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   Abstract
   Introduction
   Case report
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CASE REPORT
Year : 2006  |  Volume : 72  |  Issue : 6  |  Page : 449-451

Variant of Vohwinkel's syndrome


Department of Dermatology, Kasturba Medical College Hospital, Attavar, Mangalore, India

Correspondence Address:
Gatha M Upadya
Department of Dermatology, KMC Hospital, Attavar, Mangalore - 575 001
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0378-6323.29344

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  Abstract 

A 28-year-old female born to consanguineous parents, presented with progressive palmoplantar keratoderma since the age of six months and a constricting band on right fourth finger of one year duration. There was history of similar complaints being present in two other family members. Associated clinical findings included starfish-shaped cornified plaques on knuckles, resorption of distal phalanges and keratotic plaques on elbows, groins and knees. The patient was mentally sound and had normal audiometry. Biopsy from hyperkeratotic plaque showed hyperkeratosis, parakeratosis, increased granular layer and papillomatosis. Gene mapping for loricrin mutation was found to be negative.


Keywords: Keratoderma, Palmoplantar, Vohwinkel′s syndrome


How to cite this article:
Ali MM, Upadya GM. Variant of Vohwinkel's syndrome. Indian J Dermatol Venereol Leprol 2006;72:449-51

How to cite this URL:
Ali MM, Upadya GM. Variant of Vohwinkel's syndrome. Indian J Dermatol Venereol Leprol [serial online] 2006 [cited 2019 Oct 15];72:449-51. Available from: http://www.ijdvl.com/text.asp?2006/72/6/449/29344



  Introduction Top


Keratoderma hereditaria mutilans (KHM) was first described by Vohwinkel in the German literature in 1929.[1] This palmoplantar keratoderma is thought to be an autosomal dominant genodermatosis with defective epidermal differentiation and is quite rare.[2] A triad of clinical features is essentially pathognomonic for Vohwinkel's syndrome and this includes diffuse "honeycomb-like" thickening of palms and soles, "starfish-shaped" keratotic plaques on the dorsum of hands and feet and fibrous constricting bands (pseudo-ainhum) at the interphalangeal joints of hands and feet.[2],[3] The disease is seen in early childhood and has a familial tendency.[3] Associated findings with the disease are cicatricial alopecia,[4] ichthyosiform dermatoses, high-tone acoustic impairment, deaf mutism, spastic paraplegia and myopathy, knuckle pads and nail anomalies.[5] The hyperkeratosis in patients with KHM is difficult to treat.


  Case report Top


A 28-year-old female born to consanguineous parents presented with progressive thickening of palms and soles since the age of six months and a constricting band on the proximal interphalangeal joint of the right fourth finger of one year duration. There was no history of deaf mutism, mental retardation, spastic paralysis or myalgias, cicatricial alopecia, ichthyosiform dermatoses or autoamputation of digits. Two of her second-degree relatives had similar problems [Figure - 1]. Physical examination revealed that the volar aspect of the constricting band was opened and cracked [Figure - 2]. Associated with the keratoderma, the patient also had "starfish-shaped" cornified plaques on the knuckles, resorption of distal phalanges and keratotic papules and plaques on the elbows, groin, knees and feet [Figure - 3].

Biopsy of hyperkeratotic papules showed hyperkeratosis, parakeratosis, increased granular layer and papillomatosis. X-ray of both hands showed acral osteolysis. Audiometry revealed hearing in both ears to be within normal limits. To identify an underlying mutation in the loricrin gene in this patient, genomic DNA was isolated from peripheral blood lymphocytes of the proband using PureGene® DNA isolation kit. The entire loricrin gene was polymerase chain reaction amplified from genomic DNA and sequenced directly in an ABI Prism 310 automated sequencer, using the ABI prism big dye terminator cycle sequencing ready reaction kit, following purification with centriflex gel filtration cartridges. Gene mapping for loricrin mutation was found to be negative.


