Arteriolosclerosis with asymmetrical fibrous intimal thickening (fibrous endarteritis) and Mönckeberg medial calcinosis (calcification of the internal elastic lamina and media): A, Hematoxylin-eosin-saffron (HES)–stained (original magnification ×400); B, von Kossa–stained (original magnification ×400); C, Field-emission–scanning electron microscopy (FE-SEM). Calcific uremic arteriolopathy (CUA) hypodermic arterioles with voluminous and circumferential parietal calcium deposits: D, HES-stained (original magnification ×400); E, von Kossa–stained (original magnification ×400); F, FE-SEM.
Calcific uremic arteriolopathy (CUA) hypodermic capillaries with voluminous and circumferential parietal calcium deposits: A, hematoxylin-eosin-saffron (HES)–stained (×400), B, von Kossa-stained (original magnification ×400); C, Field-emission–scanning electron microscopy (FE-SEM). Interstitial calcific uremic arteriolopathy (CUA) deposits, aligned along the cytoplasmic membranes of adipocytes; D, HES-stained (original magnification ×400); E, von Kossa–stained (original magnification ×400); F, FE-SEM.
A, Skin biopsy of CUA; B, Infrared map of the red square area, showing an intense vascular deposit; C, Infrared spectrum of this vascular deposit: calcium–phosphate apatite spectrum with characteristic peaks (1009, 958 and 870 cm–1) in a protein matrix (skin tissue). The same spectrum was obtained for CUA and arteriolosclerosis vascular calcifications.
Micrographs (original magnifications ×10 and ×100) of (A) Periadipocyte and (B) Vascular calcifications (excitation wavelength λexc = 785 nm; numerical aperture, 0.9). The Raman bands at 960, 1076, and 590 cm–1 correspond, respectively, to the ν1, ν3 and ν4 phosphate vibrations of apatite. The low-intensity ν4 carbonate vibrations around 680 to 715 cm–1, expected for carbapatite, are not observed. The strong fluorescence background has been corrected on the presented spectra.
eTable. Univariate and Multivariate Analyses for the Risk of Death Related to CUA
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Colboc H, Moguelet P, Bazin D, et al. Localization, Morphologic Features, and Chemical Composition of Calciphylaxis-Related Skin Deposits in Patients With Calcific Uremic Arteriolopathy. JAMA Dermatol. Published online May 22, 2019155(7):789–796. doi:10.1001/jamadermatol.2019.0381
What are the precise localization, morphologic features, and chemical composition of calciphylaxis-related skin deposits?
This multicenter cohort study of 36 patients found that calcific uremic arteriolopathy calcifications are composed of pure calcium–phosphate apatite, always located circumferentially, mostly in the intima of otherwise normal-appearing vessels, and often associated with interstitial deposits, unlike calcifications observed in cutaneous arteriolosclerotic vessels, which are associated with medial hypertrophy containing the calcifications and no interstitial deposits.
The differences observed between calcific uremic arteriolopathy and cutaneous arteriolosclerosis regarding calcification location and morphologic vascular features suggest different pathogenetic mechanisms and provide new insights into the pathogenesis of calcific uremic arteriolopathy that could explain the poor efficacy of vasodilators and the therapeutic effect of calcium-solubilizing drugs.
Calcific uremic arteriolopathy (CUA), a rare, potentially fatal, disease with calcium deposits in skin, mostly affects patients with end-stage renal disease who are receiving dialysis. Chemical composition and structure of CUA calcifications have been poorly described.
To describe the localization and morphologic features and determine the precise chemical composition of CUA-related calcium deposits in skin, and identify any mortality-associated factors.
Design, Setting, and Participants
A retrospective, multicenter cohort study was conducted at 7 French hospitals including consecutive adults diagnosed with CUA between January 1, 2006, and January 1, 2017, confirmed according to Hayashi clinical and histologic criteria. Patients with normal renal function were excluded. For comparison, 5 skin samples from patients with arteriolosclerosis and 5 others from the negative margins of skin-carcinoma resection specimens were also analyzed.
Main Outcomes and Measures
Localization and morphologic features of the CUA-related cutaneous calcium deposits were assessed with optical microscopy and field-emission–scanning electron microscopy, and the chemical compositions of those deposits were evaluated with μ Fourier transform infrared spectroscopy, Raman spectroscopy, and energy dispersive radiographs.
