Kaplan K J, Goodman Z D, Ishak K G
Department of Pathology, Walter Reed Army Medical Center, Washington, DC 20307-5001, USA.
Am J Surg Pathol. 2001 Oct;25(10):1316-21. doi: 10.1097/00000478-200110000-00014.
Children with the clinical syndrome of visceral larva migrans as a result of Toxocara species have typical lesions in the liver and other viscera, consisting of palisading granulomas that contain numerous eosinophils and often Charcot-Leyden crystals; recognizable parasites are uncommon. Similar eosinophilic granulomas that are found incidentally in adults often cause diagnostic problems. To define better the clinical, laboratory, and pathologic features of these lesions, we reviewed 43 cases of hepatic eosinophilic granuloma (excluding cases of Langerhans' cell histiocytosis) collected in the files of the AFIP over a period of 31 years. The eosinophilic granulomas were found in patients of all ages (range 12 months to 77 years); 30% were younger than 20 years. There were 26 male and 17 female patients. Most patients (26 of 43; 60%) were asymptomatic, and the lesions were discovered incidentally. Others had fever (20%) or abdominal pain (20%). The granulomas were typically multiple (61%), with central necrosis surrounded by a mixed inflammatory infiltrate with numerous eosinophils and variable numbers of neutrophils. lymphocytes, and a palisade of epithelioid histiocytes and/or giant cells. Charcot-Leyden crystals were present in 19 cases (44%). Remnants of parasites (eight Toxocara sp., two Capillaria sp.) were identified in the tissue in 10 patients. There was a positive serologic test for Toxocara sp. in five additional cases. Immunohistochemical staining using polyclonal antiserum against Toxocara canis larvae demonstrated positivity in macrophages in eight of 13 cases tested. We conclude that identification of an eosinophilic granuloma in the liver should suggest the diagnosis of visceral larva migrans and prompt a search for the causative organism with serial sectioning of the block and serologic tests for Toxocara and other causative parasites.
因弓蛔虫属物种导致内脏幼虫移行临床综合征的儿童,在肝脏和其他内脏有典型病变,由含有大量嗜酸性粒细胞且常含夏科-雷登结晶的栅栏状肉芽肿组成;可识别的寄生虫并不常见。在成人中偶然发现的类似嗜酸性肉芽肿常引发诊断问题。为了更好地界定这些病变的临床、实验室和病理特征,我们回顾了31年间美国武装部队病理研究所档案中收集的43例肝嗜酸性肉芽肿病例(不包括朗格汉斯细胞组织细胞增多症病例)。嗜酸性肉芽肿见于各年龄段患者(年龄范围12个月至77岁);30%的患者年龄小于20岁。有26例男性患者和17例女性患者。大多数患者(43例中的26例,60%)无症状,病变是偶然发现的。其他患者有发热(20%)或腹痛(20%)。肉芽肿通常为多发(61%),中央坏死,周围是混合性炎症浸润,有大量嗜酸性粒细胞以及数量不等的中性粒细胞、淋巴细胞,还有一层上皮样组织细胞和/或巨细胞构成的栅栏。19例(44%)有夏科-雷登结晶。在10例患者的组织中鉴定出寄生虫残体(8例弓蛔虫属,2例毛细线虫属)。另有5例Toxocara sp.血清学检测呈阳性。用抗犬弓蛔虫幼虫的多克隆抗血清进行免疫组化染色,在13例检测病例中的8例巨噬细胞中显示阳性。我们得出结论,肝脏中嗜酸性肉芽肿的发现应提示内脏幼虫移行的诊断,并促使通过对组织块进行连续切片以及对弓蛔虫和其他致病寄生虫进行血清学检测来寻找病原体。