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CONCISE COMMUNICATION
Year : 2020  |  Volume : 11  |  Issue : 5  |  Page : 818-822  

Co-existent erythromelanosis follicularis faciei et colli and erythroses pigmentosa mediofacialis in a patient of generalized keratosis pilaris - A rare report in a young female


Department of Dermato-Venereo-Leprology, Government Medical College and Hospital, Nagpur, Maharashtra, India

Date of Submission23-Oct-2019
Date of Decision19-Jan-2019
Date of Acceptance03-Jul-2020
Date of Web Publication19-Sep-2020

Correspondence Address:
Priyanka A Kowe
Plot No. 181 A, Sumit Apartment, Pande Layout, Khamla Road, Nagpur - 440 025, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/idoj.IDOJ_535_19

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How to cite this article:
Wankhade VH, Kowe PA, Kulkarni MM, Singh RP. Co-existent erythromelanosis follicularis faciei et colli and erythroses pigmentosa mediofacialis in a patient of generalized keratosis pilaris - A rare report in a young female. Indian Dermatol Online J 2020;11:818-22

How to cite this URL:
Wankhade VH, Kowe PA, Kulkarni MM, Singh RP. Co-existent erythromelanosis follicularis faciei et colli and erythroses pigmentosa mediofacialis in a patient of generalized keratosis pilaris - A rare report in a young female. Indian Dermatol Online J [serial online] 2020 [cited 2020 Oct 30];11:818-22. Available from: https://www.idoj.in/text.asp?2020/11/5/818/295586



Sir,

Erythromelanosis Follicularis Faciei et Colli (EFFC) and Erythroses Pigmentosa Mediofacialis (EPM) are considered to be the disorders of abnormal follicular keratinization characterized by a triad of hyperpigmentation, erythema, and keratotic follicular papules. Herein, we report a young female with a features of both in association with generalized keratosis pilaris which is a rare co-occurrence, diagnosis of which was confirmed by dermoscopy and histopathology.

A 16-year-old female reported with multiple asymptomatic elevated lesions associated with darkening of skin which appeared first over the sides of cheeks, upper part of ear and gradually extended over the neck since 4 years. Similar lesions were also seen over central part of face since 2 years. Patient denied history of topical application and photosensitivity. Her past, personal, and family history was insignificant. Cutaneous examination revealed bilaterally symmetrical follicular micropapules associated with well-demarcated erythema and hyperpigmentation over the pre-auricular region, pinnae of ear and neck [Figure 1]a and [Figure 1]b. Forehead, perinasal, peribuccal region, and chin also showed lesions of similar morphology [Figure 2]. In addition, patient had keratotic papules over bilateral extremities, back, chest, abdomen, and thighs suggestive of generalized keratosis pilaris [Figure 3]a, [Figure 3]b, [Figure 3]c, [Figure 3]d. On diascopy of facial lesion erythema disappeared but pigmentation persisted. Dermoscopy using 3 Gen Dermlite DL4 (CA, USA) 10 × polarized mode, from cheeks revealed multiple small whitish rounds with keratotic follicular plugs surrounded by gray spots in a background of brownish discoloration suggestive of EFFC [Figure 4]a. Forehead lesion on dermoscopy showed numerous dilated follicles with keratotic plugging, perifollicular erythema, and scaling suggestive of EPM [Figure 4]b. Dermoscopy of the lesion from upper arm showed coiled hair, keratotic plugs, perifollicular erythema, and scaling suggestive of keratosis pilaris [Figure 4]c. Skin biopsy (one from cheek and another from forehead) with H and E staining revealed follicular hyperkeratosis with acanthosis with increased pigmentation in the basal layer. Dermis showed superficial perivascular lymphocytic infiltrate [Figure 5]a and [Figure 5]b. Based on clinical, dermoscopy and histopathology a final diagnosis of coexistent EFFC and EPM in a patient of generalized keratosis pilaris was made. The patient was counselled and started on topical tretinoin 0.025% cream and sunscreen for face and an emollient for the body. After 8 weeks of treatment patient showed only mild improvement and is under regular follow-up.
Figure 1: (a and b) Bilaterally symmetrical follicular papules, erythema, and hyperpigmentation over pre-auricular region extending over pinnae and neck

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Figure 2: Erythema, hyperpigmentation, and follicular papules over forehead, perioral region and chin

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Figure 3: (a-d) Lesions of keratosis pilaris symmetrically present over arms, back, chest and abdomen, thighs, and legs, respectively

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Figure 4: (a) Dermoscopy of EFFC revealed multiple small whitish rounds (Red arrow) with keratotic follicular plugs (Green arrow) surrounded by grey spots in a background of red-brown discolouration (Blue arrow) (b) Dermoscopy of EPM showed numerous dilated follicles (Red arrow), keratotic plugging (Green arrow) with perifollicular erythema and scaling (Blue arrow). (c) Dermoscopy of the lesion from upper arm showed coiling of hair shaft (Red arrow) with keratotic plugs (Green arrow) surrounded by perifollicular erythema and scaling (Blue arrow). (polarized; original magnification: 10X.)