Thirty-six patients (median [range] age, 64 [33-89] years; 26 [72%] female) were included, and 29 cutaneous biopsies were analyzed. Calcific uremic arteriolopathy and arteriolosclerosis skin calcifications were composed of pure calcium–phosphate apatite. Calcific uremic arteriolopathy vascular calcifications were always circumferential, found in small to medium-sized vessels, with interstitial deposits in 22 (76%) of the samples. A thrombosis, most often in noncalcified capillary lumens in the superficial dermis, was seen in 5 samples from patients with CUA. Except for calcium deposits, the vessel structure of patients with CUA appeared normal, unlike thickened arteriolosclerotic vessel walls. Twelve (33%) patients died of CUA.
Conclusions and Relevance
Calcific uremic arteriolopathy–related skin calcifications were exclusively composed of pure calcium–phosphate apatite, localized circumferentially in small to medium-sized vessels and often associated with interstitial deposits, suggesting its pathogenesis differs from that of arteriolosclerosis. Although the chemical compositions of CUA and arteriolosclerosis calcifications were similar, the vessels’ appearances and deposit localizations differed, suggesting different pathogenetic mechanisms.
Uremic calciphylaxis, also called calcific uremic arteriolopathy (CUA), is a rare and severely morbid condition that predominantly affects patients with end-stage renal disease (ESRD) receiving dialysis. Its frequency among patients with ESRD reaches 4% and its incidence increases for those on hemodialysis.1 Calcific uremic arteriolopathy’s high morbidity and mortality result from extensive skin necrosis and septic complications, with the latter being the leading cause of death. For patients with ESRD, an increased risk of subsequent CUA development has been associated with female sex, diabetes mellitus, higher body mass index, elevated serum calcium, phosphorus, and parathyroid hormone levels, nutritional status, and vitamin K-antagonist treatments.2
Although noninvasive imaging tools (eg, plain radiographs) have been reported to help diagnose CUA,3 none of those tools has been systematically evaluated.4 Definitive CUA diagnosis requires a skin biopsy. However, because biopsy of the skin is associated with the risk of new ulceration, bleeding, and infection, actually obtaining one is sometimes debated.5 When obtained, deep cutaneous biopsies of CUA lesions show calcifications, smaller than 500 μm, in hypodermal vessels, interstitial tissue or both, highly suggestive of CUA with good specificity.6
Despite well-characterized clinical and histologic descriptions of CUA, its precise pathogenetic mechanism remains unclear.7 Arteriolar calcification is probably the first event, followed by thrombosis and skin ischemia. Determination of chemical composition determination and description of the skin calcifications through physicochemical techniques could contribute to understanding CUA pathogenesis, leading to more appropriate and specific treatments.8 Nanotechnologies are receiving increased attention to improve understanding of the effects of pathologic deposits on living tissues.9,10
The aims of this study were to determine precisely the localization, morphologic features, and chemical composition of calcifications in the skin of patients with CUA, and then examine whether any association could be established between their microscopy findings and clinical characteristics.
This study followed the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline. This study was conducted in compliance with Good Clinical Practices and the Declaration of Helsinki,11 and in accordance with French law. Formal ethics committee approval of the study protocol was obtained. Patients provided written informed consent.
This retrospective study included consecutive adults diagnosed with CUA, confirmed according to Hayashi clinical and histologic criteria, and seen in 7 French hospitals between January 1, 2006, and January 1, 2017.12 Patients with normal renal function were excluded. Patients’ medical histories, treatments, and laboratory findings were extracted from their medical records. They were classified into 2 clinical subgroups, distal or proximal CUA, according to the skin lesion localizations described by Brandenburg et al.13
Five skin samples from patients with arteriolosclerosis and 5 control samples from the negative margins of skin carcinoma resections on the legs of 5 other patients were included and served as controls. All 10 control participants had normal renal function; only the 5 patients with arteriolosclerosis from among a cohort of patients with necrotic angiodermatitis underwent leg-skin biopsies.
Skin biopsy samples were sent to and centralized in Tenon Hospital, Department of Pathology. For each subject, 1.5-μm–thick sections of paraffin-embedded skin biopsy specimens were deposited on glass slides, for hematoxylin-eosin–saffron and von Kossa staining, and low-e microscope slides (MirrIR, Kevley Technologies, Tienta Sciences) for field-emission–scanning electron microscopy (FE-SEM), μ Fourier transform infrared (FT-IR) spectroscopy, and Raman spectroscopy.14 Vascular and interstitial calcifications, the caliber of calcified vessels, and the topography of deposits in skin sections were analyzed and compared between patients with CUA and control participants.
