Juvenile polyp | |
---|---|
Other names | Retention polyp [1] |
Specialty | Gastroenterology |
Symptoms |
Asymptomatic Rectal bleeding Rectal prolapse |
Usual onset | Childhood |
Types | Solitary Juvenile polyposis syndrome |
Diagnostic method | Colonoscopy |
Differential diagnosis |
Hyperplastic polyp, Inflammatory polyp,
Cowden syndrome Peutz-Jeghers syndrome |
Treatment | Polypectomy |
Frequency | 2% of children |
Juvenile polyps are a type of polyp found in the colon. While juvenile polyps are typically found in children, they may be found in people of any age. Juvenile polyps are a type of hamartomatous polyps, which consist of a disorganized mass of tissue. They occur in about two percent of children. [2] Juvenile polyps often do not cause symptoms (asymptomatic); when present, symptoms usually include gastrointestinal bleeding and prolapse through the rectum. Removal of the polyp ( polypectomy) is warranted when symptoms are present, for treatment and definite histopathological diagnosis. In the absence of symptoms, removal is not necessary. Recurrence of polyps following removal is relatively common. [3] Juvenile polyps are usually sporadic, occurring in isolation, although they may occur as a part of juvenile polyposis syndrome. Sporadic juvenile polyps may occur in any part of the colon, but are usually found in the distal colon ( rectum and sigmoid). In contrast to other types of colon polyps, juvenile polyps are not premalignant and are not usually associated with a higher risk of cancer; [4] however, individuals with juvenile polyposis syndrome are at increased risk of gastric and colorectal cancer. [2] [5] Unlike juvenile polyposis syndrome, solitary juvenile polyps do not require follow up with surveillance colonoscopy.
Juvenile polyps often do not cause symptoms (asymptomatic); when present, symptoms usually include gastrointestinal bleeding and prolapse through the rectum. Juvenile polyps are usually sporadic, occurring in isolation, although they may occur as a part of juvenile polyposis syndrome. Sporadic juvenile polyps may occur in any part of the colon, but are usually found in the distal colon ( rectum and sigmoid). [6]
Under microscopy, juvenile polyps are characterized by cystic architecture, mucus-filled glands, and prominent lamina propria. Inflammatory cells may be present. Compared with sporadic polyps, polyps that occur in juvenile polyposis syndrome tend to have more of a frond-like (resembling a leaf) growth pattern with fewer stroma, fewer dilated glands and smaller glands with more proliferation. [2] Syndrome-related juvenile polyps also demonstrate more neoplasia and increased COX-2 expression compared with sporadic juvenile polyps. [2]
Juvenile polyps are diagnosed by examination of their distinctive histopathology, generally after polypectomy via endoscopy. [7] Juvenile polyps cause fecal calprotectin level to be elevated. [8]
If symptoms are present, then removal of the polyp (polypectomy) is warranted. Recurrence of polyps following removal is relatively common. [3] Unlike juvenile polyposis syndrome, solitary juvenile polyps do not require follow up with surveillance colonoscopy. [7]
Juvenile polyps occur in about 2 percent of children. [2] In contrast to other types of colon polyps, juvenile polyps are not premalignant and are not usually associated with a higher risk of cancer; [4] however, individuals with juvenile polyposis syndrome are at increased risk of gastric and colorectal cancer. [2] [5]
Juvenile polyp | |
---|---|
Other names | Retention polyp [1] |
Specialty | Gastroenterology |
Symptoms |
Asymptomatic Rectal bleeding Rectal prolapse |
Usual onset | Childhood |
Types | Solitary Juvenile polyposis syndrome |
Diagnostic method | Colonoscopy |
Differential diagnosis |
Hyperplastic polyp, Inflammatory polyp,
Cowden syndrome Peutz-Jeghers syndrome |
Treatment | Polypectomy |
Frequency | 2% of children |
Juvenile polyps are a type of polyp found in the colon. While juvenile polyps are typically found in children, they may be found in people of any age. Juvenile polyps are a type of hamartomatous polyps, which consist of a disorganized mass of tissue. They occur in about two percent of children. [2] Juvenile polyps often do not cause symptoms (asymptomatic); when present, symptoms usually include gastrointestinal bleeding and prolapse through the rectum. Removal of the polyp ( polypectomy) is warranted when symptoms are present, for treatment and definite histopathological diagnosis. In the absence of symptoms, removal is not necessary. Recurrence of polyps following removal is relatively common. [3] Juvenile polyps are usually sporadic, occurring in isolation, although they may occur as a part of juvenile polyposis syndrome. Sporadic juvenile polyps may occur in any part of the colon, but are usually found in the distal colon ( rectum and sigmoid). In contrast to other types of colon polyps, juvenile polyps are not premalignant and are not usually associated with a higher risk of cancer; [4] however, individuals with juvenile polyposis syndrome are at increased risk of gastric and colorectal cancer. [2] [5] Unlike juvenile polyposis syndrome, solitary juvenile polyps do not require follow up with surveillance colonoscopy.
Juvenile polyps often do not cause symptoms (asymptomatic); when present, symptoms usually include gastrointestinal bleeding and prolapse through the rectum. Juvenile polyps are usually sporadic, occurring in isolation, although they may occur as a part of juvenile polyposis syndrome. Sporadic juvenile polyps may occur in any part of the colon, but are usually found in the distal colon ( rectum and sigmoid). [6]
Under microscopy, juvenile polyps are characterized by cystic architecture, mucus-filled glands, and prominent lamina propria. Inflammatory cells may be present. Compared with sporadic polyps, polyps that occur in juvenile polyposis syndrome tend to have more of a frond-like (resembling a leaf) growth pattern with fewer stroma, fewer dilated glands and smaller glands with more proliferation. [2] Syndrome-related juvenile polyps also demonstrate more neoplasia and increased COX-2 expression compared with sporadic juvenile polyps. [2]
Juvenile polyps are diagnosed by examination of their distinctive histopathology, generally after polypectomy via endoscopy. [7] Juvenile polyps cause fecal calprotectin level to be elevated. [8]
If symptoms are present, then removal of the polyp (polypectomy) is warranted. Recurrence of polyps following removal is relatively common. [3] Unlike juvenile polyposis syndrome, solitary juvenile polyps do not require follow up with surveillance colonoscopy. [7]
Juvenile polyps occur in about 2 percent of children. [2] In contrast to other types of colon polyps, juvenile polyps are not premalignant and are not usually associated with a higher risk of cancer; [4] however, individuals with juvenile polyposis syndrome are at increased risk of gastric and colorectal cancer. [2] [5]