Bogusz Agata M, Bhargava Parul
Department of Pathology, Division of Hematopathology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02115, USA.
Int J Surg Pathol. 2013 Jun;21(3):287-96. doi: 10.1177/1066896912467369. Epub 2012 Nov 29.
Kikuchi-Fujimoto disease (KFD), a histiocytic necrotizing lymphadenitis (HNL), characteristically presents as cervical lymphadenopathy in young Asian women. Most resolve spontaneously with rare recurrences described. We report a patient with biopsy-proven recurrence of KFD-like HNL after almost 8 years and analyze 65 additional published cases with recurrences. While those with recurrences similarly affect young (average age = 27 years), Asian (80%) women (76%), 73% had multiple sites of involvement and 32% of those tested had underlying autoimmune conditions. Our case is unusual with respect to the following: (a) Age: 50 years, the oldest among the reported patients with recurrences. (b) Race: African descent, with only 3 others reported with recurrent HNL. Of these 4 cases, 2 had underlying autoimmunity. (c) Underlying condition: Her clinical and laboratory features were best felt to represent Sjögren's syndrome (SjS). Only 2 other cases of SjS-associated HNL have been reported; in 2 recently reported cases SjS developed subsequently.
菊池-藤本病(KFD)是一种组织细胞坏死性淋巴结炎(HNL),典型表现为年轻亚洲女性的颈部淋巴结病。多数患者可自发缓解,复发情况罕见。我们报告了1例经活检证实的类似KFD的HNL在近8年后复发的患者,并分析了另外65例已发表的复发病例。虽然复发患者同样以年轻(平均年龄27岁)、亚洲女性(80%)为主(76%),但73%有多处受累部位,32%的检测患者有潜在自身免疫性疾病。我们的病例在以下方面较为特殊:(a)年龄:50岁,是报告的复发患者中年龄最大的。(b)种族:非洲裔,仅有另外3例报告的复发性HNL患者为此种族。在这4例中,2例有潜在自身免疫性疾病。(c)基础疾病:她的临床和实验室特征最符合干燥综合征(SjS)。仅另有2例SjS相关的HNL病例报告;在最近报告的2例病例中,SjS是后来发生的。