• Users Online: 2488
  • Print this page
  • Email this page


 
  Table of Contents  
LETTERS TO THE EDITOR
Year : 2019  |  Volume : 10  |  Issue : 2  |  Page : 183-186  

Progressive symmetrical erythrokeratoderma associated with punctate palmoplantarkeratoderma


1 Department of Dermatology and Venereology, Government Medical College and Hospital, Haldwani, Nainital, Uttarakhand, India
2 Department of Dermatology, Katihar Medical College and hospital, Katihar, Bihar, India

Date of Web Publication15-Mar-2019

Correspondence Address:
Piyush Kumar
Department of Dermatology and Venereology, Government Medical College and Hospital, Haldwani, Nainital, Uttarakhand
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/idoj.IDOJ_105_18

Rights and Permissions

How to cite this article:
Tiwary AK, Kumar P. Progressive symmetrical erythrokeratoderma associated with punctate palmoplantarkeratoderma. Indian Dermatol Online J 2019;10:183-6

How to cite this URL:
Tiwary AK, Kumar P. Progressive symmetrical erythrokeratoderma associated with punctate palmoplantarkeratoderma. Indian Dermatol Online J [serial online] 2019 [cited 2019 Aug 21];10:183-6. Available from: http://www.idoj.in/text.asp?2019/10/2/183/254280



Sir,

Progressive symmetric erythrokeratoderma (PSEK) is a rare heterogeneous genodermatoses characterized by early onset of well-defined, fixed erythematous and hyperkeratotic plaques usually affecting the extensor surface of extremities, buttocks, and sometimes face, sparing the truncal area.[1] To our knowledge, less than 100 cases have been described in the English literature.[2] Here, we report a rare presentation of PSEK associated with punctuate palmoplantarkeratoderma in a 10-year-old girl with no affection of family members.

A 10-year-old girl presented with asymptomatic erythematous lesions on her extremities and palmoplantar thickening since her early childhood. The lesions present on extensor surfaces started as erythematous, scaly macules progressing into slightly hyperkeratotic plaques covering more areas but were not migratory in nature. Her developmental milestones were normal. The child was born out of nonconsanguineous marriage, and none of her family members had similar lesions.

On cutaneous examination, there were well-defined, erythematous, hyperkeratotic, scaly, plaques symmetrically distributed over the dorsa of fingers and knuckles, knees, and dorsa of feet including toes [Figure 1]a and [Figure 1]b. Palmar lesions were seen as multiple round, keratotic, punctate lesions on palmar creases and hypothenar skin [Figure 2]a. Such lesions were also present on plantar surface, predominantly over pressure-prone areas. Many of these punctate keratotic lesions present on heel merged to form larger lesions [Figure 2]b. The mucocutaneous examination of other sites was normal. Systemic examination was unremarkable and routine laboratory parameters were within normal limits.
Figure 1: (a) Well-defined, erythematous, mildly hyperkeratotic, scaly, plaques on dorsa of fingers and knuckles, as well as knees. (b) Similar erythematous, hyperkeratotic, scaly plaques affecting the dorsa of feet including toes

Click here to view
Figure 2: (a) Multiple tiny, round, keratotic, punctate lesions on palmar creases and hypothenar skin. (b) Similar punctate keratotic lesions present on plantar surface. On heel, they merged to form larger lesions

Click here to view


Histopathological examination of the lesion on hand demonstrated orthohyperkeratosis, focal parakeratosis, acanthosis, and superficial perivascular lymphocytic infiltration [Figure 3].
Figure 3: Orthohyperkeratosis, focal parakeratosis, mild acanthosis, normal granular layer, and perivascular lymphocytic infiltration in papillary dermis (H and E,×400)

Click here to view


Clinical and histopathological features were consistent with the diagnosis of PSEK with probably autosomal recessive mode of inheritance. Genetic analysis could not be done due to unavailability of resources in our hospital. Topical keratolytics, emollients, and oral vitamin A were started, but the patient did not turn up for further evaluation.

