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Case 112

A 83-year-old male with history of skin carcinoma now presented left postauricular mass.



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The tumor was found to be tumor to be positive for CK5/6, CK19, EMA, CD117 (patchy), and BerEP4 (patchy). Occasional tumor cells are positive for p40. Considering the history, what is the most likely diagnosis?


A: Squamous cell carcinoma

B: Porocarcinoma

C: Adenoid cystic carcinoma

D: Basal cell carcinoma



Answer

The correct answer is B. Histologic sections demonstrate nests of squamoid cells with focal ductal/glandular differentiation and comedonecrosis. EMA positivity is important to highlight the ductal features.


  • Loss of diagnostic features: In poorly differentiated porocarcinoma, characteristic poroid cells and cuticular cells may no longer be recognizable, complicating classification.

  • Mimics due to necrosis: Single-cell necrosis in other tumors may form pseudoductal structures, which can resemble porocarcinoma histologically.

  • Immunohistochemistry aids distinction: Use of CEA (Carcinoembryonic Antigen) and EMA (Epithelial Membrane Antigen) can help identify true ductal structures, assisting in the differentiation from mimics.

  • Histopathologic variability: Porocarcinoma can show squamous differentiation, clear cell change, and other atypical features, leading to a broad differential diagnosis.

  • Importance of identifying parent lesion: Finding a pre-existing poroma or porocarcinoma in situ is the best strategy to confirm diagnosis and avoid misinterpretation.


  • Immunohistochemistry

    • No single marker is both completely sensitive and specific for porocarcinoma.

    • NUT (nuclear protein in testis):

      • Shows immunopositivity in ~50–58% of porocarcinomas

      • Useful for confirming diagnosis, but not reliably sensitive (PMIDs: {35158743}, {34023104})

    • Ductal differentiation can be confirmed via:

      • EMA (epithelial membrane antigen)

      • CEA (carcinoembryonic antigen)

      • These may also detect abortive intracytoplasmic lumina (PMID: {6092444})


Case credit: UCSD Pathology

Author: Wangpan Jackson Shi, MD

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