Familial adenomatous polyposis differential diagnosis: Difference between revisions
Jump to navigation
Jump to search
m (Bot: Removing from Primary care) |
|||
| (6 intermediate revisions by 3 users not shown) | |||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
[[Image:Home_logo1.png|right|250px|link=https://www.wikidoc.org/index.php/Familial_adenomatous_polyposis]] | |||
{{CMG}} {{AE}} {{SSH}}, {{MJK}} | {{CMG}} {{AE}} {{SSH}}, {{MJK}} | ||
==Overview== | ==Overview== | ||
Familial adenomatous polyposis must be differentiated from other diseases that cause multiple [[Polyp|polyps]], such as [[Peutz-Jeghers syndrome|Peutz–Jeghers syndrome]], juvenile polyposis syndrome, [[Cowden syndrome]], [[Carney syndrome]], and [[Hereditary nonpolyposis colorectal cancer|hereditary non–polyposis colon cancer]] ([[Hereditary nonpolyposis colorectal cancer|Lynch syndrome]]). | Familial adenomatous polyposis must be differentiated from other diseases that cause multiple [[Polyp|polyps]], such as [[Peutz-Jeghers syndrome|Peutz–Jeghers syndrome]], [[juvenile polyposis syndrome]], [[Cowden syndrome]], [[Carney syndrome]], and [[Hereditary nonpolyposis colorectal cancer|hereditary non–polyposis colon cancer]] ([[Hereditary nonpolyposis colorectal cancer|Lynch syndrome]]). | ||
==Differentiating familial adenomatous polyposis from other Diseases== | ==Differentiating familial adenomatous polyposis from other Diseases== | ||
Familial adenomatous polyposis must be differentiated from other diseases that cause multiple [[Polyp|polyps]] including:<ref name="pmid20301519">{{cite journal |vauthors=Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, Jasperson KW, Patel SG, Ahnen DJ |title=APC-Associated Polyposis Conditions. |journal= |volume= |issue= |pages= |year= |pmid=20301519 |doi= |url=}}</ref><ref name="pmid11446392">{{cite journal |vauthors=Beech D, Pontius A, Muni N, Long WP |title=Familial adenomatous polyposis: a case report and review of the literature |journal=J Natl Med Assoc |volume=93 |issue=6 |pages=208–13 |year=2001 |pmid=11446392 |pmc=2594024 |doi= |url=}}</ref><ref name="HalfBercovich2009">{{cite journal|last1=Half|first1=Elizabeth|last2=Bercovich|first2=Dani|last3=Rozen|first3=Paul|title=Familial adenomatous polyposis|journal=Orphanet Journal of Rare Diseases|volume=4|issue=1|year=2009|pages=22|issn=1750-1172|doi=10.1186/1750-1172-4-22}}</ref><ref name="NieuwenhuisVasen2007">{{cite journal|last1=Nieuwenhuis|first1=M.H.|last2=Vasen|first2=H.F.A.|title=Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): A review of the literature|journal=Critical Reviews in Oncology/Hematology|volume=61|issue=2|year=2007|pages=153–161|issn=10408428|doi=10.1016/j.critrevonc.2006.07.004}}</ref><ref name="KingDozois2000">{{cite journal|last1=King|first1=John E.|last2=Dozois|first2=Roger R.|last3=Lindor|first3=Noralane M.|last4=Ahlquist|first4=David A.|title=Care of Patients and Their Families With Familial Adenomatous Polyposis|journal=Mayo Clinic Proceedings|volume=75|issue=1|year=2000|pages=57–67|issn=00256196|doi=10.4065/75.1.57}}</ref> | |||
* [[Peutz-Jeghers syndrome|Peutz–Jeghers syndrome]] | |||
* | * [[Juvenile polyposis syndrome]] | ||
* | * [[Cowden syndrome]] | ||
* | * [[Carney syndrome]] | ||
* | * [[Lynch syndrome|Hereditary Non–Polyposis Colon Cancer]] ([[Hereditary nonpolyposis colorectal cancer|Lynch syndrome]]) | ||
{| | {| | ||
