Detecting the fetal abdominal circumference standard plane in low-cost obstetric blind sweeps is a highly imbalanced frame-classification problem: positive frames account for under 3% of a sequence, form short contiguous segments, and are poorly handled by off-the-shelf ultrasound and vision foundation models. We propose AnatoProto, a lightweight sequence-level framework that adapts a frozen BiomedCLIP encoder to fetal blind sweeps through four components: (i) anatomy-weighted spatial pooling that uses nnU-Net abdominal-region probabilities as a spatial prior to reweight BiomedCLIP patch tokens, so frozen semantic features are aggregated onto anatomically meaningful regions; (ii) a within-case prototype loss that pulls each frame embedding toward the mean of positive frames of the same sweep, exploiting case-level structure unavailable at the frame level; (iii) a three-stage cascade refinement (frame->segment->case-level rejecter) that lifts the prediction unit from noisy frames to structurally-constrained segments; and (iv) a hybrid prediction head that jointly models per-frame stability and inter-frame boundary transitions to suppress boundary false positives. On the ACOUSLIC-AI benchmark, AnatoProto reaches a test F1 of 67.72, outperforming the strongest foundation-model baseline (FetalCLIP + PRS, F1 = 54.52) by +13.20 F1 and the strongest video temporal-action-detection baseline (TriDet + PRS) by +15.76 F1. A synergy study, backed by embedding geometry and paired-bootstrap confidence intervals, shows that the prototype loss and anatomy-weighted pooling are not additive: applied alone the prototype loss reduces recall by 12 points, but combined with anatomy-weighted pooling it increases recall by 6.5 points -- a sign-flip we trace to the accuracy of the within-case prototype.
Foundation models such as Segment Anything Model 2 (SAM2) have transformed natural-image and video segmentation, and recent work has begun adapting them to medical imaging. These adaptations, however, are largely general-purpose models that treat MRI as one modality among many; large-scale, MRI-specific modelling and benchmarking remain limited, even though MRI's low soft-tissue contrast leaves many boundaries effectively invisible on individual slices. We present SAMRI-3D, a benchmark and method for 3D MRI segmentation with SAM2. The SAMRI-3D benchmark is the largest MRI-only evaluation to date - 10,392 volumes from 34 datasets (27 public, 7 in-house) spanning 12 anatomical domains and 10+ sequences, with explicit seen/unseen splits. Freezing the image encoder and fine-tuning only the lightweight decoder and memory modules raises mean Dice from 0.58 (zero-shot SAM2) to 0.76, surpassing recent SAM-based medical models (SAMed-2 0.69, Medical-SAM2 0.49, SAM-Med3D 0.37) with strong statistical significance. To target invisible boundaries, we introduce Global Volume Tokens (GVT): persistent memory tokens trained with a Truncated Signed Distance Field (TSDF) reconstruction objective that is discarded at inference (zero added cost). This full model, SAMRI-3D, attains the best accuracy (0.78) and lowest variance across all 34 datasets and, uniquely, shows no drop on 8 held-out datasets (0.79 unseen vs. 0.78 seen); per-sequence analysis confirms the TSDF objective helps most where per-slice contrast is weakest. We will release the benchmark, code, and models in this paper.