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PA33.1-4 | Skin — Graded Quiz
Graded
12 questions · Untimed · 2 attempts
Click any question card to reveal the correct answer.
A 63-year-old farmer presents with a 3-year-old erythematous, scaly plaque on the dorsum of his right hand. Biopsy shows: lower epidermal layer atypia with preservation of upper layers (no full-thickness involvement), solar elastosis in the dermis, and an intact basement membrane. No dermal invasion is seen. He is concerned because his neighbour had a similar lesion that became a cancer. Which statement best explains the biological behaviour of this lesion and the risk it confers?
A
This is Bowen disease (SCC in situ) — full-thickness epidermal dysplasia with a 30–50% risk of invasion within 5 years
B
This is actinic keratosis — lower-layer dysplasia only; the direct precursor of invasive SCC, carrying approximately 0.1–10% per lesion risk of progression over 10 years but with high cumulative risk given field cancerisation
✓
C
This is basal cell carcinoma in situ — the non-invasive precursor of BCC arising from hair follicle outer root sheath cells
D
This is seborrheic keratosis — a benign epidermal proliferation with no malignant potential, requiring no treatment
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A pathology report on a skin excision from the right cheek of a 70-year-old man describes: 'islands and nests of atypical basaloid cells extending from the epidermis into the dermis, with peripheral nuclear palisading, artefactual retraction clefts between tumor nests and stroma, and mucin deposition within nests.' There is no keratin pearl formation. What is the diagnosis, and what is the most important clinical fact about this tumor's behaviour?
A
Squamous cell carcinoma — metastasises in 5–10% of cases via lymphatics to regional nodes
B
Basal cell carcinoma — locally destructive but almost never metastasises; the most common malignant tumor in humans
✓
C
Merkel cell carcinoma — an aggressive neuroendocrine tumor with early lymph node and visceral metastasis
D
Sebaceous carcinoma — arises from Meibomian glands or sebaceous glands; high risk of orbital and systemic metastasis
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A 57-year-old woman presents with a pigmented lesion on her back showing asymmetry, irregular border, colour variegation (black, tan, red areas), and diameter 9 mm. Wide local excision is performed. The pathology report states: 'Breslow thickness 2.4 mm; Clark Level IV; radial growth phase absent; vertical growth phase present; no ulceration; 3 mitoses/mm²; sentinel lymph node positive for micrometastasis (0.4 mm deposit).' Which statement MOST accurately represents the prognostic hierarchy for this patient?
A
Clark Level IV is the dominant prognostic factor — it supersedes Breslow thickness because it directly measures anatomical invasion depth into the reticular dermis
B
Breslow thickness (2.4 mm) is the single most important primary tumor prognostic factor; the positive sentinel node upstages her to AJCC Stage III, which is the most important overall prognostic determinant at this point
✓
C
The number of mitoses per mm² is the dominant prognostic factor because it directly reflects proliferative index and metastatic potential
D
Ulceration is the most important prognostic factor; its absence in this case confers Stage I regardless of Breslow thickness or nodal status
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A 45-year-old woman with a history of immunosuppression following renal transplant presents with a rapidly growing, keratinising, nodular lesion on the back of her right hand. Biopsy shows well-differentiated squamous cell carcinoma with perineural invasion. Her dermatologist is concerned about high-risk features. Which combination of features in this patient confers the highest risk of nodal metastasis and locoregional recurrence?
A
UV-exposed site (dorsum of hand) + well-differentiated histology + immunosuppression
B
Immunosuppression + perineural invasion + site on hand (proximity to lymph node basin) + rapidly growing
✓
C
UV exposure + fair skin + age 45 + female sex
D
Nodular clinical morphology + keratinisation + well-differentiated histology
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A 38-year-old man develops a painful, firm nodule on his lower leg. On examination, pressing on the nodule with a finger causes it to dimple inward ('dimple sign'). Biopsy shows a dermal nodule of spindled fibroblast-like cells with storiform (cartwheel) arrangement, overlying epidermal hyperplasia, and a trapped peripheral fat lobule. No nuclear atypia, no necrosis, no mitotic figures. CD34 is negative; Factor XIIIa is focally positive. Which entity does this represent, and how does it differ from a dermatofibrosarcoma protuberans (DFSP) on both clinical and molecular grounds?