Field-emission–scanning electron microscopy (Zeiss SUPRA55-VP) was used to describe the ultrastructural characteristics of tissue sections. As previously described, high-resolution images were obtained with in-lens and Everhart-Thornley secondary electron detectors.15 Measurements were taken at low voltage (1–2 kV), without the usual carbon-coating of the sample surface. For some samples, energy-dispersive radiography (EDX) was also used to identify calcium in the abnormal deposits.
Using the same sample as for FE-SEM analyses, FT-IR and Raman spectroscopies identified the chemical compositions of the CUA calcifications. All the FT-IR hyperspectral images were recorded with a Spectrum Spotlight 400 FT-IR imaging system (Perkin–Elmer Life Sciences), with 6.25-mm spatial resolution and 8-cm–1 spectral resolution.16 Raman spectra were collected with a micro-Raman system (LabRam HR-800 Evolution) using 785-nm laser excitation wavelength, 100 × objective (Olympus, numerical aperture, 0.9) and 300 grooves per millimeter grating. Spectra were corrected at baseline to suppress the strong luminescence background.17
Data are expressed as median (range) or number (%). Fisher exact or χ2 tests were used to compare qualitative variables; Wilcoxon rank sum or Mann-Whitney tests were used to compare paired variables; and Mann-Whitney tests were used to compare nonpaired or non–normally distributed variables. Parameters with P < .20 in univariate analysis were entered into a multivariate logistic-regression model, with Y as the dependent variable. Two-tailed P <.05 was considered statistically significant Analyses were performed with JMP version 13 (SAS Institute. Inc).
Among the 36 patients with CUA, median (range) age was 64 (33-89) years and 26 (72%) were female. No data on race/ethnicity were collected. Twenty-nine skin biopsies could be analyzed by optical microscopy, FE-SEM, and spectroscopies. Clinical and histopathologic data are summarized in the Table.
Optical microscopy analysis of hematoxylin-eosin-saffron– and von Kossa–stained CUA biopsy specimens always found calcifications in small and medium-sized vessels (diameter, 10-300 μm), mostly in hypodermal arterioles and capillaries (Figure 1). These deposits occupied the entire circumference of the vessel and were located in the intima and sometimes the media. They could be associated with intimal fibrous or myxoid changes.
Those CUA vascular calcifications were associated with interstitial deposits, mainly localized to the hypodermis, in 22 (76%) of the samples. Calcification size ranged from 1 to 500 μm, sometimes becoming confluent, with clusters reaching several millimeters in diameter. They were either isolated, small clusters between adipocytes (Figure 2A and B) or aligned in a “pearl collar” along the cytoplasmic membranes of adipocytes (Figure 2D and E). Calcified elastic fibers, collagen fibers, or both were also seen in hypodermic septa or deep dermis. Thromboses were seen in 5 samples (17%), most often in noncalcified capillaries in the superficial dermis.
The 5 arteriolosclerosis-control biopsy specimens showed classic intimal fibrous endarteritis and Mönckeberg medial calcinosis associated with calcium deposits that were localized within the media along the internal elastic lamina. Those calcifications were never circumferential and no interstitial localization was observed. Negative margins of resected carcinomas contained no vascular or interstitial calcium deposits.
Twelve patients (33%) died of CUA. Poorer CUA prognosis was only associated with male sex (10 patients; P = .02) or nodular lesions (9 patients; P = .04) (eTable in the Supplement).
Subcellular calcification localization and morphologic features were assessed with FE-SEM. Vascular deposits of CUA were circumferential (Figure 1F and-Figure2C); at least 1 thrombosis in 5 of the 29 samples was located in the vessel lumen or intima, whereas the media usually appeared normal with rare calcifications. Interstitial deposits surrounded adipocytes, along the cell membranes. Morphologically, these calcifications appeared to be composed of aggregated micrometric plates (Figure 2F).
Field-emission–scanning electron microscopy analyses of control skin biopsies showing arteriolosclerosis contained vascular calcifications in the media (Figure 1C), associated with medial hypertrophy and intimal fibrosis; no interstitial deposits were seen. Field-emission–scanning electron microscopy analyses of negative resected carcinoma margins confirmed the absence of vascular and interstitial deposits.
