Literature DB >> 36012900

Dermoscopic Features of Different Forms of Cutaneous Mastocytosis: A Systematic Review.

Martyna Sławińska1, Agnieszka Kaszuba1, Magdalena Lange1, Roman J Nowicki1, Michał Sobjanek1, Enzo Errichetti2.   

Abstract

The term mastocytosis refers to a heterogeneous group of disorders characterised by accumulation of clonal mast cells in different organs, most commonly in the skin. Little is known about the role of dermoscopy in the diagnostics of mastocytosis. To date, no systematic review on the dermoscopic features of cutaneous mastocytosis has been performed. The aim of this study was to summarise the current knowledge in the field as well as to identify the knowledge gaps to show possible directions for further studies, based on a systematic search of PubMed, Scopus, and Web of Science databases and related references published before 3 January 2022. Dermoscopic features, type of dermoscope, polarisation mode, magnification, and number of cases were analysed. In total, 16 articles were included in this review (3 case series and 13 case reports), analysing 148 patients with different variants of cutaneous mastocytosis; all of the studies analysed had a low level of evidence (V). The main dermoscopic features of urticaria pigmentosa included brown structureless areas, brown lines arranged in a network, and linear vessels distributed in a reticular pattern, with this last finding also being typical of telangiectasia macularis eruptiva perstans. The presence of either circumscribed yellow structureless areas or diffuse yellowish background was a constant pattern of mastocytoma, while nodular, pseudoangiomatous xanthelasmoid, and plaque-type mastocytosis were typified by light-brown structureless areas and/or pigment network, though the first two variants also showed yellow/yellow-orange structureless areas. Finally, pigmented streaks of radial distribution surrounding hair follicles were described to be a pathognomonic dermoscopic feature of pseudoxanthomatous mastocytosis. Although this review shows that the various clinical forms of cutaneous mastocytosis may feature diagnostic dermoscopic clues, it also underlines the need for further investigation as several relevant data are missing, including evaluation of dermoscopic pattern according to anatomical locations or "lesion age", studies on rare mastocytosis variants, evaluation of the prognostic role of dermoscopy in the context of systemic involvement, and comparative analyses with common clinical mimickers.

Entities:  

Keywords:  dermatoscopy; dermoscopy; mastocytosis; review; trichoscopy

Year:  2022        PMID: 36012900      PMCID: PMC9410418          DOI: 10.3390/jcm11164649

Source DB:  PubMed          Journal:  J Clin Med        ISSN: 2077-0383            Impact factor:   4.964


1. Introduction

The term mastocytosis refers to a heterogeneous group of disorders characterised by accumulation of clonal mast cells in different organs, most commonly in the skin, bone marrow, liver, spleen, and lymph nodes. Cutaneous involvement may be either the only manifestation of the disease (Cutaneous Mastocytosis, CM) or it may be associated with systemic disease (Systemic Mastocytosis, SM) [1,2,3]. In contrast to adults, CM predominates in children [4]. According to the current World Health Organization (WHO) classification, CM is divided into three forms: maculopapular cutaneous mastocytosis (MPCM) (including clinical subtypes previously known as urticaria pigmentosa [UP] and telangiectasia macularis eruptiva perstans [TMEP]), diffuse cutaneous mastocytosis (DCM), and mastocytoma of the skin [5]. Other clinical variants of CM have been described, e.g., nodular mastocytosis, plaque-type mastocytosis, pseudoangiomatous xanthelasmoid mastocytosis, and pseudoxanthomatous localised mastocytosis, though they are no longer recognised as separate entities but as clinical subtypes of either MPCM or mastocytoma based on the number of the lesions (>5 MPCM and ≤5 mastocytoma) [2,6,7,8,9,10,11,12,13]. The diagnosis of cutaneous mastocytosis is generally based on clinical assessment (presentation of cutaneous lesions, positive Darier’s sign, and symptoms arising from mediator release) in association with additional investigations, such as histopathological, immunohistochemical, and sometimes genetic assessment. Main differential diagnoses of CM include urticaria, juvenile xanthogranuloma, arthropod bites, bullous impetigo, autoimmune bullous skin disorders, epidermolysis bullosa, staphylococcal scalded skin syndrome, and café-au-lait macules (Supplementary Table S1) [14,15]. Dermoscopy is a supportive tool in the diagnosis of different cutaneous disorders [16]. In recent years, new papers describing the dermoscopic features of mastocytosis have been published. The aim of this study was to summarise current data on the diagnostic utility of (video) dermoscopy of skin involvement in patients with mastocytosis.

