Szczurowska Agata, Pawlowski Tomasz, Halon Agnieszka, Skoczynska Anna
Department of General Radiology, Interventional Radiology and Neuroradiology, Wroclaw Medical University, University Hospital in Wroclaw, Borowska 213 50-556, Wroclaw, Poland.
Department and Clinic of Internal and Occupational Diseases and Hypertension, Wroclaw Medical University, University Hospital in Wroclaw, Borowska 213 50-556, Wroclaw, Poland.
J Med Case Rep. 2017 Feb 12;11(1):39. doi: 10.1186/s13256-017-1208-4.
Kikuchi-Fujimoto disease is a very rare cause of benign lymphadenopathy affecting mainly young Asiatic females. Little is known about the causative agent of Kikuchi-Fujimoto disease; however, there are hypotheses of infectious, autoimmune, or hyperimmune background of the disease that have not yet been confirmed in the conducted studies. Frequent episodes of tonsillitis preceding the onset of Kikuchi-Fujimoto disease have not been described as yet.
A 23-year-old white man with a history of over 20 episodes of tonsillitis in the preceding 2 years was admitted to our hospital because of cervical unilateral lymphadenopathy, fever, night sweating, weight loss, and fatigue. On admission, slight tenderness of cervical lymph nodes and asymmetric palate tonsil enlargement were noted. Owing to the patient's general symptoms and history of malignancy in his close family, a malignant disease such as lymphoma was suspected. Histopathological examination of the excised lymph node revealed areas of coagulative necrosis with abundant karyorrhectic debris, with histiocytes and lymphocytes observed at the margins of the necrotic areas. The microscopic examination led to an unexpected diagnosis of Kikuchi-Fujimoto disease. The patient was treated symptomatically. All of the patient's symptoms, excluding tonsil enlargement, retreated within 2 months.
In the differential diagnosis of cervical lymphadenopathy in patients with frequent episodes of tonsillitis, Kikuchi-Fujimoto disease should be taken into account. Kikuchi-Fujimoto disease may convincingly mimic symptoms characteristic of lymphoma.
菊池-藤本病是一种非常罕见的良性淋巴结病病因,主要影响年轻的亚洲女性。关于菊池-藤本病的病原体知之甚少;然而,有关于该疾病具有感染性、自身免疫性或超免疫背景的假说,但在已开展的研究中尚未得到证实。此前尚未有关于菊池-藤本病发病前频繁发作扁桃体炎的描述。
一名23岁的白人男性,在过去2年中有超过20次扁桃体炎发作史,因颈部单侧淋巴结病、发热、盗汗、体重减轻和疲劳入住我院。入院时,发现颈部淋巴结有轻微压痛,腭扁桃体不对称肿大。由于患者的全身症状以及其近亲中有恶性肿瘤病史,怀疑患有淋巴瘤等恶性疾病。对切除的淋巴结进行组织病理学检查,发现有凝固性坏死区域,伴有大量核碎裂碎片,在坏死区域边缘可见组织细胞和淋巴细胞。显微镜检查意外诊断为菊池-藤本病。对该患者进行了对症治疗。除扁桃体肿大外,患者的所有症状在2个月内均消退。
在对频繁发作扁桃体炎患者的颈部淋巴结病进行鉴别诊断时,应考虑菊池-藤本病。菊池-藤本病可能令人信服地模仿淋巴瘤的特征性症状。