Murase, T., Nakamura, S., Tashiro, K., Suchi, T., Hiraga, J., Hayasaki, N., Kimura, M., Murakami, M., Mizoguchi, Y., Suzuki, T. and Saito, H. (1997) Malignant histiocytosis-like b-cell lymphoma, a distinct pathologic variant of intravascular lymphomatosis: A report of five cases and review of the literature. British Journal of Haematology, 99, 656-664. doi:10.1046/j.1365-2141.1997.4623265.x

has been cited by the following article:

• TITLE: Unusual spontaneous improvement in Asian variant of intravascular large B-cell lymphoma

  AUTHORS: Takashi Ninomiya, Toru Nakamura, Nobuharu Fujii, Akio Hiraki, Shigeki Umemura, Hiromichi Yamane, Atsuko Shirakawa, Haruhito Kamei

  KEYWORDS: Lymphoma; Intravascular Large B-Cell Lymphoma; Spontaneous Improvement; Hemophagocytosis

  JOURNAL NAME: Open Journal of Internal Medicine, Vol.2 No.1, March 28, 2012

  ABSTRACT: The clinical course of the Asian variant of intravascular large B-cell lymphoma (AIVL) is generally very aggressive. We describe a case of AIVL demonstrating an unusual clinical course, with spontaneous improvement. An 81-year-old man with high-grade fever and thrombocytopenia was admitted to our hospital. Although we could not confirm the origin of his symptoms, they disappeared completely without intervention within 2 weeks. Three months later, however, thrombocytopenia reappeared and progressed. Finally, he was readmitted due to a subdural hemorrhage with high fever and he finally died of rapidly progressive multiple organ failure. Autopsy findings revealed the presence of B-cell lymphoma cells in microscopic vessels of many organs as well as hemophagocytosis in the bone marrow. He was diagnosed with AIVL with an unusual indolent clinical course with spontaneous improvement.