Erythrosis pigmentosa peribuccalis Brocq

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Abstract

Pigmented peribuccal erythrosis of Brocq is a rare disease, with less than 50 cases reported in the literature, affecting mainly women. The dermatosis manifests itself as small follicular pigmented and slightly hyperkeratotic papules that are grouped centrofacially to form plaques with clear contours around the mouth and nose, sometimes with lesions in the forehead. The color intensity may change during the day, due to the presence of a vascular component. The dermatosis does not cause subjective symptoms and the main complaints of patients are reduced to aesthetic discomfort due to the sharp transition from orange-brown coloring around the mouth and nose to the normal color of the cheeks. The etiology of this condition is currently unknown, the features of the dermatoscopic picture have not been described, and standardized and effective methods of therapy have not been developed.

This article describes the clinical manifestations and dermatoscopic picture of this rare dermatosis in a 23-year-old girl with a disease duration of 6 years and ineffectiveness of previous treatment, who had pronounced and persistent positive dynamics against the background of treatment of concomitant cystic ovarian formations, the use of external agents with a keratolytic effect and strict photoprotection.

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About the authors

Svetlana N. Shchava

Volgograd State Medical University

Email: snchava@rambler.ru
ORCID iD: 0000-0002-4946-6624
SPIN-code: 7449-7277

MD, Cand. Sci. (Medicine), Associate Professor

Russian Federation, Volgograd

Marina A. Shishkina

Volgograd State Medical University

Author for correspondence.
Email: marinashishkina_derm@mail.ru
ORCID iD: 0000-0001-5479-3075
SPIN-code: 5446-8406

assistant of the Department of Dermatovenerology

Russian Federation, Volgograd

References

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  2. Bleehan SS, Anstey AV. Disorders of skin colour. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook’s textbook of dermatology. 7th edn. Oxford: Blackwell; 2004. P. 39–42.
  3. Juhlin L, Alkemade H. Erythrosis pigmentosa mediofacialis (Brocq) and erythromelanosis follicularis faciei et colli in the same patient. Acta Derm Venereol. 1999;79(1):65–66. doi: 10.1080/000155599750011741
  4. Tüzün Y, Wolf R, Tüzün B, et al. Familial erythromelanosis follicularis and chromosomal instability. J Eur Acad Dermatol Venereol. 2001;15(2):150–152. doi: 10.1046/j.1468-3083.2001.00148.x
  5. Mekkes JR. Erythrosis pigmentosa peribuccalis (Brocq) [25 March 2024]. Available from: https://www.huidziekten.nl/zakboek/dermatosen/etxt/erythrosis-pigmentosa-peribuccalis.htm. Accessed: 15.09.2024.
  6. Li YH, Zhu X, Chen JZ, et al. Treatment of erythromelanosis follicularis faciei et colli using a dualwavelength laser system: A splitface treatment. Dermatol Surg. 2010;36(8):1344–1347. doi: 10.1111/j.1524-4725.2010.01637.x
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Supplementary files

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1. JATS XML
2. Fig. 1. Pink-brown discoloration in the perioral area, in the nose, chin and in front of the ears.

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3. Fig. 2. Symmetrical pink-brown coloring of the central part of the face spreading to the forehead.

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4. Fig. 3. Dermatoscopy: thin pointed follicular keratotic plugs; homogeneous perifollicular pigmentation; thin branching telangiectasias.

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5. Fig. 4. Clinical picture after surgery and use of agents with a keratolytic effect: facial profile (a) and frontal view (b).

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СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ЭЛ № ФС 77 - 80653 от 15.03.2021 г
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