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Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

An. Bras. Dermatol. vol.85 no.3 Rio de Janeiro June 2010

http://dx.doi.org/10.1590/S0365-05962010000300020 

WHAT IS YOUR DIAGNOSIS?

 

Case for diagnosis*

 

 

Carolina TomiyoshiI; Adma Silva de Lima WojcikII; Elisa Milani Oba VencatoIII; Guilherme Ribas TaquesIV; José Fillus NetoV; Fabiane Andrade Mulinari BrennerVI

IMedical student (6th year), Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil
IIPhysician currently undergoing medical residency in Dermatology at the Teaching Hospital of the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil
IIIPhysician currently undergoing medical residency in Dermatology at the Teaching Hospital of the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil
IVPhysician currently undergoing medical residency in Anatomopathology at the Teaching Hospital of the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil
VMaster's degree in Dermatopathology from the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil, Dermatopathologist at the Anatomopathology Department of the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil
VIMaster's degree in Dermatopathology from the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil, Head of the Dermatology Division of the Department of Clinical Medicine, Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil

Mailing Address

 

 


ABSTRACT

Localized scleroderma or morphea is a chronic disease of the connective tissue. Its etiology may be autoimmune and the condition results from a disturbance in collagen synthesis and deposition, clinically represented by sclerotic skin lesions. Some plaques may be yellowish, which can be misleading at diagnosis. This article reports the case of an adolescent girl who concomitantly presented erythematous lesions and yellowish lesions, both of which constitute clinical manifestations of the disease.

Keywords: Vitamin E; Skin and connective tissue diseases; Scleroderma, localized


 

 

HISTORY OF THE DISEASE

A 13-year old patient with lesions on the right leg for the past two years, latterly affecting her upper and lower limbs and abdomen. She reported no systemic signs or symptoms. Past history of prurigo.

Dermatological examination revealed clearly delimited, sclerotic, yellowish-brown plaques with a central depression and violet-colored border on the lower limbs and lower abdomen; erythematous lesions on the upper abdomen, livedo reticularis on the lower limbs and Raynaud's phenomenon on her hands (Figures 1, 2 and 3).

 

 

 

 

Laboratory exams were all within normal limits. Evaluation of antinuclear factor (ANF) showed titers of 1:80 with a fine dotted nuclear pattern. Biopsy of the erythematous and yellowish lesions showed skin with thickening of the collagen fibers enclosing the appendages, rare perivascular lymphocytes, thickening of connective fibers in the deep dermis and moderate perivascular lymphocytic infiltrate (Figure 4). Hematoxylin-eosin staining revealed very thick elastic fibers distributed throughout the entire dermis (Figure 5). Treatment was initiated with systemic corticosteroids, vitamin E and moisturizing cream, resulting in stabilization of the lesions.

 

 

 

COMMENTS

Localized scleroderma is a rare disease of the connective tissue, the etiology of which is probably autoimmune-related. It is characterized by a thickening of the skin that is consequent to an increase in the synthesis of collagen, glycosaminoglycans and other substances produced by the fibroblasts.1,2 It has a prevalence rate of around 0.4 – 1 cases per 100,000 individuals and affects 2-3 women for each man.1,3,4 Children are more susceptible to developing the disease. 5 It is classified into five subtypes: plaque morphea, generalized morphea, linear scleroderma, en coup de sabre and pansclerotic.6 The most common types are plaque morphea and linear scleroderma,1,3,5 the former characterized by brownish indurated patches of thickened skin occasionally surrounded by a violaceous/ erythematous "lilac" border,4,6 which is associated with active stages of the disease.7

Histologically, it has three principal characteristics: collagen deposits in the dermis and subcutaneous layer, vascular abnormalities and inflammatory cell infiltrate. The thickness of the dermis increases and collagen begins to substitute adipose tissue around the sweat glands, extending to the subcutaneous layer. There is atrophy of the appendages, with thickening of the capillary wall and narrowing of the lumen. The inflammatory infiltrate is composed of lymphocytes, macrophages and other plasma cells distributed around the vessels and diffusely through the dermis and subcutaneous layer.6,8

