Abstract

IntroductionLupus vulgaris is the most common form of cutaneous tuberculosis. It may easily be overlooked if a proper differential diagnosis is omitted.Case presentationA 46-year-old Turkish woman presented with a 42-year history of erythamatous plaque on her left arm. Ziehl–Neelsen and periodic acid-Schiff stains did not show any acid-fast bacilli. Culture from a biopsy specimen was negative for Mycobacterium tuberculosis. The result of a polymerase chain reaction-based assay for Mycobacterium was negative. Histopathologic findings revealed a tuberculoid granuloma containing epithelioid cells, lymphocytes and Langerhans-type giant cells. A diagnosis of lupus vulgaris was made by clinical and histopathologic findings.ConclusionsThe lesion improved after antituberculous therapy, confirming the diagnosis of lupus vulgaris.

Highlights

  • Lupus vulgaris is the most common form of cutaneous tuberculosis

  • The lesion improved after antituberculous therapy, confirming the diagnosis of lupus vulgaris

  • We report the case of a patient with long-lasting Lupus vulgaris (LV) mimicking hemangioma

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Summary

Introduction

Lupus vulgaris (LV) is the most common clinical type of cutaneous tuberculosis (TB) in adults [1, 2]. Case presentation A 46-year-old Turkish woman presented to our institute with a red, well-demarcated plaque on her left arm. She said the lesion had appeared when she was 4 years old. A doctor who our patient had visited when the lesion first appeared had said that the lesion was a birthmark. The results of venereal disease research laboratory (VDRL) and human immunodeficiency virus (HIV) tests were negative. Culture from the biopsy specimen was negative for Mycobacterium tuberculosis. A real-time polymerase chain reaction (PCR)-based assay of the biopsy specimen gave a negative result for Mycobacterium. Lupus vulgaris was diagnosed in our patient on the basis of the clinical and histopathologic findings. The cutaneous lesions started to regress within 3 months and had completely healed with atrophic scarring and postinflammatory hyperpigmentation after 9 months (Fig. 3)

Discussion
Conclusions

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