EQA Circulation 43 Educational Cases
Transcript of EQA Circulation 43 Educational Cases
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EQA Circulation 43 Educational Cases
E1-E2
Monica Agarwal Monklands Hospital
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E1
• 38 yrs male • Submandibular gland tumour
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E1
• Formal excision following diagnosis of poorly differentiated carcinoma on core biopsy
• 20 mm tumour • Grey/white cut surface
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p63
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CEA
EMA
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ER
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Responses Diagnoses and D/D • Salivary duct ca – 74 • Mucoepidermoid ca – 10 • Oncocytic ca – 6 • Squamous cell ca with cancerisation of salivary ducts – 2 • Malignant Warthin’s tumour – 1 • Epithelial myoepithelial ca – 1 • Micropapillary ca with squamous differentiation ?thyroid
metastasis to lymph node – 1 • Mammary analogue secretary ca – 2 • Lymphoepithelial ca – 5 • Papillary adenoca - 1 • Necrotizing sialometaplasia with marked atypia - 1
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Diagnosis
Salivary duct carcinoma
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Salivary duct carcinoma
• Uncommon salivary gland malignant tumour (about 9%)
• Frequently seen in elderly population • Commonly in 6th and 7th decades • More common in males (M:F 3-6:1) • Majority in parotid gland, some occur in
submandibular gland and rarely in minor salivary gland
• Rarely reported in longstanding chronic obstructive sialadenitis
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Salivary duct carcinoma
• One of the most aggressive salivary gland malignant tumour
• Local recurrence 33%; distant metastasis 46% • Metastasis – lymph nodes, distant • Frequent sites of distant metastasis – lung,
bone, brain, liver, skin • 65% patients die of disease usually within 4
years of diagnosis
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Salivary duct carcinoma
• Usually poorly circumscribed, tan coloured and usually solid
• Morphology resembles ductal carcinoma of breast
• Intraduct like and invasive components
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Intraduct like component Cribriform, papillary, solid with frequent comedo necrosis
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Infiltrative component • Cribriform, solid, cords,
glands • Apocrine appearance –
abundant pink cytoplasm, pleomorphic epithelioid cells, coarse chromatin and prominent nucleoli
• Squamous differentiation can be seen
• Stroma is fibrous/desmoplastic
Vascular invasion, perineural invasion commonly seen
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Variants: Micropapillary, papillary, mucin rich, spindle cells
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Salivary duct carcinoma ICC Positivity- • Low and high molecular wt cytokeratins • CEA, EMA • Androgen receptors – strong nuclear • GCDFP-15 • Her2 – commonly positive • PSA, PAP - variable Negative- • S100 • Myoepithelial markers • ER, PR
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D/D • Metastatic breast ca • High grade
mucoepidermoid carcinoma
• Oncocytic carcinoma • Cystadenocarcinoma • Intraductal
carcinoma/Low grade cribriform cystadencarcinoma (LGCCC)
Mucoepid ca
Oncocytic ca
LGCCC LGCCC
Cystadenocarcinoma
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E2
• 68 year old female • WLE right breast
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E2
• Papillary lesion seen on core biopsy • WLE showed a 22 mm nodular haemorrhagic
lesion
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p63
CK5/6
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SMM
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ER
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Responses • Encysted papillary ca – 65 • Solid papillary ca – 10 • Papillary ca – 7 • Apocrine ca – 1 • Cribriform ca – 12 • Breast ca with neuroendocrine features – 1 • Adenoca/ca – 2 • Invasive ductal ca – 1 • Intraductal papilloma/papilloma with atypical features -2 • DCIS with microinvasion – 1 • No response - 2
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Diagnosis
• Encysted papillary carcinoma
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Papillary tumours of breast WHO 4th edition
• Benign ¾ Intraductal papilloma
• Malignant - In-situ ¾ Intraductal papilloma with DCIS ¾ Intraductal papillary carcinoma ¾ Encapsulated papillary carcinoma ¾ Solid papillary carcinoma
- Invasive ¾Invasive papillary carcinoma ¾Micropapillary carcinoma
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In-situ papillary lesions
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In-situ papillary lesions
Intraductal papillomas with DCIS
• Use of atypical papilloma is discouraged • Low grade changes <3 mm ADH • Low grade changes >3 mm DCIS • Increased risk of subsequent invasive breast
cancer • Intermediate/High grade changes - DCIS
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In-situ papillary lesions
Intraductal papillary carcinoma/ Papillary DCIS • Intraductal papillary lesion with thin fibrovascular
cores • Columnar cells with nuclei aligned perpendicular
to the stromal cores • Usually lack myoepithelial cells within the lesion
(although can sometimes be demonstrated) • Myoepithelial cells are demonstrated around the
lesion
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In-situ papillary lesions
Encysted/Encapsulated papillary carcinoma
• Circumscribed papillary lesion surrounded by a thick fibrous capsule
• Complete lack of myoepithelial cells
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SMM
p63
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Encysted papillary carcinoma
• Ongoing debate regarding the true biological state
• Some of these lesions are probably low grade carcinomas growing with expansile edges