Localized scleroderma must be differentiated from systemic sclerosis. In the latter condition, there is cutaneous fibrosis and the internal organs are affected, leading to interstitial lung disease, pulmonary arterial hypertension and renal failure, among others, that are a consequence of structural and functional abnormalities of the endothelium and activation of the immune system. The histological abnormalities in the skin are similar in both the localized and systemic forms.9 Transition from localized scleroderma to systemic sclerosis is rare, with rates ranging from 0.9% to 5.7%.6,9 Recent studies have suggested that localized scleroderma is not always exclusively a skin disease, although the correlation with systemic sclerosis remains a subject of debate.9

Skin lesions in initial stages may present with edema and erythema, 6 such as in the case reported here. The yellowish coloring found here is not commonly described in this type of lesion and may be misleading at diagnosis. In this case, extremely thick elastic fibers were found distributed throughout the dermis. This abnormality is found in elastic tissue disorders such as pseudoxanthoma elasticum and may explain the xanthochromic staining of the plaques.

The pharmacological treatment of localized scleroderma represents a challenge and is generally directed towards suppressing the inflammation and the collagen alterations.6 In addition to its antioxidant effect, vitamin E stabilizes the lysosomal membrane, inhibiting autoimmune-related events. 10 Methotrexate and corticosteroids are a good alternative. Phototherapy alone or in combination with calcipotriol may be effective.1,6

 

REFERENCES

1. Zulian F, Athreya BH, Laxer R, Nelson AM, Feitosa de Oliveira SK, Puno MG, et al. Juvenile localized scleroderma: clinical and epidemiological features in 750 children. An international study. Rheumatology. 2006;45:614-20.         [ Links ]

2. Ieremia G, Raica M, Cîmpean AM, Bocan V. Morphologic and histochemical changes in the skin of patients with scleroderma. Rom J Morphol Embryol. 2007;48: 361-7.         [ Links ]

3. Christen-Zaech S, Hakim MD, Afs FS, Paller AS. Pediatric morphea (localized scleroderma): review of 136 patients. J Am Acad Dermatol. 2008;59:385-96.         [ Links ]

4. Macedo PA, Shinjo SK, Goldenstein-Schainberg. Esclerodermia Juvenil. Acta Reumatol Port. 2008;33:289-97.         [ Links ]

5. Mzano AV, Menni S, Podi A, Borghi A, Fuligni A, Fabbri P, et al. Localized scleroderma in adults and children. Clinical and laboratory investigations on 239 cases. Eur J Dermatol. 2003;13:171-6.         [ Links ]

6. Zancanaro PCQ, Isaac AR, Garcia LT, Costa IMC. Esclerodermia localizada na criança: aspectos clínicos, diagnósticos e terapêuticos. An Bras Dermatol. 2009;84:161-72.         [ Links ]

7. Sampaio AS e Rivitti EA. Dermatologia. 2ª ed.São Paulo: Artes Médicas; 2001. p. 364-70.         [ Links ]

8. Weedon D. Skin Pathology. 2nd ed. London: Churchill Livingstone;2002. p. 346-51.         [ Links ]

9. Zulian F. Systemic manifestations in localized scleroderma. Curr Rheum Rep. 2004;6:417-24.         [ Links ]

10. Gaby AR. Natural remedies for scleroderma. Altern Med Rev. 2006;11:188-95.         [ Links ]

 

 

Mailing Address:
Carolina Tomiyoshi
Serviço de Dermatologia - SAM 4
R General Carneiro número 181 Centro
80000 000 Curitiba- Paná - Brasil
e-mail: carol_tomiyoshi@uol.com.br

Approved by the Editorial Board and accepted for publication on 27.11.2009.
Conflict of interest: None
Financial funding: None

 

 

* Study conducted at the Federal University of Paraná (UFPR), Curitiba, Paraná, Brazil.