2. Materials and Methods

A comprehensive search of the literature using the PubMed, Scopus, and Web of Science electronic databases using the keywords ‘dermoscopy’ OR ‘dermatoscopy’ OR ‘trichoscopy’ OR ‘videodermoscopy’ OR ‘videodermatoscopy’ in combination with ‘mastocytosis’ OR ‘urticaria pigmentosa’ OR ‘mastocytoma’ OR ‘teleangiectasia macularis eruptiva perstans’ was performed by two investigators (M. Sławińska., A. Kaszuba) over a time period from inception to 2 January 2022. After the initial search was performed, two reviewers independently screened titles and abstracts for inclusion and exclusion criteria. In doubtful cases, decision on inclusion was based on the opinion of the third investigator (M. So). Based on title and abstract analysis, researchers selected the articles concerning dermosopic features of mastocytosis. At this step, we excluded records not related to the topic, non-English language manuscripts, review articles, and duplicates. In the relevant articles assessed full-text, references were searched for additional records. Finally, articles not containing quantitative data on dermoscopic observations were excluded. In addition to dermoscopic features, type of dermoscope, polarisation mode, magnification, and number of cases were analysed and summarised. The Oxford 2011 Levels of Evidence was used to classify the level of evidence of each article [17]. As the analysed papers concerned diagnostic studies single case reports were labelled as level of evidence V. Additionally, corresponding terminology based on the International Dermoscopy Society consensus paper has been added [18].

3. Results

Of the 245 records found initially in PubMed, Scopus, and Web of Science databases, a total of 17 articles were assessed full-text after title and abstract screening. Of these 17 articles, one was excluded as it did not meet the inclusion criteria, and none were included after reference screening. Thus, in total, 16 articles were included in this review (3 case series and 13 case reports), analysing 148 patients with different CM variants. The flow chart reporting the study selection process is presented in Figure 1.
Figure 1

PRISMA flow diagram demonstrating the selection process for study inclusion in the systematic review.

The type of dermoscope used in the study was mentioned in seven records, magnification in eight (seven used ×10 magnification and one ×50 and ×200 magnification), polarisation was mentioned in five records (polarised light was applied in all of them), and information concerning the use or not of an immersion interface was not provided in any of the analysed studies. Table 1 presents the details of the analysed studies.
Table 1

The summary of the dermoscopic features for different forms of cutaneous mastocytosis.

