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	<title>dermal backflow &#8211; Science</title>
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	<title>dermal backflow &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Contrast-enhanced ultrasound planning linked to more successful, faster venturi-like LVA in retrospective cohort of 29 women</title>
		<link>https://scienmag.com/contrast-enhanced-ultrasound-planning-linked-to-more-successful-faster-venturi-like-lva-in-retrospective-cohort-of-29-women/</link>
		
		<dc:creator><![CDATA[Nathaniel Bowman]]></dc:creator>
		<pubDate>Tue, 20 Oct 2026 20:31:38 +0000</pubDate>
				<category><![CDATA[Cancer]]></category>
		<category><![CDATA[contrast-enhanced ultrasound]]></category>
		<category><![CDATA[contrast-enhanced ultrasound lymphography]]></category>
		<category><![CDATA[dermal backflow]]></category>
		<category><![CDATA[dermal backflow detection in lymphedema stages]]></category>
		<category><![CDATA[gynecologic cancer]]></category>
		<category><![CDATA[impact of CEUS]]></category>
		<category><![CDATA[intraoperative lymphatic vessel localization]]></category>
		<category><![CDATA[lower-extremity lymphedema treatment]]></category>
		<category><![CDATA[lymphaticovenous]]></category>
		<category><![CDATA[lymphaticovenous anastomosis]]></category>
		<category><![CDATA[lymphaticovenous anastomosis efficiency]]></category>
		<category><![CDATA[lymphedema]]></category>
		<category><![CDATA[lymphography]]></category>
		<category><![CDATA[planning]]></category>
		<category><![CDATA[preoperative]]></category>
		<category><![CDATA[preoperative imaging for lymphedema]]></category>
		<category><![CDATA[retrospective cohort]]></category>
		<category><![CDATA[retrospective cohort study on lymphedema surgery]]></category>
		<category><![CDATA[surgical planning]]></category>
		<category><![CDATA[surgical success in lymphatic bypass]]></category>
		<category><![CDATA[ultrasound-guided lymphatic surgery planning]]></category>
		<category><![CDATA[venturi-like]]></category>
		<category><![CDATA[venturi-like lymphaticovenous anastomosis]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=322606</guid>

					<description><![CDATA[A retrospective cohort of 29 women found that preoperative contrast-enhanced ultrasound lymphography was associated with more successful anastomoses and a shorter median anastomosis time during venturi-like lymphaticovenous anastomosis.]]></description>
										<content:encoded><![CDATA[<p>The abstract of a retrospective cohort study reports that preoperative contrast-enhanced ultrasound lymphography (CEUS-L) was associated with more successful anastomoses and shorter median anastomosis times during venturi-like lymphaticovenous anastomosis (LVA) for lower-extremity lymphedema following gynecologic cancer treatment. The study included 29 women treated between November 2021 and August 2023, divided into 21 who underwent CEUS-L before surgery and eight who did not.</p>
<p>The primary comparison concerned surgical indicators. The CEUS-L group had a median of eight successful anastomoses per patient, compared with three in the control group, a difference reported as P &lt; 0.001. Median anastomosis time was 55 minutes in the CEUS-L group versus 97.5 minutes in the control group, also reported as P &lt; 0.001. The investigators calculated the true-positive rate of CEUS-L using successful anastomoses relative to preoperative marking-guided surgical incisions. They reported 156 successful cases among 173 such incisions, corresponding to a true-positive rate of 90.2%. These findings indicate an association between preoperative CEUS-L and the measured localization and operative efficiency indicators in this cohort.</p>
<p>The abstract also reports that the detection rate of dermal backflow differed across clinical stages of lymphedema. It was 0% in stage I, 62.5% in stage II and 90.9% in stage III. The difference between stages I and III reached statistical significance after Bonferroni adjustment, with P &lt; 0.05. This staging pattern was an additional imaging observation reported by the study; the abstract does not establish how dermal-backflow detection affected postoperative outcomes.</p>
<p>The findings remain bounded by the study design and population. It was a small retrospective cohort consisting exclusively of women with lower-extremity lymphedema after gynecologic cancer treatment, and it compared outcomes according to whether preoperative CEUS-L had been implemented. The reported endpoints focused on successful anastomoses, anastomosis time and the true-positive rate of CEUS-L. The abstract does not provide long-term follow-up or establish that the imaging approach improves patient-reported symptoms, limb volume, quality of life or other clinical benefits. Its conclusion states that larger prospective studies with long-term follow-up are required.</p>
