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Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

An. Bras. Dermatol. vol.86 no.4 supl.1 Rio de Janeiro July/Aug. 2011

http://dx.doi.org/10.1590/S0365-05962011000700007 

CASE REPORT

 

Use of dermoscopy for diagnosis of exogenous ochronosis*

 

 

Sandra Adolfina Reyes RomeroI; Priscilla Maria Rodrigues PereiraII; Adriana Valkiria de Oliveira MarianoI; Fábio FrancesconiIII; Valeska Albuquerque FrancesconiIV

IGraduation- Dermatology resident at the Getúlio Vargas University Hospital - The Federal University of Amazonas (HUGV/UFAM) - Manaus (AM), Brazil
IIGetúlio Vargas University Hospital - The Federal University of Amazonas (HUGV/UFAM) - Manaus (AM), Brazil
IIIMaster's degree - Professor at the Getúlio Vargas University Hospital - The Federal University of Amazonas (HUGV/UFAM) - Manaus (AM), Brazil
IVMaster's degree - Professor at the State of Amazonas University (UEA) - Manaus (AM), Brazil

Mailing address

 

 


ABSTRACT

Exogenous ochronosis consists of chronic hyperpigmentation of areas previously treated with topical agents such as hydroquinone, resorcinol, antimalarials and phenol. Early diagnosis allows to promptly suspend the causative agent and it is imperative since the available therapeutic options are scarce and have presented so far unsatisfactory results. Three cases of exogenous ochronosis on the face which were diagnosed with the use of dermoscopy are presented. Dermatoscopy showed blackish-gray amorphous structures, some obliterating the follicular openings. Histopathological examination confirmed the diagnosis.

Keywords: Dermoscopy; Ochronosis; Pigmentation disorders


 

 

INTRODUCTION

Exogenous ochronosis (EO), first described in selves in shapes that vary from macules to papular1906 by Pick1, is a pigmentary disorder characterized nodular lesions. 3 Dogliotti classified EO lesions by the deposit of a substance derived from polymer-according to the elementary lesion: stage I when there ized homogentisic acid in the dermis. Inhibition of the is erythema and mild hyperpigmentation; stage II enzime homogentisic-oxidase by certain substances when there is progression of hyperpigmentation, such as hydroquinone, would result in accumulation appearance of caviar-like papules and skin atrophy, of acid homogentisic that when polymerized gener-and stage III with appearance of papulonodular ates accumulation of ocher pigment in the papillary lesions with or without inflammatory process. 4 The dermis.2 The disease manifests itself through hyper-main risk factors for the development of EO are: prepigmentation in sun-exposed areas which had been vious and prolonged use of topical agents like hydropreviously treated with topical agents, showing a quinone, antimalarials, resorcinol, phenol and brownish or black-bluish color and presenting them-patients with a high phototype in Fitzpatrick scale.

 

CASE REPORTS

Three cases are described with clinical, dermoscopic and histopathological diagnoses of exogenous ochronosis due to chronic use of hydroquinone. It was considered dermatoscopic findings of EO: presence of amorphous structures of gray-blaskish color some of them obliterating the follicular openings.5 The histopathological findings that confirmed the diagnosis of EO were: ocher fibers "banana"shaped, incontinentia pigmenti and solar elastosis 6 (Figure 1).

 

 

Case 1: Thirty-eight year-old female patient, phototype V in Fitzpatrick scale who had been continously using for five years formulation containing hydroquinone 4%, tretinoin 0,05% and dexamethasone 0,05%, for treatment of melasma on the zygomatic and malar regions. It evolved with the presence of bilateral grayish hyperchromic papules on the malar region, and it received clinical, histopathological and dermoscopic diagnosis of EO, classified as Dogliotti stage 2 (Figure 2).

 

 

Case 2: Fifty-seven year-old female patient, phototype IV in Fitzpatrick scale who had been using for four years cream containing hydroquinone 2%, for treatment of melasma on the malar, temporal and zygomatic regions that evolved with the presence of grayish-blue hyperchromic papules with a mottle aspect located mainly bilaterally on the malar region. Roundish hyperchromic macules and some erythematous papules were also present in the same area. It was clinically diagnosed as leukoderma in confetti and EO.This was confirmed by dermoscopy and histopathology. EO was classified as Dogliotti stage 3 (Figure 3).

 

 

Case 3: Forty-five year-old female patient, phototype III in Fitzpatrick scale who had been using for three years, irregularly, creams containing hydroquinone varying from 4% to 6% for treatment of melasma on the malar region. It evolves with hyperchromic macule of grayish-brown color and formation of hyperchromic macules of dark-brown color bilaterally on the malar. The patient received the clinical, dermoscopic and histological diagnosis of EO, classified as Dogliotti stage 1(Ficture 4)

 

 

None of the patients had symptoms or clinical signs of EO such as: dark urine, sclera and axillae pigmentation or articular changes. 7

 

DISCUSSION

Exogenous ochronosis affects mainly patients with high phototype (IV, V and VI) in Fitzpatrick scale, after chronic use (period exceeding six months) of certain topical agents such as antimalarias, mercury, quinine, resorcinol, phenol and hydroquinone, specially if used in high concentrations and without supervision of a doctor. 8 Other complications resulting from the chronic use of hydroquinone include depigmentation in cofeti, change in skin elasticity and delayed healing. 9

