AnBrasDermatol.2020;95(4):521---523
Anais
Brasileiros
de
Dermatologia
www.anaisdedermatologia.org.brWHAT
IS
YOUR
DIAGNOSIS?
Case
for
diagnosis.
Pruritic
erythematosquamous
lesion
in
the
auricle
夽,夽夽
Elaine
Dias
Melo
a,∗,
Patrícia
Motta
de
Morais
b,
Débora
Cristina
de
Lima
Fernandes
c,
Paula
Frassinetti
Bessa
Rebello
daTeachingandResearchDepartment,Fundac¸ãodeDermatologiaTropicaleVenereologiaAlfredodaMatta,Manaus,AM,Brazil bDepartmentofHistopathology,Fundac¸ãodeDermatologiaTropicaleVenereologiaAlfredodaMatta,Manaus,AM,Brazil cLaboratoryofMycology,Fundac¸ãodeDermatologiaTropicaleVenereologiaAlfredodaMatta,Manaus,AM,Brazil
dDepartmentofTropicalDermatology,Fundac¸ãodeDermatologiaTropicaleVenereologiaAlfredodaMatta,Manaus,AM,Brazil
Received4October2019;accepted24November2019 Availableonline11May2020
KEYWORDS
Auricle;
Chromoblastomycosis; Ear,external;
Mycosis
Abstract Chromoblastomycosisisasubcutaneousmycosiswithchronicevolutionthatmainly affectsthelowerlimbsand,lessfrequently,theauricles.Clinically,itpresentswithpapillary verrucous,nodular, and/ortumorallesions,whetherisolatedorinfiltrated, formingplaques and,sometimes, atrophicinsomeareas.Histopathologically,itischaracterizedbyadermal granulomatousinflammatoryinfiltrate, andthediagnosis canbeconfirmedby thepresence of fumagoidbodiesin anatomopathological ordirect mycological exams. The treatment to beindicatedwilldependontheextentandlocationofthelesions,usingsystemicantifungals, surgicalremoval,cryotherapy,thermotherapy,andimmunoadjuvants.Thepresentstudyreports anatypicalpresentationofchromoblastomycosisontheauricle.
©2020SociedadeBrasileira deDermatologia.PublishedbyElsevierEspa˜na,S.L.U.Thisisan openaccessarticleundertheCCBYlicense(http://creativecommons.org/licenses/by/4.0/).
Case
report
A 57-year-old male farmer presented a pruritic lesion on the left auricle, with 20 years of evolution. He did not
夽 Howtocitethisarticle: MeloED,MoraisPM,FernandesDCL, RebelloPFB.Casefordiagnosis.Pruriticerythematosquamouslesion intheear.AnBrasDermatol.2020;95:521---3.
夽夽StudyconductedattheFundac¸ãodeDermatologiaTropicale VenereologiaAlfredodaMatta,Manaus,AM,Brazil.
∗Correspondingauthor.
E-mail:[email protected](E.D.Melo).
recall local trauma at the onset of the condition. Upon examination,aninfiltrated,erythematosquamouslesionwas observed on the left ear. The histopathological examina-tionpresentedagranulomatousinflammatoryinfiltratewith suppurativefoci(Fig.1AandB).
Whatisyourdiagnosis?
1. JorgeLobo’sdisease 2. Sarcoidosis
3. Paracoccidioidomycosis 4. Chromoblastomycosis https://doi.org/10.1016/j.abd.2019.11.011
0365-0596/©2020SociedadeBrasileiradeDermatologia.PublishedbyElsevierEspa˜na,S.L.U.ThisisanopenaccessarticleundertheCC BYlicense(http://creativecommons.org/licenses/by/4.0/).
522 MeloEDetal.
Figure1 (A and B)Erythematous, infiltrativelesion inthe leftear.Histopathologicalexamination:granulomatous inflam-matoryinfiltratewith suppurativefoci (Hematoxylin&eosin, ×400).
Figure 2 (A and B) Direct examination: fumagoid bodies. Microculture:septatedemaceoushyphaeandellipticalconidia intheupperportionofsimpleorslightlybranchedconidiophores --- phenotypic characteristics compatible with Rhinocladiella
spp.(KOH-20%,×400;blue,lactophenol,×400).
Thereviewofthesectionsforhistopathological examina-tionevidencedthepresenceoffumagoidbodies,compatible withchromoblastomycosis.
In the direct examination of biopsy fragments in 20% KOH,septatedemaceoushyphaeandisolatedyeastcellsin pairswereobserved,aswellassomegemmulestructures.In culture,onMycoselagar(DIFCO®)andSabourauddextrose agar(DIFCO®)withchloramphenicol(0.05g/L),ablackened colony growth wasobserved; in microculture, phenotypic findingscompatiblewithRhinocladiellasp.wereobserved (Fig.2AandB).
R.aquaspersawasconfirmedthroughamplificationand
sequencing of the intergenic spacer (ITS) region of the
Figure3 (AandB)After25daysoftreatment,andattheend oftenweeks.
ribosomalDNA(rDNA)usingthepolymerasechainreaction (PCR)technique.
Afterconfirmation ofthediagnosisof chromoblastomy-cosis,itraconazole(300mg/day)wasinitiated;thepatient presentedsignificantimprovementafter25daysandalmost completeremissionintenweeks(Fig.3AandB).Thepatient remainsunderoutpatientfollow-up.