<p><strong>Subject of Research:</strong> Preoperative ultrasound planning for venturi-like lymphaticovenous anastomosis in women with secondary lower-extremity lymphedema</p>
<p><strong>Article Title:</strong> Preoperative planning of venturi-like lymphaticovenous anastomosis for secondary lower extremity lymphedema using contrast-enhanced ultrasound</p>
<p><strong>Article References:</strong> Wei, M., Lu, K.-F., Li, Y.-F., Liu, H., Du, P., Liu, Y., Hu, Q.-H., He, H.-F., Hou, C.-J., Sun, L.-T., &amp; Tang, J.-L. (2026). Preoperative planning of venturi-like lymphaticovenous anastomosis for secondary lower extremity lymphedema using contrast-enhanced ultrasound. <em>BMC Cancer</em>. <a href="https://doi.org/10.1186/s12885-026-16707-7" rel="noopener noreferrer">https://doi.org/10.1186/s12885-026-16707-7</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12885-026-16707-7" rel="noopener noreferrer">10.1186/s12885-026-16707-7</a></p>
<p><strong>Keywords:</strong> lymphedema, lymphaticovenous anastomosis, contrast-enhanced ultrasound, lymphography, gynecologic cancer, surgical planning, retrospective cohort, dermal backflow, Preoperative, planning, venturi-like, lymphaticovenous</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">322606</post-id>	</item>
		<item>
		<title>Scientists Map Hidden Lymphatic Damage in Breast Cancer Survivors Using AI</title>
		<link>https://scienmag.com/scientists-map-hidden-lymphatic-damage-in-breast-cancer-survivors-using-ai/</link>
		
		<dc:creator><![CDATA[Nathaniel Bowman]]></dc:creator>
		<pubDate>Wed, 07 Oct 2026 10:01:30 +0000</pubDate>
				<category><![CDATA[Cancer]]></category>
		<category><![CDATA[AI in lymphatic system mapping]]></category>
		<category><![CDATA[AI-driven monitoring of lymphedema severity]]></category>
		<category><![CDATA[bioimpedance spectroscopy]]></category>
		<category><![CDATA[Breast cancer-related lymphedema]]></category>
		<category><![CDATA[breast cancer-related lymphedema diagnosis]]></category>
		<category><![CDATA[chronic complications of breast cancer treatment]]></category>
		<category><![CDATA[dermal backflow]]></category>
		<category><![CDATA[dermal backflow in lymphedema]]></category>
		<category><![CDATA[early detection]]></category>
		<category><![CDATA[ICG lymphography]]></category>
		<category><![CDATA[image segmentation]]></category>
		<category><![CDATA[indocyanine green lymphography]]></category>
		<category><![CDATA[large imaging cohort in lymphatic research]]></category>
		<category><![CDATA[lymphatic drainage]]></category>
		<category><![CDATA[lymphatic dysfunction in upper limbs]]></category>
		<category><![CDATA[lymphatic imaging in breast cancer survivors]]></category>
		<category><![CDATA[lymphatic system damage detection]]></category>
		<category><![CDATA[Machine learning]]></category>
		<category><![CDATA[machine learning for disease staging]]></category>
		<category><![CDATA[MDACC staging]]></category>
		<category><![CDATA[Random Forest]]></category>
		<category><![CDATA[spatial atlas]]></category>
		<category><![CDATA[spatial atlas of lymphatic dysfunction]]></category>
		<category><![CDATA[upper limb]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=244001</guid>

					<description><![CDATA[Researchers have built the first spatial atlas of dermal backflow in breast cancer-related lymphedema from 282 patients and shown that machine learning models stage the disease more accurately when quantitative imaging features are included.]]></description>
										<content:encoded><![CDATA[<p>Breast cancer saves lives, but for roughly one in five survivors, the treatment that cures the tumor leaves behind a quieter, chronic burden: breast cancer-related lymphedema, or BCRL. This condition arises when surgery or radiotherapy disrupts the lymphatic drainage of the arm, causing fluid to accumulate, fat tissue to proliferate, and lymph to reflux backward into the skin, a phenomenon clinicians call dermal backflow. Now, a research team spanning the University of Auckland in New Zealand and Macquarie University in Australia has transformed hundreds of clinician-drawn diagnostic diagrams into something unprecedented: a spatial atlas of where lymphatic dysfunction strikes the upper limb, paired with machine learning models that can stage disease severity objectively. The study, published in Breast Cancer Research and Treatment, draws on one of the largest imaging cohorts ever assembled for this purpose and could reshape how a debilitating complication is detected and monitored.</p>
