Gilsanz V, Harris G B
Radiology. 1978 Feb;126(2):463-5. doi: 10.1148/126.2.463.
The clinical, radiographic and pathologic findings of two children (ages 6 months and 5 1/2 years) with histiocytic medullary reticulosis are reviewed. Chest radiographs, excretory urograms, and skeletal survey revealed involvement of the mediastinum, lung parenchyma, pleural space, liver, spleen, kidneys, retroperitoneal lymph nodes, and long bones. This condition has rarely been reported in children and never during the first year of life. Histiocytic medullary reticulosis can occur in the very young; familiarity with its presentation at an early age helps to differentiate it from other infiltrative disorders of childhood.
对两名患有组织细胞性髓性网状细胞增多症的儿童（年龄分别为6个月和5岁半）的临床、影像学和病理学检查结果进行了回顾。胸部X光片、排泄性尿路造影和骨骼检查显示纵隔、肺实质、胸腔、肝脏、脾脏、肾脏、腹膜后淋巴结和长骨均有受累。这种疾病在儿童中很少见，在生命的第一年从未出现过。组织细胞性髓性网状细胞增多症可发生于幼儿期；熟悉其早期表现有助于将其与儿童期其他浸润性疾病区分开来。
