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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 6

Schematic representation of hypothesized mechanism leading to blood-filled lymphatic vessels.

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Schematic representation of hypothesized mechanism leading to blood-fill...
(A) In contrast to blood endothelial cells (BECs), lymphatic endothelial cells (LECs) lining lymphatic vessels express the lymphatic markers PROX1 and Podoplanin (PDPN) (blue LECs, right). PDPN, a surface protein, binds platelets, resulting in their activation, which enables them to bind any red blood cells entering the lymphatic vessel. It is assumed that under normal physiological conditions if a shunt appears between a blood vessel and a lymphatic vessel in the skin, blood with all its components (including red blood cells and platelets) can escape into the lymphatic vessels. However, due to the immediate PDPN activation of the platelets, red blood cells will be bound, and filling of the lymphatic vessels with red blood cells is prevented. (B) In the hypothesized model, if a shunt appears between a blood vessel and a lymphatic vessel, which do not express PDPN (green LECs, middle), the platelets entering the lymphatics are not activated and therefore will not bind the entering red blood cells. This way blood filling of the lymphatic capillaries can happen, which make them appear as an erythematous cutaneous capillary malformation (nevus). Arrow, direction of flow of red blood cells/blood.

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