CC BY-NC-ND 4.0 · Arch Plast Surg 2022; 49(05): 701-702
DOI: 10.1055/s-0042-1756504
Extremity/Lymphedema: Image

Does Lymphangiogenesis Occur through Incisional Scars?

Seungjun Lee*
1   Department of Plastic and Reconstructive Surgery, Seoul National University Bundang Hospital, Seongnam-si, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Seoul National University Bundang Hospital, Seongnam-si, Republic of Korea
,
2   Department of Plastic and Reconstructive Surgery, Seoul National University School of Medicine, Seoul, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Seoul National University Bundang Hospital, Seongnam-si, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Seoul National University Bundang Hospital, Seongnam-si, Republic of Korea
› Author Affiliations
 

Lymphangiogenesis is crucial in the homeostasis of interstitial fluids, immunity, and metabolism. Also, its importance in wound healing has been reported in animal models and clinical studies.[1] [2] However, the current understanding of lymphangiogenesis through incisional scars is still limited. We present indocyanine green (ICG) lymphography images near a 16-year-old Pfannenstiel scar of a 43-year-old female patient. Informed consent was obtained from the patient for publication of this image report and accompanying images.

The patient underwent a total mastectomy and immediate breast reconstruction using a free transverse rectus abdominis myocutaneous flap. ICG was injected intradermally at seven points: three points superior to, three points superolateral to, and one below the inguinal ligament. Drainage of the ICG was captured using Fluobeam near-infrared fluorescence imaging camera (Fluoptics, Cambridge, MA). Lymphatic drainage from injection point 1 traveled in the cephalic direction, while injection points 2 and 3 (above the scar) formed collaterals with injection point 3 (which is not above the scar). Other injection points showed the inguinal area's previously known lymphatic drainage ([Fig. 1]).

Zoom Image
Fig. 1 (A) A schematic illustration of the lymphatic drainage of the inguinal area: indocyanine green (ICG) was injected intradermally at 7 points (numbered). The blue line illustrates the drainage. (B) ICG lymphangiogram of the inguinal area during 10 minutes immediately after injection of the ICG.

One hour delayed ICG lymphography after flap elevation showed multiple lymphatic vessels near the superficial fascia. Interestingly, no lymphatic vessel was visible near the Pfannenstiel scar ([Fig. 2], above the line). ICG quantification showed pooling of the ICG in points 1 and 2, as well as collateral drainage in the cephalic direction ([Fig. 3]).

Zoom Image
Fig. 2 Indocyanine green (ICG) lymphangiogram of the inguinal area 1 hour after injection. After flap elevation, multiple lymphatics were seen near the superficial fascia. However, no lymphatics were found near the Pfannenstiel scar.
Zoom Image
Fig. 3 Indocyanine green (ICG) quantification: Pooling of the ICG was observed in the first and second injection points. Also, only cephalic (but no caudal) collateral drainages were observed.

In animal models, lymphangiogenesis has been evident near the wound edge 3 to 5 days after incision[3] with a temporary increase of new sprouts from existing lymphatic vessels.[2] On the contrary, our images show that human lymphangiogenesis does not occur through incisional scars. Further animal and clinical studies on lymphangiogenesis near incisional scars are needed.


#

Conflict of Interest

None declared.

Authors' Contributions

S.L. contributed with data curation and writing the original draft. B.N. took part in writing the original draft. C.Y.H. was involved in conceptualization and reviewing and editing the manuscript. J.K.-h.P. took part in conceptualization, data curation, and reviewing and editing the manuscript. Y.M. was involved in conceptualization, and reviewing and editing the manuscript.


Ethical Approval

This study was approved by the Institutional Review Board of Seoul National University Bundang Hospital (IRB# B2202-739-701). Written informed consent was obtained for this article.


* Both authors contributed equally as the first authors.


  • References

  • 1 Asahara T, Masuda H, Takahashi T. et al. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ Res 1999; 85 (03) 221-228
  • 2 Paavonen K, Puolakkainen P, Jussila L, Jahkola T, Alitalo K. Vascular endothelial growth factor receptor-3 in lymphangiogenesis in wound healing. Am J Pathol 2000; 156 (05) 1499-1504
  • 3 Ji RC, Miura M, Qu P, Kato S. Expression of VEGFR-3 and 5′-nase in regenerating lymphatic vessels of the cutaneous wound healing. Microsc Res Tech 2004; 64 (03) 279-286

Address for correspondence

Joseph Kyu-hyung Park, M.D.
Department of Plastic and Reconstructive Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital
82 Gumi-ro 173beon-gil, Bundang-gu, Seongnam-si 463-707
Republic of Korea   
Yujin Myung, M.D., Ph.D.
Department of Plastic and Reconstructive Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital
82 Gumi-ro 173beon-gil, Bundang-gu, Seongnam-si 463-707
Republic of Korea   

Publication History

Received: 12 January 2022

Accepted: 08 July 2022

Article published online:
23 September 2022

© 2022. The Korean Society of Plastic and Reconstructive Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Asahara T, Masuda H, Takahashi T. et al. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ Res 1999; 85 (03) 221-228
  • 2 Paavonen K, Puolakkainen P, Jussila L, Jahkola T, Alitalo K. Vascular endothelial growth factor receptor-3 in lymphangiogenesis in wound healing. Am J Pathol 2000; 156 (05) 1499-1504
  • 3 Ji RC, Miura M, Qu P, Kato S. Expression of VEGFR-3 and 5′-nase in regenerating lymphatic vessels of the cutaneous wound healing. Microsc Res Tech 2004; 64 (03) 279-286

Zoom Image
Fig. 1 (A) A schematic illustration of the lymphatic drainage of the inguinal area: indocyanine green (ICG) was injected intradermally at 7 points (numbered). The blue line illustrates the drainage. (B) ICG lymphangiogram of the inguinal area during 10 minutes immediately after injection of the ICG.
Zoom Image
Fig. 2 Indocyanine green (ICG) lymphangiogram of the inguinal area 1 hour after injection. After flap elevation, multiple lymphatics were seen near the superficial fascia. However, no lymphatics were found near the Pfannenstiel scar.
Zoom Image
Fig. 3 Indocyanine green (ICG) quantification: Pooling of the ICG was observed in the first and second injection points. Also, only cephalic (but no caudal) collateral drainages were observed.