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我们曾收治骨嗜酸粒细胞淋巴肉芽肿1例、汉-许-克氏综合征2例、累-赛氏征1例。现摘要报告并讨论如下: [例1]张×,男,1岁半。硬腭有红枣大,无痛性肿物两个月,表面溃疡状,有黄色伪膜覆盖,松动,两颌下各有一肿大淋巴结。近月余时有低热。病理报告为骨嗜酸粒细胞淋巴肉芽肿。入院后检查其他脏器无异常。给抗生素、强的松10天。于全麻下行肿物刮除术,术中见硬腭呈圆形破坏3×3×1厘米,边缘锐利,骨板未穿通,拔除,创面填碘仿纱条缝合固定。术后热退,9天拆线,骨创肉芽组织新生,拔牙创愈合出院。一个月后复查腭粘膜完全愈合。术后病理报告:粘膜下见大量嗜酸粒细胞和组织细胞浸
We have received bone eosinophilic granulomatosis in 1 case, 2 cases of Han - Xu - Kline’s syndrome, tired - Sae’s syndrome in 1 case. The summary report is presented and discussed below: [Example 1] Zhang ×, male, 1 year and a half. Hard palate jujube, painless mass two months, the surface of ulcers, yellow pseudomembranous cover, loose, two enlarged jaw lymph nodes. Low heat in recent months. Pathological report of bone eosinophilic granulomatosis. After admission check other organs without exception. To antibiotics, prednisone 10 days. Under general anesthesia for tumor curettage, intraoperative see the hard palate was a circular damage 3 × 3 × 1 cm, sharp edges, bone plate is not perforated, unplug, wound fill iodine gauze suture fixation. After the heat back, 9 days stitches, bone granulation tissue regeneration, tooth extraction and healing. After a month review the palate mucosa completely healed. Postoperative pathology report: Submucosal see a large number of eosinophils and somatic cell immersion