Kikuchi’s disease (necrotizing lymphadenitis) presenting as acneiform eruption

Sahar H. Al-Natour, Najla Zabeeri
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引用次数: 1

Abstract

We report a case of Kikuchi’s disease (KD) in a 19 year old Saudi woman who initially presented with fever, myalgia, headaches and cervical and supraclavicular lymphadenopathy at the age of 10 years. A lymph node biopsy demonstrated the typical necrotizing lymphadenitis of KD. Her disease was controlled with oral corticosteroids and remained quiescent for 7 years without treatment. Recently, her systemic symptoms reappeared and she developed an acneiform eruption consisting of scaly, erythematous macules and indurated papules, with no comedones, over face, neck and mid chest. Skin biopsy was consistent with the diagnosis of KD. The majority of cutaneous lesions of KD show the characteristic histological changes that parallel those of the lymph nodes. Few have non-specific clinical and histological findings as this case, and are a diagnostic challenge. Dermatologists should be aware of this rare entity when evaluating acneiform eruptions with concomitant systemic symptoms. Screening and intermittent observation and evaluation for autoimmune disease, specifically systemic lupus erythematosus (SLE) is recommended in confirmed KD.

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菊池氏病(坏死性淋巴结炎)表现为针状疹
我们报告一例菊池病(KD)在一个19岁的沙特妇女谁最初表现为发烧,肌痛,头痛和颈部和锁骨上淋巴结病在10岁。淋巴结活检显示典型的KD坏死性淋巴结炎。她的疾病经口服皮质类固醇控制,在未经治疗的情况下保持了7年的静止状态。最近,她的全身性症状再次出现,她在面部、颈部和胸部中部出现鳞状红斑和硬化丘疹,无粉刺。皮肤活检符合KD的诊断。KD的大多数皮肤病变表现出与淋巴结相似的特征性组织学改变。很少有非特异性的临床和组织学表现,如本病例,是一个诊断挑战。皮肤科医生应该意识到这种罕见的实体时,评估痤疮疹伴随全身症状。对于确诊的KD患者,推荐筛查、间歇性观察和评估自身免疫性疾病,特别是系统性红斑狼疮(SLE)。
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