Afonso Anaísa, Cachão Joana, Pinto Junior Vitor Laerte, Gouveia Teresa
Department of Pediatrics, Centro Hospitalar de Setúbal EPE, Setúbal, Portugal.
Department of Pediatrics, Centro Hospitalar de Setúbal EPE, Setúbal, Portugal
BMJ Case Rep. 2021 Apr 1;14(4):e240747. doi: 10.1136/bcr-2020-240747.
Gianotti-Crosti syndrome (GCS) is a self-limited condition, mainly affecting children younger than 6 years, less common in adolescents and adults. It consists of a viral exanthema with papular lesions with a flat top and symmetrical distribution, affecting predominantly extremities, gluteal region and extensor surfaces. It is often associated with viral infections but can also be related to bacterial infections, vaccination or be idiopathic. In this report, we present a case of GCS in a 13-year-old healthy female adolescent who presented with fever, odynophagia, prostration and diffuse maculopapular rash. The diagnosis of infectious mononucleosis due to infection by the Epstein-Barr virus was established. On the second week of the disease, a clinical recrudescence occurred, with worsening of the fever and modification of the exanthema characteristics. GCS is often an underdiagnosed entity. The differential diagnosis of viral exanthema can prove to be challenging and clinical suspicion is essential to achieve the diagnosis.
詹诺蒂-克罗西综合征(GCS)是一种自限性疾病,主要影响6岁以下儿童,在青少年和成人中较少见。它表现为一种病毒性皮疹,伴有平顶丘疹性病变,分布对称,主要累及四肢、臀部和伸侧皮肤表面。它常与病毒感染有关,但也可能与细菌感染、疫苗接种或病因不明有关。在本报告中,我们介绍了一例13岁健康女性青少年患GCS的病例,该患者出现发热、吞咽疼痛、极度虚弱和弥漫性斑丘疹。确诊为由爱泼斯坦-巴尔病毒感染引起的传染性单核细胞增多症。在疾病的第二周,出现了临床复发,发热加重,皮疹特征改变。GCS常常是一种诊断不足的疾病。病毒性皮疹的鉴别诊断可能具有挑战性,临床怀疑对于做出诊断至关重要。