In the reported cases all used hydroquinone, with average treatment time of four years (3 to 5 years) and average concentration of 4% (6% to 2%). Some reports describe cases of EO with use of concentrations of hydroquinone 2%, suggesting that in some patients the concentration of the substance is not the most important risk factor.10,11 The high prevalence of pigmentary disorders in patients with high phtotype in Fitzpatrick scale would be one of the factors for a greater number of described cases in this population. However, there are reports in patients who are Asian and Caucasian descendants.12

The clinical diagnosis of EO can be challenging mainly when it occurs concomitantly with other pigmentary disorder implying the need for diagnostic confirmation. Histopathology when demonstrated the presence of ocher color "banana" shaped fibers still is the gold standard for the diagnosis of such dermatosis.6 Melasma was present in all reported cases and the appearance of EO occured during the clinical evolution of the disease. The change in the clinical pattern perceived by the patients made them sought for a new dermatological consultation.

Dermatoscopy has proved to be an useful tool for a noninvasive diagnosis of many pathologies, among them EO.5 Our demoscopic analysis made it possible to distinguish the melasma area from the EO area. We observed in EO blackish-gray amorphous structures, some obliterating the follicular openings. On the other hand, in the melasma area it is possible to observe a reticular pattern of brownish color (Figure 5). These findings were similar to the ones found by Berman et al. 13

Many therapeutic options are described for the treatment of EO such as retinoic acid, glycolic acid, azelaic acid, Q-switched (755nm) laser, but all them with unsatisfactory results.10,14 As most EO cases are iatrogenic resulting from inadequate use of hydroquinone for the treatment of melasma, dermatologists should pay attention not only to prevention but also to early diagnosis of EO. As there are few reports about the use of dermoscopy to help to diagnose EO the authors present three cases where dermoscopy was efficient in the differentiation between pre-existing melasma and exogenous ochronosis.

 

REFERENCES

1. Pick L. Uber die Ochronose. Klin Wochenschr. 1906;43:478-80.         [ Links ]

2. Penneys NS. Ochronosis-like pigmentation from bleaching creams. Arch Dermatol. 1985;121:1239-40.         [ Links ]

3. Levin CY, Maibac H. Exogenous ochronosis and update on clinical features, causative agents and treatment options. Am J Clin Dermatol. 2001;2:213-7.         [ Links ]

4. Dogliotti M, Leibowitz M. Granulomatous Ochronosis a Cosmetic-Induced Skin Disorder in Blacks. S Afr Med J. 1970;9:757-60.         [ Links ]

5. Charlín R, Barcaui CB, Kac BK, Soares DB, Rabello-Fonseca R, Azulay-Abulafia L. Hydroquinone-induced exogenous ochronosis: a report of four cases and useful ness of dermoscopy. Int J Dermatol. 2008;47:19-23.         [ Links ]

6. Elder DS, Elenitsas R, Johnson Jr B, Murphy GH, Xu XW, editors. Lever's Histopathology of the skin. 10th ed. Philadelphia: Lippincott Williams & Wilkins; 2007. p.440        [ Links ]

7. Turgay E, Canat D, Gurel MS, Yuksel T, Baran MF, Demirkesen C. Endogenous ochronosis. Clin Exp Dermatol. 2009; 34:865-868        [ Links ]

8. Katsambas AD, Stratigos AJ. Depigmenting and bleaching agents: coping with hyperpigmentation. Clin Dermatol. 2001;19:483-8.         [ Links ]

9. Olumide YM, Akinkugbe AO, Altraide D, Mohammed T, Ahamefule N, Ayanlowo S, et al. Complications of chronic use of skin lightening cosmetics. Int J Dermatol. 2008;47:344-53.         [ Links ]

10. Ribas J, Schettini APM, Cavalcante MSM. Ocronose exógena induzida por hidroquinona: relato de quatro casos. An Bras Dermatol. 2010;85:699-703.         [ Links ]

11. Huerta Brogeras M, Sánchez-Viera M. Exogenous Ochronosis. J Drugs Dermatol. 2006;5:80-1        [ Links ]

12. Tan SK, Goh CL. Hydroquinone-induced exogenous ochronosis in Chinese - two case reports and a review. Int J Dermatol. 2008;47:639-40.         [ Links ]

13. Berman B, Ricotti C, Vieira M, Amini S. Diferentiation of exogenous ochronosis from melasma by dermoscopy. J Am Acad Dermatol. 2009;60(Suppl1):AB2.         [ Links ]

14. Merola JF, Meehan S, Walters RF, Brown L. Exogenous ochronosis. Dermatol Online J. 2008;14:6        [ Links ]

 

 

Mailing address:
Sandra Adolfina Reyes Romero
Rua Alexandre magno, q. 01, c. 14. Shangrila 4 - Pq 10
69054-723 - Manaus - AM, Brazil
E-mail: sandra.rreyes@gmail.com

Received on 25.07.2010.
Approved by the Advisory Board and accepted for publication on 21.10.2010
Conflict of interest: None
Financial funding: None

 

 

* Work carried out at the Getúlio Vargas University Hospital - The Federal University of Amazonas (HUGV - UFAM) - Manaus (AM), Brazil.