“Erythrokeratodermas” are a group of rare genodermatosis which includes two major nonsyndromic entities –progressive symmetric erythrokeratoderma (PSEK) and erythrokeratoderma variabilis (EKV) – and some syndromes such as KID (keratitis, ichthyosis, deafness) syndrome and HID (hystrix-like ichthyosis withdeafness) syndrome.[3] Although PSEK was first described by Darier, the term was coined by Gottron, hence eponymically also known as “Darier–Gottron syndrome.”[4]

Most cases of PSEK follow an autosomal dominant mode of inheritance with incomplete penetrance and variable expressivity, however, sporadic cases do occur frequently and few autosomal recessive cases have also been reported (as in our case). The molecular basis of PSEK is still obscure with no confirmed candidate gene. Of note, in a single case of PSEK, mutation in GJB4 gene encoding connexin 30.3 protein (often seen in cases of EKV) was found.[5] No genetic mutation was identified in all other cases.[6],[7],[8]

The classical presentation of PSEK consists of symmetrically distributed, nonmigratory, large, well-defined, erythematous, hyperkeratotic plaques with marked peripheral erythema.[1] The sites of predilection are extensors of extremities and sometimes face.[1] The trunk is usually spared. Mostly, PSEK has infantile or childhood onset with no gender predilection. The lesions progress slowly during childhood and tend to stabilize during teenage years.[2]

The histopathological features of PSEK are orthokeratotic hyperkeratosis, focal parakeratosis, mild or moderate acanthosis, normal or prominent granular layer, and perivascular lymphocytic infiltration in papillary dermis.[3]

EKV, psoriasis, and pityriasis rubra pilaris are close differential diagnosis of PSEK.[3] The latter two entities can easily be ruled out by clinical and histopathological evaluation. The clinical, histological, and genetic overlapping between EKV and PSEK questioned their separate existence. Consequently, an alternative term EKV progressiva was suggested in past years in place of PSEK and EKV.[9] Whatever be the different school of thoughts, this dispute can only be puzzled out with reporting of more cases and their genetic studies. Till then, it is reasonable to know the existing distinguishable features between the two, which are summarized in [Table 1].
Table 1: Distinguishing features between PSEK and EKV

Click here to view


PSEK has been reported to be associated with PPK and many other conditions.[3] In our case, it was interesting to find the punctate type of PPK which also involved palmar creases. Of note, we have not been able to find any case of PSEK in previous literature which had this association. Reporting of such cases widen the clinical spectrum of PSEK and lessen the chances of misdiagnosis and the urge of correlating with a syndrome.

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.
Verma SB, Uwe W. Progressive symmetric erythrokeratodermia with delayed intellectual milestones and convulsions. Indian Dermatol Online J 2012;3:54-6.  Back to cited text no. 1
[PUBMED]  [Full text]  
2.
Tarikci N, Göncü EK, Yüksel T, Singer R, TopalİO, Şahin İM. Progressive symmetrical erythrokeratoderma on the face: A rare condition and successful treatment with calcipotriol. JAAD Case Reports 2016;2:70-1.  Back to cited text no. 2
    
3.
Sacchidanand S, Sahana MS, Kamoji SG, Asha GS. Progressive symmetric erythrokeratoderma with nephrotic syndrome: Coincidence or new association?. Indian Dermatol Online J 2013;4:347-9.  Back to cited text no. 3
[PUBMED]  [Full text]  
4.
Gottron HA. Congenital symmetrical progressive erythrokeratoderma. Arch DermatolSyph 1923;7:416.  Back to cited text no. 4
    
5.
Van Steensel MA, Oranje AP, van der Schroeff JG, Wagner A, vanGeel M. The missense mutation G12D in connexin30.3 can cause both erythrokeratodermiavariablis of Mendes da Costa and progressive erythrokeratodermia of Gottron. Am J Med Genet A 2009;149A:657-61.  Back to cited text no. 5
    
6.
Guo BR, Sun LD, Cui Y, Yang S, Zhang XJ. Progressive symmetrical erythrokeratoderma: Report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes. Clin Exp Dermatol 2013;38:925-7.  Back to cited text no. 6
    
7.
Cui Y, Yang S, Gao M, Zhou WM, Li M, Wang Y, et al. Identification of a novel locus for progressive symmetric erythrokeratodermia to a 19.02-cM interval at 21q11.2-21q21.2. J Invest Dermatol 2006;126:2136-9.  Back to cited text no. 7
    
8.
Wei S, Zhou Y, Zhang TD, Huang ZM, Zhang XB, Zhu HL, et al. Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia. ClinExp Dermatol 2011;36:399-405.  Back to cited text no. 8
    
9.
Mahajan VK, Khatri G, Chauhan PS, Mehta KS, Raina R, Mrinal G. Progressive symmetric erythrokeratoderma having overlapping features with erythrokeratodermavariabilis and lesional hyperkeratosis: Is nomenclature “Erythrokeratodermavariabilis progressive” More appropriate? Indian J Dermatol 2015;60:410-1.  Back to cited text no. 9
[PUBMED]  [Full text]  


    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
    Tables

  [Table 1]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed162    
    Printed2    
    Emailed0    
    PDF Downloaded32    
    Comments [Add]    

Recommend this journal