Houcine Y, Sassi A, Mlika M, Yassine H, Mezni F
Pathology Department, Abderrahmen Mami Hospital, Ariana, Tunisia.
LR18SP06, Tunisia.
Heliyon. 2020 Jun 24;6(6):e04225. doi: 10.1016/j.heliyon.2020.e04225. eCollection 2020 Jun.
A 38-year-old man, with no history of malignancy, was found to have a 2 cm jugular lymph node, for which a lymph node tuberculosis was suspected. The specimen revealed a cystic structure lined by mature keratinizing squamous epithelium with a prominent granular cell layer consistent with a squamous inclusion cyst in a lymph node, but a metastatic squamous cell carcinoma could not be excluded. This is the first case report of a rapidly enlarging squamous inclusion cyst in a jugular lymph node. Our case demonstrates the diagnostic challenges related to a squamous inclusion cyst in cervical lymph node and serves to inform the readers to consider this lesion in the differential diagnosis for similar situations.
一名38岁男性,无恶性肿瘤病史,发现有一个2厘米的颈静脉淋巴结,怀疑为淋巴结结核。标本显示为一个囊性结构,内衬成熟的角化鳞状上皮,有明显的颗粒细胞层,符合淋巴结中的鳞状上皮包涵囊肿,但不能排除转移性鳞状细胞癌。这是颈静脉淋巴结中快速增大的鳞状上皮包涵囊肿的首例病例报告。我们的病例展示了与颈部淋巴结鳞状上皮包涵囊肿相关的诊断挑战,并提醒读者在类似情况的鉴别诊断中考虑这种病变。