## Case of Schwachman's Syndrome With Intermittent Neutropenia and Lymphocyte Subset Disturbances To the Editor: Schwachman's syndrome, a familial disease transmitted as an autosomal-recessive trait, is characterized by moderate chronic neutropenia, marked marrow hypocellularity, occasional thromb
Simultaneous detection of MYC, BVR1, and PVT1 translocations in lymphoid malignancies by fluorescence in situ hybridization
✍ Scribed by Katrina Rack; Eric Delabesse; Isabelle Radford-Weiss; Priscille Bourquelot; Gaëlle Le Guyader; Michel Vekemans; Elizabeth Macintyre
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 232 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
✦ Synopsis
The rapid detection of chromosome band 8q24 rearrangements, including classical translocations involving MYC and variant 3Ј translocations, is important for the accurate diagnosis and appropriate treatment of lymphoid malignancies. We have identified and characterized a CEPH YAC, 934e1, which extends from at least 190 kbp upstream to over 280 kbp downstream to MYC, allowing detection of classical t(8;14)(q24;q32) and variant t(8;22)(q24;q11) and t(8;14)(q24;q11), extending distal to PVT1 and therefore, by extrapolation, to BVR1. This YAC also allowed clarification of complex chromosome 8 abnormalities and the identification of translocations in interphase nuclei. A second CEPH YAC, 904c3, previously shown to contain the PVT1 locus but not MYC, allowed distinction between translocations occurring centromeric and telomeric to MYC. Use of the 934e1 YAC will aid classification of a variety of lymphoid proliferations and further characterization of rearranged cases with the 904c3 YAC will simplify mapping of their diverse breakpoints.
📜 SIMILAR VOLUMES
## BACKGROUND. Atypical and anaplastic meningiomas tend to recur and to invade adjacent brain, bone, and skin. They also can metastasize to extracranial organs such as the lung, liver, or bone, causing death. Recent reports have indicated that allelic deletion of chromosome 1p is associated with m
## BACKGROUND. Benign body cavity effusions sometimes cannot be distinguished from malignant ones by conventional cytology. The authors performed fluores-Barry Sanchez, B
By two-color fluorescence in situ hybridization (FISH), der(16)t(1;16) or der(1;16) was frequently detected in low-grade papillary carcinoma but not in benign intraductal papilloma of the breast. In order to clarify the incidence and clinicopathological significance of der(16)t(1;16)/der(1;16) in co