Energy-dispersive radiograph analyses of CUA samples verified the calcium and phosphate composition of vascular and interstitial deposits, with similar calcium to phosphate ratios in both sites. Energy-dispersive radiograph analyses showed the composition of vascular deposits in control arteriolosclerosis biopsies to be similar to that found in CUA.
μ Fourier transform infrared (FT-IR) analyses of CUA and arteriolosclerosis skin calcifications showed that all were composed of calcium–phosphate apatite (Figure 3). Careful examination of 3 CUA samples identified the presence of amorphous carbonated calcium–phosphate associated with calcium–phosphate apatite that was not seen in any samples from patients with arteriolosclerosis.
Raman spectroscopy confirmed the similar calcium–phosphate-apatite compositions of vascular and interstitial calcifications (Figure 4).17
These FE-SEM, EDX, and spectroscopic analyses were able to finally specify the localization and the complete chemical composition of skin calcifications in patients with CUA. Our spectroscopic analyses demonstrated that those circumferential calcifications, located in the intima and media of skin vessels in patients with CUA, were composed exclusively of calcium–phosphate apatite. In 22 (76%) of these samples, calcium–phosphate apatite was also found in interstitial tissue of the deep dermis and hypodermis, along the cytoplasmic membranes of adipocytes, and elastic and collagen fibers.
The chemical composition and localization of cutaneous CUA calcifications have been investigated in only a few small series. Using EDX and FE-SEM, Kramann et al18 found calcium/phosphate accumulations, with a molar ratio matching that of hydroxyapatite, in the hypodermis of 7 patients with CUA. Two other studies used mass spectrometry and Raman spectroscopy to detect and characterize CUA skin calcifications. Using mass spectrometry, Amuluru et al19 showed that tissue samples from 12 CUA patients had high iron and aluminum contents, suggesting a role of metal deposition in CUA pathogenesis. Using microcomputed-tomography and Raman spectroscopy, Lloyd et al20 confirmed the presence carbonated apatite in debrided CUA tissues from 6 patients. However, those studies included small numbers of samples and performed only chemical analyses. To the best of our knowledge, the precise localization and exact morphologic features of these abnormal deposits have not yet been reported.
Patients with proximal lesions, body mass index greater than 30, ulcerated lesions, and female sex were reported to have poorer prognoses.21 Our univariate and multivariate analyses did not identify those factors as having a relationship with shorter survival, and retained only male sex and nodular lesions as being significantly associated with mortality. However, the relatively small number of patients included makes those findings less relevant than risk factors identified in larger studies.
Skin deposits in patients with CUA or arteriolosclerosis were always composed of calcium–phosphate apatite, but their different localizations in the vessel walls could indicate different pathogenetic mechanisms. Indeed, arteriolosclerotic vessel walls are thickened, with media hypertrophy, suggestive of slowly progressive thickening and degeneration of the arteriolar wall with secondary calcium–phosphate apatite accumulation. Circumferential CUA vascular deposits were located mostly in the intima of otherwise normal-appearing vessels, suggesting a faster and global process, with primary calcium deposition.
Ellis et al recently showed that pathognomonic cutaneous calcifications associated with CUA could also occur in viable tissue from patients with ESRD who did not have CUA, amputated because of peripheral arterial disease.22,23 However, Ellis et al did not consider that some of their controls might have had undiagnosed acral calciphylaxis and undergone amputations for distal ischemia. Those possibilities might explain some of their histopathologic observations of calciphylaxis in their controls. Our histologic findings (circumferential calcifications of small to medium-sized vessels often associated with interstitial calcifications) and high-technology tools, such as FE-SEM, enabled us to demonstrate several differences between the vascular calcifications seen in CUA and arteriolosclerosis, thereby confirming our previous results and those of Chen et al.6,24
Patients with calciphylaxis probably develop skin calcifications subsequent to a disequilibrium between calcification promoters and inhibitors. Calcium-inhibitor deficiency, such as matrix Gla protein, impaired inhibition of calcium–phosphate precipitation, thereby leading to skin calcifications.21
Chronic inflammatory states, including ESRD, are associated with increased levels of reactive oxygen species that impair endothelial function.25 ESRD-related endothelial dysfunction engenders vessel-wall abnormalities, including the presence of bone morphogenetic protein in medial and intimal layers.26 Such vascular protein modification, associated with increased calcium × phosphate products, might explain the intimal and medial calcifications observed in CUA.
