Bouhafs Nadia, N'joumi Chaimae, Elouali Aziza, Babakhouya Abdeladim, Rkain Maria, Benajiba Noufissa
Department of Pediatrics, Centre Hospitalier Universitaire Mohammed VI Oujda, Oujda, MAR.
Department of Pediatrics, Faculty of Medicine and Pharmacy of Oujda, Mohammed I University, Oujda, MAR.
Cureus. 2024 Jun 11;16(6):e62178. doi: 10.7759/cureus.62178. eCollection 2024 Jun.
Griscelli syndrome (GS) type II is a rare hereditary disorder characterized by partial albinism, immunodeficiency, and the subsequent development of hemophagocytic syndrome (HPS). Herein, we present a case involving a four-month-old infant admitted to our facility due to a prolonged fever complicated by HPS. The diagnosis of GS type 2 was established based on a constellation of clinical and laboratory findings: consanguinity, familial history of early infectious fatalities, ocular-cutaneous hypopigmentation, characteristic silvery hair sheen, onset of HPS, and notably, the pathognomonic appearance upon microscopic examination of a hair sample. The absence of giant granules within nucleated cells helped exclude Chediak-Higashi syndrome.
II型格里斯切利综合征(GS)是一种罕见的遗传性疾病,其特征为部分白化病、免疫缺陷以及随后发生的噬血细胞综合征(HPS)。在此,我们报告一例病例,一名4个月大的婴儿因长期发热并伴有HPS而入住我院。根据一系列临床和实验室检查结果确诊为2型GS:近亲结婚、有早期感染致死的家族史、眼皮肤色素减退、特征性的银发光泽、HPS的发作,特别是毛发样本显微镜检查时具有诊断意义的外观。有核细胞内无巨大颗粒有助于排除切迪阿克-东综合征。