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Figure 5: (a) Scanner view, showing follicular hyperkeratosis (Red arrow), acanthosis (Green arrow) (H and E, 10X). (b) Dermis showing increased pigmentation of basal cell layer (Blue arrow), mild perivascular lymphocytic infiltrate (yellow arrow) (H and E 40X)

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EFFC is an unfamiliar syndrome described by Kitamura, in 1960, with well-demarcated erythema, telangiectasia, hyperpigmentation, and follicular papules primarily on lateral aspect of the face, with an extension on to the lateral half of the neck, thus the name et colli (in Latin”et”=”and”,”colli”=”neck”). It affects patients of all ethnic group but majorly seen in Asian or Middle Eastern men.[1] The male to female ratio is observed to be 2:1.[2] However, it is increasingly reported in female patients as noticed in our case.[3] EPM as described by Brocq, is erythematous to hyperpigmented, rough skin over midline of the face. It is synonymously called as erythrose pigmentaire faciale, dermatose pigmentée médiofaciale, erythrosis pigmentosa peribuccalis, erythrosis pigmentata faciei, erythromelanosis follicularis faciei and erythrosis pigmentosa faciei colli.[4] The etiology of EFFC is multifactorial and includes genetic (autosomal recessive) and hereditary components.[5] Previous data suggest spontaneous mutation in EFFC.[6] Tuzun and Wolf et al. postulated that EFFC to be a chromosomal instability syndrome.[7] It is hypothesized that various environmental factors such as cosmetics, ultraviolet radiation, and topical formulations can cause hyperpigmentation over the period of years. Dermoscopy of EFFC shows multiple round whitish areas with follicular plugs, some shows central hair, surrounded by blue gray spots or peppering in a reddish-brown background.[8] Dermoscopy of EPM includes follicular dilatation with yellowish keratotic plugs, perifollicular erythema, and scaling surrounded by slate-gray globules.[9] Histology of EFFC and EPM is similar and shows follicular hyperkeratosis, increased basal layer pigmentation, and incontinence of melanin pigment with dermal melanophages. Dermis shows perivascular and periadnexal lymphocytic infiltrate with vasodilatation.[8] EFFC has been found to be associated with keratosis pilaris of different body parts which postulated that EFFC is a variant of keratosis pilaris.[3],[4],[6],[7],[10],[11] Juhlin et al. has reported a single case of EFFC and EPM occurring in a 34-year-old female postulating that the two conditions are same.[12] Our case is unique since she had concurrent EFFC, EPM, and generalized KP. It can be stated that both EFFC and EPM are etiologically same conditions manifesting at different sites. Dermoscopy plays an important beside tool to identify these entities. Differential diagnosis of EFFC and EPM includes ulerythema ophryogenes, atrophoderma vermiculatum, Riehl's melanosis, poikiloderma of Civatte, tricostasis spinulosa, lichen spinulosus [Table 1]. Treatment of EFFC and EPM is same but unsatisfactory. Various topical keratolytics such as tretinoin, glycolic acid, salicylic acid (20–30%), urea, ammonium lactate, vitamin C can be used assuming it to be a disorder of keratinization. Oral isotretinoin (0.1–1 mg/kg/d) can be tried for extensive involvement. Topical tacalcitol ointment was found to be a successful therapeutic option for EFFC in recent years.[13] Multiple sessions of long-pulsed dye laser for erythema and Q-switched Nd: YAG laser (1,064 nm) for hyperpigmentation are mentioned in the treatment of EFFC by Li et al.[14] EFFC and EPM are underreported disorders which can be easily diagnosed with the help of a dermoscope. Also, it is the rarity of EFFC and EPM associated with generalized KP which prompted us to report this case.
Table 1: Differential diagnosis of erythrosis pigmentosa mediofacialis and erythromelanosis follicularis faciei et colli

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Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Judge MR, McLean WH, Munro CS. Disorders of keratinization. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook's Textbook of Dermatology. 8th ed. vol 1. U.K: Wiley-Blackwell; 2010. p. 19.72-3.  Back to cited text no. 1
    
2.
Al Hawsawi K, Aljuhani O, Niaz G, Fallatah H, Alhawsawi A. Erythromelanosis follicularis faciei: A case report and review of the literature. Case Rep Dermatol 2015;7:335-9.  Back to cited text no. 2
    
