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Inflammatory fibroid polyp

Summary

An inflammatory fibroid polyp (IFP) is an uncommon digestive system tumor.[1] J. Vanek initially identified it as a separate pathological entity in 1949 when he reported six case reports of eosinophilic infiltration in gastric submucosal granulomas.[2] It is a single, non-encapsulated polypoid lesion that is typically submucosal. It is characterized by a large number of small blood vessels, oedematous connective tissue, and an inflammatory eosinophilic infiltrate.[3]

Inflammatory fibroid polyp
Other namesIFP, Eosinophilic granulomatous polyp, Vanek's tumor.
Low magnification micrograph of an inflammatory fibroid polyp. H&E stain.
SpecialtyGastroenterology

Inflammatory fibroid polyp has also been referred to as polypoid myo-endothelioma,[4] fibroma with eosinophilic infiltration,[5] inflammatory pseudotumour,[5] myxoma,[6] haemangiopericytoma,[7] eosinophilic granuloma,[5] Vanek's tumour,[8] and gastric eosinophilic submucosal granuloma.[2]

When the lesions are symptomatic, they typically measure less than 3 cm in size and are linked to symptoms such as iron deficiency anemia, bleeding, weight loss, and dyspeptic symptoms. Significant complications like obstruction, intussusception, and even hypovolemic shock can result from larger lesions.[9]

Signs and symptoms edit

The tumor's size, location, and complications will affect how it presents itself.[1] Common symptoms include epigastric pain and bleeding in the stomach and intestinal symptoms.[10] When it is in the esophagus, symptoms such as bleeding,[11] gastroesophageal reflux,[12] and dysphagia may occur.[13]

Although the inflammatory fibroid polyp's natural history is unknown, it has been known to grow quickly, within a few months,[1] and to reach sizes of up to 20 cm.[14]

Complications edit

Inflammatory fibroid polyps emerge from the submucosa and pierce the lamina propria, causing the mucosal layer to bulge. On rare occasions, they may develop ulcers through the mucosa, resulting in bleeding and symptoms similar to hypovolemic shock.[15]

Causes edit

The inflammatory fibroid polyp is a benign lesion whose cause is unknown;[13] some reports attribute its genesis to myofibroblasts,[16] while others propose vascular or perivascular tissue.[17] It is widely acknowledged that this is a reactive process to chemical, physical, or microbiological stimuli rather than a neoplasm.[18] In the past, it was believed that the etiology was caused by an inflammatory reaction to an underlying granuloma.[15] An irritating stimulus is frequently linked to the development of a submucosal granuloma (such as trauma, tuberculosis, helicobacter pylori, Crohn's disease, or sarcoidosis).[19]

Parasites have also been implicated as a potential cause of inflammatory fibroid polyps.[20]

There have been suggestions that a factor that has not yet been identified[21] may cause hyperplasia of vessels and stromal cells, leading to localized vascular inflammation.[22]

Risk factors edit

The inflammatory fibroid polyp may be connected to neoplastic and neoplastic GI lesions occurring simultaneously or synchronously, but the literature does not support a causal relationship.[23][24] Isolated reports have been made of inflammatory fibroid polyps at different locations coexisting with granular cell tumors[25] and certain immune system conditions, such as neurofibromatosis,[26] Crohn's disease,[10][27] ankylosing spondylitis,[22] and human immunodeficiency virus infection,[28] however, these results are inconsistent and most likely coincidental.[10]

Genetics edit

Inflammatory fibroid polyps have demonstrated a higher incidence in individuals with a family history of gastrointestinal polyps.[29] Activating mutations in the platelet-derived growth factor receptor alpha (PDGFRA) gene were found in 70% of cases in a genetic study involving inflammatory fibroid polyps.[30]

Diagnosis edit

Over 90% of gastrointestinal polyps found during routine endoscopic examination are present in patients who are asymptomatic and do not appear to be cancerous.[31] By using a gross examination alone, these polyps cannot be identified from those that need additional treatment.[15] Consequently, to identify the type of polyp and whether underlying dysplasia is present, histological analysis is always recommended.[32] To accurately determine the type of polyp, additional diagnostic techniques such as tandem biopsies, immunohistochemistry staining, and endoscopic ultrasound (EUS) may also be required.[31]

