Histiocytosis X; follow-up of 43 cases.
Open Access
- 1 June 1977
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 52 (6) , 433-440
- https://doi.org/10.1136/adc.52.6.433
Abstract
Over a 29-year period, 43 cases of histiocytosis X presented in children under the age of 12 years. 29 patients (67%) have survived, and of these, 15 (52%) have a detectable disability. It was confirmed that young age at presentation and evidence of soft tissue involvement were associated with a worse prognosis. The majority of deaths were associated with pulmonary involvement. 14 patients developed diabetes insipidus. 5 of the surviving adults have heights below the 3rd centile. Puberty usually occurred at a normal age. Follow-up studies on 12 survivors showed no evidence of residual abnormality of haematology, deficient lymphocyte function, or yeast opsonization. HLA typing showed no unusual pattern. Mild carbon monoxide diffusion deffects were present in 4 patients and other abnormalities were detected on lung function tests.Keywords
This publication has 19 references indexed in Scilit:
- Histiocytosis X—an analysis of prognostic factorsThe Journal of Pediatrics, 1975
- Histiocytosis X—comparison of three treatment regimensThe Journal of Pediatrics, 1975
- Familial opsonization defect associated with fatal infantile dermatitis, infections, and histiocytosis.Archives of Disease in Childhood, 1975
- Response of Growth-Retarded Patients with Hand–Schüller–Christian Disease to Growth Hormone TherapyNew England Journal of Medicine, 1975
- Pulmonary manifestations of histiocytosis X.1971
- HISTIOCYTIC REACTION IN DYSGAMMAGLOBULINEMIA AND CONGENITAL RUBELLAPediatrics, 1970
- Acute disseminated histiocytosis X: a case with transition from eosinophilic granuloma of bone to Letterer-Siwe disease.1969
- Prognosis in reticuloendotheliosis in childrenThe Journal of Pediatrics, 1962
- A clinicopathologic study of 40 cases and review of the literature on eosinophilic granuloma of bone. Hand-Schuller-Christian disease and Letterer-Siwe disease.1961
- HISTIOCYTOSIS-X - INTEGRATION OF EOSINOPHILIC GRANULOMA OF BONE LETTERER-SIWE DISEASE, AND SCHULLER-CHRISTIAN DISEASE AS RELATED MANIFESTATIONS OF A SINGLE NOSOLOGIC ENTITY1953