Head and Neck #20

Clinical Data

3-year-old male:

  • With left-sided dyspraxia

Indicate the abnormality:

Description:

  • Well-defined cystic lesion in subcutaneous plane of lateral margins of orbit on left

  • Underlying bone and adjacent lacrimal gland are unremarkable

Differential diagnosis includes:

  • Orbital dermoid cyst

  • Orbital teratoma

  • Orbital dermolipoma

  • Orbital hemangioma

  • Orbital rhabdomyosarcoma

Differential diagnosis includes:

Description:

    Possible differential considerations include:

    • Orbital dermoid cyst – TRUE

    • Orbital teratoma – TRUE

    • Orbital dermolipoma – TRUE

    • Orbital hemangioma – TRUE

    • Orbital rhabdomyosarcoma – FALSE

Dermoid cysts

  • They are thought to occur as a developmental anomaly in which embryonic ectoderm and mesoderm are trapped in the closing neural tube between the 5th and 6th weeks of gestation

  • These lesions are usually extraconal, non-enhancing masses with smooth margins, cystic, and/or solid components

  • They are typically heterogeneous with soft tissue, fluid, and fatty (sebum) components; occasionally calcifications may be present

  • They are most commonly located superotemporally, arising from the zygomaticofrontal suture, followed by superonasally, arising from the frontoethmoidal or frontolacrimal sutures

  • Ruptured dermoids may show adjacent inflammatory changes

  • Superficial lesions barely require cosmetic excision, while a deeper lesions may require more invasive methods involving micro-dissection and orbitotomy

References:

  • Kudo K, Tsutsumi S, Suga Y et al. Orbital dermoid cyst with intratumoral inflammatory hemorrhage: case report. Neurol. Med. Chir. (Tokyo). 2008;48 (8): 359-62. Pubmed citation

  • Ahmed RA, Eltanamly RM. Orbital epidermoid cysts: a diagnosis to consider. J Ophthalmol. 08;2014: 508425. doi:10.1155/2014/508425 – Free text at pubmed – Pubmed citation

  • Chaudhry IA. Management of deep orbital dermoid cysts. Middle East Afr J Ophthalmol. 2008;15 (1): 43-5. doi:10.4103/0974-9233.53376 – Free text at pubmed – Pubmed citation

Head and Neck #19

Clinical Data

80-year-old female:

  • With left-sided dyspraxia

  • Duration uncertain

What do you see?

The case was initially interpreted as CSF seeding by a malignant choroid plexus tumor.

However, retrospective investigation of CTA showed another pathology.

  • This case demonstrates several small areas of cortical enhancement in the right hemisphere. These enhancing areas correspond to small regions of subacute cortical ischemia in the right MCA territory, caused by a ruptured carotid plaque with an intraluminal thrombus. The mass in the antrum of the left ventricle is an incidental intraventricular meningioma. Follow-up scans showed regression of the cortical enhancement and stable intraventricular meningioma on the left.

  • Teaching points:

    • Subacute ischemia may enhance and in some cases mimic tumors or CSF seeding.

    • Ruptured carotid plaque with intraluminal thrombus presents with finger-like filling defect of the internal carotid.

    • Choroid plexus carcinomas are rare in elderly patients with an intraventricular meningioma being way more common. Typical location, sharp tumor-brain interface, homogeneous enhancement and T2 hypointensity allow for a confident diagnosis of an intraventricular meningioma.

Head and Neck #18

Clinical Data

73-year-old male:

  • With worsening paresis of cranial nerves CN3-7







What do you see?


Axial T2 image on the left shows partial obliteration of the right Meckel’s cave and an ill-defined T2 hypointense lesion on the right temporal fossa.

Axial T2 image on the right shows atrophy of the right-sided masticatory muscles.



