Isolated central nervous system Aspergillosis infection in a chronic lymphocytic leukemia patient on Ibrutinib: A case report

Invasive Aspergillosis (IA) is an opportunistic infection caused by the fungus Aspergillus [1]. Immunocompromised patients are at risk; however, in patients with Chronic Lymphocytic Leukemia (CLL) per se are not thought to be at a higher risk of IA. A 2016 correspondence in New England Journal of Medicine (NEJM) alerted clinicians to be aware of the possibility that ibrutinib use in CLL, even without neutropenia, is rarely associated with CNS-A [2]. Either the lung or paranasal sinuses are typically infected prior to or concomitant with CNS-A and therefore may serve as an etiological clinical clue to the correct diagnosis.

The diagnosis of isolated CNS-A is challenging. Neurological symptoms and signs are variable and an intracranial mass, detected by Computed Tomography (CT) or MRI, is not pathognomonic and easily misattributed to malignancy or abscess. Criteria for proven invasive fungal disease is by tissue biopsy histopathology and culture [3], but may not be possible or deemed safe to accomplish. Early diagnosis and prompt surgical and medical treatment reduces morbidity and mortality. Treatment of CNS-A is surgical excision (resection or removal if possible) of the Aspergillus granuloma and necrotic tissue treatment with anti-aspergillus therapy [4]. Current Infectious Diseases Society of America (IDSA) guidelines recommend voriconazole as the preferred first line anti-aspergillus therapy [5]. Amphotericin B may also be considered in patients intolerant to voriconzole [5].

A 74-year-old Caucasian male with CLL and no prior chemotherapy on ibrutinib for 6 months, presented with 3 months of fluctuating, slowly progressive imbalance, unsteady gait, left occipital headache and 1 week of intermittent confusion prior to neurological evaluation. Medical history included: COPD, non-valvular atrial fibrillation (novel oral anticoagulant treated), and pulmonary sarcoidosis on chronic prednisone 5 mg daily. Neurological exam revealed a right upper hemianopsia, unsteady wide based gait. He was afebrile and alert, but mildly confused. Sino- pulmonary exam was normal and no lymphadenopathy or hepatosplenomegaly detected. Basic lab work showed no neutropenia. Head MRI showed a ring enhancing lesion (Fig. 1a) in the left occipital region without sinus abnormalities. An emergent craniotomy to evacuate the brain “abscess” revealed acute 45-degree angle branching hyphae (Fig. 1b), consistent with Aspergillus and confirmed with silver stain and positive culture. Chest CT was without signs of pulmonary aspergillosis or pneumonia and blood cultures were without growth. Transthoracic Echocardiogram performed showed no definitive vegetations. Serum galactomannan levels were not drawn due to lab limitations; however, B-D Glucan levels were positive. Within 72 h of postoperatively initiated voriconazole, his neurological symptoms dramatically improved. At six-month follow-up, repeat MRI confirmed complete resolution of the central nervous system (CNS) lesion and absence of neurological signs and symptoms.

Our patient on ibrutinib for CLL and low dose steroids for pulmonary sarcoidosis presented with subacute, neurological symptoms and signs attributed to isolated CNS-A. Aggressive diagnostic surgical and medical treatment led to complete cure.

Case reports predominate the literature. A 2012 meta-analysis compared cases of CNS-A at Massachusetts General Hospital (MGH) (n = 14) with globally published cases (n = 123) from 2000 to 2011 [6]. Of the 14 cases at MGH, none had isolated CNS-A (only 1 had primary discitis) without antecedent pulmonary or paranasal sinus infection. Of the 123 global cases, 22.8% (n = 28/123) did not have an apparent site of extra-CNS infection^. Hematogenous dissemination was confirmed from a pulmonary focus in 26.8% (n = 33/123) of cases and direct extension from paranasal sinus infection in 27.6% (n = 34/123) of cases. None had CLL or ibrutinib exposure [6].

Isolated CNS-A cases are rarely documented in CLL patients [7]. Three CNS-A cases were reported in 2016 from the international RESONATE-2 trial, a prospective observational cohort study of 1149 CLL patients in the United States on ibrutinib therapy. All three patients were on steroids and developed CNS-A within 2 months of initiating Ibrutinib [2]. Our case reinforces the importance of being vigilant for isolated CNS-A in CLL patients on ibrutinib who present with neurological symptoms and signs, even without prior or co-infection of sino-pulmonary tissue, as early recognition and treatment can be lifesaving. Prompt neuroimaging prudent to identify if a CNS space occupying lesion was accessible to biopsy.

Management included surgical evacuation with an attempt to remove or at least reduce the infection and voriconazole for 6 months, consistent with IDSA guidelines [5]. Due to limited access to serum voriconazole level testing and slow turnaround time, serum levels were unable to be monitored. However, adequate CNS penetration was clinically documented by absence of neurological signs and symptoms on physical exam with resolution of CNS lesion on MRI at follow-up.