HISTIOCYTOSIS-X (LANGERHANS-CELL HISTIOCYTOSIS) OF THE PALATE - CASE-REPORT

被引：3

作者：

LOH, HS

QUAH, TC

机构：

[1] Department of Oral Surgery, National University of Singapore

[2] Department of Paediatrics, National University of Singapore

来源：

AUSTRALIAN DENTAL JOURNAL | 1990年 / 35卷 / 02期

关键词：

Histiocytosis X; Langerhans‐cell histiocytosis;

D O I：

10.1111/j.1834-7819.1990.tb05874.x

中图分类号：

R78 [口腔科学];

学科分类号：

1003 ;

摘要：

A case of histiocytosis X (Langerhans‐cell histiocytosis) occurring in the maxilla of a two‐year‐old boy is presented. Common dental and oral conditions were considered and eliminated. Diagnosis was made through a biopsy which showed aggregates of histiocytes. Management consisted of multi‐modal treatment. Full skeletal radiographic survey and review were essential to detect other possible sites of involvement. None was found in this case over a four‐year review. 1990 Australian Dental Association

引用

页码：117 / 120

页数：4

共 5 条

[1] Lichtenstein L., Integration of eosinophilic granuloma of bone, Letterer‐Siwe disease and Hand‐Schuller‐Christian disease as related manifestations of a single nosologic entity, Arch Pathol, 56, pp. 84-102, (1953)
[2] Histiocytosis syndromes in children, Lancet, pp. 208-209, (1987)
[3] Grimm RA, Muss HB, Patterson RB, Et al., Reactivation of Hand‐Schuller‐Christian disease, six and thirteen years after discontinuation of systemic therapy, Med Pediatr Oncol, 9, pp. 17-21, (1981)
[4] Hartman KS., Histiocytosis X: A review of 114 cases with oral involvement, Oral Surg Oral Med Oral Pathol, 49, pp. 38-53, (1980)
[5] Matus-Ridley M., Raney RB, Thaweranti H., Et al., Histiocytosis X in children — patterns of disease and results of treatment, Medical and Pediatric Oncology, 11, pp. 99-105, (1983)

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