  Discussion Top


There are thought to be two different forms of Vohwinkel's syndrome. The type that is associated with sensorineural hearing loss is thought to result from a mutation of GJB2 gene that codes for the gap junction protein, connexin 26.[6] Cases of connexin 26 mutations causing autosomal dominant palmoplantar keratoderma with deafness but without other clinical features of Vohwinkel's syndrome have also been reported.[7] The other clinical variant of Vohwinkel's syndrome associated with generalized ichthyosis without deafness is caused by mutations of the gene encoding loricrin.[8]

The differential diagnosis of Vohwinkel's syndrome includes other types of hereditary keratodermas that may be associated with autoamputation of the digits. These are Olmsted's syndrome, acral keratoderma of Sybert,  Mal de Meleda More Details and palmoplantar keratoderma of Gamborg Nielsen.[9]

Vohwinkel's syndrome has variable expression and treatment should focus on palliation of the keratoderma and prevention of autoamputation. Surgical release of the constricting bands may be used to prevent autoamputation. Treatment options for keratoderma include keratolytics and retinoids. Etretinate and isotretinoin have been used successfully in several patients with Vohwinkel's syndrome to reverse both the keratoderma and pseudoainhum; however, the condition recurred once the medication was discontinued.[2],[3],[10],[11]

Our patient had neither ichthyosis nor deafness. There was no evidence of mutation in the loricrin gene. So this may be considered as a new variant of Vohwinkel's syndrome. As our patient was in the reproductive age she refused any treatment with systemic retinoids. However, keratolytics were tried with partial benefit.


  Acknowledgments Top


We would like to acknowledge Dr. Angela Christiano for the help rendered by her in gene mapping of the loricrin mutation.

 
  References Top

1.Vohwinkel KH. Keratoderma hereditarium meditans. Arch Dermatol Syphil 1929;158:354-64.  Back to cited text no. 1    
2.Camisa C, Rossana C. Variant of Keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin. Arch Dermatol 1984;120:1323-8.  Back to cited text no. 2    
3.Chang Sing Pang AF, Oranje AP, Vuzevki VD, Stolz E. Successful treatment of keratoderma hereditaria mutilans with an aromatic retinoid. Arch Dermatol 1981;117:225-8.  Back to cited text no. 3  [PUBMED]  
4.Gibbs RC, Frank SB. Keratoderma hereditaria mutilans (Vohwinkel): Differentiating features of conditions with constriction of digits. Arch Dermatol 1966;94:619-25.  Back to cited text no. 4  [PUBMED]  
5.Wirz F. Keratoma hereditarium mutilans. Arch Dermatol Syphil 1930;159:311-2.  Back to cited text no. 5    
6.Maestrini E, Korge BP, Ocana-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, et al . A missense mutation in connexim 26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Hum Mol Genet 1999;8:1237-43.  Back to cited text no. 6    
7.Richard G, White TW, Smith LE, Bailey RA, Compton JG, Paul DL, et al . Functional defects in a family with deaf mutism and palmoplantar keratodermm. Human Genet 1998;103:393-9.  Back to cited text no. 7    
8.Maestrini E, Monaco AP, McGrath JA, Ishida-Yamamoto A, Camisa C, Hovnanian A, et al . A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet 1996;13:70-7.  Back to cited text no. 8    
9.Peris K, Salvati EF, Torlone G, Chimenti S. Keratoderma hereditaria mutilans (Vohwinkel's syndrome) associated with congenital deaf mutism. Br J Dermatol 1995;132:617-20.  Back to cited text no. 9    
10.Wereide K. Mutilating palmoplantar keratoderma successfully treated with etretinate. Acta Derm Venerol 1984;64:566-9.  Back to cited text no. 10    
11.Rivers JK, Duke EE, Justus DW. Etretinate: Management of keratoma hereditaria mutilans in four family members. J Am Acad Dermatol 1985;13:43-9.  Back to cited text no. 11    


    Figures

[Figure - 1], [Figure - 2], [Figure - 3]

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