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Mortazavi M, Saad El-Din SA. Bilateral linear lichen planus along the lines of Blaschko: Report of a rare case and brief review. Our Dermatol Online. 2017;8(3):322-325. |
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Bilateral linear lichen planus along the lines of Blaschko: Report of a rare case and brief review
Mohammadreza Mortazavi1, Somaia Ahmed Saad El-Din2
1Department of Dermatology, Hayat International Hospital, Muscat, Oman; 2Department of Pathology, Faculty of Medicine, Ain Shams University, Cairo, Egypt
Corresponding author: Dr. Mohammadreza Mortazavi, E-mail: mmortazavir@gmail.com
Submission: 12.12.2016; Acceptance: 01.02.2017
DOI: 10.7241/ourd.20173.92
ABSTRACT
Linear lichen planus (LP) is a rare variant of lichen planus that may present in a dermatomal or zosteriform distribution or develop along the lines of Blaschko. Blaschkoid linear LP is a rarer distinct variant of LP and should be differentiated from other linear subtypes of LP and other Blaschkoid dermatoses. A 24-year-old male patient presented with multiple shiny, purple, polygonal papules arranged perpendicularly over the right lower extremity and also in shorter curvilinear (S-shaped) lesions on the left side of the abdomen and left flank along the lines of Blaschko. The histopathological findings of a biopsy specimen were compatible with the clinical diagnosis of lichen planus. To date, almost all of the reported cases of linear lichen planus along the lines of Blaschko have had unilateral presentations. We herein report a rare case of bilateral linear Blaschkoid lichen planus and review the literature briefly.
Key words: Lichen planus, Linear lichen planus, Blaschkoid lichen planus, Bilateral
INTRODUCTION
Lichen planus (LP) is a common cutaneous disorder that usually presents as pruritic, purple or violaceous, polygonal, planar (flat-topped) papular skin lesions, but it may also affect the mucous membranes, nails and hairs. The clinical presentation of lichen planus includes several different morphological variants such as hypertrophic, atrophic, actinic, pigmented (LP pigmentosus), annular, follicular (lichenplanopilaris), and linear LP [1]. Linear LP may arise in a dermatomal or zosteriform distribution (i.e. following the course of a peripheral nerve) either de novo or at the sites of trauma (isomorphic response or Koebnerization) [2] or as Wolf’s isotopic response at the site of healed herpes zoster [3]. In addition, linear LP may present with development of lesions along the lines of Blaschko [3,4]. Blaschko’s lines do not correspond to the nervous, vascular or lymphatic structures and represent a form of mosaicism that develops during the embryonic period [5]. Linear LP has been described in less than 1% of all LP patients [3]. Almost all of the reported cases of linear lichen planus along the lines of Blaschko presented unilaterally [3–5,8–10]. We herein report a rare case of bilateral linear Blaschkoid lichen planus.
CASE REPORT
A 24-year-old man presented with multiple itchy, purple lesions on the right lower extremity since five months ago. The lesions started from his right lower leg, gradually extended to the right thigh and buttock area in a linear manner and recently appeared on the left side of his abdomen. The patient had history of glucose-6-phosphate dehydrogenase (G6PD) deficiency, migraine headaches and has been recently diagnosed with mild familial antithrombin III deficiency without any thrombotic event up to now. He had family history of serious and even fatal thromboembolism due to antithrombin III deficiency. After full medical investigations, he was advised to take prophylactic anticoagulants just for travel and major surgery. He has not been on any regular medications during last 5 to 6 months, except occasional and random intake of NSAIDs (Ibuprofen & Mefenamic acid), Paracetamol and Naratriptan for a sport left knee injury and for his migraine headaches.
The findings in general physical examination were unremarkable and the skin examination showed multiple shiny, purple, polygonal flat-topped papules distributed from the right lower leg to the medial and then lateral sides of the right thigh, up to the right buttock in a linear pattern along the lines of Blaschko (Fig. 1a and b). Also, there were a few shorter curvilinear (S-shaped) lesions consist of flat violaceous papules on the left side of the abdomen and left flank (Fig. 1c). In addition, the arrangement of several similar micropapules in a short vertical line on the right elbow was noted as an isomorphic response to scratching (Koebner phenomenon) (Fig. 1d). Other areas of the skin including scalp, nails, and also genital and oral mucosa were spared.
The results of routine laboratory tests including complete CBC and liver function tests were all within normal limits and the serology tests for hepatitis B and C were reported negative.