<p>The data came from the Australian Lymphedema Education, Research and Treatment (ALERT) Centre Databank at Macquarie University in Sydney. The researchers extracted records from 282 female patients with confirmed BCRL, covering 289 affected limbs, including seven patients with lymphedema on both sides. Each patient had undergone indocyanine green (ICG) lymphography, an imaging technique in which a fluorescent tracer is injected into the skin and visualized with a near-infrared camera. During these sessions, four trained clinicians drew the observed lymphatic drainage pathways directly onto paper templates of the patient&#8217;s arm, marking regions of dermal backflow in red once the signal stabilized after roughly an hour. These annotated summary diagrams, digitized as high-resolution images, became the raw material for the atlas. Alongside the images, the databank provided rich clinical information: age, duration of lymphedema, cancer treatment history, limb volume difference, bioimpedance spectroscopy scores known as L-Dex, body mass index, and the clinician-assigned MD Anderson Cancer Center (MDACC) stage of lymphedema severity.</p>
<p>Turning hand-drawn diagrams from hundreds of patients into a single coherent map posed a genuine computational challenge. The team chose a left-arm template as the reference space and horizontally flipped diagrams from right-sided cases, an approach justified by the known symmetry of normal upper-limb lymphatic drainage when assessed by nodal basin. Each diagram was then aligned to the template using feature-based image co-registration: the ORB algorithm, which combines the FAST keypoint detector with the BRIEF descriptor, identified matching landmarks, while the RANSAC algorithm estimated the geometric transformation needed to overlay every image onto the common frame. Segmentation of the red dermal backflow regions was performed semi-automatically by thresholding in the CIELAB perceptual color space, exploiting the fact that the A-channel captures the green-red axis of an image. Morphological operations cleaned up small artifacts, and the researchers manually corrected masks where necessary using image editing software before quality checks.</p>
<p>Once every diagram was registered and segmented, the binary masks, marking background as zero and dermal backflow as one, were stacked into a three-dimensional volume with one slice per patient study. A pixel-wise mean across the stack produced a frequency map: for every anatomical location on the arm, the proportion of patients exhibiting dermal backflow at that spot. The result is, in effect, a probabilistic heat map of lymphatic failure painted onto the anatomy of the upper limb. The team also generated subgroup-specific heat maps stratified by MDACC stage, L-Dex ratio, limb volume difference, lymphatic drainage region, and the presence of backflow in the hand, allowing them to see how the geography of disease shifts as severity increases.</p>
<p>The atlas revealed striking and reproducible spatial patterns. In the anterior view, dermal backflow reached its highest prevalence, up to roughly 80 percent, in the medial wrist and forearm, then faded progressively toward the elbow and upper arm. In the posterior view, prevalence climbed even higher, approaching 90 percent in the olecranon region and forearm. By contrast, the fingers, the shoulder, and, notably, the region near the axilla showed the lowest frequencies, below 10 percent. The thenar eminence at the base of the thumb was the most commonly affected part of the hand. This distal-to-proximal gradient suggests that lymphatic dysfunction in BCRL is not a diffuse, uniform process but a regionally patterned one, with certain anatomical zones acting as consistent hotspots of failure across hundreds of individuals.</p>
<p>The subgroup analyses added clinical depth. As MDACC stage increased from 1 to 4, dermal backflow became more extensive and spread more proximally up the limb. Higher L-Dex ratios and greater limb volume differences were likewise associated with broader regions of involvement. Patients whose lymph drained through alternative routes beyond the predominant ipsilateral axilla showed distinct patterns, and those with hand involvement displayed more distally concentrated backflow with less upper-arm involvement. Perhaps most clinically provocative, dermal backflow was frequently observed in limbs with minimal or even negative limb volume difference, hinting that lymphatic dysfunction can precede measurable swelling. Because negative volume differences can arise from arm dominance and baseline variability, the finding underscores a key limitation of conventional volume- and impedance-based assessments: they may underestimate early or spatially localized disease that a spatial heat map can capture as a continuous probability signal.</p>
