Tumours of the upper resp tract Flashcards

1
Q

Epidemiology of papilloma?

A

Most common benign neoplasm of the nasal cavity & paranasal sinuses; more common in men aged 50-60 years.

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2
Q

Clinical feature of papillomas

A

Nasal obstruction & epistaxis.

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3
Q

Types of papilloma

A

Exophytic
Endophytic

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4
Q

Grows outward from the epithelial surface, commonly on lateral walls.

A

Exophytic

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5
Q

Grows inward into tissues in finger-like projections, commonly at the nasal diaphragm.

A

Endophytic

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6
Q

Microscopic Features of papilloma?

A

Cylindrical epithelium with increased cellular rows.
Squamous metaplasia.
Resemblance to transitional epithelium

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7
Q

What is angiofibroma and its clinical manifestation?

A

Rare vascularized lesion, common in adolescent males.
Clinical manifestation: Epistaxis.

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8
Q

What are the microscopic findings of angiofibroma?

A

Numerous blood vessels in a fibrotic matrix.

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9
Q

Prognosis of angiofibroma

A

Good

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10
Q

What is squamous cell carcinoma of the nose and its microscopic findings?

A

Most common malignant nasal tumour.
Microscopic findings: Large eosinophilic cells, keratin production, & keratin pearl

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11
Q

What causes nasopharyngeal carcinoma?

A

Caused by Epstein-Barr virus.

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12
Q

Localisation of nasopharyngeal carcinoma

A

Localized in the pharyngeal fossa of Rosenmüller.

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13
Q

What are the microscopic features of nasopharyngeal carcinoma?

A

Sheets of undifferentiated cells with non-neoplastic T lymphocytes.
Vesicular nuclei and prominent cytoplasm.
No keratinization.

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14
Q

What is adenocarcinoma of the nose and its types?

A

5% of malignant nasal tumours.
Types: Intestinal-type adenocarcinoma (resembling colon cancer) and non-intestinal type (e.g., adenoid cystic carcinoma).

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15
Q

What is olfactory neuroblastoma (aesthesioneuroblastoma)?

A

Tumour in older male patients.

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16
Q

Microscopic findings of olfactory neuroblastoma

A

Small round blue cells with Flexner-Wintersteiner rosettes.

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17
Q

olfactory neuroblastoma is +ve for

A

Chromogranin, ACTH, Neurofilament (NF), Neuron Specific Enolase (NSE), S-100 & Cytokeratins

18
Q

What are the immunohistochemistry findings in plasmacytoma?

A

Positive for one light chain (κ, λ), IgG, IgM, CD38, CD79A, CD138, and VS38c.

18
Q

What is plasmacytoma and its localization?

A

Localized in the upper airway tract.
Most common extra-medullary site.
Can be a manifestation of multiple myeloma or primary.

19
Q

Macroscopic features of plasmacytoma

A

Sub-mucosal localisation
Airway tract obstruction
Ulceration and haemorrhage
Diffuse cellular population
Round to ovoid cells “Cart-wheel” chromatin
Basophilic cytoplasm

20
Q

Supra & subglottic carcinomas proognosis

A

Less common and worse

21
Q

Where does glotiic carcinoma originate from & whats the prognosis?

A

Origin: true vocal cords
Most common and best prognosis

22
Q

Cause of vocal cord nodule

A

Chronic irritation

23
Q

Vocal cord nodule is ass w

A

heavy smoking

24
Localisation of vocal cord nodules
True vocal cords
25
Squamous Papilloma of the larynx is ass w
Association with low-risk HPV-6 and -11 benign
26
Squamous Papilloma of the larynx localisation
Centered around true vocal cords
27
Risk factors of Squamous Papilloma of the larynx
Airway obstruction
28
Epidemiology of squamous cell carcinoma of the larynx
Most common malignant tumour of the larynx - Men >40 years
29
Squamous cell carcinoma of the larynx predisposing factors
Combination of cigarette smoking and alcoholism NO association to HPV infection
30
Clinical picture of Squamous cell carcinoma of the larynx
Persistent hoarseness
31
Squamous cell carcinoma of the oropharynx is ass w
High risk HPV
32
Localisation of Squamous cell carcinoma of the oropharynx
Palatine & lingual tonsils
33
Histopathology of Squamous cell carcinoma of the oropharynx
Non-keratinising squamous cell carcinomas with basaloid morphology
34
What is Embryonal Rhabdomyosarcoma?
An aggressive mesenchymal malignancy of skeletal muscle origin, & the most common soft tissue sarcoma in children & adolescents.
35
Epidemiology of Embryonal Rhabdomyosarcoma
Most common in children and adolescents (<15 years: ~87% of cases). Annual incidence: 6 cases per 100,000 in the US.
36
What are the common sites of occurrence for Embryonal Rhabdomyosarcoma?
Occur in any anatomic site. Most common in the head, neck, and genitourinary tract.
37
What are the microscopic findings in Embryonal Rhabdomyosarcoma?
Small, round blue cell tumour with high cytologic variability. Differentiated neoplasms: Rhabdomyoblasts with eosinophilic cytoplasm and cross striations. Poorly differentiated cells: Elongated pleomorphic tumour cells, hyperchromatic nuclei, and variable pleomorphism. Loose, myxoid, or collagenous stroma. High mitotic index and prominent nucleoli.
38
What are the clinical features of Embryonal Rhabdomyosarcoma?
Expanding mass with pain and compression symptoms. Metastases may cause: Bone pain. Anaemia, thrombocytopenia, and neutropenia. Respiratory difficulty due to lung nodules or pleural effusion.
39
What is the prognosis of Embryonal Rhabdomyosarcoma for metastatic and localized disease?
Metastatic disease: 5-year survival rate <30%. Localized disease: 5-year survival rate >80% with combined surgery, radiation, and chemotherapy.