|- style="background: #4479BA; color: #FFFFFF; text-align: center;" | |- style="background: #4479BA; color: #FFFFFF; text-align: center;" | ||
| Line 42: | Line 41: | ||
* [[APC (gene)|''APC'' gene]] | * [[APC (gene)|''APC'' gene]] | ||
* [[MUTYH|''MUTYH'' gene]] | * [[MUTYH|''MUTYH'' gene]] | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" |[[Adenoma]]+++ | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[Adenoma]]+++ | |||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[Colon (anatomy)|Colon]] | * [[Colon (anatomy)|Colon]] | ||
| Line 60: | Line 60: | ||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | | | style="background: #F5F5F5; padding: 5px; text-align: center;" | | ||
* [[STK11]] (LBK1) gene | * [[STK11]] (LBK1) gene | ||
| style="background: #F5F5F5; padding: 5px; text-align: | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
[[Hamartoma]]+++ | * [[Adenoma]]+ | ||
| style="background: #F5F5F5; padding: 5px; text-align: | * [[Hamartoma]]+++ | ||
* Breast | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* Lung | * [[Breast]] | ||
* Pancreas | * [[Lung]] | ||
* [[Pancreas]] | |||
* [[Ovaries]] | * [[Ovaries]] | ||
* Sertoli cells | * [[Sertoli cell|Sertoli cells]] | ||
* | * [[Uterus]] | ||
| style="background: #F5F5F5; padding: 5px; text-align: | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |'''Juvenile Polyposis Syndrome''' | | style="background: #DCDCDC; padding: 5px; text-align: center;" |'''[[Juvenile polyposis syndrome|Juvenile Polyposis Syndrome]]''' | ||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | + | | style="background: #F5F5F5; padding: 5px; text-align: center;" | + | ||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | | | style="background: #F5F5F5; padding: 5px; text-align: center;" | | ||
| Line 82: | Line 83: | ||
* [[BMPR1A]] | * [[BMPR1A]] | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
[[Adenoma]]+ | * [[Adenoma]]+ | ||
[[Hamartoma]]+++ | * [[Hamartoma]]+++ | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[Colon (anatomy)|Colon]] | * [[Colon (anatomy)|Colon]] | ||
| Line 94: | Line 95: | ||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | – | | style="background: #F5F5F5; padding: 5px; text-align: center;" | – | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
[[Axillary]]+ | * [[Axillary]]+ [[Inguinal region|Inguinal]]+ [[Facial]]+ | ||
[[Inguinal region|Inguinal]]+ | |||
[[Facial]]+ | |||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | – | | style="background: #F5F5F5; padding: 5px; text-align: center;" | – | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[PTEN (gene)|PTEN]] | * [[PTEN (gene)|PTEN]] | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
[[Adenoma]]+ | * [[Adenoma]]+ | ||
[[Hamartoma]]+++ | * [[Hamartoma]]+++ | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[Breast]] | * [[Breast]] | ||
| Line 109: | Line 108: | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[Trichilemmoma]] | * [[Trichilemmoma]] | ||
* Skin hamartoma | * Skin [[hamartoma]] | ||
* Hyperplastic polyp | * [[Colon polyps|Hyperplastic polyp]] | ||
* Macrocephaly | * [[Macrocephaly]] | ||
* Breast fibrosis | * Breast [[fibrosis]] | ||
|- | |- | ||
| style="background: #DCDCDC; padding: 5px; text-align: center;" |[[Carney syndrome|'''Carney Syndrome''']] | | style="background: #DCDCDC; padding: 5px; text-align: center;" |[[Carney syndrome|'''Carney Syndrome''']] | ||