Discussion
Chromoblastomycosis is a subcutaneous mycosis caused by demaceous fungi of the order Chaetothyriales, family Herpotrichiellaceae, found in decomposing soil, vegeta-bles, plants,andwood.1,2 The mainetiological agentsare
fromthegeneraFonsecaea,Cladophialophora,Phialophora,
Rhinocladiella, and Exophiala. Inoculation occurs after
traumawithcontaminatedmaterial.1,3,4
Theconditionmost frequentlyaffectsmenbetween 40 and50yearsofage, beingconsidered acosmopolitan dis-ease, with greater prevalence in tropical and subtropical regions.2InBrazil,itoccursinmoststates,witha
predom-inance in the Amazon region, particularly in the state of Pará.2,5
Thediseasemainlyaffectsthelowerlimbs.Incaseswith longevolution,associationwithlymphedemaiscommon.1,4,6
InJapan,themostcommonlocationsinvolvedaretheupper limbs,face,andcervicalregion.2Reportsofmanifestations
exclusivelyontheauriclearerare.1,3,6---10 Amongthecases
reported in this topography, Fonsecaea pedrosoi1,3,10 and
Phialophoraverrucosa7werethemostcommonlyidentified
agents, followed byFonsecaea nubica6 and Rhinocladiella
aquaspersa.8
Accordingtotheliteratureconsulted,thisisthesecond casewithisolatedinvolvementoftheauriclecausedbyR. aquaspersa.
In the Amazon region, the differential diagnosis must include Jorge Lobo’s disease, leprosy, anergic leishmani-asis, cutaneous tuberculosis, and paracoccidioidomycosis. Histopathologicaland mycologicalexams areessentialfor diagnosis.
Several treatments are indicated for chromoblastomy-cosis.Forlocalizedlesions,surgical excision,cryotherapy, or thermotherapy are recommended; for more exten-sive cases, systemic and immunoadjuvant antifungals are recommended.2,4Amongsystemicantifungals,itraconazole,
Casefordiagnosis.Pruriticerythematosquamouslesionintheauricle 523 posaconazole, voriconazole, and isavuconazole are used.4
Theliteraturereportstwocasesofchromoblastomycosisin auricular locations, which presented complete regression aftertreatment withflucytosine3and itraconazole1 for 12
and10weeks,respectively.
Therearereportsofagoodtherapeuticresponsewiththe association ofsystemicantifungalsandtopical immunoad-juvants,suchasimiquimod.4
Financial
support
Nonedeclared.
Authors’
contributions
Elaine Dias Melo: Conception and planning of the study; elaborationandwritingofthemanuscript;obtaining, ana-lyzing,andinterpretingthedata;intellectualparticipation in propaedeutic and/or therapeutic conduct of studied cases;criticalreviewoftheliterature.
PatríciaMottadeMorais:Approvalofthefinalversionof the manuscript;intellectual participation in propaedeutic and/ortherapeuticconductofstudiedcases;criticalreview oftheliterature;criticalreviewofthemanuscript.
DéboraCristinadeLimaFernandes:Elaborationand writ-ingofthemanuscript;criticalreviewoftheliterature.
Paula Frassinetti Bessa Rebello: Approval of the final version of the manuscript; intellectual participation in propaedeuticand/ortherapeuticconductofstudiedcases.
Conflicts
of
interest
Nonedeclared.
Acknowledgements
Thanks toprofessorAntônio Pedro Mendes Schettini, der-matopathologist, head of the histopathology laboratory
at the Fundac¸ão deDermatologia Tropicale Venereologia AlfredodaMatta;Dr.SinésioTalhari,dermatologist atthe Fundac¸ãodeDermatologia TropicaleVenereologiaAlfredo daMatta;andDr.MariaZeliMoreiraFrota,biochemical phar-macistattheUniversidadeFederaldoAmazonas.
References
1.Estrada VFM, Paz GAV, Tolosa MR. Chromomycosis: report of a case with unusual topography. Rev Iberoam Micol. 2011;28:50---2.
2.BritoAC,BittencourtMJS.Chromoblastomycosis:anetiological, epidemiological,clinical,diagnostic,andtreatmentupdate.An BrasDermatol.2018;93:495---506.
3.IwatsuT,TakanoM,OkamotoS.Auricularchromomycosis.Arch Dermatol.1983;119:88---9.
4.Queiroz-TellesF,deHoogS,SantosDW,SalgadoCG,Vicente VA,BonifazA,etal.Chromoblastomycosis.ClinMicrobiolRer. 2017;30:233---76.
5.TalhariS,CunhaMG,SchettiniAP,TalhariAC.Deepmycosesin Amazonregion.IntJDermatol.1988;27:481---4.
6.ChenY, Yin S, Li M, ChenR, WeiL, Ma H, et al.A caseof chromoblastomycosisbyFonsecaeanubicaindicatingapossible insectrouteoftransmission.Mycoses.2016;59:662---7.
7.BittencourtAL,LonderoAT,AndradeJA.Auricular chromoblas-tomycosis. A case report. Rev Inst Med Trop São Paulo. 1994;36:381---3.
8.ArangoM,JaramilloC,Cortés A,RestrepoA. Auricular chro-moblastomycosis caused by Rhinocladiella aquaspersa. Med Mycol.1998;36:43---5.
9.MinottoR,BernardiCD,MallmannLF,EdelweissMI,Scroferneker ML.Chromoblastomycosis:areviewof100casesinthestateof RioGrandedoSul,Brazil.JAmAcadDermatol.2001;44:585---92.
10.Franc¸a K, Villa RT, Bastos VR, Almeida AC, Massucatti K, Fukumaru D, et al. Auricular chromoblastomycosis: a case report and review of published literature. Mycopathologia. 2011;172:69---72.