Inflammatory fibroid polyp: Difference between revisions
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{{SI}} {{Infobox medical condition | |||
| name = Inflammatory fibroid polyp | |||
| image = [[File:Inflammatory_fibroid_polyp_-_low_mag.jpg|thumb|Inflammatory fibroid polyp under low magnification]] | |||
| caption = Histological image of an inflammatory fibroid polyp | |||
| field = [[Gastroenterology]] | |||
| synonyms = Vanek's tumor | |||
| symptoms = [[Abdominal pain]], [[intestinal obstruction]], [[gastrointestinal bleeding]] | |||
| complications = [[Intestinal obstruction]] | |||
| onset = Typically in adults, most common in 5th to 7th decades | |||
| duration = Chronic | |||
| causes = Unknown, possibly [[inflammatory]] or [[reactive]] | |||
| risks = No specific risk factors identified | |||
| diagnosis = [[Endoscopy]], [[biopsy]], [[histopathology]] | |||
| differential = [[Gastrointestinal stromal tumor]], [[adenomatous polyp]], [[lipoma]] | |||
| treatment = [[Surgical resection]] | |||
| medication = None specific | |||
| prognosis = Excellent with surgical removal | |||
| frequency = Rare | |||
| deaths = None directly attributable | |||
}} | |||
'''Inflammatory fibroid polyp''' ('''IFP''') is a benign [[neoplasm]] that can occur in various parts of the [[gastrointestinal tract]], but is most commonly found in the [[stomach]] and [[small intestine]]. It was first described by the Austrian pathologist [[Hans Chiari]] in 1949. | '''Inflammatory fibroid polyp''' ('''IFP''') is a benign [[neoplasm]] that can occur in various parts of the [[gastrointestinal tract]], but is most commonly found in the [[stomach]] and [[small intestine]]. It was first described by the Austrian pathologist [[Hans Chiari]] in 1949. | ||
== History == | == History == | ||
The term "inflammatory fibroid polyp" was first used by [[John Helwig]] and [[Franklin F. M. Bosman]] in 1953. They described it as a distinct pathological entity characterized by a proliferation of connective tissue, blood vessels, and a prominent inflammatory infiltrate. | The term "inflammatory fibroid polyp" was first used by [[John Helwig]] and [[Franklin F. M. Bosman]] in 1953. They described it as a distinct pathological entity characterized by a proliferation of connective tissue, blood vessels, and a prominent inflammatory infiltrate. | ||
== Pathogenesis == | == Pathogenesis == | ||
The exact cause of IFP is unknown. However, it is believed to be a reactive process rather than a true neoplasm. Some studies suggest that it may be related to chronic inflammation or irritation. Genetic factors may also play a role, as some cases have been associated with specific genetic mutations. | The exact cause of IFP is unknown. However, it is believed to be a reactive process rather than a true neoplasm. Some studies suggest that it may be related to chronic inflammation or irritation. Genetic factors may also play a role, as some cases have been associated with specific genetic mutations. | ||
== Clinical features == | == Clinical features == | ||
IFPs can occur at any age, but they are most common in middle-aged adults. They can cause various symptoms depending on their location. In the stomach, they may cause abdominal pain, nausea, vomiting, or bleeding. In the small intestine, they may cause abdominal pain, diarrhea, or intestinal obstruction. | IFPs can occur at any age, but they are most common in middle-aged adults. They can cause various symptoms depending on their location. In the stomach, they may cause abdominal pain, nausea, vomiting, or bleeding. In the small intestine, they may cause abdominal pain, diarrhea, or intestinal obstruction. | ||
== Diagnosis == | == Diagnosis == | ||
The diagnosis of IFP is usually made by endoscopic biopsy. The histological features include a proliferation of spindle cells, blood vessels, and inflammatory cells, with a characteristic "onion-skin" pattern around the blood vessels. Immunohistochemical staining can help to confirm the diagnosis. | The diagnosis of IFP is usually made by endoscopic biopsy. The histological features include a proliferation of spindle cells, blood vessels, and inflammatory cells, with a characteristic "onion-skin" pattern around the blood vessels. Immunohistochemical staining can help to confirm the diagnosis. | ||
== Treatment == | == Treatment == | ||
The treatment of choice for IFP is surgical removal. This can usually be done by endoscopic resection. In some cases, open surgery may be required. The prognosis after treatment is excellent, with a very low risk of recurrence. | The treatment of choice for IFP is surgical removal. This can usually be done by endoscopic resection. In some cases, open surgery may be required. The prognosis after treatment is excellent, with a very low risk of recurrence. | ||
== See also == | == See also == | ||
* [[Gastrointestinal neoplasm]] | * [[Gastrointestinal neoplasm]] | ||
* [[Stomach cancer]] | * [[Stomach cancer]] | ||
* [[Small intestine cancer]] | * [[Small intestine cancer]] | ||
[[Category:Gastrointestinal neoplasms]] | [[Category:Gastrointestinal neoplasms]] | ||
[[Category:Stomach disorders]] | [[Category:Stomach disorders]] | ||
| Line 32: | Line 39: | ||
{{Gastroenterology-stub}} | {{Gastroenterology-stub}} | ||
{{Medicine-stub}} | {{Medicine-stub}} | ||
Latest revision as of 03:21, 6 April 2025
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Obesity, Sleep & Internal medicine
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| Inflammatory fibroid polyp | |
|---|---|
 | |
| Synonyms | Vanek's tumor |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Abdominal pain, intestinal obstruction, gastrointestinal bleeding |
| Complications | Intestinal obstruction |
| Onset | Typically in adults, most common in 5th to 7th decades |
| Duration | Chronic |
| Types | N/A |
| Causes | Unknown, possibly inflammatory or reactive |
| Risks | No specific risk factors identified |
| Diagnosis | Endoscopy, biopsy, histopathology |
| Differential diagnosis | Gastrointestinal stromal tumor, adenomatous polyp, lipoma |
| Prevention | N/A |
| Treatment | Surgical resection |
| Medication | None specific |
| Prognosis | Excellent with surgical removal |
| Frequency | Rare |
| Deaths | None directly attributable |
Inflammatory fibroid polyp (IFP) is a benign neoplasm that can occur in various parts of the gastrointestinal tract, but is most commonly found in the stomach and small intestine. It was first described by the Austrian pathologist Hans Chiari in 1949.
History[edit]
The term "inflammatory fibroid polyp" was first used by John Helwig and Franklin F. M. Bosman in 1953. They described it as a distinct pathological entity characterized by a proliferation of connective tissue, blood vessels, and a prominent inflammatory infiltrate.
Pathogenesis[edit]
The exact cause of IFP is unknown. However, it is believed to be a reactive process rather than a true neoplasm. Some studies suggest that it may be related to chronic inflammation or irritation. Genetic factors may also play a role, as some cases have been associated with specific genetic mutations.
Clinical features[edit]
IFPs can occur at any age, but they are most common in middle-aged adults. They can cause various symptoms depending on their location. In the stomach, they may cause abdominal pain, nausea, vomiting, or bleeding. In the small intestine, they may cause abdominal pain, diarrhea, or intestinal obstruction.
Diagnosis[edit]
The diagnosis of IFP is usually made by endoscopic biopsy. The histological features include a proliferation of spindle cells, blood vessels, and inflammatory cells, with a characteristic "onion-skin" pattern around the blood vessels. Immunohistochemical staining can help to confirm the diagnosis.
Treatment[edit]
The treatment of choice for IFP is surgical removal. This can usually be done by endoscopic resection. In some cases, open surgery may be required. The prognosis after treatment is excellent, with a very low risk of recurrence.
See also[edit]
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