Primary cutaneous amyloidosis: Difference between revisions
Content deleted Content added
+Image |
Blue-Sonnet (talk | contribs) →See also: Added hidden headings to try to fix infobox, which is appearing halfway down when viewing the page on mobile versions. Tags: Mobile edit Mobile web edit Advanced mobile edit |
||
| Line 22: | Line 22: | ||
| deaths = |
| deaths = |
||
}} |
}} |
||
<!-- Definition --> |
|||
'''Primary cutaneous amyloidosis''' is a form of [[amyloidosis]] associated with [[oncostatin M receptor]].<ref name="urlAmyloid">{{cite web |url=http://neuromuscular.wustl.edu/nother/amyloid.htm |title=Amyloid |website= |accessdate=}}</ref><ref name="pmid18179886">{{cite journal |vauthors=Arita K, South AP, Hans-Filho G, etal |title=Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis |journal=Am. J. Hum. Genet. |volume=82 |issue=1 |pages=73–80 |date=January 2008 |pmid=18179886 |doi=10.1016/j.ajhg.2007.09.002 |url= |pmc=2253984}}</ref> |
'''Primary cutaneous amyloidosis''' is a form of [[amyloidosis]] associated with [[oncostatin M receptor]].<ref name="urlAmyloid">{{cite web |url=http://neuromuscular.wustl.edu/nother/amyloid.htm |title=Amyloid |website= |accessdate=}}</ref><ref name="pmid18179886">{{cite journal |vauthors=Arita K, South AP, Hans-Filho G, etal |title=Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis |journal=Am. J. Hum. Genet. |volume=82 |issue=1 |pages=73–80 |date=January 2008 |pmid=18179886 |doi=10.1016/j.ajhg.2007.09.002 |url= |pmc=2253984}}</ref> |
||
<!-- Subtypes --> |
|||
This type of amyloidosis has been divided into the following types:<ref name="Andrews">{{cite book |author1=James, William D. |author2=Berger, Timothy G. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=978-0-7216-2921-6 |oclc= |doi= |accessdate=|display-authors=etal}}</ref>{{rp|520}} |
|||
* '''Macular amyloidosis''' is a cutaneous condition characterized by itchy, brown, rippled [[macule]]s usually located on the interscapular region of the back.<ref name="Andrews" />{{rp|521}} Combined cases of lichen and macular amyloidosis are termed biphasic amyloidosis, and provide support to the theory that these two variants of amyloidosis exist on the same disease spectrum.<ref name="Craig">[http://dermatology-s10.cdlib.org/125/UCDcases/amlyoid/craig.html Lichen amyloidosis of the auricular concha] Craig, E. (2006) Dermatology Online Journal 12 (5): 1, University of California, Davis Department of Dermatology</ref> |
* '''Macular amyloidosis''' is a cutaneous condition characterized by itchy, brown, rippled [[macule]]s usually located on the interscapular region of the back.<ref name="Andrews" />{{rp|521}} Combined cases of lichen and macular amyloidosis are termed biphasic amyloidosis, and provide support to the theory that these two variants of amyloidosis exist on the same disease spectrum.<ref name="Craig">[http://dermatology-s10.cdlib.org/125/UCDcases/amlyoid/craig.html Lichen amyloidosis of the auricular concha] Craig, E. (2006) Dermatology Online Journal 12 (5): 1, University of California, Davis Department of Dermatology</ref> |
||
Revision as of 19:58, 17 January 2020
| Primary cutaneous amyloidosis | |
|---|---|
| Other names | Primary localized cutaneous amyloidosis[1] |
 | |
| Macular amyloidosis, located on the right lumbar region of the back | |
| Specialty | Dermatology |
Primary cutaneous amyloidosis is a form of amyloidosis associated with oncostatin M receptor.[2][3] This type of amyloidosis has been divided into the following types:[4]: 520
- Macular amyloidosis is a cutaneous condition characterized by itchy, brown, rippled macules usually located on the interscapular region of the back.[4]: 521 Combined cases of lichen and macular amyloidosis are termed biphasic amyloidosis, and provide support to the theory that these two variants of amyloidosis exist on the same disease spectrum.[5]
- Lichen amyloidosis is a cutaneous condition characterized by the appearance of occasionally itchy lichenoid papules, typically appearing bilaterally on the shins.[4]: 521
-
Histopathology of lichen amyloidosis, with subepithelial Congo red-positive deposits
- Nodular amyloidosis is a rare cutaneous condition characterized by nodules that involve the acral areas.[4]: 521
See also
References
- ^ "Primary cutaneous amyloidosis | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 18 April 2019.
- ^ "Amyloid".
- ^ Arita K, South AP, Hans-Filho G, et al. (January 2008). "Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis". Am. J. Hum. Genet. 82 (1): 73–80. doi:10.1016/j.ajhg.2007.09.002. PMC 2253984. PMID 18179886.
- ^ a b c d James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
- ^ Lichen amyloidosis of the auricular concha Craig, E. (2006) Dermatology Online Journal 12 (5): 1, University of California, Davis Department of Dermatology
External links
 | This cutaneous condition article is a stub. You can help Wikipedia by expanding it. |