| Line 120: | Line 119: | ||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | – | | style="background: #F5F5F5; padding: 5px; text-align: center;" | – | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
[[Facial]]+ | * [[Facial]]+ [[Mucous membrane|Mucosal]]+ | ||
[[Mucous membrane|Mucosal]]+ | |||
| style="background: #F5F5F5; padding: 5px; text-align: center;" | – | | style="background: #F5F5F5; padding: 5px; text-align: center;" | – | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
| Line 148: | Line 146: | ||
* [[PMS2]] | * [[PMS2]] | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
[[Adenoma]]+ | * [[Adenoma]]+ | ||
| style="background: #F5F5F5; padding: 5px; text-align: left;" | | | style="background: #F5F5F5; padding: 5px; text-align: left;" | | ||
* [[Endometrium]] | * [[Endometrium]] | ||
| Line 161: | Line 159: | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
| |||
| |||
[[Category:Medicine]] | |||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] | ||
[[Category:Oncology]] | [[Category:Oncology]] | ||
[[Category: | [[Category:Up-To-Date]] | ||
Latest revision as of 21:43, 29 July 2020
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2], Mohamad Alkateb, MBBCh [3]
Overview
Familial adenomatous polyposis must be differentiated from other diseases that cause multiple polyps, such as Peutz–Jeghers syndrome, juvenile polyposis syndrome, Cowden syndrome, Carney syndrome, and hereditary non–polyposis colon cancer (Lynch syndrome).
Differentiating familial adenomatous polyposis from other Diseases
Familial adenomatous polyposis must be differentiated from other diseases that cause multiple polyps including:[1][2][3][4][5]
- Peutz–Jeghers syndrome
- Juvenile polyposis syndrome
- Cowden syndrome
- Carney syndrome
- Hereditary Non–Polyposis Colon Cancer (Lynch syndrome)
| Diseases | History and Symptoms | Physical Examination | Laboratory Findings | Other Findings | ||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Abdominal Pain | Rectal Bleeding | Fatigue | Abdominal Tenderness | Hyperpigmentation | Anemia | Gene(s) | Gastrointestinal Tumors | Cancers | ||
| Familial Adenomatous Polyposis | + | + | + | +/– | – | + |
|
|||
| Peutz–Jeghers syndrome | + | + | + | + | + | + |
|
|||
| Juvenile Polyposis Syndrome | + | + | – | – | – |
|
||||
| Cowden Syndrome | – | – | – | – | – |
| ||||
| Carney Syndrome | – | – | – | – | – | |||||
| Hereditary Non–Polyposis Colon Cancer | – | + | + | +/– | – | + | ||||
References
- ↑ Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean L, Stephens K, Amemiya A, Jasperson KW, Patel SG, Ahnen DJ. "APC-Associated Polyposis Conditions". PMID 20301519. Vancouver style error: initials (help)
- ↑ Beech D, Pontius A, Muni N, Long WP (2001). "Familial adenomatous polyposis: a case report and review of the literature". J Natl Med Assoc. 93 (6): 208–13. PMC 2594024. PMID 11446392.
- ↑ Half, Elizabeth; Bercovich, Dani; Rozen, Paul (2009). "Familial adenomatous polyposis". Orphanet Journal of Rare Diseases. 4 (1): 22. doi:10.1186/1750-1172-4-22. ISSN 1750-1172.
- ↑ Nieuwenhuis, M.H.; Vasen, H.F.A. (2007). "Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): A review of the literature". Critical Reviews in Oncology/Hematology. 61 (2): 153–161. doi:10.1016/j.critrevonc.2006.07.004. ISSN 1040-8428.
- ↑ King, John E.; Dozois, Roger R.; Lindor, Noralane M.; Ahlquist, David A. (2000). "Care of Patients and Their Families With Familial Adenomatous Polyposis". Mayo Clinic Proceedings. 75 (1): 57–67. doi:10.4065/75.1.57. ISSN 0025-6196.