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Adrenal histoplasmosis: unusual presentations.

The Journal of the Association of Physicians of India (2013-06-20)
Anil Bhansali, Sambit Das, Pinaki Dutta, Rama Walia, Uma Nahar, S K Singh, P Vellayutham, Shanmugasundar Gopal
ABSTRACT

Histoplasmosis has been sporadically reported from India. Though asymptomatic adrenal involvement has been described in patients with disseminated histoplasmosis; isolated adrenal involvement with adrenal insufficiency (AI) as the presenting manifestation of the disease is rare. We describe 5 immunocompetent men (mean age 55.6 yrs) from a nonendemic area with adrenal histoplasmosis presenting with constitutional symptoms. Three patients had AI at presentation with bilateral adrenal involvement and the other two developed AI during the course of the illness and had unilateral adrenal mass . All the patients had histopathological/cytologically proven adrenal histoplasmosis. 18FDG-PET done in 3 patients helped in delineating the extent of the disease. Adrenalectomy was done in 2 patients who presented with unilateral adrenal mass. All these patients received Amphotericin B and/or itraconazole treatment which led to symptomatic improvement but AI persisted in all at the end of the follow up of 6 to 18 months. The diagnosis of adrenal histoplasmosis should be considered in patients presenting with constitutional symptoms and unilateral or bilateral adrenal mass/es with or without AI.

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Sigma-Aldrich
Amfotericina B, 250 μg/mL in deionized water, 0.1 μm filtered, BioReagent, suitable for cell culture
Sigma-Aldrich
Amfotericina B, soluzione, powder, γ-irradiated, BioXtra, suitable for cell culture
Sigma-Aldrich
Amfotericina B, ~80% (HPLC), powder
Sigma-Aldrich
Amfotericina B, BioReagent, suitable for cell culture, ~80% (HPLC)
Amphotericin B for peak identification, European Pharmacopoeia (EP) Reference Standard