Clinical Manifestation of CMFirst Author, Journal, YearDermoscopic Features per Diagnosis (Number/%) Corresponding Terminology Based on International Dermoscopy Society Consensus DocumentDermoscopic-Histopathological Correlation Discussed in the ArticleType of Dermoscope/MagnificationPolarisation/ImmersionStudy DesignNumber of Cases of Specific Mastocytosis SubtypeLevel of EvidenceAspects Important for Clinical Practice
Maculopapular CM (MPCM) urticaria pigmentosa clinical subtype Akay, Dermatology,2008 [10]brown reticular linesbrown lines arranged in a network-like structurebasal hyperpigmentation and increase in mast cells in the dermisDermLite II Pro HR 3Gen/NRNR/NRcase series3Vbrown reticular lines seen on dermoscopy may be present also in melanocytic lesion, dermatofibroma, solar lentigo, ink-spot lentigo, seborrheic keratosis, accessory nipple
Vano-Galvan,Arch Dermatol, 2011 [9]light-brown blot (43/90;47.8%);pigment network (36/90; 40.0%);vascular pattern (11/90; 12.2%)brown structureless areas;brown lines arranged in a network-like structure;linear vessels arranged in a reticular pattern; dotted vesselshyperpigmentation of basal layer (mild and homogenous); mast cells in the dermis;hyperpigmentation of the basal layer (marked on the rete ridges); mast cells in the dermis;blood vessel dilatationDermLite 3Gen/×10NR/NRcase series90Vvascular pattern was an independent predictive factor for the need for daily anti-mediator therapy
Gutiérrez-González, Dermatol Online J, 2011[19]brown reticular linesbrown lines arranged in a network-like structureincrease in melanocytes and melanin deposits in the basal layer, mast cells in the dermisNR/NRNR/NRcase report1Vpapules dermoscopically mimicked melanocytic nevi
Miller, An Bras Dermatol, 2013[20]pigment network,light-brownish blotbrown lines arranged in a network-like structure,brown structureless areasbasal cell layer hyperpigmentation, mast cells and lymphocytes in dermisNR/×10NR/NRcase report1V
Nirmal,Indian Dermatol Online J, 2019[21]brown reticular linesbrown lines arranged in a network-like structure basal cell layer hyperpigmentation;mast cells in dermisDermLite DL3,3Gen/×10polarised/NRcase series2Vbrownish lines seen on dermoscopy were darker in case of mastocytosis with positive Darier sign
Chauhan,Indian Dermatol Online J, 2020[22]brown reticular lines,reddish backgroundbrown lines arranged in a network-like structure-basal cell layer hyperpigmentation, mild epidermal spongiosis, increase in mast cells and lymphocytes in dermisDermLite II hybrid m; 3Gen/×10polarised/NRcase report1Vreddish background was suggested by the authors as a feature helpful in differentiation between mastocytosis and melanocytic nevi
Amorim,Int J Dermatol,2021[23]reticular lines (pigmented network)brown lines arranged in a network-like structuremastocytes on superficial dermisNR/NRNR/NRcase report1V
MPCM telangiectasia macularis eruptiva perstans clinical subtype Akay, Dermatology, 2008[10]thin reticular telangiectasias (3/3);erythematous background (2/3);brown reticular lines (1/3)linear vessels arranged in a reticular pattern-brown lines arranged in a network-like structuredilated dermal vessels; mast cells in superficial dermis;NRDermLite II Pro HR 3Gen/NRNR/NRcase series3Vreticular vascular pattern may be helpful in differentiation between TMEP and other eruptions
Vano-Galvan, Arch Dermatol,2011 [9]reticular vascular pattern (7/7; 100%)linear vessels arranged in a reticular patterndilation of the blood vesselsDermLite 3Gen/×10NR/NRcase series7V
Unterstell, An Bras Dermatol,2013[12]thin and tortuous linear vessels,mild erythema,fine pigment networklinear-curved vessels-brown lines arranged in a network-like structuredilatation and vascular proliferation associated with the presence of mast cells in the dermis,NRNR/NRNR/NRcase report1V
Kumar, Indian Dermatol Online J, 2019[11]reticular vascular pattern of linear and branching vessels,brownish backgroundlinear vessels and linear vessels with branches in a reticular distribution,brown structureless areasdilated superficial capillaries surrounded by mast cells in the papillary dermis;NRDino Lite AM413ZT Digital Microscope/×50polarised/NRcase report1Vat higher magnification (200×), branching vessels encircled the eccrine glands (visible as white dots)
