Ram Rapur, Swarnalatha Gudithi, Adiraju Krishna Prasad, Srinivasan Vangipurapu Rangacharlu, Dakshinamurty Kaligotla Venkata
Department of Nephrology, Nizam's Institute of Medical Sciences, Hyderabad, India.
Department of General Medicine, Nizam's Institute of Medical Sciences, Hyderabad, India.
NDT Plus. 2011 Aug;4(4):238-40. doi: 10.1093/ndtplus/sfr033. Epub 2011 Apr 6.
A cervical lymph node biopsy from a 38-year-old woman initially revealed necrotising lymphadenitis. Her case is presented herein. An exhaustive examination that included renal biopsy did not suggest systemic lupus erythematosus (SLE). She was diagnosed with Kikuchi-Fujimoto Disease (KFD) and was treated with prednisone. One year later, a renal biopsy performed for renal failure revealed Class IV SLE. It was proposed that lymphadenitis in this KFD patient should be considered as SLE so that the SLE would be properly treated. In our patient, this hypothesis was partially correct, because even though SLE could not be verified at initial presentation, it evolved into full SLE after a year interval.
一名38岁女性的颈部淋巴结活检最初显示为坏死性淋巴结炎。本文介绍了她的病例。包括肾活检在内的详尽检查未提示系统性红斑狼疮(SLE)。她被诊断为菊池-藤本病(KFD),并接受了泼尼松治疗。一年后,因肾衰竭进行的肾活检显示为IV级SLE。有人提出,该KFD患者的淋巴结炎应被视为SLE,以便对SLE进行恰当治疗。在我们的患者中,这一假设部分正确,因为尽管在初次就诊时无法证实为SLE,但一年后它发展为典型的SLE。