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Laser speckle contrast imaging of perfusion in oncological clinical applications: a literature review Cover

Laser speckle contrast imaging of perfusion in oncological clinical applications: a literature review

Open Access
|Sep 2024

Figures & Tables

Figure 1.

Schematic representation of the laser speckle contrast imaging (LSCI) method. (A) The technique relies on the interference of light backscattered from moving particles, creating distinct dark and bright areas (speckle pattern) captured by a camera. (B) Variations in the speckle pattern are predominantly driven by the movement of red blood cells, enabling interpretation as perfusion. (C) Analysis of speckle-pattern variations yields an image displayed on the monitor, where white and yellow depict areas with high perfusion, contrasting with darker areas indicating lower perfusion areas. Taken from Berggren et al.19 and reprinted with permission from the publisher.
Schematic representation of the laser speckle contrast imaging (LSCI) method. (A) The technique relies on the interference of light backscattered from moving particles, creating distinct dark and bright areas (speckle pattern) captured by a camera. (B) Variations in the speckle pattern are predominantly driven by the movement of red blood cells, enabling interpretation as perfusion. (C) Analysis of speckle-pattern variations yields an image displayed on the monitor, where white and yellow depict areas with high perfusion, contrasting with darker areas indicating lower perfusion areas. Taken from Berggren et al.19 and reprinted with permission from the publisher.

Figure 2.

Speckle contrast demonstrates lower values for well-vascularized parathyroid glands. Lower speckle contrast values indicate greater blood flow due to more blurring of the speckle pattern, while higher contrast values indicate less blood flow. The top row displays representative white light images, and the bottom row shows speckle contrast images of a well-vascularized (left), a compromised (middle), and a devascularized (right) parathyroid gland, with parathyroid glands marked with ellipses. The corresponding speckle contrast values were 0.11, 0.18, and 0.21, respectively. Taken from Mannoh et al.33 and reprinted with permission from the publisher.
Speckle contrast demonstrates lower values for well-vascularized parathyroid glands. Lower speckle contrast values indicate greater blood flow due to more blurring of the speckle pattern, while higher contrast values indicate less blood flow. The top row displays representative white light images, and the bottom row shows speckle contrast images of a well-vascularized (left), a compromised (middle), and a devascularized (right) parathyroid gland, with parathyroid glands marked with ellipses. The corresponding speckle contrast values were 0.11, 0.18, and 0.21, respectively. Taken from Mannoh et al.33 and reprinted with permission from the publisher.

Figure 3.

Representative examples of laser speckle contrast images, showing the blood perfusion in the free skin grafts, immediately postoperatively (0 weeks), and at follow-up after 1, 3, and 7 weeks. It can be seen that reperfusion occurred simultaneously in the center and periphery of the graft, and that complete reperfusion was achieved after 7 weeks. Taken from Berggren et al.43 and reprinted with permission from the publisher.
Representative examples of laser speckle contrast images, showing the blood perfusion in the free skin grafts, immediately postoperatively (0 weeks), and at follow-up after 1, 3, and 7 weeks. It can be seen that reperfusion occurred simultaneously in the center and periphery of the graft, and that complete reperfusion was achieved after 7 weeks. Taken from Berggren et al.43 and reprinted with permission from the publisher.

Figure 4.

Typical laser speckle images in two patients. High-resolution laser speckle contrast imaging (LSCI) can indicate the bowel demarcation line at the point of ligation of the marginal vessels. (A) Normal color image before ligating the marginal vessels. (B) LSCI image before ligating the marginal vessels. (C) LSCI image after ligating the marginal vessels. Taken from Kojima et al.56 and reprinted with permission from the publisher.
Typical laser speckle images in two patients. High-resolution laser speckle contrast imaging (LSCI) can indicate the bowel demarcation line at the point of ligation of the marginal vessels. (A) Normal color image before ligating the marginal vessels. (B) LSCI image before ligating the marginal vessels. (C) LSCI image after ligating the marginal vessels. Taken from Kojima et al.56 and reprinted with permission from the publisher.

Included articles reporting the use of laser speckle contrast imaging (LSCI) to quantify perfusion in clinical applications in oncology

ReferenceYear of publicationNumber of patientsOncologic setting
Brain
Parthasarathy et al.2120103Tumor resection
Richards et al.22201410Tumor resection
Richards et al.2720178Tumor resection
Klijn et al.2520138Tumor resection
Ideguchi et al.28201712Tumor resection
Breasts
Tesselaar et al.29201715Adjuvant radiotherapy for stage I-II breast cancer
Zötterman et al.30202023Deep inferior epigastric artery perforator (DIEP) flap surgery
Endocrine glands
de Paula et al.31202142Non-functioning adrenal incidentaloma
Mannoh et al.32201728Thyroidectomy/parathyroidectomy
Mannoh et al.33202172Thyroidectomy
Mannoh et al.34202321Thyroidectomy/parathyroidectomy
Skin
Tchvialeva et al.352012214 lesionsMalignant melanoma, squamous cell carcinoma, basal cell carcinoma, melanocytic nevus, seborrheic keratosis
Reyal et al.36201212Basal cell carcinoma
Zhang et al.37201912 (total 143)Facial nerve palsy due to nerve tumor (also including other etiology)
Zieger et al.3820219Basal cell carcinoma
Tenland et al.39201913Oculoplastic reconstructive surgery (tarsoconjunctival flaps)
Berggren et al.4020199Oculoplastic reconstructive surgery (tarsoconjunctival flaps)
Tenland et al.41202112Oculoplastic reconstructive surgery after squamous cell carcinoma, basal cell carcinoma, and intradermal nevus
Berggren et al.4220217Oculoplastic reconstructive surgery after squamous cell carcinoma and basal cell carcinoma
Berggren et al.4320217Oculoplastic reconstructive surgery after squamous cell carcinoma and basal cell carcinoma
Berggren et al.4420211Oculoplastic reconstructive surgery
Berggren et al.4520227Oculoplastic reconstructive surgery after squamous cell carcinoma and basal cell carcinoma
Stridh et al.4620241Cutaneous angio-sarcoma
Gastrointestinal tract (open surgical setting)
Eriksson et al.47201410Liver resection
Milstein et al.48201611Esophagectomy
Ambrus et al.49201745Esophagectomy
Ambrus et al.50201725Ivor-Lewis esophagectomy
Di Maria et al.5120172Colorectal resection
Jansen et al.52201826Esophagectomy
Kojima et al.5320198Colorectal resection
Kaneko et al.54202036Colorectal resection (34 due to colorectal carcinoma)
Gastrointestinal tract (laparoscopic/thoracoscopic setting)
Heeman et al.55201910Colorectal resection
Kojima et al.56202027Colorectal resection
Slooter et al.57202024Esophagectomy
Heeman et al.58202367Hemicolectomy and sigmoid resection
Nwaiwu et al.59202340Colectomy, also non-oncological interventions (Roux-en-Y gastric bypass and sleeve gastrectomy)
DOI: https://doi.org/10.2478/raon-2024-0042 | Journal eISSN: 1581-3207 | Journal ISSN: 1318-2099
Language: English
Page range: 326 - 334
Submitted on: Jul 16, 2024
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Accepted on: Jul 26, 2024
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Published on: Sep 15, 2024
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2024 Rok Hren, Simona Kranjc Brezar, Urban Marhl, Gregor Sersa, published by Association of Radiology and Oncology
This work is licensed under the Creative Commons Attribution 4.0 License.