Gastrointestinal Pathology. Группа авторов

Gastrointestinal Pathology - Группа авторов


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presence of rings, furrows, plaques, and strictures.

GERD
Medications
Infection
Motility disorders
Immune‐mediated disorders (e.g. CVID)
Lichen planus/lichenoid esophagitis
Crohn's disease (pediatric)
Celiac disease (pediatric)
Photo depicts characteristic histology of lymphocytic esophagitis.

      Microscopic Features

      Immunohistochemical Studies and Molecular Features

      Ancillary testing, including the subtyping of the intraepithelial CD3, CD4, and CD8 T cells is generally noncontributory and not required for the diagnosis. A subset of cases with CD4 predominant T cells and dysmotility has been reported.

      Differential Diagnosis

      The clinical and endoscopic differential diagnosis includes EOE, although by definition eosinophils are rare or absent. If neutrophils are present, special stains for candida may be warranted. Intraepithelial lymphocytes may be prominent in lichen planus esophagitis/lichenoid esophagitis, although the additional presence of a band‐like lymphocytic infiltrate in the lamina propria and necrotic keratinocytes is a distinguishing feature. Characteristic direct immunofluorescence findings of lichen planus DIF may or may not be demonstrated. Lymphocytosis may also be associated with esophageal involvement by Crohn’s disease in children, although other histologic and clinical features of Crohn’s disease are typically present, particularly elsewhere in the gut.

      Prognosis

      Follow‐up clinical and biopsy data are limited, although in some patients sequential biopsies have demonstrated persistent lymphocytosis, suggesting a chronic process.

      Definition, General Features, Predisposing Factors

      Elderly patients and women are most commonly affected. The elderly often have multiple underlying risk factors, and the female predominance is attributed to the more common use of certain medications in this group, such as iron supplements and bisphosphonates. Risk factors include pills taken with little or no water or while recumbent, underlying disorders of esophageal motility (e.g. diabetes, strictures, achalasia) and disorders of local anatomy causing external compression (enlarged left atrium, aortic aneurism). However, many patients do not exhibit abnormal esophageal function or other risk factors.

      Clinical and Endoscopic Characteristics

Medication Histologic features
NSAIDs Nonspecific, ± crystalline debris
Antibiotics (e.g. tetracyclines/doxycycline, clindamycin) Doxycycline—vascular injury
Potassium chloride Nonspecific
Iron Bluish‐brown crystalline debris, Fe stain +
Bisphosphonates (e.g. alendronate) Nonspecific, ± crystalline debris and multinucleated squamous cells
Quinidine Nonspecific
Resins (e.g. kayexalate, bile acid sequestrants) Kayexalate: Basophilic crystals with “fish scales,” AFB (black), PAD, Diff‐quick bile acid sequestrants:Orange‐black crystals, lack “fish scales,” AFB (yellow)
Mycophenolate Increased apoptosis (GVHD‐like)
Taxanes Mitotic arrest, ring mitoses

      Microscopic Features (Table 2.7)

      Biopsies most commonly show nonspecific esophagitis characterized by erosions, ulcers, active inflammation with neutrophils and occasionally eosinophils, surface epithelial damage, and granulation tissue. Adjacent mucosa is relatively normal. A careful search of the exudate and ulcer bed for refractile or polarizable foreign material is warranted, which may be an important diagnostic clue. However, in most cases the clinical history is necessary to make the diagnosis.


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