Multifocal stenosing ulceration of the small intestine
Multifocal stenosing ulceration of the small intestine is a rare condition that is characterised by recurrent ulcers of the small intestine.
Signs and symptoms
The clinical features of this condition are variable. Features associated with it include:Faecal occult blood testing is usually positive.
Laboratory investigations normally show anaemia and low albumin.
Cause
A mutation in the cytosolic phospholipase A2-α gene has been identified as the cause of this disease in one family. In this family the mutation was inherited as an autosomal recessive. It is not yet known if this gene is the cause of this disease in other families.The gene encoding cytosolic phospholipase A2-α is found on chromosome 1. Cytosolic phospholipase A2-α acts on membrane phospholipids to release arachidonic acid a precursor in the synthesis of eicosanoids. The eicosanoids are involved in multiple regulatory pathways.
Pathology
This disease is characterised by multifocal stenosing ulceration of the small intestine. The ulcers are circular or irregular in shape and their margins are always clear. The lesions involve only the mucosa and submucosa and are confined to the jejunum and proximal ileum. The intervening mucosa appears normal. Nonspecific inflammatory changes are present. Giant cells or other typical features of granulomatous inflammation are not found. Multiple stenoses are typically present.Diagnosis
This may be difficult given the non specific nature of the presenting symptoms and the rarity of the condition itself. It is normally made by the combination of the clinical picture, endoscopic findings and typical histology. Radiology may also be helpful. Other conditions such as infections and vasculitis should be ruled out with the relevant laboratory investigations.Differential diagnosis
- Idiopathic ulcerative jejunoileitis
- Lymphoma
- Infectious agents
- Infections in the immunosuppressed with unusual organismsTropheryma whipplei, Mycobacterium avium intracellulare
- Drug induced
- Zollinger-Ellison syndrome
- Heterotopic functioning gastric mucosa
- Meckel's diverticulum
- Crohn's disease
- Traumatic injury
- Ischemia
- Thrombotic diseases
- Degos disease
- Pseudoxanthoma elasticum
- Myeloproliferative disorders
- Antithrombin III deficiency
- Vasculitis
- Coeliac disease
- Behçet's disease