Freiman Anatoli, Ting Patricia, Miller Mark, Greenaway Christina
Division of Dermatology, McGill University Health Centre, Montreal, Canada.
Cutis. 2005 Jun;75(6):341-6.
We describe a case of papulonecrotic tuberculid, a rare form of cutaneous tuberculosis, in a 25-year-old Philippino woman who had immigrated to Canada 8 years previously. The patient presented with a 3-week history of tender left cervical adenopathy; 1 week later, she developed multiple ulcerated erythematous nodules and emboluslike lesions scattered over her fingers. Results of a biopsy performed on the lymph node revealed granulomatous lymphadenitis, and Mycobacterium tuberculosis grew from the lymph node. Histopathologic analysis of an ulcerative finger lesion demonstrated nonnecrotizing granulomas with dense lymphocytic inflammation of the superficial dermis; however, results of acid-fast staining, mycobacterial culture, and polymerase chain reaction for M tuberculosis complex were all negative. Different conditions can mimic papulonecrotic tuberculid. Therefore, the diagnosis can be difficult unless M tuberculosis is isolated from a site other than the skin, because stain and culture results from skin biopsy specimens are typically negative and the polymerase chain reaction is positive in only 50% of cases. We review the epidemiology, clinicopathologic features, and differential diagnosis of papulonecrotic tuberculid. Awareness of this entity is important to distinguish it from other conditions and to institute appropriate therapy in a timely fashion.
我们描述了一例丘疹坏死性结核疹病例,这是一种罕见的皮肤结核形式,患者为一名25岁的菲律宾女性,8年前移民至加拿大。患者出现左侧颈部淋巴结压痛3周病史;1周后,她手指上出现多个溃疡的红斑结节及栓子样损害。对淋巴结进行活检的结果显示为肉芽肿性淋巴结炎,且从淋巴结中培养出结核分枝杆菌。对手指溃疡病变进行组织病理学分析显示为非坏死性肉芽肿,伴有浅表真皮致密的淋巴细胞炎症;然而,抗酸染色、分枝杆菌培养及结核分枝杆菌复合群聚合酶链反应的结果均为阴性。不同疾病可酷似丘疹坏死性结核疹。因此,除非从皮肤以外的部位分离出结核分枝杆菌,否则诊断可能会很困难,因为皮肤活检标本的染色和培养结果通常为阴性,聚合酶链反应仅在50%的病例中呈阳性。我们回顾了丘疹坏死性结核疹的流行病学、临床病理特征及鉴别诊断。认识这一疾病对于将其与其他疾病相鉴别并及时进行适当治疗很重要。