Punch biopsy of a papule on the right thigh was performed with the clinical diagnosis of linear Blaschkoid lichen planus and to rule out linear psoriasis, lichen striatus and other linear lesions. The specimen was stained with Hematoxylin & Eosin (H & E). The histopathological examination (Figs. 2a–c) revealed mild hyperkeratosis (orthokeratosis) with occasional foci of parakeratosis, prominent granular cell layer, foci of irregular acanthosis with saw-tooth appearance of the rete ridges; dense band-like lymphocytic inflammatory infiltrate, obscuring the dermal-epidermal junction associated with basal cell vacuolization, apoptosis of the basal cells with formation of the characteristic eosinophilic Civatte (colloid) bodies. The lymphocytes in the infiltrate were intermingled with some macrophages, melanophages and eosinophils. These histopathological findings were compatible with the clinical diagnosis of linear lichen planus. Moreover, the absence of the features such as psoriasiform epidermal hyperplasia, thinning out of the supra-papillary epidermis, neutrophilic epidermal exocytosis, and deep reticular dermal perifollicular and perieccrine inflammatory infiltrate excluded other clinical differential diagnoses, i.e., linear psoriasis and lichen striatus, respectively.
With a final diagnosis of linear Blaschkoid lichen planus, treatment was started by oral antihistamines, topical Betamethasone valerate (Betnovate cream) and emollients. After 2 weeks, topical Betamethasone was replaced by topical Clobetasol propionate (Dermovate cream) to accelerate his improvement. The patient responded well to topical corticosteroid therapy.
DISCUSSION
Linear lichen planus along the lines of Blaschko is one of the rare morphological presentations of LP [5]. The lines of Blaschko were described in 1901 by the German dermatologist, Alfred Blaschko as the linear developmental patterns of epidermal and sebaceous nevi in more than 150 patients [6]. Jackson, after 75 years, provided a detailed review of the concept of Balschko lines [6]. The lines of Blaschko represent a classic pattern of mosaicism, arises from two or more genetically different cutaneous cell populations in an individual derived from a single zygote, that can be seen in a wide variety of not only congenital but also acquired skin disorders, including lichen planus [3,7]. It is hypothesized that the mosaicism may increase susceptibility of the skin in that specific area to develop a particular multifactorial cutaneous disease. Establishing the diagnosis of an inflammatory acquired skin disease that follows the Blaschko lines requires careful consideration of the history (age of onset, symptoms, natural course, etc.) as well as the clinical and histologic features [7].
A review of the reported linear LP cases in the literature reveals a controversy about the use of the terms zosteriform LP versus Blaschkoid (or Blaschkoian) LP. Some of the reported “zosteriform” LP cases need to be revised as Blaschkoid LP [4,8]. To solve this controversy, Blaschko lines should be clearly distinguished from other linear patterns such as lines of innervation of spinal nerves (dermatomes), Langer’s lines, etc. [5,9]. Zosteriform (dermatomal) patterns consistently correspond to the areas that are innervated by the spinal nerves but Blaschko lines follow some distinct developmental patterns and are V-shape over the upper spine, S-shape on the abdomen, inverted U-shape from the breast area onto the upper arm and perpendicular over the front and back of the lower extremities [10]. Another source of confusion is the role of Koebner phenomenon in development of linear LP lesions. The koebner phenomenon satisfactorily explains most cases with linear as well as the zosteriform distribution of LP because they have appeared either secondary to a known trauma or in the healed lesions of a preexisting disease such as herpes zoster [2,3,9]. The exact cause of the Blaschkoid pattern of LP has not yet been verified but there is no evidence to support the role of Koebner phenomenon in its etiology.
Most of the reported Blaschkoid LP cases (including our case) present with typical papular lesions, but there are rare reports of other variants of LP in the literature such as LP pigmentosus [11], lichenplanopilaris, atrophic LP [12], and drug-induced LP [13] with linear Blaschkoid pattern.
Lichen planus is generally a cell-mediated immune reaction of unknown cause. An association between lichen planus and hepatitis C virus infection, chronic active hepatitis, and primary biliary cirrhosis has been reported [14]. In one meta-analysis, 16% of LP patients had hepatitis C infection [14]. To date, no systemic associations, including hepatitis C have been reported with Blaschkoid LP [9], while other variants of linear LP may show such associations [15]. In our reported case, serology tests for hepatitis B and C were negative.
Our reported case was recently diagnosed with asymptomatic hereditary antithrombin III deficiency and glucose-6-phosphate dehydrogenase (G6PD) deficiency. The authors believe that this is the first reported comorbidity of these medical conditions and Blaschkoid type of LP in the literature. Considering the very high prevalence of erythrocyte G6PD deficiency in Oman’s male population (up to 25%) [16], the concurrent presence of it and LP in our reported case seems to be merely a co-incidence.
Bilateral linear presentation of Blashkoid skin diseases other than LP, such as linear Grover’s Disease [17], lichen striatus [18] and linear morphea [19] have rarely been reported in the literature. Almost all of the reported Blaschkoid LP cases had presented with unilateral lesions. To the best of our knowledge, this is the second reported case of bilateral Blaschkoid LP after the Long & Finlay’s case [20].
Consent
The evaluation and examination of the patient was conducted according to the Declaration of Helsinki principles.
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Notes
Source of Support: Nil
Conflict of Interest: None declared.
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