A Solitary Variant of Congenital Self‐healing Reticulohistiocytosis: Solitary Hasimoto‐Prltzker Disease
- 1 June 1986
- journal article
- case report
- Published by Wiley in Pediatric Dermatology
- Vol. 3 (3) , 230-236
- https://doi.org/10.1111/j.1525-1470.1986.tb00519.x
Abstract
Four neonates had solitary, congenital, rapidly growing, spontaneously ulcerating tumors of the face, trunk, and extremities. No extracutaneous involvement was found, and all lesions spontaneously involuted. Mononuclear cells of the cutaneous infiltrate were Langerhans'cells. These findings expand the spectrum of congenital self-healing reticulohistiocytosisKeywords
This publication has 20 references indexed in Scilit:
- Congenital self-healing reticulohistiocytosis: Report of the seventh case with histochemical and ultrastructural studiesJournal of the American Academy of Dermatology, 1984
- Benign cephalic histiocytosisArchives of Dermatology, 1984
- Cutaneous histiocytosis X. The presence of S-100 protein and its use in diagnosisArchives of Dermatology, 1983
- Congenital self-healing histiocytosisArchives of Dermatology, 1982
- Histiocytosis-XNew England Journal of Medicine, 1981
- Histiocytosis X: natural history and management in childhoodClinical and Experimental Dermatology, 1979
- Epidermal Langerhans cells are derived from cells originating in bone marrowNature, 1979
- Histiocytosis X—an analysis of prognostic factorsThe Journal of Pediatrics, 1975
- An Electron Microscope Study of Basal Melanocytes and High-Level Clear Cells (Langerhans Cells) in Vitiligo**From the Chester Beatty Research Institute, Royal Cancer Hospital, London, S.W. 3, and the Departments of Anatomy, and Dermatology, St. Mary's Hospital Medical School (University of London) London, W. 2, England.Journal of Investigative Dermatology, 1961