Post-contrast 3D T1 FSE fat-saturated images showing an enhancing lesion overlying the right temporal fossa, with perineural spread along CN7, the auriculotemporal nerve and continuing intracranially via the right foramen ovale (note the asymmetry in enhancement).



3D bSSFP images (CISS) before (left) and after (right) contrast administration. bSSFP images contain both T1 and T2 information, therefore showing enhancement after contrast administration.

While pre-contrast image doesn’t depict any obvious pathology, the post-contrast image on the right clearly highlights tumor deposits (red arrows) along the lateral aspect of the right cavernous sinus. The tumor has encased the cranial nerves, leading to the patient’s symptoms. For comparison, the normal anatomy of the cranial nerves is shown on the left (green arrows).

  • This case shows a histologically verified squamous cell carcinoma of the temporal fossa spreading along the CN7, auriculotemporal nerve, mandibular nerve and into the right cavernous sinus.

  • Teaching points:

    • Multiple CN palsies of CN3-6 should raise a suspicion of cavernous sinus pathology.

    • Auriculotemporal nerve is an important connection between the facial and mandibular nerves.

    • bSSFP sequences like CISS contain both T1 and T2 information and therefore show post-contrast enhancement which can be diagnostically useful in conjunction to their excellent spatial resolution.

Head and Neck #15

What do you see in the following images?

Click here to see the answer

Scalp haemangioma
Right parietal subcutaneous well-defined soft tissue oval lesion. It demonstrates low signal on T1W image, Intermediate signal on T2W image with prominent vascular flow voids, and avid enhancement on the post contrast image. No adjacent osseous or soft tissue abnormality. No intracranial extension.

More information

Infantile hemangiomas are benign vascular tumours, most of these tumours arise in the craniofacial region. Most of them are not present at birth but they increase in size during the first year of life, with a subsequent progressive involution during early childhood.

Differential diagnosis includes: epidermoid cyst, lymphatic malformation,  and sinus pericranii.

Head and Neck #14

What do you see in the following images?

Click here to see the answer

Nasolabial cyst
Right nasolabial lesion with remodeling of the maxillary alveolus bone. On MRI it shows high signal intensity on both T1- and T2-weighted images with no signal suppression on the T2 FLAIR with Fat saturation sequence.
Differential Diagnosis:
Nasolabial cyst with hemorrhage
Epidermal inclusion cyst
Dermoid cyst
Dentigerous cyst

Head and Neck #13

What do you see?

Labyrinthitis Ossificans

Ossification of the membranous labyrinth, high-density bone deposition involving all the cochlear turns.

This usually occurs as a complication of suppurative labyrinthitis, either due to otomastoiditis or meningitis. Other causes include trauma, autoimmune diseases, and surgery.

Head and Neck #12

24-year-old male:
– Feels a lump in the upper lateral corner of right eye.
– MRI was made.

What do you see?

Preseptal lesion right supero-lateral corner, lateral to lacrimal gland.
T2 and T1 hyperintense, low signal after fat suppression.
No enhancement (right upper picture).
Slight remodeling of bone.
No invasive growth no post-septal component.

What is the most likely diagnosis?

Diagnosis: dermoid cyst, also fits with age and location of lesion.

Head and Neck #9

47-year-old male:
– Headache since 2 months, nausea, and vomiting.
– Papilledema but no loss of vision.
– MRI is made.

What is the most likely diagnosis?

Expansive mass in the midline centered in the clivus (basiocciput and basisphenoid) with high signal on FLAIR (upper left), intermediate to low T1 signal, high T2 signal, and moderate heterogeneous enhancement after contrast administration.

No diffusion restriction.
ADC value is around 1350. No dural tail.
No encasement of basilar artery.
Compression on pons but no invasive growth.
Upward displacement of chaism, anterior displacement of pituitary gland and stalk.

Diagnosis: chordoma.

Does not fit with meningioma, pituitary macroadenoma, chondrosarcoma, lymphoma, or plasmacytoma.This
was histologically proven.