Abstract

A 42-
After 14 days of unsuccessful empirical antibacterial therapy she was hospitalized. A computed tomography (CT) scan showed multiple bilateral ground glass opacities and enlarged mediastinal and pulmonary hilar lymph nodes. We performed several invasive diagnostic procedures that were negative for Mycobacterium tuberculosis and other infectious agents [bronchoalveolar lavage (BAL), cerebrospinal fluid, and lymph node biopsy].
The lymphoid population on the BAL sample consisted mainly of CD3+ T cells, with a CD4/CD8 ratio of 5.6. The transbronchial biopsy showed inflammatory lymph granulocytic infiltrates. The mediastinal lymph node transbronchial needle aspiration revealed sparse histiocytes without epithelioid cell granulomas. Finally, the mediastinal lymph node biopsy showed necrosis with confluent granulomas without acid-fast bacilli. Concomitantly, the patient developed interstitial nephritis with renal impairment without hypercalciuria and/or hypercalcemia.
Consistent with the presence of two major diagnostic criteria (noncaseating granulomas and lack of acid-fast bacilli on biopsy) 1 and a CD4/CD8 ratio greater than 4:1 on BAL, 2 we diagnosed a multisystemic sarcoidosis. A baseline [18F]fluorodeoxyglucose positron emission tomography-computed tomography (18FDG-PET/TC) showed intense FDG uptake in several lymph node stations on both sides of the diaphragm (Fig. 1A). High-dose prednisone (1 mg/kg/daily) was then started with rapid clinical improvement and weight gain; after a few weeks, steroid treatment was slowly tapered to 7.5 mg/daily. Five months later, a second 18FDG-PET/TC revealed partial resolution of the nodal disease; tissue-specific glucose uptake semiquantitative analysis revealed a partial metabolic response. Conversely, splenic uptake was inhomogeneously increased (Fig. 1B). The prednisone dosage was then increased to 50 mg/day and subsequently tapered off slowly to 10 mg/day. A third 18FDG-PET/TC, performed 10 months after the start of prednisone, showed a complete metabolic response in all tissues (Fig. 1C). At the same time, the CD4 T cell count rose to 389/mm3 (23.6%). Renal function remained stable, although altered.

Granulomatous disease in HIV-infected patients needs a multidisciplinary approach and nuclear medicine could be a valid support. 3 Sarcoidosis is rare in HIV; no diagnostic criteria are tailored in this setting and this make the diagnosis challenging. To our knowledge, only one case of sarcoidosis had previously been reported in HIV-2 infection. 4 Moreover, starting high-dose steroid treatment in the presence of HIV infection and a low CD4 T cell count is a cause for concern. Longitudinal assessment of serial 18FDG-PET/TC is a valuable imaging tool in assessing treatment efficacy, especially in the case of extrapulmonary unusual features such as diffuse FDG splenic uptake.
Footnotes
Author Disclosure Statement
No competing financial interests exist.
