## Abstract A 55‐year‐old Caribbean woman with a 6‐year history of smoldering adult T‐cell leukemia/lymphoma presented with clinical and biological symptoms of hemophagocytic syndrome. An extensive search for infectious diseases was negative. A lymph node biopsy showing large T‐cell lymphoma (CD4^−
Pancytopenia due to hemophagocytic syndrome as the presenting manifestation of babesiosis
✍ Scribed by Pankaj Gupta; Randolph W. Hurley; Peter H. Helseth; Jesse L. Goodman; Dale E. Hammerschmidt
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 516 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
✦ Synopsis
We present a case of hemophagocytosis during infection with the intraerythrocytic protozoan Babesia microti in a 47-year-old splenectomized renal allograft recipient. After therapy with clindamycin and quinine a relapse responded to atovaquone; durable remission was not achieved until trimethoprim/sulfa was added. We postulate the severity of our patient's syndrome was due to splenectomy and chronic immunosuppression. Babesiosis should be considered when immunocompromised patients develop pancytopenia.
📜 SIMILAR VOLUMES
## Abstract We report here a new case of oculomasticatory syndrome related to systemic Whipple's disease. The patient presented typical ophthalmoparesis associated with ocular myorhythmia consisting of 1 Hz convergent oscillations of both eyes. The masticatory involvement was remarkable and consist