Ann Dermatol. 2018 Feb;30(1):114-116. English.
Published online Dec 26, 2017.
Copyright © 2018 The Korean Dermatological Association and The Korean Society for Investigative Dermatology
Brief Communication

Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles

Jin-Hwa Son,1 Hyunju Jin,1 Hyang-Suk You,1 Woo-Haing Shim,2 Jeong-Min Kim,2 Gun-Wook Kim,1 Hoon-Soo Kim,1 Byung-Soo Kim,1 Moon-Bum Kim,1 and Hyun-Chang Ko1,2,3
    • 1Department of Dermatology, Pusan National University School of Medicine, Busan, Korea.
    • 2Department of Dermatology, Pusan National University Yangsan Hospital, Yangsan, Korea.
    • 3Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea.
Received November 03, 2016; Revised December 14, 2016; Accepted February 01, 2017.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Dear Editor:

Smooth muscle hamartoma (SMH) is a rare benign tumor of the skin, characterized by the proliferation of smooth muscle bundles within the reticular dermis1, 2.

A 5-month-old girl presented with multiple skin-colored patches with hypertrichosis on the left upper back since birth (Fig. 1A). The lesions were composed of three patches with linear distribution (Fig. 1B). The mother of the infant had noted transient induration with piloerection of the lesions when exposed to cool air and rubbing, called a “pseudo-Darier sign.” Dermoscopic findings showed different types of hypertrichosis in the three patches (Fig. 1D~F). Histopathological examination revealed numerous haphazardly arranged smooth muscle bundles in the dermis (Fig. 1C), and immunohistochemical staining showed diffusely stained smooth muscle actin (Fig. 1G~I). These findings suggested a diagnosis of congenital SMH.

Fig. 1
(A) Multiple linear scattered skin-colored patches with hypertrichosis on left upper back were observed. (B) Close-up view of left upper back. (C) Numerous smooth muscle bundles with various direction throughout dermis were shown (H&E, ×40). (D~F) In three sites, hypertrichosis with various density was shown on dermoscopy. (G~I) Different amount of smooth muscles according to hypertrichosis was observed in the reticular dermis (smooth muscle actin, ×20).

Gagné and Su3 suggested that hypertrichosis or prominent overlying hair in congenital SMH was usually present, but hair density was unchanged besides increased hair diameter and length. However, we speculated that there is a relation between hypertrichosis including hair density and the amount of smooth muscle bundle. Interestingly, dermoscopy revealed hypertrichosis with varying densities at the different sites (Fig. 1D~F), and histopathological examination revealed different numbers of smooth muscle in the reticular dermis (Fig. 1G~I). Thus, we measured the density of the hair (/mm3) in each lesion by using dermoscopy and the area of smooth muscle in the reticular dermis (%) by using a digital image analysis software (ImageJ 1.01 version; National Institutes of Health, Bethesda, MD, USA). The density of hair was 0.27/mm3 in the lateral hairy patch (Fig. 1D), 0.44/mm3 in the middle patch (Fig. 1E), and 1.40/mm3 in the medial patch (Fig. 1F), and the number of smooth muscle bundles in the reticular dermis was 9.5%, 24.6%, and 31.0% in each patch (Fig. 1G~I). Therefore, we believed that the number of hair in multiple patches, as observed using dermoscopy, was in proportion with the number of smooth muscle bundles in each lesion, as observed in the histopathological examination (Fig. 2).

Fig. 2
Correlation between hypertrichosis and the amount of smooth muscle bundle.

In the literature, SMH probably represents aberrant development of the arrector pilorum during fetal maturation. In human skin, it may develop at the time of mesodermal maturation4. Koizumi et al.5 suggested that numerous CD34-positive cells may be present in the stroma surrounding the smooth muscle bundles. It has been speculated that dermal dendritic cells release growth factors or directly contact the epithelial cells of the bulge, a region considered to represent a reservoir of hair follicle stem cells.

We speculate that dermal dendritic cells situated in the SMH might have a role in the hypertrichosis. However, the definite relation between SMH and hypertrichosis remains to be established.

Though it was focused one case to generalize the results, it is not possible to generalize the results. However, our case shows that a simple, non-invasive dermoscopic examination to determine hair density could be an ancillary method to predict the number of smooth muscle bundle in the dermis.

Notes

CONFLICTS OF INTEREST:The authors have nothing to disclose.

References

    1. Kwon SB, Lee SJ, Kim DW, Jun JB. Congenital smooth muscle hamartoma: a patchy follicular variant. Ann Dermatol 2000;12:231–234.
    1. Gerdsen R, Lagarde C, Steen A, Steen KH, Uerlich M, Bieber T. Congenital smooth muscle hamartoma of the skin: clinical classification. Acta Derm Venereol 1999;79:408–409.
    1. Gagné EJ, Su WP. Congenital smooth muscle hamartoma of the skin. Pediatr Dermatol 1993;10:142–145.
    1. Huffman DW, Mallory SB. Congenital smooth muscle hamartoma. Am Fam Physician 1989;39:117–120.
    1. Koizumi H, Kodama K, Tsuji Y, Matsumura T, Nabeshima M, Ohkawara A. CD34-positive dendritic cells are an intrinsic part of smooth muscle hamartoma. Br J Dermatol 1999;140:172–174.

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