• However managed as in-situ lesions as behaviour is similar to DCIS
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In-situ papillary lesions
Solid papillary carcinoma • Single or multiple nodules • Usually multiple expansile cellular nodules with
smooth contours • Solid papillary growth pattern • Myoepithelial cells can be demonstrated at the
periphery • More commonly associated with invasive
component
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Solid papillary carcinoma
• In cases lacking mantle of myoepithelial cells – if the tumour islands are irregular with jagged edges and surrounded by desmoplastic stroma, consider diagnosis of invasive malignancy
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In-situ papillary lesions
When diagnosis of papillary carcinoma is made, it is imperative to clarify in the report whether the lesion is in-situ or invasive
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Reference
Review article Papillary and neuroendocrine breast lesions: the WHO stance. Tan PH et al, Histopathology, 2015, 66, 761-770
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Thank you
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GENERAL EQA CIRCULATION 43
Educational Cases E3 & E4
Dr John Robert Millar Monklands General Hospital
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CASE E3
• F 35 • Hx of pulsatile tinnitus • Bx red mass behind eardrum
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CD34
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S100
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CD56
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SMA
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ANSWERS • Jugulotympanic paraganglioma, paraganglioma (57)
• Glomus tympanicum (2)
• Glomus tumour/glomangioma (27)
• Haemangioma (8)
• Carotid body paraganglioma (1)
• Glomus carotid body tumour (2)
• Adenoma (1)
• Pecoma (1)
TOTAL: 99
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JUGOLOTYMPANIC PARAGANGLIOMA
• Also called glomus jugulare tumour or glomus tympanicum tumour
• Most common tumour of middle ear
• Usually women, ages 40-69 years – 85% arise in jugular bulb, causing mass in middle ear or external auditory canal – 12% arise from tympanic branch of glossopharyngeal nerve, causing middle ear
mass; – 3% arise from posterior auricular branch of vagus nerve, causing external
auditory canal mass
• Usually cause conductive hearing loss/tinnitus • Tumours are fed by branches of nearby large arteries; may bleed profusely at biopsy
• Histology usually benign, but this does not predict behaviour
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DIAGNOSTIC FEATURES • Classic organoid (zellballen) or nesting pattern of
paragangliomas with central round/oval chief cells containing abundant eosinophilic granular or vacuolated cytoplasm, uniform nuclei with dispersed chromatin
• Sustentacular cells (spindled, basophilic, difficult to see with H&E) are present at periphery of nests
• Prominent fibrovascular stroma separates nests
• No glandular or alveolar differentiation, although alveolar pattern like in middle ear adenoma has been described
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IMMUNOHISTOCHEMISTRY
• Chromogranin and synaptophysin+ (chief cells), S100+ (sustentacular cells)
• Reticulin+ (stains stroma and delineates nesting pattern, particularly helpful with crushed specimens)
• Keratin, EMA, HMB45, desmin/other myogenic markers, PAS, mucicarmine -
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DIFFERENTIAL
• Middle ear adenoma (glandular & NE differentiation, keratin/CK7/chromo+, intraluminal mucin+, non-vascular )
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CASE E4
• F 79 • Large polyp prepyloric area at endoscopy
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CD34
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CD117
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ANSWERS • Inflammatory fibroid tumour/myofibroblastic (90)
• GIST (2)
• Inflammatory pseudopolyp/tumour (3)
• Eosinophilic granuloma (1)
• NF (1)
• Hamartoma (1)
• Schwannoma (1)
TOTAL: 99
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INFLAMMATORY FIBROID TUMOUR/POLYP
• Gastrointestinal tract tumour characterised by spindle and stellate cells set in an inflammatory, myxoid stroma
• Most common in antrum, followed by small intestine
• 3rd t0 8th decades of life (mean age 60) – May present with intussusception, obstruction, bleeding – Infrequently recurs – No metastases or local aggressive recurrences
• Most are semi-pedunculated polyps arising in the submucosa
– Covered by mucosa or may be eroded – Occasional tumours may be restricted to the lamina propria and muscularis
mucosae – Larger tumours may extend into muscularis propria – Most <5 cm, rarely up to 20 cm
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DIAGNOSTIC FEATURES • Composed of bland, uniform spindled/stellate cells
– The lesional cells may be lost in the background and difficult to identify – Multinucleated giant cells in 1/3 of cases
• Loose fibromyxoid background with regular vascular pattern
– Regular small to medium sized vessels throughout – May have granulation tissue appearance
• Eosinophil rich mixed inflammatory infiltrate
– Also includes lymphocytes, plasma cells, macrophages, mast cells – Lymphoid aggregates may be seen
• Frequent whorled, concentric “onion skin” pattern centred on
blood vessels and glands – 10% of cases may lack this pattern, but may be accentuated by CD34
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DIFFERENTIAL • GIST – CD117+, infrequent eosinophils, lacks regular vascular
pattern
• Solitary fibrous tumour – arises in serosa, ropey collagen, inflammation infrequent
• Schwannoma – peripheral lymphoid cuff, lacks regular vascular pattern
• Inflammatory myofibroblastic tumour – children, plasma cells >eosinophils, desmin/keratin/ALK1+, CD34 -, lacks regular vascular pattern, nuclear pleomorphism
• Leiomyoma – desmin +, CD34-, infrequent eosinophils