Interstitial calcifications were also seen in 22 (76%) of CUA samples. Voluminous calcifications of the subcutaneous tissue or dystrophic and metastatic calcinosis cutis are known to occur in a variety of disorders, including dermatomyositis, lupus, or trauma. The ectopic calcified masses, composed of hydroxyapatite and amorphous calcium–phosphate apatite, were disseminated throughout the dermis and hypodermis that appeared petrified, involving interstitial tissue and vessels.27 The pathophysiologic development is still unclear but it has been hypothesized that hypodermal inflammation might release the phosphate bound to denatured proteins and serve as a niche for ectopic calcifications.27 However, despite clinical and pathologic differences, the physiology of these calcifying disorders might be similar, and calcium deposits obstructing some hypodermis vessels in CUA might lead to detrimental adipocyte, collagen and elastic fiber alterations, and the release of the phosphate bound to denatured proteins and ectopic interstitial calcifications. According to that hypothesis, interstitial calcifications might be a secondary phenomenon, thereby explaining the inconstant interstitial localization. The constant presence of vascular deposits could suggest a primary vascular trigger of CUA.
Our finding that CUA vascular calcifications were always circumferential suggests that therapeutic strategies with vasodilators might be less relevant than those using calcium-solubilizing drugs. Therefore, drugs that act on calcium–phosphate precipitation, such as sodium thiosulfate, bisphosphonates, and vitamin K supplements, would seem to be more appropriate and a rational approach for future therapeutic studies on CUA.27,28 Along the same line, Dedinszki et al,29 who studied other calcifying disorders, including pseudoxanthoma elasticum and generalized arterial calcifications of infancy, reported that oral pyrophosphate inhibited tissue calcifications.30
Because our study was retrospective, some information, including vital status, was missing for some patients. Our failure to identify factors associated with greater mortality in larger studies might be explained by the relatively small size of our series. It is worth highlighting that morphologic features of calcification can be modified by sectioning paraffin-embedded skin biopsy specimens and that the appearance of these deposits may differ between glass and low-e slides, making it more difficult to discern the association between optical microscopy and electronic microscopy.
Our histologic, FE-SEM, EDX, and spectroscopy results provide a better understanding of the morphologic, ultrastructural, and chemical characteristics of skin calcium–phosphate-apatite deposits in patients with CUA. Those deposits appear to be initially vascular and develop rapidly in normal vessel walls. Circumferential vascular and interstitial deposits, albeit inconstant, were specific to CUA. Although the chemical compositions of the calcifications were similar in CUA and arteriolosclerosis, the vessels’ appearances and deposit localizations differed, suggesting different pathogenetic mechanisms.
Accepted for Publication: February 15, 2019.
Corresponding Author: Hester Colboc, APHP, Service Plaies et Cicatrisation, Hôpital Rothschild, 5, Rue Santerre, 75012 Paris, France (firstname.lastname@example.org).
Published Online: May 22, 2019. doi:10.1001/jamadermatol.2019.0381
Author Contributions: Dr Colboc had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Drs Moguelet and Bazin are co–second authors.
Concept and design: Colboc, Moguelet, Bazin, Frochot, Letavernier, Senet.
Acquisition, analysis, or interpretation of data: All authors.
Drafting of the manuscript: Colboc, Bazin, Dillies, Frochot, Senet.
Critical revision of the manuscript for important intellectual content: Colboc, Moguelet, Bazin, Carvalho, Chaby, Maillard, Diane, Goujon, Jurus, Panaye, Frochot, Letavernier, Daudon, Lucas, Weil, Courville, Monfort, Chasset, Senet.
Statistical analysis: Chasset.
Obtained funding: Bazin, Dillies, Chaby, Frochot, Courville.
Administrative, technical, or material support: Colboc, Moguelet, Bazin, Carvalho, Maillard, Jurus, Frochot, Weil, Monfort, Senet.
Supervision: Colboc, Moguelet, Bazin, Frochot, Letavernier, Daudon, Lucas, Monfort, Senet.
Conflict of Interest Disclosures: Dr. Senet reported receiving personal fees from URGO, personal fees from SERVIER, and personal fees from SIGVARIS outside the submitted work. No other disclosures were reported.
