The edition · Pathology
In phyllodes tumours, mitoses and heterologous elements predicted metastasis better than reclassification
A Brazilian series found the Refined Criteria upgraded half of borderline tumours without picking out the ones that spread. Plus a SOX10 map for salivary tumours, and what smears do to NGS coverage.
The edition in brief
A single-centre review of 58 borderline and malignant phyllodes tumours found that stromal mitoses of 30 or more per 10 high-power fields and malignant heterologous elements were independently associated with metastasis. The Tan classification agreed with WHO 2019 in 97% of cases, while the Refined Criteria reclassified 52% of borderline tumours as malignant and none of those metastasised during follow-up. A meta-analysis of 35 studies listed salivary gland tumours by SOX10 positivity: pleomorphic adenoma, adenoid cystic, acinic cell and polymorphous carcinoma are almost always positive; Warthin tumour, oncocytoma and salivary duct carcinoma are almost always negative; clone BC34 stained fewer tumours. In 666 resected gastric cancers, the 27 with a neuroendocrine carcinoma component had worse survival, and nodal metastases were mostly neuroendocrine. Cytology cell blocks matched FFPE tissue for hybrid-capture NGS coverage, while stained smears gave less uniform coverage. The pearl covers how to report a mixed neuroendocrine component.
SOX10 in salivary tumours: a pooled positive and negative list
Use SOX10 in a salivary panel to split lineages, and state the clone, especially if it is BC34.
Gastric cancers with a neuroendocrine component did worse, and spread as NEC
Report any neuroendocrine carcinoma component in gastric cancer with its proportion and its share of nodal metastases.
Cell blocks sequenced like FFPE; stained smears gave patchier coverage
Make a cell block when sequencing is likely, and validate smears as a separate specimen type.
Reporting a mixed neuroendocrine component
Report the neuroendocrine component's grade, proportion, Ki-67 and presence in metastases, even below the mixed-tumour threshold.
Phyllodes tumours: the Refined Criteria upgraded half the borderlines without predicting spread
Report mitotic count and heterologous elements in every phyllodes tumour, and be cautious about upgrading on the Refined Criteria alone.
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