Levine S, Smith V V, Malone M, Sebire N J
Department of Paediatric Histopathology, Great Ormond Street Hospital, London, UK.
Histopathology. 2005 Nov;47(5):508-16. doi: 10.1111/j.1365-2559.2005.02258.x.
To describe the spectrum of histopathological features encountered in children with chronic granulomatous disease (CGD) at a specialist centre.
The histopathological findings of 88 surgical pathology requests from a range of organ systems including upper and lower gastrointestinal tract biopsy series, liver, bladder, bone, lung, skin, soft tissue, bone marrow and lymph node biopsy specimens, in 32 patients aged 4 months to 18 years (median 7 years) with CGD were reviewed. In most tissues the features were those of active chronic inflammation, with or without abscess or granuloma formation, often associated with fungal infection. In some tissues, more characteristic findings were identified, including the presence of pigmented macrophages, especially in hepatic sinusoids and colonic mucosa, where active chronic eosinophil predominant colitis was also observed.
Chronic granulomatous disease may present to histopathologists in a wide range of tissue specimens most often demonstrating features of active chronic inflammation with or without granuloma formation. The presence of numerous pigmented macrophages in association with such inflammation should raise suspicion of the diagnosis. In addition, diffuse granulomatous inflammation of the lung and hepatic abscess formation should be regarded as suggestive of the diagnosis.
描述在一家专科中心慢性肉芽肿病(CGD)患儿中所遇到的组织病理学特征谱。
回顾了32例年龄在4个月至18岁(中位年龄7岁)的CGD患者的88份手术病理申请的组织病理学结果,这些申请来自一系列器官系统,包括上、下消化道活检系列、肝脏、膀胱、骨骼、肺、皮肤、软组织、骨髓和淋巴结活检标本。在大多数组织中,特征为活动性慢性炎症,伴有或不伴有脓肿或肉芽肿形成,常与真菌感染相关。在一些组织中,发现了更具特征性的表现,包括色素沉着巨噬细胞的存在,特别是在肝血窦和结肠黏膜中,在结肠黏膜中还观察到活动性慢性嗜酸性粒细胞为主的结肠炎。
慢性肉芽肿病可能在多种组织标本中呈现给组织病理学家,最常表现为伴有或不伴有肉芽肿形成的活动性慢性炎症特征。伴有此类炎症的大量色素沉着巨噬细胞的存在应引起对该诊断的怀疑。此外,肺部弥漫性肉芽肿性炎症和肝脓肿形成应被视为提示该诊断。