Group Information: The Groupe Angio-Dermatologie of the French Society of Dermatology members are Stéphane Barete, MD (Service de Dermatologie, Hôpital Pitié-Salpêtrière, Paris); Nathalie Baudot, MD (Service de Dermatologie, Hôpital Tenon, Paris, France); Nathalie Beneton, MD (Service de Dermatologie, Centre Hospitalier du Mans, Le Mans, France); Maud Bezier, MD (Service de Dermatologie, Hôpital Saint-Louis, Paris, France); Paul Bilan, MD (Service de Dermatologie, Hôpital Robert Ballanger, Aulnay-sous-Bois, France); Sophie Blaise, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Grenoble, France); Thierry Boye, MD (Service de Dermatologie, Hôpital d'Instruction des Armées, Toulon, France); Priscille Carvalho, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Rouen, France); Michel Colomb, MD (Service de Dermatologie, Polyclinique Reims, Bezannes, France); Patrick Combemale, MD (Service de Dermatologie, Centre Léon Berard, Lyon, France); Jean-François Cuny, MD (Service de Dermatologie, Centre Hospitalier Régional, Metz, France); Olivier Dereure, MD, PhD (Service de Dermatologie, Centre Hospitalo-Universitaire, Montpellier, France); Anne-Sophie Dillies, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Amiens, France); Anne Dopmartin, MD, PhD (Service de Dermatologie, Centre Hospitalo-Universitaire, Caen, France); Brigitte Faivre, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Besançon, France); Juliette Fontaine, MD (Service Plaies et Cicatrisation, Hôpital Rothschild, Paris, France); Camille Frances, MD, PhD (Service de Dermatologie, Hôpital Tenon, Paris, France); Elisa Goujon, MD (Service de Dermatologie, Centre Hospitalier, Chalon-Sur-Saône, France); Bernard Guillot, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Montpellier, France); Romain Jacquet, MD (Médecine Vasculaire, Private Practice, Reims, France); Julie Journet, MD (Service de Dermatologie, Centre Hospitalier, Chalon-Sur-Saône, France); Diane Kottler, MD (Service de Dermatologie, Hôpital Bichat, Paris, France); Isabelle Lazareth, MD (Service de Médecine Vasculaire, Hôpital Saint-Joseph, Paris, France); Marie-Thérèse Leccia, MD, PhD (Service de Dermatologie, Centre Hospitalo-Universitaire, Grenoble, France); Véronique LeCerf, MD (Dermatologie, Private Practice, Paris, France); Anne-Laure Liegon, MD (Service de Dermatologie, Centre Hospitalier, Valence, France); Catherine Lok, MD, PhD (Service de Dermatologie, Centre Hospitalo-Universitaire, Amiens, France); Emmanuel Mahe, MD (Service de Dermatologie, Centre Hospitalier Régional, Argenteuil, France); Hervé Maillard, MD (Service de Dermatologie, Centre Hospitalier du Mans, Le Mans, France); Jacques Martel, MD (Dermatologie, Private practice, Cenon, France); Sylvie Meaume, MD (Service Plaies et Cicatrisation, Hôpital Rothschild, Paris, France); Philippe Modiano, MD, PhD (Service de Dermatologie, Hôpital Saint Vincent de Paul, Lille, France); Jean-Benoît Monfort, MD (Service de Dermatologie, Hôpital Tenon, Paris, France); Christine Moulinier, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Amiens, France); Géraldine Perceau, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Reims, France); Bruno Sassolas, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Brest, France); Amélie Schoeffler, MD (Service de Dermatologie, Centre Hospitalier Régional, Metz, France); Magali Segard, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Lille, France); Jean-Luc Schmutz, MD, PhD (Service de Dermatologie, Centre Hospitalo-Universitaire, Nancy, France); Patricia Senet, MD (Service de Dermatologie, Hôpital Tenon, Paris, France); Emilie Tella, MD (Service de Dermatologie, Centre Hospitalier Régional, Argenteuil, France); Pascal Toussaint, MD (Service de Dermatologie, Maison de Santé Protestante de Bordeaux-Bagatelle, Talence, France); François Truchetet, MD (Service de Dermatologie, Centre Hospitalier Régional, Metz, France); Loïc Vaillant, MD, PhD (Service de Dermatologie, Centre Hospitalo-Universitaire, Tours, France); and Béatrice Villemur, MD (Service de Dermatologie, Centre Hospitalo-Universitaire, Grenoble, France).
Additional Contributions: We thank LabEx MICHEM (ANR-11-IDEX-0004-02) for allowing us to use their nano/micro-Raman facilities in UPMC. We thank Quentin Rezard, MS, from CNRS, LPC, Ba340, Université Paris XI, and Chantal Jouanneau, MS, from INSERM, Hôpital Tenon, for their help and support in this study. They were not compensated for their contributions.
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