3.
Augustine M, Jayaseelan E. Erythromelanosis follicularis faciei et colli: Relationship with keratosis pilaris. Indian J Dermatol Venereol Leprol 2008;74:47-9.  Back to cited text no. 3
[PUBMED]  [Full text]  
4.
Kalwaniya S, Morgaonkar M, Gupta S, Jain SK. Co-occurrence of erythrosis pigmentosa mediofacialis and erythromelanosis follicularis faciei et colli associated with keratosis pilaris in an adolescent female. Indian J Dermatol 2016;61:467.  Back to cited text no. 4
[PUBMED]  [Full text]  
5.
Yanez S, Velasco JA, Gonzalez MP. Familial erythromelanosis follicularis faciei et colli-an autosomal recessive mode of inheritance. Clin Exp Dermatol 1993;18:283-5.  Back to cited text no. 5
    
6.
Arif T. Generalized keratosis pilaris associated with erythromelanosis follicularis faciei et colli: A rare coexistence. Indian J Paediatr Dermatol 2015;16:149-51.  Back to cited text no. 6
  [Full text]  
7.
Tüzün Y, Wolf R, Tüzün B, Ozdemir M, Demirkesen C, Deviren A, et al. Familial erythromelanosis follicularis and chromosomal instability. J Eur Acad Dermatol Venereol 2001;15:150-2.  Back to cited text no. 7
    
8.
Maouni S, El Anzi O, Sqalli A, Znati K, Meziane M, Hassam B. Erythromelanosis follicularis faciei et colli: Dermoscopy and dermatopathology correlates. JAAD Case Rep 2019;5:535-6.  Back to cited text no. 8
    
9.
Luna PC, Abad ME, González VM, Vigovich F, Casas JG, Larralde M, et al. Erythrosis pigmentosa peribuccalis in an adolescent: Dermoscopic description and management. Pediatr Dermatol 2016;33:e65-8.  Back to cited text no. 9
    
10.
Ermertcan AT, Oztürkcan S, Sahin MT, Türkdogan P, Saçar T. Erythromelanosis follicularis faciei et colli associated with keratosis pilaris in two brothers. Pediatr Dermatol 2006;23:31-4.  Back to cited text no. 10
    
11.
Elghblawi E. Erythromelanosis follicularis faciei et colli: A first female case report from the outskirts of Libya and literature review. Indian J Paediatr Dermatol 2017;18:53-9.  Back to cited text no. 11
  [Full text]  
12.
Juhlin L, Alkemade H. Erythrosis pigmentosa mediofacialis (Brocq) and erythromelanosis follicularis faciei et colli in the same patient. Acta Derm Venereol 1999;79:65-6.  Back to cited text no. 12
    
13.
Kim WJ, Song M, Ko HC, Kim BS, Kim MB. Topical tacalcitol ointment can be a good therapeutic choice in erythromelanosis follicularis faciei et colli. J Am Acad Dermatol 2012;67:320-1.  Back to cited text no. 13
    
14.
Li YH, Zhu X, Chen JZ, Wu Y, Wei HC, Gao XH, et al. Treatment of erythromelanosis follicularis faciei et colli using a dualwavelength laser system: A splitface treatment. Dermatol Surg 2010;36:1344-7.  Back to cited text no. 14
    
15.
Sonthalia S, Bhatia J, Thomas M. Dermoscopy of keratosis pilaris. Indian Dermatol Online J 2019;10:613-4.  Back to cited text no. 15
[PUBMED]  [Full text]  
16.
Coelho De Sousa V, Pinheiro R, Cunha N, Lencastre A, Cabete J. And next…Adnexa: Ulerythema ophryogenes and keratosis pilaris. Eur J Dermatol. 2018 Aug 1;28(4):566-7.  Back to cited text no. 16
    
17.
Panchaprateep R, Tanus A, Tosti A. Clinical, dermoscopic, and histopathologic features of body hair disorders. J Am Acad Dermatol. 2015 May;72(5):890-900.  Back to cited text no. 17
    
18.
Katoulis AC, Stavrianeas NG, Panayiotides JG, Bozi E, Vamvasakis E, Kalogeromitros D, Georgala S. Poikiloderma of Civatte: a histopathological and ultrastructural study. Dermatology. 2007;214(2):177-82.  Back to cited text no. 18
    
19.
Errichetti E, Stinco G. Dermoscopy in Facilitating the Recognition of Poikiloderma of Civatte. Dermatol Surg. 2018 Mar;44(3):446-7.  Back to cited text no. 19
    
20.
Wang L, Xu AE. Four views of Riehl's melanosis: clinical appearance, dermoscopy, confocal microscopy and histopathology. J Eur Acad Dermatol Venereol 2014 Sep; 28(9):1199-206.  Back to cited text no. 20
    
21.
Vora RV, Kota RS, Sheth NK. Dermoscopy of nevus comedonicus. Indian Dermatol Online J 2017;8:388-9.  Back to cited text no. 21
[PUBMED]  [Full text]  


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