|Year : 2019 | Volume
| Issue : 1 | Page : 67-69
Eosinophilic gastroenteritis: Atypical cause for chronic diarrhea in human immunodeficiency virus-associated immunosuppression
Om Shrivastav1, Nirzar Samir Parikh2, Ajay Bharat Jhaveri2, Rajni Ahlawat3
1 Department of Infectious Diseases, Jaslok Hospital and Research Centre, Mumbai, Maharashtra, India
2 Department of Gastroenterology, Jaslok Hospital and Research Centre, Mumbai, Maharashtra, India
3 Department of Pediatric Gastroenterology, Marshfield Clinic Children's Medical Center, Marshfield, Wisconsin, USA
|Date of Web Publication||10-May-2019|
Nirzar Samir Parikh
Department of Gastroenterology, Jaslok Hospital and Research Centre, Mumbai, Maharashtra
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Eosinophilic gastroenteritis (EGE) is an uncommon disease in both immunocompetent and immunocompromised. We describe a 57-year-old male with human immunodeficiency virus who presented to us with chronic diarrhea. He had no history of allergies and had significant weight loss, normal systemic examination, and a complete blood count showing no eosinophilia. After an esophagogastroduodenoscopy, the diagnosis of EGE was made by histopathological findings. The symptoms started improving with the initiation of treatment with oral prednisolone.
Keywords: Cachexia, esophagogastroduodenoscopy, prednisolone
|How to cite this article:|
Shrivastav O, Parikh NS, Jhaveri AB, Ahlawat R. Eosinophilic gastroenteritis: Atypical cause for chronic diarrhea in human immunodeficiency virus-associated immunosuppression. Indian J Sex Transm Dis 2019;40:67-9
|How to cite this URL:|
Shrivastav O, Parikh NS, Jhaveri AB, Ahlawat R. Eosinophilic gastroenteritis: Atypical cause for chronic diarrhea in human immunodeficiency virus-associated immunosuppression. Indian J Sex Transm Dis [serial online] 2019 [cited 2019 May 19];40:67-9. Available from: http://www.ijstd.org/text.asp?2019/40/1/67/256248
| Introduction|| |
Primary eosinophilic gastroenteritis (EGE) has not been reported before as an etiology for chronic diarrhea in patients infected with human immunodeficiency virus (HIV). After ruling out common etiologies such as infections and drugs, EGE should be considered as a differential diagnosis despite the patient being immunosuppressed.
| Case Report|| |
A 57-year-old Indian male with HIV-positive status was admitted to our hospital with chief complaints of large-volume watery stools without blood or mucus, 3–4 times a day for 4 months with recent exacerbation for 1 week. This was also associated with nausea, loss of appetite, significant weight loss, generalized weakness, and dysphagia to solids. He denied personal or family history of allergies. He was diagnosed with HIV infection 17 years ago and was on treatment with antiretroviral drugs, namely raltegravir, lamivudine, and efavirenz. He was also diagnosed with pulmonary tuberculosis 5 months back for which he was on treatment with isoniazid, rifampicin, pyrazinamide, and ethambutol. He unintentionally lost 20 kg of weight over the past 4 months. He further denied the use of laxatives or any complementary or alternative medications. He had stable vital signs, was cachectic, and had a normal systemic examination. His workup for chronic diarrhea included a normal thyroid function test and no opportunistic infections or helminthic infestation. Stool analysis including culture was negative for Clostridium difficile toxin, Cryptosporidium, Vibrio cholerae, acid-fast bacteria, or any other parasites. Serum IgE concentration was also within the normal range. Other investigations revealed hemoglobin 11.4 g/dL (13–18 g/dL), platelets 244,000/uL (140,000–440,000/uL), and total leukocyte count 4880/mm3 (4000–10000/mm3) with neutrophils 78.5% (40%–75%), lymphocytes 16.2% (20%–45%), and eosinophils 0.8% (1%–6%). His total protein was 5.4 g/dL (6.60–8.70 g/dL), albumin 1.8 g/dL (3.97–4.94 g/dL), absolute CD4 count 89.91/mm3 of blood (400–1600/mm3 of blood), absolute CD8 count 427.68/mm3 of blood (280–1400/mm3 of blood), CD4 (helper T-cells)% 11.1% (28–58%), CD8 (suppressor T-cells)% 52.8% (19–49%), CD4/CD8 0.21 (1.2–3.3), and HIV-1 viral load by TaqMan plasma (quantitative) 12,59,309 copies/mL.
