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A case of eosinophilic granuloma of the skull in an adult man: a case report

机译:一例成年男子颅骨嗜酸性肉芽肿1例

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Eosinophilic granuloma is very rare benign bone tumor which presents in more than 90% in children under the age of ten. There is predominance for males. It is usually found at flat and long bones. The skull and vertebral spine is often affected. We report a case of 57 year-old man who gradually developed local pain at his skull and orbit. A soft, movable, palpable and tender mass was found at the left temporal bone. The pain deteriorated after an accidental injury at skull and remained so. The clinical examination revealed no pathological findings. The patient was a doctor who smoked and consumed alcohol daily. He had a history of cardial infraction and psoriatic arthritis. X-rays and CT revealed a round lytic defect at the skull. Its borders were sharp and its size was 1.6 × 1.8 cm. No periostic reaction or bone formation was noted. Scintigraphy depicted a lytic lesion without radionuclide enhancement. Thus we suspected an eosinophilic granuloma. An attempt to excise the tumor failed as it had already eroded the underlying temporal bone. The external meninga was affected but not the internal one. Histological diagnosis with dominance of Langerhans cells set the diagnosis. A second surgery was done and the eosinophilic granuloma was extracted. After eight months the gap was bridged with plastic heterologous transplant. After the curettage the patient received antibiotics and five cycles of radiotherapy. The aesthetic result was excellent. The patient's head has a normal hairy appearance. No tenderness, swelling or recurrence is recorded until now. Eosinophilic granuloma is of unknown aetiology but uncontrolled proliferation of Langerhans cells, previous inflammations or tumors and autoimmune disorders are suspected. Due to the co-existence of psoriatic arthritis and eosinophilic granuloma to our patient we assume that an autoimmune mechanism is probable.
机译:嗜酸性肉芽肿是一种非常罕见的良性骨肿瘤,在10岁以下的儿童中占90%以上。男性占主导地位。通常在扁平和长骨处发现。头骨和椎骨经常受到影响。我们报告了一例57岁的男子,他的头骨和眶部逐渐出现局部疼痛。在左颞骨发现了一块柔软,可移动,可触及的嫩块。颅骨意外受伤后疼痛加剧,并且一直持续到现在。临床检查未发现病理发现。该患者是一位每天吸烟和饮酒的医生。他有心脏梗塞和牛皮癣关节炎的病史。 X射线和CT显示颅骨有一个圆形的溶解缺陷。它的边界很锋利,大小为1.6×1.8厘米。没有观察到骨膜反应或骨形成。闪烁扫描显示溶胞性病变没有放射性核素增强。因此我们怀疑是嗜酸性肉芽肿。切除肿瘤的尝试失败了,因为它已经侵蚀了下面的颞骨。外部脑膜受到影响,但内部脑膜未受影响。组织学诊断以朗格汉斯细胞为主导设置了诊断。进行第二次手术并提取嗜酸性肉芽肿。八个月后,用异源塑料移植弥合了缺口。刮宫后,患者接受了抗生素和五个放疗周期。美学效果极好。病人的头部有多毛的外观。迄今为止,没有压痛,肿胀或复发的记录。嗜酸性肉芽肿的病因不明,但怀疑是朗格汉斯细胞增殖失控,先前的炎症或肿瘤以及自身免疫性疾病。由于银屑病关节炎和嗜酸性肉芽肿并存于我们的患者,我们认为自身免疫机制是可能的。

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