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Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies
René Hägerling, Malou Van Zanten, Rose Yinghan Behncke, Sascha Ulferts, Nils R. Hansmeier, Bruno Märkl, Christian Witzel, Bernard Ho, Vaughan Keeley, Katie Riches, Sahar Mansour, Kristiana Gordon, Pia Ostergaard, Peter S. Mortimer
René Hägerling, Malou Van Zanten, Rose Yinghan Behncke, Sascha Ulferts, Nils R. Hansmeier, Bruno Märkl, Christian Witzel, Bernard Ho, Vaughan Keeley, Katie Riches, Sahar Mansour, Kristiana Gordon, Pia Ostergaard, Peter S. Mortimer
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Research Article Angiogenesis Cell biology

Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies

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Abstract

Superficial erythematous cutaneous vascular malformations are assumed to be blood vascular in origin, but cutaneous lymphatic malformations can contain blood and appear red. Management may be different and so an accurate diagnosis is important. Cutaneous malformations were investigated through 2D histology and 3D whole-mount histology. Two lesions were clinically considered as port-wine birthmarks and another 3 lesions as erythematous telangiectasias. The aims were (i) to demonstrate that cutaneous erythematous malformations including telangiectasia can represent a lymphatic phenotype, (ii) to determine if lesions represent expanded but otherwise normal or malformed lymphatics, and (iii) to determine if the presence of erythrocytes explained the red color. Microscopy revealed all lesions as lymphatic structures. Port-wine birthmarks proved to be cystic lesions, with nonuniform lymphatic marker expression and a disconnected lymphatic network suggesting a lymphatic malformation. Erythematous telangiectasias represented expanded but nonmalformed lymphatics. Blood within lymphatics appeared to explain the color. Blood-lymphatic shunts could be detected in the erythematous telangiectasia. In conclusion, erythematous cutaneous capillary lesions may be lymphatic in origin but clinically indistinguishable from blood vascular malformations. Biopsy is advised for correct phenotyping and management. Erythrocytes are the likely explanation for color accessing lymphatics through lympho-venous shunts.

Authors

René Hägerling, Malou Van Zanten, Rose Yinghan Behncke, Sascha Ulferts, Nils R. Hansmeier, Bruno Märkl, Christian Witzel, Bernard Ho, Vaughan Keeley, Katie Riches, Sahar Mansour, Kristiana Gordon, Pia Ostergaard, Peter S. Mortimer

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Figure 2

Macroscopic as well as 2D and 3D microscopic manifestations of a patient (case 2) with KTS and port-wine birthmark.

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Macroscopic as well as 2D and 3D microscopic manifestations of a patient...
(A and B) Clinical manifestations of patient with KTS presenting with extensive port-wine birthmarks associated with segmental overgrowth, scoliosis, venous disease, and foot swelling. (C) Standard histological analysis of a skin biopsy with port-wine birthmark using hematoxylin and eosin stain of microtome sections. (D–H) 2D optical section (D) as well as 3D reconstruction (E–H) of lymphatic vessels of whole-mount immunostained affected patient tissue (port-wine birthmark) imaged using light sheet microscopy. Podoplanin (PDPN) served as a lymphatic endothelial cell membrane marker and the transcription factor PROX1 as a lymphatic endothelial nuclei marker. Detected antigens and respective colors are indicated. (D) Representative 2D optical sections of whole-mount immunostained affected patient tissue. Blood-filled lymphatic vessel is marked by white arrowhead. Dilated PDPN-negative, PROX1-positive vessels are marked by white arrows. (E–G) Maximum-intensity projections of 3D reconstructed lymphatic vasculature. Visualization of the tissue volume with the papillary dermis located at top and cutaneous plexus at bottom of dermis (DM). PDPN-negative, PROX1-positive cystic vascular lesions located underneath the epidermis (ED) are highlighted using red arrows. Red arrowheads: fragmented vessels. (H) Digitally rotated view of the same specimen, showing the vessels of the papillary plexus viewed en face through the epidermis. White arrows: PROX1-positive, PDPN-negative cystic vascular lesions. Red arrowheads: fragmented vessels. Scale bars: 200 μm.

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