Navigating the complexities: a case report on the varied presentation of lupus vulgaris

Ashima R. Chandran
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Abstract

A 16-year-old female presented with an asymptomatic lesion in the right axilla, evolving over six months into a scaly, erythematous to brownish-colored plaque with associated axillary lymphadenopathy. Routine investigations revealed mild anemia, elevated erythrocyte sedimentation rate (ESR), and a positive Mantoux test. Histopathological examination confirmed lupus vulgaris, characterized by tuberculoid granulomas within the superficial dermis. Treatment with anti-tubercular therapy led to significant lesion improvement. Lupus vulgaris, a form of cutaneous tuberculosis, presents varied clinical features and poses diagnostic challenges. Early recognition and prompt treatment are essential to prevent morbidity and scarring. This case highlights the importance of considering lupus vulgaris in differential diagnosis of atypical cutaneous lesions, contributing to better disease management and reduced morbidity.
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驾驭复杂情况:关于寻常狼疮各种表现的病例报告
一名 16 岁的女性患者因右腋窝出现无症状病变而就诊,病变在 6 个月后演变为鳞屑状、红斑至棕褐色斑块,并伴有腋窝淋巴结肿大。常规检查显示患者有轻度贫血、红细胞沉降率(ESR)升高以及曼氏试验阳性。组织病理学检查证实患者患有寻常狼疮,真皮浅层出现结核性肉芽肿。经过抗结核治疗后,患者的皮损明显好转。寻常狼疮是一种皮肤结核病,临床表现多种多样,给诊断带来了挑战。早期识别和及时治疗对防止发病和疤痕形成至关重要。本病例强调了在鉴别诊断不典型皮肤病变时考虑寻常狼疮的重要性,有助于更好地管理疾病和降低发病率。
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