Asia Oceania Journal of Nuclear Medicine and Biology

Asia Oceania Journal of Nuclear Medicine and Biology

Bilateral adrenal histoplasmosis incidentally detected on 18F-FDG PET/CT in an immunocompetent man with primary adrenal insufficiency: A case report

Document Type : Case report

Authors
1 Department of Nuclear Medicine, Dr Rajendra Prasad Government Medical College (RPGMC), Tanda, Kangra, Himachal Pradesh, India
2 Department of Oncology, Dr Rajendra Prasad Government Medical College (RPGMC), Tanda, Kangra, Himachal Pradesh, India
Abstract
Adrenal histoplasmosis is an uncommon manifestation of Histoplasma capsulatum infection and may closely mimic malignancy or granulomatous diseases on imaging. We describe an immunocompetent 51 year old man with 5 months of constitutional symptoms who underwent 18F-FDG PET/CT for evaluation of occult disease. The scan revealed intensely FDG avid bilateral adrenal masses with necrotic components, with no other abnormal sites. Biochemical testing confirmed primary adrenal insufficiency. CT guided adrenal biopsy, targeted to the most FDG-avid viable component, demonstrated necrotizing granulomatous inflammation with intracellular yeast forms consistent with Histoplasma capsulatum. Antifungal therapy with itraconazole plus glucocorticoid replacement led to clinical improvement and interval regression of adrenal lesions on follow-up. This case highlights the value of 18F-FDG PET/CT for detecting unsuspected adrenal histoplasmosis, localizing optimal biopsy targets, and facilitating timely treatment even in immunocompetent patients presenting with nonspecific symptoms.
Keywords
Subjects

1.    Kauffman CA. Histoplasmosis: a clinical and laboratory update. Clinical microbiology reviews. 2007; 20(1):115-32. 
2.    Wheat LJ, Freifeld AG, Kleiman MB, Baddley JW, McKinsey DS, Loyd JE, et al. Clinical practice guidelines for the management of patients with histoplasmosis: 2007 update by the Infectious Diseases Society of America. Clinical Infectious Diseases. 2007: 
807-25. 
3.    Singh M, Chandy DD, Bharani T, Marak RS, Yadav S, Dabadghao P, et al. Clinical outcomes and cortical reserve in adrenal histoplasmosis- A retrospective follow‐up study of 40 patients. Clinical Endocrinology. 2019; 90(4): 534-41. 
4.    Kumar N, Singh S, Govil S. Adrenal histoplasmosis: clinical presentation and imaging features in nine cases. Abdominal imaging. 2003; 28(5):703-8. 
5.    Vyas S, Kalra N, Das PJ, Lal A, Radhika S, Bhansali A, et al. Adrenal histoplasmosis: an unusual cause of adrenomegaly. Indian Journal of Nephrology. 2011; 21(4): 283-5. 
6.    Rozenblit AM, Kim A, Tuvia J, Wenig BM. Adrenal histoplasmosis manifested as Addison’s disease: unusual CT features with magnetic resonance imaging correlation. Clinical radiology. 2001; 56(8):682-4. 
7.    Radin DR. Disseminated histoplasmosis: abdominal CT findings in 16 patients. AJR. American journal of roentgenology. 1991; 157(5):955-8. 
8.    Sharma P, Mukherjee A, Karunanithi S, Bal C, Kumar R. Potential role of 18F-FDG PET/CT in patients with fungal infections. American Journal of Roentgenology. 2014; 203(1): 180-9. 
9.    Kalathoorakath RR, Sharma A, Sood A, Nahar U, Gorla AK, Mittal BR. 18F-FDG PET/CT imaging and PET-guided biopsy in evaluation and treatment decision in adrenal histoplasmosis. BJR| case reports. 2016; 2(3): 20150451. 
10.Wandler E, Kramer EL, Sherman O, Babb J, Scarola J, Rafii M. Diffuse FDG shoulder uptake on PET is associated with clinical findings of osteoarthritis. American Journal of Roentgenology. 2005; 185(3): 797-803.
11.Ochsner JE, Sewall SA, Brooks GN, Agni R. Elastofibroma dorsi. Radiographics. 2006; 26(6):1873-6.
12.Patrikeos A, Breidahl W, Robins P. F-18 FDG uptake associated with elastofibroma dorsi. Clinical nuclear medicine. 2005; 30(9): 617-8. 
13.Pierce III JC, Henderson R. Hyper metabolism of elastofibroma dorsi on PET–CT. American Journal of Roentgenology. 2004; 183(1): 35-7.