MPCM telangiectasia macularis eruptiva perstans clinical subtype—limited to acral areas Sammut, Int J Dermatol,2019[8]reticular vascular patternlinear vessels arranged in a reticular patternprominent ectatic blood vessels in the upper and mid dermisNR/NRNR/NRcase report1V
Mastocytoma Vano-Galvan, Arch Dermatol,2011[9]yellow-orange blot (11/11; 100%)yellow-orange structureless areasdense infiltration ofmast cells along the papillary and reticular dermisDermLite 3Gen/×10NR/NRcase series11Vin differential diagnosis of lesions presenting with yellow-orange structureless pattern on dermoscopy consider: juvenile/adult xanthogranuloma, sebaceous hyperplasia, reticulohistiocytoma, xanthomatous dermatofibroma
Adya,Indian Dermatol Online J, 2018[24]central white structureless area,yellow background,peripheral brown reticular linescentral white structureless area,diffuse yellow structureless area,brown lines arranged in a network-like structureaccumulation of serosanguineous fluid produced due to excoriation of the epidermis in the centre of the lesion,diffuse mononuclear cell infiltrate involving the dermis extending into and expanding the dermal papillae,increased melanisation of the basal layerDermLite DL3/×10polarised/NRcase report1Vdermoscopy is helpful in differentiation with juvenile xanthogranuloma
Gündüz, Dermatol Pract Concept,2019 [25]central vascular structures *peripheral yellow structureless area-peripheral yellow structureless areacentral vascular structure might reflect the detachment of epidermis due to the bullous reaction,dense mast cell infiltration in dermisNR/×10NR/NRcase report1V
Kumar, BMJ Case Reports, 2020[26]central whitish area, reticulate light brown rim,yellowish backgroundcentral white structureless area,brown lines arranged in a network-like structure,diffuse yellow structureless areaNR,basal layer melanisation,diffuse infiltration of the superficial epidermis by mastocytesNR/NRNR/NRcase report1V
Mukherje, Dermatol Pract Concept, 2021[27]pigment network,yellow backgroundbrown lines arranged in a network-like structure,diffuse yellow structureless areabasal layer hyperpigmentation, mast cells in dermisDermLite DL4/×10polarised/NRcase report1Vprovocation of Darier sign on dermoscopy shows decrease in yellow colour and pigment network intensity with appearance of peripheral erythema
Other clinical forms Plaque-type mastocytosis Vano-Galvan, Arch Dermatol,2011[9]light-brown blot (5/8; 62.5%);pigment network (3/18; 37.5%)brown structureless areas;brown lines arranged in a network-like structurehyperpigmentation of basal layer (mild and homogenous), mast cells in the dermis;hyperpigmentation of the basal layer (marked on the rete ridges), mast cells in the dermisDermLite 3Gen/×10NR/NRcase series8V
Other clinical forms Nodular mastocytosis Vano-Galvan, Arch Dermatol, 2011[9]light-brown blot (3/11; 27.3%);pigment network (5/11; 45.5%);yellow-orange blot (6/11; 54.6%)brown structureless areas;brown lines arranged in a network-like structure;yellow-orange structureless areashyperpigmentation of basal layer (mild and homogenous), mast cells in the dermis;hyperpigmentation of the basal layer (marked on the rete ridges), mast cells in the dermis;dense infiltration of mast cells along the papillary and reticular dermisDermLite 3Gen/×10NR/NRcase series11V
Other clinical forms Pseudoangiomatous xanthelasmoid mastocytosis Salah, J Eur Acad Dermatol,2016[7]brown reticular pattern,yellow blotsbrown lines arranged in a network-like structure.yellow structureless areaspatchy basal hyperpigmentation,mast cells in dermisNR/NRNR/NRcase report1Vmain clinical differential diagnoses: xanthoma, vascular tumour/malformation, xanthogranuloma
Other clinical forms Pseudoxanthomatous localised mastocytosis Li, An Bras Dermatol, 2018[6]pigmented stripes radiating from hair follicles,pink background,linear branched vessels,reticular vesselsspecific clue,-linear vessels with branches,linear vessels arranged in a reticular patternhyperpigmentation of keratinocytes in the basal layer,dense infiltration of mast cells,NR,NRNR/NRNR/NRcase report1Vvulva may be predilection site for localised cases;clinical differential diagnoses include pseudoxanthoma elasticum, juvenile xanthogranuloma, xanthoma;pigmented lines arranged radially around hair follicles may be a specific feature