<p>Why the forearm and wrist should be so vulnerable remains an open question, but the authors point to the underlying organization of upper-extremity lymphatic drainage and the lymphosome concept, which divides the body into discrete lymphatic territories. The antecubital region is associated with drainage toward the epitrochlear nodes en route to the axilla, while the low prevalence near the axilla itself may simply reflect the normal convergence of superficial lymphatics into deeper nodal structures as they approach their destination. The patterns also echo earlier physiological work: a study by Mayrovitz and colleagues reported regional variability in superficial tissue water content in women treated for breast cancer even before overt lymphedema appeared. The new atlas suggests that this regional susceptibility is preserved, and possibly amplified, in established disease, with distal regions showing roughly 70 percent prevalence compared with about 30 percent proximally.</p>
<p>The second half of the study translated these imaging insights into prediction. Using Spearman&#8217;s rank correlation, the team narrowed 28 clinical variables down to 13 statistically significant and clinically relevant features. Dermal backflow percentage, calculated as the segmented backflow area divided by the total upper-limb area across anterior and posterior views, showed the strongest correlation with MDACC stage at rho equals 0.90, far exceeding L-Dex at 0.67 and limb volume difference at 0.65. Five machine learning models were then trained to classify stage: multinomial logistic regression, random forest, multi-layer perceptron, k-nearest neighbors, and support vector machine, evaluated with five-fold stratified cross-validation under a one-versus-rest framework.</p>
<p>The results were clear. When dermal backflow percentage was included, random forest achieved the highest area under the curve at 0.94 with precision of 0.768, while multinomial logistic regression posted the best F1 score at 0.926 and sensitivity of 0.735, both with accuracy around 0.737 and specificity above 0.92. The neural network and support vector machine performed at an intermediate level, and k-nearest neighbors lagged throughout. Critically, removing dermal backflow from the feature set degraded every model, with random forest&#8217;s AUC falling to 0.832. The authors note that the simpler, interpretable models outperforming deep architectures is good news for clinical translation, where understanding why a model assigns a stage matters as much as the assignment itself. Interestingly, the non-linear models showed higher sensitivity for advanced stage 4 disease, though by that point lymphedema is typically clinically obvious anyway.</p>
<p>The study has limitations the authors acknowledge candidly. The atlas reflects clinician interpretation of ICG studies rather than raw imaging data, and although standardized training reduced variability among the four annotators, differences in interpretation may have influenced the maps. A U-Net deep learning segmentation model was trialed to automate the pipeline but degraded on the full dataset, particularly in the small and variable hand regions, so manual correction remained necessary. The two-dimensional diagrams also approximate, rather than perfectly capture, the curved three-dimensional skin surface. Still, the framework opens concrete paths forward: external validation in multi-centre cohorts, fully automated registration and segmentation, three-dimensional volumetric analysis, and investigation of whether sentinel versus axillary lymph node dissection produce different backflow patterns. For now, the atlas offers clinicians a reference for what typical lymphatic failure looks like across a large cohort, and a quantitative, reproducible measure of severity that could complement, rather than replace, existing assessment, potentially catching the disease before the tape measure can.</p>
<p><strong>Subject of Research:</strong> Spatial mapping of dermal backflow and machine learning-based staging of breast cancer-related lymphedema</p>
<p><strong>Article Title:</strong> A dermal backflow atlas of lymphatic dysfunction in breast cancer-related lymphedema with machine learning-based stage prediction</p>
<p><strong>Article References:</strong> Sutejitsiri, L., Suami, H., Nielsen, P. M. F., Phillips, A. R. J., &amp; Reynolds, H. M. (2026). A dermal backflow atlas of lymphatic dysfunction in breast cancer-related lymphedema with machine learning-based stage prediction. <em>Breast Cancer Research and Treatment, 219</em>(3), Article 28. <a href="https://doi.org/10.1007/s10549-026-08093-2" rel="noopener noreferrer">https://doi.org/10.1007/s10549-026-08093-2</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s10549-026-08093-2" rel="noopener noreferrer">10.1007/s10549-026-08093-2</a></p>
<p><strong>Keywords:</strong> breast cancer-related lymphedema, dermal backflow, ICG lymphography, machine learning, spatial atlas, MDACC staging, lymphatic drainage, random forest, bioimpedance spectroscopy, upper limb, image segmentation, early detection</p>
]]></content:encoded>
					
		
		
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