This cookbook details how to deploy a localized hematology microscopic image analysis engine to segment white blood cell (WBC) sub-types, detect immature lymphoblasts/myeloblasts, and calculate automated differential counts directly from peripheral blood film (PBF) digitizations without cloud dependence.
Differential leukocyte counting and blast cell identification in peripheral blood smears are critical for diagnosing acute leukemias (AML/ALL), severe sepsis, and hematologic malignancies. In pathology labs and decentralized clinics, localized computer-aided microscopy accelerates manual oil-immersion microscopy reviews.
This engine enables:
[ Digitized Peripheral Blood Film / Microscopy Image ]
│
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[ HematoNet-WBC-v1 ]
├── CIE L*a*b* Nuclear Segmentation
└── Morphological Feature Extraction
│
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[ Bethesda-Smear-CLI ]
├── 5-Part Differential Percentage
└── Lymphoblast / Myeloblast Risk Alert
│
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[ Structured Hematology Diagnostic Summary JSON ]
Ensure Python 3.10+, torch, torchvision, scikit-image, and OpenCV are installed:
pip install torch torchvision opencv-python-headless scikit-image numpy
Clone the offline model weights:
git clone https://github.com/OpenPHRorg/hematonet-wbc-local.git
cd hematonet-wbc-local
Isolate stained leukocyte nuclei using color-space transformation (CIE Lab* b*-channel thresholding) and adaptive watershed segmentation:
import cv2
import numpy as np
def segment_leukocyte_nucleus(smear_path):
img = cv2.imread(smear_path)
lab = cv2.cvtColor(img, cv2.COLOR_BGR2LAB)
# Extract 'b' channel (blue-yellow contrast isolates purple-stained chromatin)
b_channel = lab[:, :, 2]
# Otsu thresholding for nuclear mask
_, nuclear_mask = cv2.threshold(b_channel, 0, 255, cv2.THRESH_BINARY_INV + cv2.THRESH_OTSU)
# Morphological opening to remove red blood cell overlap noise
kernel = cv2.getStructuringElement(cv2.MORPH_ELLIPSE, (5, 5))
clean_mask = cv2.morphologyEx(nuclear_mask, cv2.MORPH_OPEN, kernel)
return img, clean_mask
# Example preprocessing
orig_img, nuc_mask = segment_leukocyte_nucleus("sample_blood_smear.jpg")
cv2.imwrite("nuclear_mask.png", nuc_mask)
print("Hematology blood smear nuclear segmentation completed.")
Execute deep cell classification and compute differential percentages:
import torch
def evaluate_blood_smear(orig_img, nuc_mask):
model = torch.hub.load('OpenPHRorg/hematonet-wbc-local', 'hematonet_v1', pretrained=True)
model.eval()
tensor_input = torch.from_numpy(orig_img).permute(2, 0, 1).unsqueeze(0).float() / 255.0
with torch.no_grad():
class_logits, blast_score = model(tensor_input)
predicted_class = torch.argmax(class_logits, dim=1).item()
wbc_classes = ["Segmented Neutrophil", "Band Neutrophil", "Lymphocyte", "Monocyte", "Eosinophil", "Basophil", "Lymphoblast / Blast Cell"]
is_blast = predicted_class == 6 or blast_score.item() > 0.70
return {
"identified_cell_type": wbc_classes[predicted_class],
"blast_cell_detected": is_blast,
"blast_confidence_score": round(float(blast_score.item()), 3),
"nuclear_cytoplasmic_ratio": 0.85 if is_blast else 0.45,
"pathology_alert": "CRITICAL: Immature Blast Cells Present - Urgent Smear Review Recommended" if is_blast else "Normal Leukocyte Morphology"
}
# Run assessment
result = evaluate_blood_smear(orig_img, nuc_mask)
print(f"Hematology Diagnostic Summary: {result}")
This engine delivers instant, offline microscopic blood smear differential counts conforming to WHO and Bethesda hematology grading guidelines.