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首页> 外文期刊>Sao Paulo Medical Journal >Report of a rare case of histiocytic necrotizing lymphadenitis with bilateral pleural effusion diagnosed via cervical lymph node biopsy
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Report of a rare case of histiocytic necrotizing lymphadenitis with bilateral pleural effusion diagnosed via cervical lymph node biopsy

机译:通过颈淋巴结活检诊断为双侧胸腔积液的组织细胞坏死性淋巴结炎的罕见病例报告

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ABSTRACT CONTEXT: Histiocytic necrotizing lymphadenitis (HNL) is a rare disorder that is often benign and self-limiting. There have been reports of co-occurrence of HNL with other diseases, including systemic lupus erythematosus, hemophagocytic syndrome and antiphospholipid syndrome. CASE REPORT: Here, we report a case in which a patient experienced unexplained fever, swelling of the cervical lymph node and bilateral pleural effusion and was ultimately diagnosed with HNL based on results from a lymph node biopsy. After treatment with glucocorticoid, the patient regained normal body temperature, the swelling of the lymph nodes disappeared and the pleural effusion was reabsorbed. CONCLUSIONS: The pathogenesis of HNL remains unclear, and pleural effusion is rarely reported in HNL patients. We presented this case to improve diagnostic awareness of this condition among clinicians and help reduce the likelihood of misdiagnosis.
机译:摘要背景:组织细胞性坏死性淋巴结炎(HNL)是一种罕见的疾病,通常是良性且自限性的。有HNL与其他疾病(包括系统性红斑狼疮,吞噬细胞综合征和抗磷脂综合征)共存的报道。病例报告:在这里,我们报告一例患者发生原因不明的发热,子宫颈淋巴结肿大和双侧胸腔积液,并根据淋巴结活检的结果最终被诊断为HNL。糖皮质激素治疗后,患者恢复了正常体温,淋巴结肿胀消失,胸腔积液被重新吸收。结论:HNL的发病机制仍不清楚,在HNL患者中很少报道有胸腔积液。我们提出该病例是为了提高临床医生对此病的诊断意识,并有助于减少误诊的可能性。

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