Huang Pengling, Ma Chao, Pei Guanghua, Sun Daqing
Department of Ultrasound, Tianjin Children's Hospital, Tianjin, China.
Department of General Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Transl Pediatr. 2022 Jul;11(7):1274-1280. doi: 10.21037/tp-22-255.
A squamous epithelial inclusion cyst in a lymph node is a rare heterotopic phenomenon. Heterotopic squamous inclusion cysts in cervical lymph nodes are even rarer, and to date, only 3 such cases have been reported in the literature, none of which have described the ultrasound features. Here, we report a pediatric case, focusing on the ultrasonographic manifestations of the disease and the differential diagnosis of cervical space-occupying lesions in children.
We report the case of a 6-year-old boy in good health, who presented with a non-tender mass on the right side of the neck 1 month earlier. Some 7 days before admission, the mass gradually increased in size and became tender. Laboratory tests showed an increase in C-reactive protein of 17 mg/L (normal range: 0-8 mg/L). The physical examination revealed a palpable 3.0 cm × 2.0 cm mass with tenderness and poor mobility in the right submandibular region. Doppler ultrasonography showed an oval, ill-defined mass in the right submandibular area, consisting of a peripheral homogeneous hypoechoic component with hilar-like vascularity and an internal heterogeneous very hypoechoic component with patchy hyperechoic areas. The computed tomography (CT) scan showed a heterogeneously hypodense mass with irregular annular enhancement in the right submandibular region. Lymph node tuberculosis or space-occupying lesions were suspected based on the clinical and imaging findings. The mass was completely excised by surgery. The pathological diagnosis was a secondary infection of squamous epithelial inclusion cysts in the right cervical lymph node. The peripheral homogeneous hypoechoic component was normal lymph node tissue, and the internal heterogeneous very hypoechoic component was a squamous inclusion cyst with keratin debris. The patient was followed up for a total of 3 times after surgery, and no recurrence of the tumor was found.
Ultrasonography can help in the early diagnosis of heterotopic squamous inclusion cysts in children's cervical lymph nodes, and can be used to differentiate other cervical lesions. We reviewed the literature and found that this heterotopic phenomenon was more likely to occur in the submandibular region of the neck in younger patients. Surgery may be an effective treatment for this disease.
淋巴结内的鳞状上皮包涵囊肿是一种罕见的异位现象。宫颈淋巴结内的异位鳞状包涵囊肿更为罕见,迄今为止,文献中仅报道了3例此类病例,均未描述其超声特征。在此,我们报告1例儿科病例,重点关注该疾病的超声表现及儿童颈部占位性病变的鉴别诊断。
我们报告1例6岁健康男孩,1个月前右侧颈部出现无痛性肿块。入院前约7天,肿块逐渐增大并出现压痛。实验室检查显示C反应蛋白升高至17mg/L(正常范围:0 - 8mg/L)。体格检查发现右下颌下区可触及一个3.0cm×2.0cm的肿块,有压痛,活动度差。多普勒超声显示右下颌下区有一个椭圆形、边界不清的肿块,由周边均匀的低回声成分伴门样血管分布以及内部不均匀的极低回声成分伴片状高回声区组成。计算机断层扫描(CT)显示右下颌下区有一个不均匀低密度肿块,呈不规则环形强化。根据临床和影像学表现怀疑为淋巴结结核或占位性病变。通过手术将肿块完整切除。病理诊断为右颈部淋巴结鳞状上皮包涵囊肿继发感染。周边均匀的低回声成分是正常淋巴结组织,内部不均匀的极低回声成分是含有角蛋白碎屑的鳞状包涵囊肿。患者术后共随访3次,未发现肿瘤复发。
超声检查有助于儿童宫颈淋巴结内异位鳞状包涵囊肿的早期诊断,并可用于鉴别其他宫颈病变。我们查阅文献发现,这种异位现象在年轻患者中更易发生于颈部下颌下区。手术可能是治疗该疾病的有效方法。