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
Q

Localisation of vocal cord nodules

A

True vocal cords

25
Q

Squamous Papilloma of the larynx is ass w

A

Association with low-risk HPV-6 and -11 benign

26
Q

Squamous Papilloma of the larynx localisation

A

Centered around true vocal cords

27
Q

Risk factors of Squamous Papilloma of the larynx

A

Airway obstruction

28
Q

Epidemiology of squamous cell carcinoma of the larynx

A

Most common malignant tumour of the larynx
- Men >40 years

29
Q

Squamous cell carcinoma of the larynx predisposing factors

A

Combination of cigarette smoking and alcoholism NO association to HPV infection

30
Q

Clinical picture of Squamous cell carcinoma of the larynx

A

Persistent hoarseness

31
Q

Squamous cell carcinoma of the oropharynx is ass w

A

High risk HPV

32
Q

Localisation of Squamous cell carcinoma of the oropharynx

A

Palatine & lingual tonsils

33
Q

Histopathology of Squamous cell carcinoma of the oropharynx

A

Non-keratinising squamous cell carcinomas with basaloid
morphology

34
Q

What is Embryonal Rhabdomyosarcoma?

A

An aggressive mesenchymal malignancy of skeletal muscle origin, & the most common soft tissue sarcoma in children & adolescents.

35
Q

Epidemiology of Embryonal Rhabdomyosarcoma

A

Most common in children and adolescents (<15 years: ~87% of cases).
Annual incidence: 6 cases per 100,000 in the US.

36
Q

What are the common sites of occurrence for Embryonal Rhabdomyosarcoma?

A

Occur in any anatomic site.
Most common in the head, neck, and genitourinary tract.

37
Q

What are the microscopic findings in Embryonal Rhabdomyosarcoma?

A

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
Q

What are the clinical features of Embryonal Rhabdomyosarcoma?

A

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
Q

What is the prognosis of Embryonal Rhabdomyosarcoma for metastatic and localized disease?

A

Metastatic disease: 5-year survival rate <30%.
Localized disease: 5-year survival rate >80% with combined surgery, radiation, and chemotherapy.