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组织细胞增多症X的罕见表现。

Uncommon manifestations of histiocytosis X.

作者信息

Zachariades N, Anastasea-Vlachou K, Xypolyta A, Kattamis C

出版信息

Int J Oral Maxillofac Surg. 1987 Jun;16(3):355-62. doi: 10.1016/s0901-5027(87)80159-5.

DOI:10.1016/s0901-5027(87)80159-5
PMID:3112267
Abstract

Histiocytosis X is a group of disorders of uncertain etiology with a variety of manifestations that are usually related to the age of the patient. Treatment consists of local curettage, irradiation and chemotherapy. The prognosis depends on the systems involved. The oral and perioral tissues are occasionally involved and often lead to the diagnosis. We report a case with spinal cord involvement and a case of facial nerve paralysis secondary to involvement of the petrosal bone. Also included is a case of involvement of the mandibular condyle.

摘要

组织细胞增多症X是一组病因不明的疾病,有多种临床表现,通常与患者年龄有关。治疗方法包括局部刮除术、放疗和化疗。预后取决于受累系统。口腔及口周组织偶尔受累,常可由此作出诊断。我们报告1例脊髓受累病例、1例因岩骨受累继发面神经麻痹的病例,还包括1例下颌髁突受累的病例。

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Uncommon manifestations of histiocytosis X.组织细胞增多症X的罕见表现。
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引用本文的文献

1
A rare occurrence of Langerhans cell histiocytosis in an adult.成人罕见的朗格汉斯细胞组织细胞增多症病例。
J Oral Maxillofac Pathol. 2014 Sep-Dec;18(3):415-9. doi: 10.4103/0973-029X.151335.
2
Solitary eosinophilic granuloma of mandibular condyle: literature review and report of a rare case.下颌骨髁突孤立性嗜酸性肉芽肿:文献综述及1例罕见病例报告
J Maxillofac Oral Surg. 2015 Mar;14(Suppl 1):209-14. doi: 10.1007/s12663-012-0438-7. Epub 2012 Sep 15.
3
Eosinophilic granuloma of mandibular condyle: resection and complete regeneration.
下颌髁突嗜酸性肉芽肿:切除与完全再生
J Maxillofac Oral Surg. 2015 Mar;14(1):107-10. doi: 10.1007/s12663-013-0581-9. Epub 2013 Sep 13.