On further investigations, esophagogastro duodenoscopy revealed white mucosal plaques in the esophagus consistent with esophageal candidiasis. The mucosa of the duodenum showed focal erosions with blunting of the villi as seen in [Figure 1]. Urease test was negative for Helicobacter pylori. Mucosal biopsies from the stomach and duodenum were taken. Histopathology study shown in [Figure 2] revealed active inflammation in the gastric and duodenal mucosa with excess eosinophils (20 eosinophils/high-power field) and no microorganisms. This was consistent with EGE. He also had a colonoscopy which was normal. Rifampicin was stopped during this admission for a period of 2 weeks. However, the persistence of diarrhea ruled out drug-induced EGE. He was then started on oral prednisolone 40 mg once daily. The frequency of stools decreased and consistency improved. Prednisolone was gradually tapered over a period of 2 months. This was associated with an increase in the frequency of watery stools like before resulting in a readmission with dehydration and weight loss.
|Figure 1: On esophagogastroduodenoscopy, mucosa of the duodenum shows (a) focal erosions and (b) blunting of the villi|
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|Figure 2: Histopathology (magnification: ×40). (a) More than 20 eosinophils seen around the mucous glands and (b) the eosinophils are focally forming crypt abscesses|
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The patient was restarted on oral prednisolone 60 mg once daily. Along with cessation of diarrhea, his appetite and weight improved during follow-up after 30 days. On 6-month follow-up, he has regained 18 kg and has normal stools. He is currently on oral prednisolone 40 mg once daily.
| Discussion|| |
Primary eosinophilic gastrointestinal disorders are disorders of the gastrointestinal tract that include eosinophilic esophagitis, eosinophilic gastritis, EGE, eosinophilic enteritis, and eosinophilic colitis, characterized by eosinophilic-rich inflammation in the absence of any known causes of eosinophilia. Eosinophils are present in the mucosal, muscular, or subserosal layers in excess of 20 per high-power field and more commonly involve the stomach and duodenum as seen in our patient. Although serum eosinophil counts are frequently elevated, up to 20% of patients have been reported to have normal counts. Large-scale population studies in the US have estimated the prevalence of EGE to be 28/100,000 persons. Eosinophilic gastrointestinal disorders affect all ethnic groups between 20 and 50 years of age but more commonly around the third decade of life. Unlike in the esophagus, baseline eosinophils are detected in the stomach and intestine under healthy conditions as a part of the host-defense mechanism., However, their infiltration to the deeper layers is considered abnormal. Eosinophilia in the intestinal mucosa is not seen with infections caused by common bacteria, viruses, and fungus. Eosinophils play an important role against infections caused by helminths, Dientamoeba fragilis, Mycobacterium spp., Isospora belli, Sarcocystis, Coccidioidomycosis, and HIV.
In our patient, diarrhea persisted even after stopping antituberculosis therapy, thus ruling out secondary causes of EGE. Primary EGE has not been reported before in HIV-associated immunosuppression and should be kept as a differential diagnosis in patients with HIV presenting with chronic diarrhea.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
We extend our thanks to our patient and his family.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Rothenberg ME. Eosinophilic gastrointestinal disorders (EGID). J Allergy Clin Immunol 2004;113:11-28.
Martillo M, Abed J, Herman M, Abed E, Shi W, Munot K, et al.
An atypical case of eosinophilic gastroenteritis presenting as hypovolemic shock. Case Rep Gastroenterol 2015;9:142-51.
Ingle SB, Hinge Ingle CR. Eosinophilic gastroenteritis: An unusual type of gastroenteritis. World J Gastroenterol 2013;19:5061-6.
Conner JR, Kirsch R. The pathology and causes of tissue eosinophilia in the gastrointestinal tract. Histopathology 2017;71:177-99.
López-Medina G, Gallo M, Prado A, Vicuña-Honorato I, Castillo Díaz de León R. Eosinophilic gastroenteritis: Case report and review in search for diagnostic key points. Case Rep Gastrointest Med 2015;2015:239506.
[Figure 1], [Figure 2]