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对称性面部中央红斑及丘疹:一项临床病理挑战

Symmetrical Centrofacial Erythematous Plaques and Papules: A Clinicopathological Challenge.

作者信息

Sahni Kanika, Yadav Deepika, Ahuja Rhea, Agarwal Shipra

机构信息

Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India.

Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Indian Dermatol Online J. 2022 Jan 24;13(1):102-104. doi: 10.4103/idoj.IDOJ_66_21. eCollection 2022 Jan-Feb.

Abstract

Facial papular eruptions remain a diagnostic dilemma for the dermatologist with a wide range of inflammatory and infectious conditions manifesting in this manner. Here, we present a case of a 29-year-old, otherwise healthy man from North India with asymptomatic well-defined normoaesthetic symmetrical papules and plaques over the upper and mid-face of 3 months duration. Skin biopsy showed perivascular and periappendageal well-defined collections of foamy macrophages and epithelioid cells in superficial and deep dermis, characteristic of borderline lepromatous leprosy. Though acid-fast stain for lepra bacilli was negative both on lesional biopsy specimen and lesional and ear lobe slit skin smear, a 16s ribosomal ribonucleic acid (16s-r-RNA) polymerase chain reaction on skin biopsy specimen was found to be positive for lepra bacilli. A final diagnosis of borderline lepromatous leprosy in type I reaction was made and the patient received World Health Organization (WHO) multibacillary (MB) multidrug therapy along with oral steroids. This case highlights the unusual localized involvement in a case of MB leprosy lacking all the three cardinal features of leprosy, i.e. sensory loss, peripheral nerve involvement, and acid-fast bacilli positivity on biopsy or slit skin smear but diagnosed on the basis of characteristic histology and positive polymerase chain reaction results.

摘要

面部丘疹性皮疹对于皮肤科医生来说仍然是一个诊断难题,因为有多种炎症性和感染性疾病会以这种方式表现出来。在此,我们报告一例来自印度北部的29岁健康男性病例,其面部上半部分和中部出现无症状、边界清晰、感觉正常的对称性丘疹和斑块,病程3个月。皮肤活检显示,在浅真皮层和深真皮层有血管周围和附属器周围边界清晰的泡沫状巨噬细胞和上皮样细胞聚集,这是界线类偏瘤型麻风的特征。尽管在病变活检标本以及病变处和耳垂皮肤切片涂片上,麻风杆菌的抗酸染色均为阴性,但皮肤活检标本的16s核糖体核糖核酸(16s-r-RNA)聚合酶链反应检测发现麻风杆菌呈阳性。最终诊断为I型反应中的界线类偏瘤型麻风,患者接受了世界卫生组织(WHO)的多菌型(MB)联合化疗以及口服类固醇治疗。该病例突出了MB型麻风的一种不寻常的局限性表现,该病例缺乏麻风的所有三个主要特征,即感觉丧失、周围神经受累以及活检或皮肤切片涂片上抗酸杆菌阳性,但根据特征性组织学和聚合酶链反应阳性结果得以确诊。

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