Evidence map›Paper›PMID 42761181›Full record

ArticleClinical case reports2026

Gastrointestinal Histoplasmosis Mimicking Intestinal Tuberculosis and Crohn's Disease: Ileocecal Involvement in an Immunocompetent Host.

Rashid Shahriar Sazal, Sayma Samia Esha, Abdullah Al Faisal, Md Abul Kalam Azad, Khaled Mahbub Murshed, Kazi Ali Aftab

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Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rashid Shahriar SazalDepartment of Internal Medicine Bangladesh Medical University Dhaka Bangladesh.ORCID https://orcid.org/0009-0008-2515-3042
Sayma Samia EshaDepartment of Internal Medicine Bangladesh Medical University Dhaka Bangladesh.ORCID https://orcid.org/0009-0002-7595-0150
Abdullah Al FaisalDepartment of Internal Medicine Bangladesh Medical University Dhaka Bangladesh.ORCID https://orcid.org/0009-0001-4496-8932
Md Abul Kalam AzadDepartment of Internal Medicine Bangladesh Medical University Dhaka Bangladesh.ORCID https://orcid.org/0009-0002-7771-1065
Khaled Mahbub MurshedDepartment of Internal Medicine Bangladesh Medical University Dhaka Bangladesh.ORCID https://orcid.org/0009-0006-6204-0501
Kazi Ali AftabDepartment of Internal Medicine Bangladesh Medical University Dhaka Bangladesh.ORCID https://orcid.org/0009-0001-5221-0021

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastrointestinal histoplasmosis is an under-recognized manifestation of disseminated Histoplasma capsulatum infection. Its ileocecal predilection closely mimics intestinal tuberculosis (TB) and Crohn's disease, posing serious diagnostic challenges, particularly in TB-endemic regions. A 26-year-old immunocompetent male presented with a 3-month history of diffuse abdominal pain, hematochezia, and 16 kg weight loss. He had received 60 days of empirical four-drug anti-tubercular therapy (ATT) without improvement. Examination revealed cachexia, pallor, digital clubbing, pedal oedema, a hard palate ulcer, and small cervical lymphadenopathy. Investigations showed microcytic anemia, C-reactive protein (CRP) 143.35 mg/L, hypoalbuminemia (2 g/dL), hyponatremia, and fecal calprotectin of 1849.47 μg/g. Magnetic resonance enterography (MRE) suggested multi-segmental small bowel disease consistent with Crohn's disease. Sequential colonoscopies revealed ulcero-nodular lesions involving the distal ileum, ileocecal valve, and caecum. Initial biopsies were inconclusive. Repeat deep tissue biopsy from the caecum and ileocecal valve identified intracellular narrow-based budding yeast forms with eccentric nuclei, consistent with H. capsulatum. GeneXpert and Quantiferon-TB gold plus were negative. Cervical lymph node fine-needle aspiration cytology (FNAC) confirmed disseminated disease. HIV testing was negative. Itraconazole was initiated, followed by liposomal amphotericin B. On day 15, the patient developed catastrophic lower gastrointestinal hemorrhage, resulting in refractory hemodynamic collapse and death. Disseminated histoplasmosis should be considered in the differential diagnosis of ileocecal disease even in immunocompetent patients from TB-endemic regions. Histopathological confirmation through deep tissue biopsy is critical prior to immunosuppressive therapy. Delayed diagnosis carries significant mortality risk.

Indexed as

Crohn's diseasediagnostic mimicrydisseminated histoplasmosisfungal infectiongastrointestinal histoplasmosishistopathologyHistoplasma capsulatumileocecal diseaseimmunocompetent hostintestinal tuberculosis

Identifiers

PMID42761181
PMCPMC13586439

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