mass - Ectopic Thyroid Tissue in the base of the tongue or floor of the mouth
  • 42. Differential Diagnosis 2) Laryngocele - Traces back to the Larynx - Air and fluid
  • 43. Differential Diagnosis 3) Median Sub-Lingual Abscess - Clinical: associated Odontogenic or salivary gland infection - Thick enhancing wall, DWI restriction in MRI Harnsberger 2004
  • 44. NB: most frequent location of an abscess in neck is retropharyngeal space
  • 45.  Congenital malformations during development of the branchial apparatus  4 types of branchial cleft anomalies: cysts, sinuses, fistulas from the 1st , 2nd, 3rd and 4th branchial arches  2nd branchial cleft anomaly is the most common: 95% Branchial Cleft Anomalies Head and neck region at 4 weeks gestation (Meuwly et al 2005)
  • 46.  Unilocular cysts with thin wall  Fluid content: CT hypodense, T1 hypohintense, T2 hyperintense  No enhancement or subtle wall enhancement  If infected: wall thickening/enhancement, increase density of the fluid  Neoplastic degeneration: enhancing nodules along the wall Branchial Cleft Anomalies
  • 47. 1st Branchial Cleft Anomaly  Benign, congenital cyst in or adjacent to parotid gland, EAC, or pinna  Several classifications related to embryology or location Postero-inferior to auricle Adjacent to parotid gl./mandible angle B. Koch 2015
  • 48.
  • 49. 2nd Branchial Cleft Anomaly  Typical location: Antero-medially to the SCM (superior 1/3), posteriorly to the submandibular gland, laterally to the carotid space B. Koch 2015
  • 50.
  • 51. 3rd Branchial Cleft Anomaly -Medially to the middle 1/3 of the SCM -Lower than 2nd BCC -In the posterior cervical space Carotid sp 3BCC SCM Post Cerv Sp 4th Branchial Cleft Anomaly It is a tract from the pyriform sinus to the Superior aspect of the thyroid Thyroid B. Koch 2015
  • 52.  Uni- or multiloculated, non-enhancing, cystic neck mass.  Micro- and macro cystic  Often trans-spatial, with fluid-fluid levels (hemorrhage and high proteinaceous components)  Venolymphatic Malf. : Combined elements of venous malformation & lymphatic malformation (contrast enhancement of the venous elements) Lymphatic Malformation
  • 53.
  • 54.  2nd BCC: unilocular cyst, typical location, no fluid- fluid levels  Abscess/suppurative nodes: clinical signs of infection, peripheral enhancement and cellulitis  Thyroglossal duct cyst: typical (midline) location, single cyst Differential Diagnosis
  • 55. Dermoid/Epidermoid Cyst  Definition: Cystic mass resulting from congenital epithelial inclusion or rest  Epidermoid: Epithelial elements only, fluid content  Dermoid: Epithelial elements plus dermal substructure, fluid, fatty or mixed content  Location: oral cavity (DD with Ranula and TGDC), midline anterior neck (DD with TGDC), orbit (DD with abscess and lymphatic malf.), nasal with associated nasal dermal sinus ± intracranial extension
  • 56. Imaging Epidermoid: homogeneous T1 hypo and T2 hyper. Increase T1 signal if high protein fluid Dermoid: heterogeneous signal. Fatty elements are T1 hyper and low in fat sat T2. Possible Ca++ Both can have DWI restriction and thin rim enhancement T1 T2 fat-sat T1
  • 57. Dermoid: tyipical “sac of marbles” appearance due to area of fatty attentuation Malik et al. 2012
  • 58. Differential Diagnosis  Ranula: salivary gland retention cyst in sublingual space.  Can be indistinguishable from epidermoid cyst which doesn’t show restriction.  Often is ruptured into the submandibular space (diving ranula) which shows typical “comet shape” (body in the SMS and tail in the SLS)  No fat, no Ca++ and no DWI restriction
  • 59. Malik et al. 2012 Tail Body
  • 60. Teratoma  Anterior neck, midline mass containing all 3 germ layers  Mixed (cystic and solid) with fat and calcium  DD: Lymphatic Malf (fluid with no fat, calcium or solid components), Goiter (homogeneous, respects limits of the thyroid gland)
  • 61. Mixed solido-cystic mass with fat content
  • 62.
  • 63.
  • 64.  Neck masses are common findings in children and can be a diagnostic challenge  Often trans-spatial  No space-specificity  Distinction in Solid or Cystic (or mixed) can help in the differential diagnosis Conclusion

Hinweis der Redaktion

  1. Posteriorly there it surrounds the trapezious
  2. Visceral space: Thyroid, esophagus, larhynx,trachea.
  3. Posteriorly there it surrounds the trapezious
  4. Primary Neck Neuroblastoma : anywhere from neck to pelvis along sympathetic chain.
  5. NOTE: MOST OF THE MASSES IN THE NECK CAN BE TRANSPATIAL(THIS IS WHY I CHOSE TO DESCRIBE THE SINGLE ENTITY AND NOT THE DIFFERENT ENTITY FOR EVERY SPACE) PPS: rare primary tumors but can important to understand the origin of other tumours invading/compressing this space. RMV : retromandibular vein thrombosis Goiter: gozzo, enlargement of the thyroid.
  6. Note ADC has been described as useful to distinguish metastatic nodes form reactive but this is controversial since the ADC values of the normal nodes are already low due to packed cells.
  7. Noteimaging cannot distinguish NHL from HL
  8. If no clinical suspect, radiologist should suggest biopsy. As you can see Size is important (these are very large nodes) as well as bilateral disease and involvement of the posterior space (level V / spinal accessory chain)
  9. CT homogeneously enhancing infantile hemangioma involving the left parapharyngeal, carotid, deep parotid, masticator, and perivertebral spaces of the neck Axial T1WI C+ FS MR shows intense post-contrast enhancement, typical of infantile hemangioma.
  10. Noteimaging cannot distinguish NHL from HL
  11. Differentiation between tumor and hyper intense mucosal tissue
  12. Note the displacement of the carotid artery, nodes around tumor and calcium. Mass like that: biopsy
  13. Graphic shows the course of thyroglossal duct cyst
  14. Claw sign
  15. Position is similar but is enhancing and solid mass
  16. Sinus means 1 communication Fistual: several communications
  17. Type 1:Duplication of membranous EAC; ectodermal (cleft) origin Type 2: Duplication of membranous EAC & cartilaginous pinna (ecftodermal and mesodermal origin)
  18. sublingual other differential are with lymphatic malf (orbital and sublingual) which is multilocular,transspatial and has fluid fluid level; and abscess (clinical and thick wall enhancement)