• Sonuç bulunamadı

Sebaceous Hyperplasia en plaque: A Rare Variant

N/A
N/A
Protected

Academic year: 2021

Share "Sebaceous Hyperplasia en plaque: A Rare Variant"

Copied!
2
0
0

Yükleniyor.... (view fulltext now)

Tam metin

(1)

Sebaceous Hyperplasia en plaque: A Rare Variant

Aslı Hapa,1MD, Duygu Gülseren,2MD, Gül Erkin,3MD, Özay Gököz,4MD

Address: 1Sifa University, Faculty of Medicine, Department of Dermatology, Gaziemir, İzmir, 2Polatlı Duatepe State Hospital, Polatlı, 3Private Güven Hospital, Dermatology Clinic, 4Hacettepe University, Faculty of Medicine,

Department of Pathology, Ankara, Turkey.

E-mail: draltaykan@yahoo.com

* Corresponding Author: Dr. Aslı Hapa, Sifa University, Faculty of Medicine, Department of Dermatology, Gaziemir, İzmir, Turkey.

Case Report DOI: 10.6003/jtad.16103c4

Published:

J Turk Acad Dermatol 2016; 10 (3): 16103c4

This article is available from: http://www.jtad.org/2016/3/jtad16103c4.pdf Keywords: Sebaceous hyperplasia, plaque

Abstract

Observation: We present a rare variant of sebaceous hyperplasia in the postauricular area presenting with yellowish papules coalescing to form a plaque. We would like to present this unique case because of its plaque like formation of the sebaceous papules as well as its rare localization in the retroauricular region.

Introduction

Sebaceous hyperplasia (SH) occurs frequently as solitary or multiple yellowish papules on the face in adults of middle age and older [1].

We present here a rare variant of sebaceous hyperplasia in the postauricular area presen- ting with yellowish papules coalescing to form a plaque.

Case Report

A 20- year- old female presented with asymptoma- tic skin lesions in the postauricular area for 2 years. She was otherwise healthy. Dermatological examination revealed multiple yellowish papules coalescing to form plaque on the left postauricular region (Figure 1). A- 4mm- punch biopsy was made from one of the yellowish papules which re- vealed hyperplastic sebaceous glands (Figure 2).

The diagnosis was sebaceous hyperplasia en pla- que.

Discussion

Sebaceous hyperplasia occurs frequently as solitary or multiple yellowish papules on the face in adults of middle age and older [1]. Re- cently, several cases in adolescence and Page 1 of 2

(page number not for citation purposes) Figure 1. Multiple yellowish papules coalescing to form plaques on the left postauricular region (4 mm-punch

biopsy site is seen on the middle of the plaque)

(2)

young adult patients have been described and identified as premature sebaceous gland hyperplasia [2]. The pathogenesis of this early clinical variant seems to be different from the senile type and it is poorly understood. Some reports have documented a family history [3].

In addition to this early clinical variant of se- baceous hyperplasia, several more clinical va- riants have been reported. There are patients with a giant form [4] on the cheek and also with linear arrangement [5]. Similiar to our case, patients who had grouped hyperplastic sebaceous glands in a plaque pattern were rarely described [6].

The most frequent localizations of the senile and premature type of SH are the face, neck and upper thorax [2]. However, reports of SH

on atypical localizations such as areola [7], vulva [8] and penis [9] have been described.

To the best of our knowledge, the only report with SH forming a plaque around auricular region apart from our case is the one descri- bed by Kim et al [6].

However, SH is thought to be associated with decreased androgen levels in aging individu- als and the pathogenesis of these early and unusual variants remain unknown. In con- clusion, we would like to present this unique case because of its plaque like formation of the sebaceous papules as well as its rare lo- calization in the retroauricular region.

References

1. McCalmont TM. Adnexal neoplasms. In: Dermato- logy. Bolognia JL, Jorizzo JL, Schaffer JV, editors.

3rd ed. China: Elsevier, 2012, 1839-1840.

2. Turan H1, Erdem H, Turan A, Kadioglu N, Basar F.

Premature sebaceous hyperplasia with pre-pubertal onset. Int J Dermatol 2014; 53: e224-226. PMID:

23829474

3. Boochai W, Leenutophong V. Familial presenile se- baceous gland hyperplasia. J Am Acad Dermatol 1997; 36: 120-122. PMID: 8996280

4. Kato N, Yasuoka A. Giant senile sebaceous hyperp- lasia. J Dermatol 1992, 19: 238-241. PMID: 1607487 5. Jeong TJ, Shin MK, Lee MH. Linear sebaceous hyperplasia on the chest. Clin Exp Dermatol 2009, 34: e366-367. PMID: 19489857

6. Kim HS, Lee HJ, Lee JY, Kim HO, Park YM. Papular skin lesions in the retroauricular area: A quiz. Pre- mature sebaceous hyperplasia en plaque. Acta Derm Venereol 2010; 90: 223-224. PMID: 20169325 7. Carmen FM, Luisa SM, Pilar E, Enric P, Lucia M,

Unilateral areolar sebaceous hyperplasia in a male.

Am J Dermatopathol 1996; 18: 417-419.

8. Malliah R, Gilhooly P, Lambert WC, Heller DS. Seba- ceous hyperplasia of the vulva: Case report and re- view of the literatüre. J Low Gen Tract Disease 2006;

10: 55-57. PMID: 16378033

9. Kumar A, Kossard S. Band-like sebaceous hyperpla- sia over the penis. Aust J Dermatol 1999; 40: 47-48.

PMID: 10098291

J Turk Acad Dermatol 2016; 10 (3): 16103c4. http://www.jtad.org/2016/3/jtad16103c4.pdf

Page 2 of 2

(page number not for citation purposes) Figure 2. A conspicious sebaceous gland with holoc-

rine degeneration on the background of normal skin (HEX100)

Referanslar

Benzer Belgeler

In this thesis, we present a survey on the well-posedness of the Cauchy problems for peridynamic equations with different initial data spaces.. These kind of equations can be

Our proposed Heart Rate Measuring device is economical and user friendly and uses optical technology to detect the flow of blood through index finger and that it is

Hemochromatosis is a multisystem disease with excess iron deposition in several organs such as the liver, heart, pancreas, joints, skin, and endocrine system that damages

Zakir Avşar, Cengiz Mutlu, Mücahit Özçelik, Cihan Özgün, Aysun Sarıbey Haykıran, Ali Özkan, Mustafa Salep, Cemal Sezer, Tahir Sevinç, Bülent Şener,

In contrast to the sporadic CJD, clinical presentation of variant CJD is unique almost in all cases, and diagnosis could be predicted confidently by clinical findings and

Heterozygous Beta Chain Variant Hemoglobin Pusan: A Rare Case Report in Turkish

Mucosal involvement is usually characterized by oral mucosal lesions and involvement of other mucosal surfaces such of vulvovaginal region is rare and may also be challenging in

This upward migration of dermal papilla is crucial for continuation of hair cycle [3]. In AP, there is failure of proper involution of lower segment of hair follicle and of