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   Abstract
   Introduction
   Case Report
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CASE REPORTS
Year : 2005  |  Volume : 71  |  Issue : 6  |  Page : 421-422

Linear scleroderma following Blaschko's lines


Consultant dermatologist, Asansol, West Bengal, India

Correspondence Address:
Amiya Kumar Mukhopadhyay
"Pranab", Ismile (near Dharmaraj mandir), Asansol, District Burdwan, West Bengal-713301
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0378-6323.18949

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  Abstract 

Blaschko's lines form a pattern, which many diseases are found to follow, but linear scleroderma following Blaschko's lines is a controversial entity rarely reported in the literature. A 24-year-old man presented with multiple linear, atrophic, hyperpigmented lesions punctuated by areas of depigmentations on the left half of the trunk distributed on the anterior, lateral and posterior aspects. The lesions were distributed in a typical S-shaped line. Antinuclear antibody and antihistone antibody tests were negative. Histopathological examination of the skin from the affected area showed features suggestive of scleroderma. Here, we present a case of linear scleroderma following Blaschko's lines in a male patient - an entity reported only three times so far.


Keywords: Scleroderma, Linear, Lines of Blaschko


How to cite this article:
Mukhopadhyay AK. Linear scleroderma following Blaschko's lines. Indian J Dermatol Venereol Leprol 2005;71:421-2

How to cite this URL:
Mukhopadhyay AK. Linear scleroderma following Blaschko's lines. Indian J Dermatol Venereol Leprol [serial online] 2005 [cited 2020 Feb 29];71:421-2. Available from: http://www.ijdvl.com/text.asp?2005/71/6/421/18949



  Introduction Top


Blaschko's lines (BL) are the pattern assumed by many congenital as well as acquired disorders. They do not follow any known nervous, vascular or lymphatic distribution.[1]

Localized scleroderma (LS) is divided clinically into three subclasses: (1) circumscribed plaques or band; (2) linear morphea; and (3) fronto-parietal lesions, with or without hemiatrophy of the face.[2] LS following BL is a controversial entity.[3] Of the five patients reported, only one was male. Here, we describe a male patient whose lesions were distributed along the lines of Blaschko.


  Case Report Top


A 24-year-old man presented with multiple hyperpigmented, atrophic lesions on the left side of his body for the last six years. He gave a history of erythematous, indurated lesions that started spontaneously and gradually transformed into the present picture. He denied any history of trauma, disease or drug administration preceding his present problem. Other members of his family were normal.

On examination, there were atrophied, hyperpigmented lesions punctuated by areas of depigmentation present on the left half of the trunk distributed on the anterior, lateral and posterior aspects [Figure - 1]. They followed a typical S-shaped line at places. They were sclerotic but non-tender and did not show any lilac border.

Routine examination of the blood and urinalysis was normal. Antinuclear antibody and antihistone antibody tests were negative. Histopathological examination of the skin from the affected area showed that the entire dermis was markedly thickened and had partially replaced the subcutaneous fat, causing the adnexal structures to appear to lie higher up in the dermis than usual. The upper dermis had a sparse perivascular lymphocytic infiltrate. Thus the findings were consistent with the diagnosis of an old lesion of scleroderma.


  Discussion Top


The lines of Blaschko represent a pattern followed by many skin diseases, both congenital and acquired. They are commonly confused with dermatomes, but the difference between dermatomes and BL are most apparent on the trunk because arcs on the upper chest, S-shapes on the abdomen and V-shapes as the lesions approach to the posterior midlines are noted in BL.[4] Linear skin diseases that follow the BL are thought to be a consequence of mosaicism.[5]

LS occurs as a linear band, usually with a single unilateral lesion. The lower extremities are most often involved, followed, in frequency of occurrence, by the upper extremities, frontal area of the head, and anterior thorax.[6] The female-to-male ratio is 4:1. Whether LS follows BL is controversial.[3] Jackson first described it,[1] but later observed that although LS was thought to follow BL it was probably dermatomal.[7] Linear atrophoderma of Moulin is an acquired condition where pigmented atrophy of the superficial dermis occurs along the BL. However, there is no history of inflammatory changes preceding the atrophic changes and also features like sclerosis and depigmentation that are seen in scleroderma are absent.[5],[8] Our patient gave a history suggestive of an inflammatory phase in the beginning of his disease and clinically as well as histologically differed from linear atrophoderma of Moulin. In a detailed review, Bolognia et al could not find a single case of LS following BL.[4] Subsequently, only three papers described this finding.[5],[9],[10] Our case is the fourth such report to the best of our knowledge.

Regarding the development of LS following BL, it has been speculated that the tendency for the development of scleroderma is predetermined during embryogenesis, with the formation of a clone of vulnerable cells. Exposure to an appropriate trigger such as an autoimmune phenomenon may result in the development of full-blown disease.[9]

The most striking feature in our patient is the very well demarcated distribution of the lesions following BL, which we believe will settle the controversy regarding linear scleroderma along Blaschko's lines.



 
  References Top

1.Jackson R. The lines of Blaschko: a review and reconsideration. Br J Dermatol 1976;95:349-60.  Back to cited text no. 1      
2.Rowell NR, Goodfield MJ. The 'connective tissue diseases.' In: Champion RH, Burton JL, Burns DA, Breathnach SM, editors. Rook/ Wilkinson/ Ebling Textbook of dermatology. 6th ed. Oxford: Blackwell Science; 1998. p. 2437-575.  Back to cited text no. 2      
3.Habif TP. Clinical dermatology: A color guide to diagnosis and therapy. 4th ed. Edinburgh: Mosby; 2004. p. 622.  Back to cited text no. 3      
4.Bolognia JL, Seth JO, Sharon AG. Lines of Blaschko. J Am Acad Dermatol 1994;31:157-90.  Back to cited text no. 4      
5.Hauser C, Skaria A, Harms M, Saurat JH. Morphea following Blaschko's line. Br J Dermatol 1996;134:594-5.  Back to cited text no. 5      
6.Tu JH, Eisen AZ. Scleroderma. In: Freedberg IM, Eisen AZ, Wolff K, Austen KF, Goldsmith AL, Katz SI, et al . editors. Fitzpatrick's Dermatology in general medicine. 5th ed. New York: McGraw-Hill; 1999. p. 2023-33.  Back to cited text no. 6      
7.Jackson R. Observations on the site, size shape and arrangement of lesions in the human skin. Int J Dermatol 1984;23:370-5.   Back to cited text no. 7      
8.Wollenberg A, Baumann L, Plewig G. Linear atrophoderma of Moulin: a disease which follows Blaschko's lines. Br J Dermatol 1996;135:277-9.  Back to cited text no. 8      
9.Soma Y, Fujimoto M. Frontoparietal scleroderma (en coup de sabre) following Blaschko's lines. J Am Acad Dermatol 1998;38:366-8.  Back to cited text no. 9      
10.Soma Y, Kawakami T, Yamasaki E, Sasakai R. Linear scleroderma along Blaschko's lines in a patient with systematized morphea. Acta Derm Venereol 2003;83:362-4.  Back to cited text no. 10      


    Figures

  [Figure - 1]

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