## Abstract A new Tβcell line (Amsalem) was established from the peripheral blood of a patient with preβT leukemia. Amsalem cells are unique in that they possess antigenic determinants associated with the Eβreceptor, yet fail to form rosettes with sheep red blood cells (SRBC). Amsalem cells were fo
Electron microscopy of E-rosette-forming leukemic monocytes in a child with acute monocytic leukemia
β Scribed by Masahige Tsukada; Hiroharu Saitoh; Toshihiro Hara; Atsushi Komiyama; Taro Akabane
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 378 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
A 7-year-old boy with acute monocytic leukemia (AMoL) had leukemic monocytes that formed spontaneous rosettes with sheep red blood cells (E-rosette). The E-rosette formation was observed in 75% of leukemic monocytes at 4 C and in 37% at 37 C. Cytochemical and ultrastructural studies confirmed that the rosette-forming cells were leukemic monocytes. The leukemic monocytes attached to the red blood cells at a portion of their surface and did not show any phagocytic processes at the electron microscopic level. The data from this patient seem to indicate that in a rare case of AMoL, abnormal myeloid lymphoid stem cells can differentiate to monocytes while retaining lymphoid properties.
Cancer 4731800-1103, 1981.
L I M A N MONOCYTES have Fc and C3 receptors on
H their surface, and leukemic monocytes in acute monocytic leukemia (AMoL) usually retain such receptors.'-3 However, they do not form rosettes with sheep red blood cells (SRBC), a specific marker for T-lymphocytes.
Reported here is an unusual case of childhood AMoL, in which leukemic cells formed spontaneous rosettes with SRBC (E-rosette). The E-rosette formation by leukemic monocytes has been confirmed at the electron microscopic level.
Case Report
A 7-year-old boy was admitted to Shinshu University Hospital in September 1978. At the age of 6 years, 9 months, he had visited another hospital with complaints of fever and cervical lymphadenopathy, and was diagnosed as having acute leukemia. Complete remission was attained with a combination of vincristine, 6-mercaptopurine (6-MP), and prednisolone, and was maintained with 6-MP and methotrexate.
In September 1978, he was sent to Shinshu University Hospital because of relapse of the leukemia. On admission. hemoglobin was 12.8 d m l , red blood cells 3.86 x IO'Vcu nim, platelets 20,OOO/cu mm. leukocytes 750/cu mm with a differential count of 44% lymphocytes and 56% nionocytic
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