An inflammatory fibroid polyp presents histologically as an exuberant,[10] non-encapsulated, localized proliferation of spindle-shaped mononuclear cells,[4] with an inflammatory infiltrate that is frequently dominated by eosinophils.[33] The fuzzy borders visible on endoscopic ultrasound correspond with the non-encapsulated proliferating spindle cells.[34] Most inflammatory fibroid polyps are vascular, consisting of a network of varying diameter blood vessels.[35] Occasionally, the spindle-shaped cells are arranged in a concentric pattern that resembles "onion skin".[36][4] Surface ulceration in focal areas can occasionally be observed.[6] Though usually polypoidal,[7] the lesion is thought to originate in the lower layer of the lamina propria[23] and may be sessile.[24][7] The layers of the muscle wall atrophy, fraying, and splitting are brought on by inflammatory fibroid polyps.[6]

When inflammatory fibroid polyps from different GI sites are stained with immunohistochemistry, the spindle cell component exhibits nearly 100% positivity for vimentin[5] and CD34,[17] but varying staining for smooth muscle actin, HHF-35, KP1, and Mac 387.[23]

Classification edit

The literature describes four histopathological groups into which inflammatory fibroid polyps can be divided: classical fibrovascular, nodular, sclerotic, and edematous.[3]

Treatment edit

The only available treatment option is surgical excision of the lesion using either an open or endoscopic approach, depending on the location and size of the tumor.[1] In certain instances, a formal oesophagectomy or lateral oesophagotomy was required for resection.[37] Moreover, reports of using Nd YAG laser and thermocautery to treat tiny polyps exist.[1]

Epidemiology edit

Individuals who have inflammatory fibroid polyps usually show up in their fifth or seventh decade of life.[38] In children, it is uncommon.[39] Even though the female-to-male ratio has varied from 2.8:1[24] to 0.7:1,[7] both sexes seem to be equally affected.[38]

See also edit

References edit

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  2. ^ a b J, Vanek (1949). "Gastric submucosal granuloma with eosinophilic infiltration". The American Journal of Pathology. 25 (3). Am J Pathol: 397–411. ISSN 0002-9440. PMC 1942901. PMID 18127133.
  3. ^ a b Wysocki, A. Peter; Taylor, Graeme; Windsor, John A. (2007). "Inflammatory fibroid polyps of the duodenum: a review of the literature". Digestive Surgery. 24 (3): 162–168. doi:10.1159/000102099. ISSN 0253-4886. PMID 17476106.
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  25. ^ Bickel, A; Szvalb, S; Eitan, A; Cohen, I (November 1994). "The coexistence of inflammatory fibroid polyp and granular cell tumor in the same gastric lesion". The American Journal of Gastroenterology. 89 (11): 2090–2091. PMID 7942750.
  26. ^ Goto, Keisuke; Hirosaki, Takuya; Masubuchi, Mariko (February 2017). "Neurofibromatosis Type 1-Associated Inflammatory Polyp of the Gastrointestinal Tract". International Journal of Surgical Pathology. 25 (1): 65–68. doi:10.1177/1066896916648772. ISSN 1940-2465. PMID 27170677. S2CID 37595484.
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Further reading edit

  • Harima, Hirofumi; Kimura, Tokuhiro; Hamabe, Kouichi; Hisano, Fusako; Matsuzaki, Yuko; Sanuki, Kazutoshi; Itoh, Tadahiko; Tada, Kohsuke; Sakaida, Isao (2018). "Invasive inflammatory fibroid polyp of the stomach: a case report and literature review". BMC Gastroenterology. 18 (1): 74. doi:10.1186/s12876-018-0808-9. ISSN 1471-230X. PMC 5984322. PMID 29855265.
  • Adams, Haley S.; Bergstrom, Brian; Haines, Bret; Roberts, Nathan (2017). "Inflammatory Fibroid Polyp: An Unusual Cause of Ileoileal Intussusception". Case Reports in Surgery. 2017. Hindawi Limited: 1–4. doi:10.1155/2017/6315934. ISSN 2090-6900. PMC 5733754. PMID 29348960.

External links edit

  • Pathology Outlines

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