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LETTER TO THE EDITOR
Year : 2011  |  Volume : 77  |  Issue : 1  |  Page : 64-66

The successful treatment of palmoplantar hyperkeratotic lichen planus with enoxaparin


1 Department of Dermatology, Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey
2 Department of Pathology, Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey

Date of Web Publication6-Jan-2011

Correspondence Address:
Sirin Yasar
Haydarpasa Numune Egitim ve Arastirma Hastanesi, Dermatoloji Bolumu, 34746 Uskudar, Istanbul
Turkey
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0378-6323.74989

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How to cite this article:
Yasar S, Serdar ZA, Goktay F, Doner N, Tanzer C, Akkaya D, Gunes P. The successful treatment of palmoplantar hyperkeratotic lichen planus with enoxaparin. Indian J Dermatol Venereol Leprol 2011;77:64-6

How to cite this URL:
Yasar S, Serdar ZA, Goktay F, Doner N, Tanzer C, Akkaya D, Gunes P. The successful treatment of palmoplantar hyperkeratotic lichen planus with enoxaparin. Indian J Dermatol Venereol Leprol [serial online] 2011 [cited 2019 Aug 18];77:64-6. Available from: http://www.ijdvl.com/text.asp?2011/77/1/64/74989


Sir,

The palmoplantar hyperkeratotic variant of lichen planus (PHLP) is a rare entity. The clinical features of PHLP do not resemble classic lichen planus (LP), and the disease is mostly resistant to treatment. In approximately one-quarter of PHLP cases, typical lichen lesions can also be seen on other skin and mucosal surfaces. [1] Two cases of PHLP, which were successfully treated by subcutaneous enoxaparin without any subsequent adverse effects, are presented below.

Case 1: A 24-year-old male patient was admitted with complaints of thick plaques existing on the palms of his hands. During the physical examination of the patient, yellowish, solid, thick plaque lesions surrounded by a livid margin were observed on both palms and soles [Figure 1]a, b. No pit formation was observed on the solid and thick areas. While no change was observed on the nails, a bilateral reticular appearance on the oral mucosa and scattered livid colored bright papules on the trunk were seen.
Figure 1 :(a,b) Yellow thick plaques existing on palms of the hands and soles of the feet; (c) hyperkeratosis, acanthosis, wedge-shaped hypergranulosis within epidermis, degeneration in basal layer and lichenoid pattern of lymphocytic infiltration at the dermoepidermal junction (H and E, ×200)

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Case 2: A 45-year-old male patient was admitted, who had suffered from yellowish solid lesions on his hands and feet for 10 years. During the dermatological examination of the patient, a white reticular appearance was observed bilaterally on the buccal mucosa, and multiple solid hyperkeratotic papular lesions livid in color, which included Wickham striae, were detected on the flexor surfaces of the arms and on the anterior surface of the tibia.

Common histopathologic features of biopsies taken from the palms of both cases revealed hyperkeratosis, acanthosis, wedge-shaped hypergranulosis within the epidermis, degeneration in the basal layer, and a lichenoid pattern of lymphocytic infiltration at the dermo-epidermal junction [Figure 1]c. These findings were consistent with PHLP.

Enoxaparin (Clexane; , Rhone Poulenc-Cedex-F, France) was administered at a dose of 3 mg subcutaneously into the abdominal wall once a week, after receiving written and verbal informed consent from the patients. HCV, anti-HBs and HBs antigens were found to be negative in laboratory examinations. Platelet count assays and coagulation parameters of the patients (activated partial thromboplastin time, international normalized ratio, prothrombin time) were within normal limits. At the end of 12 sessions, all the skin lesions were seen to heal, leaving postlesional hyperpigmentation [Figure 2]a-c, but oral mucosa lesions remained stable. No local or systemic adverse effects were seen in the patients. No recurrence was seen during a 1-year follow-up of the patients.
Figure 2 :(a– c) Complete response to enoxaparin treatment

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The PHLP is a rare variant of lichen which can be easily misdiagnosed as palmoplantar keratoderma, psoriasis, verruca vulgaris, callus, punctate porokeratosis, arsenic keratosis, and lichen simplex chronicus. [2] In PHLP, lesions are frequently highly pruritic, erythematous, squamous and/or hyperkeratotic, well-defined, usually not involving the digits and resemble plaques located on the internal plantar arch. [3] Apart from this classic appearance, PHLP can also be seen with erythematous plaques, punctate keratosis, diffuse keratoderma and ulcerated lesions. [3] The determination of classic LP findings during a histopathologic examination enables a diagnosis.

Enoxaparin was administered for the first time in 1988 by Hodak et al. in Israel. Administration was successfully carried out at a dose of 3 mg via subcutaneous injection once a week to 10 LP patients with diffuse skin involvements. [4]

Enoxaparin's mechanism of action is based on the inhibition of the heparanase enzyme released by active T lymphocytes. The heparanase enzyme emerging on the surface of T lymphocyte passes through blood, cleaves heparan sulfate side chains that have a supporting role in the extracellular matrix, and thus enables the T lymphocyte to penetrate through the upper dermis. Since the heparanase enzyme is inhibited by low-dose, low-molecular-weight heparin, T lymphocytes cannot reach their target tissue. [4],[5] Because of the disaccharide structure of enoxaparin, it also inhibits the cytokines' role in inflammation, and especially the expression of tumor necrosis factor alpha. [4]

The lesions in PHLP tend to regress spontaneously within 6-18 months. Topical-systemic corticosteroids and other treatment regimens provide healing within 2-9 months in most cases, but recurrence is frequently seen after discontinuation of the drug. [3]

In our cases, complete cure was obtained using enoxaparin administered once a week for 3 months, and no adverse effects were seen. No recurrence was seen in follow-ups performed for 1 year.

Therefore, enoxaparin can offer a successful, particularly safe and long-term therapeutic alternative in PHLP treatment when its adverse effects are compared to those of long-term corticosteroid use.

 
  References Top

1.Black MM. Lichen planus and lichenoid disorders. In: Champion RH, Burton JL, Bruns DA, Breathnach SM, editors. Textbook of Dermatology. 6 th ed., Vol. 41. Oxford, England: Blackwell Science Inc; 1998. p. 1899-926.  Back to cited text no. 1
    
2.Rotunda AM, Craft N, Haley JC. Hyperkeratotic plaques on the palms and soles. Arch Dermatol 2004;140:1275-80.  Back to cited text no. 2
    
3.Sαnchez-Pιrez J, Rios Buceta L, Fraga J, Garcνa-Dνez A. Lichen planus with lesions on the palms and/or soles: Prevalence and clinicopathological study of 36 patients. Br J Dermatol 2000;142:310-3.   Back to cited text no. 3
    
4.Hodak E, Yosipovitch G, David M, Ingber A, Ingber A, Chorev L, et al. Low-dose low-molecular-weight heparin (enoxaparin) is beneficial in lichen planus: A preliminary report. J Am Acad Dermatol 1998;38:564-8.  Back to cited text no. 4
    
5.Stefanidou MP, Ioannidou DJ, Panayiotides JG, Tosca AD. Low molecular weight heparin; a novel alternative therapeutic approach for lichen planus. Br J Dermatol 1999;141:1040-5.  Back to cited text no. 5
    


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