NR—not reported; *—vessel morphology not provided.

3.1. Maculopapular Cutaneous Mastocytosis (UP Clinical Subtype)

The systematic review revealed 99 cases in seven studies. Most data on dermoscopy of this mastocytosis variant came from a study by Vano-Galvan et al. [9], who analysed 90 patients with MPCM. The most prevalent dermoscopic findings were light-brown blots (structureless areas) (43/90; 47.8%), pigment networks (36/90; 40.0%), and vascular patterns including linear vessels in reticular distribution—described as reticular vessels—and dotted vessels (11/90; 12.2%). Interestingly, the study showed that the vascular dermoscopic pattern was an independent predictive factor for the need for daily anti-mediator therapy. The remaining data from smaller case reports/case series (six studies, nine patients) confirmed the presence of pigment network (brown reticular lines) in all cases (in two of them associated with a red or light-brown background) [9,10,19,20,21,22,23] (Figure 2).
Figure 2

(a) Maculopapular cutaneous mastocytosis (urticaria pigmentosa clinical subtype)—clinical presentation. (b–d) Dermoscopy shows brown reticular lines (pigment network)(FotoFinder, Medicam 800 HD, FotoFinder Systems GmbH, Bad Birnbach, Germany; ×20 magnification, immersion gel).

3.2. Maculopapular Cutaneous Mastocytosis (TMEP Clinical Subtype)

When it comes to TMEP, a systematic review revealed 13 cases from five studies, including one case limited only to acral areas. The three main dermoscopic patterns were reticular vascular pattern (thin reticular telangiectasias) observed in all cases, in three cases associated with an erythematous background, in two cases with pigment network (brown reticular lines), and in one with brownish background [9,10,11,12] (Figure 3).
Figure 3

(a) Maculopapular cutaneous mastocytosis (telangiectasia macularis eruptiva perstans clinical subtype)—clinical presentation. (b–d). Dermoscopy shows reticular vascular pattern (thin reticular telangiectasias) over erythematous background (FotoFinder, Medicam 800 HD, FotoFinder Systems GmbH, Bad Birnbach, Germany; ×20 magnification, immersion gel).

3.3. Mastocytoma

The systematic review revealed 15 cases from five studies. In all cases, the authors described the presence of yellow structureless areas (blot)/yellowish background. In most of them (11/13; 84.6%), it was the only observed pattern [9,24,25,26,27]. Additional structures were peripheral brown reticular lines (3/13), a central white structureless area (2/13), and vessels in a central distribution (vessel morphology was not described; 1/13) (Figure 4).
Figure 4

(a) Mastocytoma—clinical presentation. (b) Dermoscopy shows central polymorphic vessels and peripheral yellow brownish structureless area (FotoFinder, Medicam 800 HD, FotoFinder Systems GmbH, Bad Birnbach, Germany; ×20 magnification, immersion gel). (c) Mastocytoma—clinical presentation. (d) Dermoscopy shows yellow structureless pattern (FotoFinder, Medicam 800 HD, FotoFinder Systems GmbH, Bad Birnbach, Germany; ×20 magnification, immersion gel).

3.4. Other Clinical Forms of CM

With regard to nodular mastocytosis and plaque-type mastocytosis, Vano-Galvan et al. [9] in their study analysed eleven and eight instances of the former and latter variant, respectively. In detail, the main dermoscopic features of nodular mastocytosis were yellow-orange structureless areas (6/11; 54.6%), pigment networks (5/11; 45.5%), and light-brown structureless areas (3/11; 27.3%), while plaque-type mastocytosis was associated with light-brown structureless areas (5/8; 62.5%) and pigment networks (3/18; 37.5%) [9] (Figure 5).
Figure 5

(a,c) Maculopapular cutaneous mastocytosis (plaque-type mastocytosis clinical subtype)—clinical presentation. (b) Dermoscopy shows reticular vascular pattern (thin reticular telangiectasias) over yellow background. (d) Dermoscopy shows yellow structureless areas (FotoFinder, Medicam 800 HD, FotoFinder Systems GmbH, Bad Birnbach, Germany; ×20 magnification, immersion gel).

Considering pseudoangiomatous xanthelasmoid mastocytosis, only one dermoscopic case of this rare entity was published revealing a pigment network (brown reticular lines) and yellow blots (structureless areas) [7]. Finally, an instance of pseudoxanthomatous localised mastocytosis involving the vulva showed pigmented streaks with radial distribution surrounding hair follicles, and this pattern was considered pathognomonic by the authors [6].

4. Discussion

The aim of this review was to summarise the current knowledge on the role of dermoscopy in diagnosis of mastocytosis. The analysis of published studies revealed that almost all data (127 out of 148 patients) came from one large case series, and the remaining were small case series/case reports. All of the analysed studies showed a low level of evidence (V). Based on this review, the main dermoscopic features of UP included brown structureless areas, brown lines arranged in a network, and linear vessels distributed in a reticular pattern. The first two findings were due to basal cell layer hyperpigmentation, a typical histological feature of this form of mastocytosis, while the vascular pattern was the result of dermal vessel dilation. This last histological finding was also responsible for the main dermoscopic feature of TMEP—the so-called “vascular reticular pattern” (thin reticular telangiectasias). By contrast, the presence of either circumscribed yellow structureless areas or diffuse yellowish background was a repetitive dermoscopic pattern of mastocytoma histologically resulting from a compact mast cell infiltration of the dermis. Moving to nodular, pseudoangiomatous xanthelasmoid, and plaque-type mastocytosis, all of them may be typified by light-brown structureless areas and/or pigment network as a result of basal cell layer hyperpigmentation, yet only the first two variants may also show yellow/yellow-orange structureless areas, likely due to a denser cellular infiltration. Finally, pigmented streaks of radial distribution surrounding hair follicles were described as being a pathognomonic dermoscopic feature of pseudoxanthomatous mastocytosis, though this observation needs to be confirmed in further studies as it came from a single report [28]. Importantly, most of the remaining mentioned findings were not specific to mastocytosis and thus, should be interpreted carefully along with clinical and histopathological findings. Brown lines arranged in a network should be differentiated from melanocytic lesions or dermatofibroma, while in cases of yellow-orange structureless areas, diagnosis of juvenile xanthogranuloma, xanthoma, solitary reticulohistiocytoma, sebaceous tumours, keratin accumulation or scaly disorders, elastic fibres disorders, and others should be considered [29].

