Nocardia otitidiscaviarum meningitis in a diffuse large B-cell lymphoma patient with CD4-positive lymphocytopenia and persistent oligoclonal CD8-positive lymphocytes in the peripheral blood

• Published in: International journal of clinical and experimental pathology Vol. 11; no. 1; pp. 455 - 461
• Main Authors: Tajima, Katsushi, Terada, Taichi, Okuyama, Shuhei, Akaneya, Daisuke, Hori, Ryuichiro, Abe, Shuichi, Osakabe, Mitsumasa, Kumagai, Hiroaki, Tsumanuma, Riko, Omoto, Eijiro, Ito, Junko, Gonoi, Tohru
• Format: Journal Article
• Language: English
• Published: United States e-Century Publishing Corporation 2018
• Subjects: Case Report; granulomatous lesions; idiopathic CD4-positive T-lymphocytopenia; Nocardia otitidiscaviarum; oligoclonal CD8-positive T-lymphocytes; meningitis
• ISSN: 1936-2625

Nocardiosis, sometimes presenting with multiple granulomatous lesions, is a rare opportunistic infection occurring in immunocompromised patients. However, its immunological features remain largely unaddressed. We investigated the immunological characteristics of human nocardiosis and examined the component cells of the granulomatous lesions. A 66-year-old man with diffuse large B-cell lymphoma presented with fever and multiple nodules in the lung during chemotherapy. The blood culture formed white colonies, but their characterization was difficult by routine microbiological laboratory methods. Matrix-assisted laser desorption ionization-time of flight mass spectrometry identified the colonies as
. Meanwhile, the patient suddenly experienced an epileptic seizure without a brain abscess. His cerebrospinal fluid (CSF) showed neutrophilic pleocytosis (108/mm
). The conventional agar culturing failed to isolate colonies, but culturing with brain-heart infusion agar generated colonies. These colonies were completely concordant with those from the blood, as confirmed by 16S rRNA gene sequencing. Therefore, the patient had developed meningitis through sepsis induced by
. His CD4-positive T-lymphocyte counts were low, and oligoclonal CD8-positive αβ T-lymphocytes were present in the blood prior to the first and after three cycles of chemotherapy. He had bone marrow granulomatous lesions comprising lymphoma and CD8-positive αβ T-cells. Treatment with sulfamethoxazole/trimethoprim relieved all of his symptoms. The combined analysis by microbiological and molecular methods determined the cause of his epileptic seizure. His immunological characteristics, including low CD4-positive or CD8-positive αβ T-lymphocytes, may have contributed to the unusual clinical presentations by
, which rarely involves the central nervous system.