Case 677 17.1.13 (H. Diwan) M 79 chronic leg wound
Some LP views missing. Infiltrative BCC pattern with adjacent mucin. Chromogranin stain +ve.
Case 2426 17.10.19 (S. Taibjee) F 70 cheek lesion
Looked like secondary from carcinoma
BerEP4 strong +ve; CD56 +ve; chromogranin patchy +ve
EMA, synaptophysin, CK20, TTF-1, CK7, Cam 5.2 all –ve
BCC with NE differentiation has good prognosis
Case 2656 10.9.20 (S. Taibjee) M 91 cheek
LP BCC architecture. However, palisading is not well seen and there is no retraction artefact. Some cells show bubbly cytoplasm. I suspected this was a BCC mimic such as sebaceous carcinoma or basaloid SCC. S. Taibjee makes the point that the nuclei are larger and “high grade” compared to common BCC. He feels these may be more common than recognised and often signed out as ordinary BCC. They don’t seem to have a propensity for metastasis i.e. don’t behave like MCC.
IH: showed strong BerEP4, chromogranin and CD56. Pronounced lymphocytic infiltrate as far down as the fat was reactive and not a sign of other pathology such as CLL.
Case 2751 21.1.21 (S. Taibjee) F 84 lesion behind ear
Epidermally derived cords and strands suggesting porocarcinoma. Areas of more typical BCC including retraction artefact contrasting with a 'high grade' cytology.
BerEP4 +ve; EMA -ve; neuroendocrine markers CD56, synaptophysin and chromogranin +ve. CK20-ve. Some do express CAM5.2, but without dot positivity
Ref: Review: Neuroendocrine differentiation of skin tumours.
Hamie, L et al . Am J Derm Path Dec 2020 42: (12), p 899–910
Case 2816 22.4.21 (S. Taibjee) M elderly
Ulcerated BCC pattern with cytology suggesting neuroendocrine differentiation. Confrmed by IH: BerEP4+ve; EMA -ve; CK20 -ve; chromogranin and synaptophysin +ve.
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