5. Conclusions

Despite several articles being published on the dermoscopy of CM, there is still a need for further investigations in this regard as the current evidence was from low-quality studies. Additionally, there were various aspects that have not been investigated so far, including evaluation according to anatomical locations or “lesion age”, studies on rare mastocytosis variants, evaluation of the prognostic role of dermoscopy in the context of systemic involvement, and comparative analyses with common clinical mimickers. Based on current knowledge, it seems that dermoscopy will remain a complementary technique in mastocytosis diagnosis, as potential overlap with structures observed in other entities exists.
  41 in total

1.  Evolution of urticarial vasculitis: a clinical, dermoscopic and histopathological study.

Authors:  K S Suh; D Y Kang; K H Lee; S H Han; J B Park; S T Kim; M S Jang
Journal:  J Eur Acad Dermatol Venereol       Date:  2013-09-03       Impact factor: 6.166

2.  Pseudoangiomatous Xanthelasmoid Mastocytosis - a new histopathological entity.

Authors:  L A Salah; O Ljungberg; Å Svensson; A T Rubin
Journal:  J Eur Acad Dermatol Venereol       Date:  2016-10-28       Impact factor: 6.166

3.  Solitary Bullous Mastocytoma with Dermoscopic Features in a Neonate.

Authors:  Özge Gündüz; Dilsun Yıldırım; F Gülru Erdoğan; Başar Kaya; Handan Doğan
Journal:  Dermatol Pract Concept       Date:  2019-10-31

Review 4.  Dermoscopy in general dermatology.

Authors:  Iris Zalaudek; Giuseppe Argenziano; Alessandro Di Stefani; Gerardo Ferrara; Ashfaq A Marghoob; Rainer Hofmann-Wellenhof; H Peter Soyer; Ralph Braun; Helmut Kerl
Journal:  Dermatology       Date:  2006       Impact factor: 5.366

Review 5.  Epidemiology, prognosis, and risk factors in mastocytosis.

Authors:  Knut Brockow
Journal:  Immunol Allergy Clin North Am       Date:  2014-05       Impact factor: 3.479

6.  Dermoscopy for the screening of common urticaria and urticaria vasculitis.

Authors:  Francisco Vázquez-López; Alejandro Fueyo; Jesus Sánchez-Martín; Narciso Pérez-Oliva
Journal:  Arch Dermatol       Date:  2008-04

7.  Dermatoscopy in life-threatening and severe acute rashes.

Authors:  Enzo Errichetti; Giuseppe Stinco
Journal:  Clin Dermatol       Date:  2019-11-11       Impact factor: 3.541

8.  Dermatoscopic findings of urticaria pigmentosa.

Authors:  Marcela Duarte Benez Miller; Natália Solon Nery; Alexandre Carlos Gripp; Juan Piñeiro Maceira; Gisele Moro do Nascimento
Journal:  An Bras Dermatol       Date:  2013 Nov-Dec       Impact factor: 1.896

9.  Bullous mastocytosis mimicking congenital epidermolysis bullosa.

Authors:  Julio Cesar Salas-Alanis; Cesar Eduard Rosales-Mendoza; Jorge Ocampo-Candiani
Journal:  Case Rep Dermatol       Date:  2014-05-08

10.  Dermatoscopic findings in telangiectasia macularis eruptiva perstans.

Authors:  Natasha Unterstell; Fernanda Guedes Lavorato; Natália Solon Nery; Danielle Mann; Maria de Fátima Scotelaro Guimarães Alves; Carlos Barcauí
Journal:  An Bras Dermatol       Date:  2013 Jul-Aug       Impact factor: 1.896

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