A
Dermatofibroma — benign; DFSP is malignant, characterized by COL1A1-PDGFB fusion from t(17;22), CD34-positive, with infiltrative growth and high local recurrence rate
✓
B
DFSP — diagnosed by Factor XIIIa positivity, with t(17;22); dermatofibroma is CD34-positive and locally aggressive
C
Dermatofibroma — benign; DFSP is benign but locally aggressive, distinguished by lack of dimple sign and CD34 positivity with no specific translocation
D
Nodular fasciitis — benign self-limiting reactive proliferation with USP6 translocation; DFSP is distinguished by storiform pattern and Factor XIIIa positivity
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A 32-year-old woman has a 4 mm brown-black lesion on her right shoulder. Dermoscopy shows irregular network, asymmetric pigmentation, and a notched border. Excision biopsy is performed. Histology shows: pleomorphic melanocytes in nests at the dermal-epidermal junction with pagetoid spread (single cells throughout the epidermis), and minimal dermal invasion limited to the papillary dermis (Breslow thickness 0.35 mm). Mitoses: 0/mm². Margins clear. Sentinel node is not performed. What is the CORRECT management rationale, and which histological feature provides the most diagnostic weight for melanoma vs a dysplastic naevus?
A
Pagetoid spread (single melanocytes scattered upward through the full epidermis) — most specific for melanoma; sentinel node biopsy should be performed because Breslow >0.1 mm
B
Pagetoid spread (single melanocytes scattered throughout the epidermis beyond the junctional nests) — most diagnostically weighted feature for melanoma; sentinel node biopsy is NOT indicated at Breslow 0.35 mm (threshold 0.8 mm with adverse features or 1.0 mm unconditionally)
✓
C
Breslow thickness 0.35 mm with 0 mitoses — the primary determinant; sentinel node biopsy is mandatory at any Breslow depth exceeding 0.25 mm
D
Irregular dermoscopic network — the most diagnostically weighted feature; sentinel node biopsy is indicated because dermoscopy showed asymmetry and notched border
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A 29-year-old woman with BRAF V600E-positive metastatic melanoma is started on a BRAF inhibitor. Her oncologist explains that despite initial dramatic response, most patients relapse within 6–12 months. A pathologist examining biopsy from a regrown lesion finds increased expression of MEK-ERK pathway proteins. Which of the following pathological and molecular reasoning chains MOST accurately explains both (1) why BRAF V600E drives melanoma and (2) why resistance develops through MEK-ERK reactivation?
A
(1) BRAF V600E constitutively activates the MAPK pathway → uncontrolled proliferation; (2) Resistance: alternative splicing of BRAF V600E produces a truncated form that dimerizes and reactivates ERK independently of upstream BRAF inhibition
✓
B
(1) BRAF V600E suppresses p16/CDKN2A → releases CDK4/6 from inhibition → direct G1-S bypass; (2) Resistance: compensatory TP53 amplification restores G1 checkpoint and selects resistant clones
C
(1) BRAF V600E activates PI3K/AKT exclusively → activates mTOR → protein synthesis drives proliferation; (2) Resistance: PTEN loss reduces AKT phosphorylation and bypasses BRAF inhibition via mTORC2
D
(1) BRAF V600E methylates promoters of DNA repair genes → genomic instability → rapid accumulation of driver mutations; (2) Resistance: acquired PD-L1 overexpression impairs BRAF inhibitor uptake by tumor cells
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A dermatopathologist reviews a slide from a 65-year-old man's facial skin lesion. The slide shows: islands of basaloid cells, peripheral palisading of nuclei at the edge of each island, artefactual retraction spaces between islands and adjacent stroma, abundant mucin within the tumor nests, and no intercellular bridges or keratin pearls. In the same session, another slide from a 58-year-old woman's back shows: tongues of squamous cells infiltrating the dermis with abundant eosinophilic cytoplasm, central concentric keratin whorl formation ('pearl'), visible intercellular bridges (desmosomes), and a desmoplastic stroma. Which diagnostic pairing MOST accurately identifies both tumors, differentiates them histologically, and predicts their differing propensity for metastasis?
A
Slide 1 = SCC (peripheral palisading is seen in poorly differentiated SCC); Slide 2 = BCC (keratin pearls appear in the sclerosing BCC subtype); both rarely metastasize
B
Slide 1 = BCC (palisading + retraction + mucin; no keratin pearls); Slide 2 = SCC (keratin pearls + desmosomes + desmoplastic stroma); BCC almost never metastasises (<0.1%), SCC metastasises in 5–10% of cases via regional lymphatics
✓
C
Slide 1 = BCC; Slide 2 = SCC; both metastasize at equivalent rates (~5%) because both arise from keratinocytes exposed to the same UV-induced TP53 mutations
D
Slide 1 = Merkel cell carcinoma (peripheral palisading + retraction); Slide 2 = SCC (keratin pearls); Merkel cell has higher metastatic rate than SCC
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A 55-year-old man had a Clark Level II, Breslow 0.4 mm melanoma on his left shoulder excised 18 months ago with clear margins. He now presents with a painful 2 cm nodule in the left axilla. Fine needle aspiration of the axillary nodule shows large pleomorphic cells with prominent nucleoli, intracytoplasmic melanin granules, and abundant mitoses. He has no other sites of disease. Which sequence of events best explains the progression from the primary melanoma to the current axillary presentation?
