CNS histoplasmosis coexisting with pulmonary tuberculosis in a HIV negative patient: case report.

Publication date: Nov 14, 2024

Tuberculosis is a highly prevalent disease in India, while Histoplasmosis, an emerging disease, is often underreported due to limited resources in developing countries. Coinfection with both these organisms is rarely documented in immunocompetent host. Due to overlapping symptoms, it can be easily missed and treatment delays are not uncommon. Here, we report a case of a 62-year-old male with a chronic history of intermittent fever and dry cough, splenomegaly, lymphadenopathy, and persistent pancytopenia. He was diagnosed with tuberculosis with cartridge-based nucleic acid amplification test (CBNAAT) positivity from a paratracheal lymph node biopsy. Simultaneously, a bone marrow biopsy revealed Histoplasmosis and the patient was started on dual treatment (Itraconazole and antitubercular drugs). After an initial response, the patient developed new space-occupying cerebral lesions. CSF histoplasma antigen was also positive. The reason for treatment failure was likely to be drug interaction (suboptimal levels of itraconazole due to rifampicin). The patient received liposomal amphotericin and subsequently put on a modified antitubercular treatment regimen to avoid interaction with itraconazole. At 2-month follow-up, the patient’s condition significantly improved with a substantial resolution in CNS lesions. Histoplasmosis and tuberculosis have overlapping symptoms, diagnosing one does not preclude the possibility of other, even in non-HIV patients. Clinicians should also be vigilant about potential drug interactions.

Open Access PDF

Concepts Keywords
Biopsy Brain abscess
Easily CNS histoplasmosis
Immunocompetent Coinfection
Liposomal Immunocompetent
Tuberculosis Tuberculosis

Semantics

Type Source Name
disease MESH histoplasmosis
disease MESH pulmonary tuberculosis
disease MESH Tuberculosis
pathway KEGG Tuberculosis
disease MESH Coinfection
disease IDO host
disease MESH treatment delays
disease IDO history
disease MESH splenomegaly
disease MESH lymphadenopathy
disease MESH pancytopenia
disease IDO nucleic acid
drug DRUGBANK Itraconazole
disease MESH treatment failure
disease MESH drug interaction
drug DRUGBANK Rifampicin
drug DRUGBANK Amphotericin B
pathway REACTOME Reproduction
disease MESH Infectious Diseases
drug DRUGBANK Coenzyme M
disease MESH Brain abscess
drug DRUGBANK Inosine pranobex
drug DRUGBANK Stavudine
disease MESH infections
disease MESH fungal infection
disease MESH immunocompromised patients
disease MESH weight loss
disease MESH ulcers
disease MESH hypertension
disease MESH acute kidney injury
drug DRUGBANK Creatinine
disease MESH dengue
disease MESH malaria
pathway KEGG Malaria
disease IDO blood
disease MESH leptospirosis
disease MESH scrub typhus
disease MESH brucellosis
disease IDO protein
drug DRUGBANK Dextrose unspecified form
disease MESH hypercalcemia
drug DRUGBANK Parathyroid hormone
drug DRUGBANK Angiotensin II
disease MESH hyperferritinemia
disease MESH sarcoidosis
drug DRUGBANK Prednisolone
disease MESH tachycardia
drug DRUGBANK Dimercaprol
disease MESH granuloma
drug DRUGBANK Trestolone
drug DRUGBANK 5-amino-1 3 4-thiadiazole-2-thiol
disease MESH recurrence
drug DRUGBANK Silver
disease MESH necrosis
disease MESH fibrosis
disease MESH syndrome
disease MESH pneumonia
drug DRUGBANK Calcium
disease MESH edema
disease MESH abscess
drug DRUGBANK Levofloxacin
drug DRUGBANK Isoniazid
drug DRUGBANK Pyrazinamide
disease IDO primary infection
disease IDO immunodeficiency
disease IDO cell
disease MESH AIDS
disease MESH opportunistic infections
disease IDO infection
disease MESH dual diagnosis
pathway REACTOME Metabolism
disease MESH confusion
disease MESH Immune reconstitution inflammatory syndrome
drug DRUGBANK Guanosine
drug DRUGBANK p-Phenylenediamine

Original Article

Leave a Comment

Your email address will not be published. Required fields are marked *