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The edition · Pathology

In small-bowel NETs, only the Ki67 of the mesenteric deposit predicted progression — stain the deposit, not only the primary

A Histopathology cohort on where to grade jejunoileal NETs, evidence that MTAP loss does not stand in for CDKN2A deletion in peritoneal mesothelioma, a methylation triage meta-analysis for HPV-positive women, and a copy-number split within TP53-mutated multiple-classifier endometrial cancer.

The edition in brief

Today's pathology edition closes on a Histopathology cohort (15 September) of 75 node-positive or deposit-bearing jejunoileal neuroendocrine tumours: in 68% the node or deposit Ki67 exceeded the primary's, and only the Ki67 of the largest mesenteric deposit predicted progression on multivariable analysis (HR 1.22 per 1% rise, 1.02 to 1.46). The lead is a Histopathology study (21 September) showing that in peritoneal mesothelioma, MTAP immunohistochemistry agreed with MTAP FISH but poorly with CDKN2A deletion (kappa 0.21), unlike pleural disease — so MTAP loss cannot be read as a CDKN2A surrogate in the peritoneum, though it may still support malignancy. A meta-analysis of 8 studies and 7494 women (Medicine, 18 September) reported PAX1/JAM3 methylation sensitivity 0.81 and specificity 0.95 for CIN2+, promising for HPV-positive triage but drawn largely from single-population studies. A Modern Pathology cohort (17 September) of 33 TP53-mutated multiple-classifier endometrial carcinomas found a copy-number-high third that carried all six recurrences, a hypothesis for now. The pearl is on naming the block you stained for Ki67.

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