Santa Cruz Liliana, Martins Ana Sofia, Guedes Ana Salomé, Mendonça Mariana, Carvalho Liliane
General and Family Medicine, USF (Unidade de Saúde Familiar) Coimbra Sul, Coimbra, PRT.
General and Family Medicine, USF (Unidade de Saúde Familiar) Mondego, Coimbra, PRT.
Cureus. 2023 Jul 18;15(7):e42091. doi: 10.7759/cureus.42091. eCollection 2023 Jul.
Many cases of adenopathies, whose differential diagnosis includes a wide spectrum of pathologies (including some malignant conditions like lymphoproliferative diseases, e.g., lymphomas), resort to primary healthcare. Kikuchi-Fujimoto disease is a rare, benign, self-limiting entity characterized by adenopathies, mainly in the cervical region, which may be associated with constitutional symptoms. This specific pathology is very rare in primary care and is often overlooked. That is why it is essential to promote medical literacy and provide support in managing these cases, which we want to emphasize through this case presentation. This case report presents a 24-year-old female patient who sought a consultation at the Family Health Unit due to a painful swelling in the right cervical region that lasted two weeks. She denied a history of recent infections or constitutional symptoms. A painful and hard right submaxillary mass, measuring 2 cm in diameter, was identified upon palpation. An analytical study and ultrasound of the soft tissues of the cervical region were initially required. Analytically, there were no relevant changes; however, the ultrasound revealed "hypoechoic ganglion formations in the right laterocervical chains, from the retroauricular region to the lower region of the neck, the largest measuring 19x7mm". The patient was reassessed one month later, due to an increase in the number of adenopathies, and a new ultrasound was performed that revealed "supraclavicular adenopathy". After that, she was referred to Secondary Healthcare (Central Hospital), where a lymph node biopsy was performed, with histological results of Kikuchi-Fujimoto disease. The patient maintains a follow-up in a hemato-oncology consultation, with painless adenopathies that, according to her, get worse with anxiety symptoms. Currently, the patient is being treated symptomatically, with stabilization of adenopathies and anxious manifestations. These patients need long-term follow-up due to the possibility of disease recurrence or the development of autoimmune processes. Although it is a diagnosis of exclusion, this disease must always be considered, since it can be mistaken with other serious pathologies that require aggressive treatments. Regarding the relationship between anxiety disorder and the worsening of adenopathies, although no conclusive evidence was found in the literature, there are some studies that have established a connection between inflammation and the deterioration of certain depressive symptoms.
许多淋巴结病病例,其鉴别诊断涵盖广泛的病理情况(包括一些恶性疾病,如淋巴增殖性疾病,如淋巴瘤),会求助于初级医疗保健。菊池-藤本病是一种罕见的、良性的、自限性疾病,其特征为淋巴结病,主要位于颈部,可能伴有全身症状。这种特定的病理情况在初级医疗保健中非常罕见,常被忽视。这就是为什么提高医学素养并在处理这些病例时提供支持至关重要,我们希望通过这个病例介绍来强调这一点。本病例报告介绍了一名24岁女性患者,她因右侧颈部疼痛性肿胀持续两周而到家庭健康中心就诊。她否认近期有感染史或全身症状。触诊时发现一个直径2厘米的右侧颌下疼痛性硬结。最初需要对颈部软组织进行分析研究和超声检查。分析结果无相关异常;然而,超声显示“右侧颈外侧链从耳后区域至颈部下部有低回声淋巴结形成,最大者为19×7毫米”。一个月后,由于淋巴结病数量增加,对患者进行了重新评估,并再次进行超声检查,结果显示“锁骨上淋巴结病”。之后,她被转诊至二级医疗保健机构(中心医院),在那里进行了淋巴结活检,组织学结果为菊池-藤本病。患者在血液肿瘤门诊接受随访,有无痛性淋巴结病,据她所说,焦虑症状会使其加重。目前,患者正在接受对症治疗,淋巴结病和焦虑表现已稳定。由于疾病复发或自身免疫过程发展的可能性,这些患者需要长期随访。尽管这是一种排除性诊断,但必须始终考虑到这种疾病,因为它可能被误诊为其他需要积极治疗的严重疾病。关于焦虑症与淋巴结病加重之间的关系,尽管文献中未找到确凿证据,但有一些研究已证实炎症与某些抑郁症状的恶化之间存在联系。