Delcourt-Debruyne E M, Boutigny H R, Hildebrand H F
Faculté d'Odontologie, Département de Parodontologie, Université Lille, France.
J Periodontol. 2000 May;71(5):816-24. doi: 10.1902/jop.2000.71.5.816.
Chédiak-Higashi syndrome (C-HS) is a rare congenital disease characterized by defective neutrophil function with abnormal lysosomal inclusions, neutropenia, and reduced chemotaxis. The complete syndrome includes oculocutaneous albinism with photophobia, neurologic features, recurrent infections, and enterocolitis.
A 14-year-old male C-HS patient was referred to us because of serious periodontal destruction with acute inflamed gingiva and ulcers. Clinical and biological investigations were performed, leading to the diagnosis of C-HS.
Laboratory findings included neutropenia and hypergammaglobulinemia. Peripheral blood smears showed giant granules in neutrophils, eosinophils, and granulocytes. Bone marrow smears showed giant inclusions in leukocyte precursor cells. These granules and inclusions were characteristic of Chédiak-Higashi syndrome. Oral radiographic status showed extensive loss of alveolar bone leading, in most cases, to tooth exfoliation. Bacteria often associated with periodontitis were detected in subgingival plaque samples, including Fusobacterium nucleatum, Campylobacter rectus, Prevotella melaninogenica, Peptostreptococcus anaerobius, and Clostridium sp. Biopsies of periodontal tissues for light and electronic microscopic examinations revealed massive bacterial invasion of the epithelial tissue, epithelial cells, and connective tissue. Ultrastructural observations of periodontal polymorphonuclear leukocytes showed defective granulation, with abnormal granules not discharging their lysosomal content against engulfed bacteria. Viable dividing bacteria were found in the cytoplasm.
In this case, early-onset periodontitis seems to be the expression of C-HS granulocyte deficiency. Periodontal treatment of these patients is often unsuccessful. This case report illustrates the importance of the dentist in initiating clinical and biological investigations in such early aggressive periodontitis in young patients.
切-希综合征(C-HS)是一种罕见的先天性疾病,其特征为中性粒细胞功能缺陷,伴有异常溶酶体包涵体、中性粒细胞减少和趋化性降低。完整的综合征包括畏光性眼皮肤白化病、神经学特征、反复感染和小肠结肠炎。
一名14岁男性C-HS患者因严重的牙周破坏、急性牙龈发炎和溃疡转诊至我院。进行了临床和生物学检查,从而诊断为C-HS。
实验室检查结果包括中性粒细胞减少和高球蛋白血症。外周血涂片显示中性粒细胞、嗜酸性粒细胞和粒细胞中有巨大颗粒。骨髓涂片显示白细胞前体细胞中有巨大包涵体。这些颗粒和包涵体是切-希综合征的特征。口腔X线片显示牙槽骨广泛丧失,在大多数情况下导致牙齿脱落。在龈下菌斑样本中检测到了通常与牙周炎相关的细菌,包括具核梭杆菌、直肠弯曲菌、产黑色素普雷沃菌、厌氧消化链球菌和梭菌属。对牙周组织进行光镜和电镜检查的活检显示,上皮组织、上皮细胞和结缔组织有大量细菌侵入。对牙周多形核白细胞的超微结构观察显示颗粒形成缺陷,异常颗粒未对吞噬的细菌释放其溶酶体内容物。在细胞质中发现了存活的正在分裂的细菌。
在本病例中,早发性牙周炎似乎是C-HS粒细胞缺乏的表现。这些患者的牙周治疗通常不成功。本病例报告说明了牙医对年轻患者这种早期侵袭性牙周炎开展临床和生物学检查的重要性。