Hereditary progressive mucinous histiocytosis explained
Hereditary progressive mucinous histiocytosis is a very rare, benign, non-Langerhans' cell histiocytosis. An autosomal dominant or X-linked hereditary disease described on the skin, it has been found almost exclusively in women.[1] [2] One case of the disease in a male patient has been reported.[3]
See also
Notes and References
- Book: James, William D. . Berger, Timothy G. . Andrews' Diseases of the Skin: clinical Dermatology . limited . Saunders Elsevier . 2006 . 718. 978-0-7216-2921-6 . etal.
- 10844262. 2000. Antoni-Bach. N. Hereditary progressive mucinous histiocytosis. Annales de Dermatologie et de Vénéréologie. 127. 4. 400–4. Pfister. R. Grosshans. E. Kleinclaus. I. Boehm. N. Grange. F. Guillaume. J.
- 20107728. 2010. Schlegel. C. Hereditary progressive mucinous histiocytosis: First report in a male patient. Acta Dermato Venereologica. 90. 1. 65–7. Metzler. G. Burgdorf. W. Schaller. M. 10.2340/00015555-0763. free.