A
Hematogenous spread from the primary tumor to the axilla — melanoma preferentially seeds capillary beds in muscle, explaining the painful nodule
B
Lymphatic spread from the primary shoulder melanoma via the ipsilateral lymphatic drainage network to the left axillary sentinel lymph node basin, with subsequent nodal metastasis
✓
C
Direct local extension of the primary melanoma along deep fascia planes to the axilla — a form of satellite lesion formation
D
A second primary melanoma arising de novo in an axillary hair follicle melanocyte — more likely given the 18-month gap and low Breslow depth of the primary
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A 51-year-old man presents with a 1.5 cm nodule on the medial aspect of his right thigh that has been present for 8 years. It is firm, non-tender, moves with overlying skin, and dimples inward when the skin is pinched. Biopsy shows a dermal proliferation of spindled cells in a storiform pattern, with trapped fat at the periphery, overlying epidermal hyperplasia, and no cytological atypia. Factor XIIIa is positive; CD34 is negative. He asks: 'Will this come back after removal, and could it become cancer?' What is the accurate answer?
A
Dermatofibrosarcoma protuberans (DFSP) — high local recurrence rate (20-50%), rare metastasis, should be treated with wide excision or Mohs surgery
B
Dermatofibroma — benign, low recurrence rate after simple excision, essentially no malignant potential; reassurance is appropriate
✓
C
Dermatofibroma — but in rare cases undergoes malignant transformation to DFSP when Factor XIIIa expression is lost and CD34 is acquired
D
Nodular fasciitis — self-limiting reactive fibroblastic proliferation; spontaneous regression expected; no excision needed
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A 48-year-old man has a 7 mm pigmented lesion removed from his upper back. Histology: junctional nests of melanocytes confined to the dermal-epidermal junction with mild nuclear enlargement and irregular spacing; scattered single melanocytes along the basal layer confined to the junctional zone (no pagetoid spread); no dermal invasion; architectural disorder present but atypia is mild. A second lesion from the same patient's forearm shows: compound naevus with intradermal nests, mononuclear melanocytes with small nuclei, 'maturation' (decreasing cell size with depth), and no mitoses. Which statement MOST accurately summarises the biological distinction between these two lesions?
A
Lesion 1 is a compound naevus; Lesion 2 is a dysplastic naevus — both are entirely benign with no melanoma risk
B
Lesion 1 is a dysplastic naevus (architectural disorder + mild cytological atypia, confined junctional single cells, no pagetoid spread) — a melanoma precursor with intermediate risk; Lesion 2 is an intradermal naevus — a benign, mature naevus with essentially no malignant risk
✓
C
Lesion 1 is a dysplastic naevus; Lesion 2 is a compound naevus — both carry equivalent risk of progression to melanoma, requiring annual surveillance
D
Lesion 1 is an early radial growth phase melanoma (junctional single cells); Lesion 2 is a regression-phase melanoma (maturation pattern indicates spontaneous regression)
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A 75-year-old man with a 50-pack-year smoking history and type 2 diabetes presents with a 3 cm ulcerated tumor on his lower lip. Biopsy shows invasive SCC with perineural invasion and poorly differentiated areas. Sentinel lymph node biopsy of the ipsilateral cervical nodes is performed; the pathologist identifies a 3 mm deposit of SCC in one of four nodes examined. The multidisciplinary team is deciding on adjuvant therapy. Which pathological feature combination in this case represents the highest-risk category, and what is the primary route of lymphatic drainage from lip SCCs?
A
Poorest prognostic combination: lip location + ulceration + size >2 cm; primary lymphatic drainage: bilateral submental and parotid nodes
B
Poorest prognostic combination: perineural invasion + poorly differentiated histology + nodal metastasis (pN1); primary lymphatic drainage of lower lip: submental (midline) and submandibular nodes (ipsilateral)
✓
C
Poorest prognostic combination: tobacco history + diabetes + age >70; primary lymphatic drainage: superficial parotid and pre-auricular nodes
D
Poorest prognostic combination: poorly differentiated + nodal metastasis; primary lymphatic drainage: deep cervical chain directly (bypassing level I-II nodes)
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