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29 results

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Page 1
IgM Plasma Cell Myeloma.
Lu H, Durkin L, Zhao X, Nakashima MO. Lu H, et al. Am J Clin Pathol. 2022 Jan 6;157(1):47-53. doi: 10.1093/ajcp/aqab095. Am J Clin Pathol. 2022. PMID: 34508562
Three of four tested cases were positive for t(11;14) by fluorescence in situ hybridization, one with monosomy 13. The remaining case was positive for del13q14. All were negative for MYD88 L265P and WHIM-like CXCR4 mutations. ...
Three of four tested cases were positive for t(11;14) by fluorescence in situ hybridization, one with monosomy 13. The remaini …
Prognostic significance of acquired 1q22 gain in multiple myeloma.
Audil HY, Cook JM, Greipp PT, Kapoor P, Baughn LB, Dispenzieri A, Gertz MA, Buadi FK, Lacy MQ, Dingli D, Fonder AL, Hayman SR, Hobbs MA, Muchtar E, Siddiqui M, Gonsalves WI, Hwa YL, Leung N, Lin Y, Kourelis TV, Warsame R, Kyle RA, Ketterling RP, Rajkumar SV, Kumar SK. Audil HY, et al. Am J Hematol. 2022 Jan 1;97(1):52-59. doi: 10.1002/ajh.26391. Epub 2021 Nov 3. Am J Hematol. 2022. PMID: 34710241 Free article.
Abnormalities on baseline fluorescence in situ hybridization (FISH) included trisomies (54%) and monosomy 13 (39%); 16 (25%) had high-risk (HR) translocations or del(17p). ...
Abnormalities on baseline fluorescence in situ hybridization (FISH) included trisomies (54%) and monosomy 13 (39%); 16 (25%) h …
Pathologic, cytogenetic, and molecular features of acute myeloid leukemia with megakaryocytic differentiation: A report from the Children's Oncology Group.
Chisholm KM, Smith J, Heerema-McKenney AE, Choi JK, Ries RE, Hirsch BA, Raimondi SC, Wang YC, Dang A, Alonzo TA, Sung L, Aplenc R, Gamis AS, Meshinchi S, Kahwash SB. Chisholm KM, et al. Pediatr Blood Cancer. 2023 May;70(5):e30251. doi: 10.1002/pbc.30251. Epub 2023 Feb 15. Pediatr Blood Cancer. 2023. PMID: 36789545 Free PMC article.
Cases with NUP98 fusions were enriched in trisomy 6 (p < .001), monosomy 13/del(13q) (p < .001), trisomy 21 (p = .026), and/or complex karyotypes (p = .026). ...

Cases with NUP98 fusions were enriched in trisomy 6 (p < .001), monosomy 13/del(13q) (p < .001), trisomy 21 (p = .026),

…
Prognostic Implications of Monosomies in Patients With Multiple Myeloma.
Shin SY, Eom HS, Sohn JY, Lee H, Park B, Joo J, Jang JH, Lee MN, Kim JK, Kong SY. Shin SY, et al. Clin Lymphoma Myeloma Leuk. 2017 Mar;17(3):159-164.e2. doi: 10.1016/j.clml.2016.12.001. Epub 2016 Dec 26. Clin Lymphoma Myeloma Leuk. 2017. PMID: 28089441
CONCLUSION: In addition to known cytogenetic abnormalities, such as monosomy 13, hypodiploidy, and TP53 (17p) deletion, monosomy 16 and loss of the Y chromosome have adverse prognostic implications in patients with MM....
CONCLUSION: In addition to known cytogenetic abnormalities, such as monosomy 13, hypodiploidy, and TP53 (17p) deletion, monoso …
In vitro fertilization and preimplantation genetic diagnosis outcomes in mosaic Turner's syndrome: A retrospective cohort study from a single referral center experience.
Acet F, Sahin G, Ucar AAO, Emirdar V, Karaca E, Durmaz B, Goker ENT, Tavmergen E. Acet F, et al. J Gynecol Obstet Hum Reprod. 2022 Sep;51(7):102405. doi: 10.1016/j.jogoh.2022.102405. Epub 2022 May 13. J Gynecol Obstet Hum Reprod. 2022. PMID: 35569796
In embryos with 2 abnormal chromosomes, the most common 2 abnormalities were monosomy 13 and trisomy 21, while trisomy 13, trisomy X and monosomy 18 were found in 3 or more abnormalities, respectively. ...
In embryos with 2 abnormal chromosomes, the most common 2 abnormalities were monosomy 13 and trisomy 21, while trisomy 13, tri …
Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India.
Govindasamy P, Pandurangan P, Tarigopula A, Mani R, R Samuel C. Govindasamy P, et al. Asian Pac J Cancer Prev. 2019 Jan 25;20(1):235-241. doi: 10.31557/APJCP.2019.20.1.235. Asian Pac J Cancer Prev. 2019. PMID: 30678438 Free PMC article.
A translocation involving the IGH gene alone or accompanied by trisomy(ies) or by monosomy 13/13q deletion or by both was registered in 80 (37.2%) patients. Atypical patterns such as a deletion of the IGH variable segment (IGHv) on the derivative chromosome 14 or on …
A translocation involving the IGH gene alone or accompanied by trisomy(ies) or by monosomy 13/13q deletion or by both was regi …
Prenatal diagnosis of a case of partial monosomy/monosomy 13 mosaicism: 46,XX,r(13)(p11q33)/45,XX,-13 suspected by nuchal fold translucency increasing.
Kataoka A, Hirakawa S, Iwamoto M, Sakumura Y, Yoshinaga R, Ohba T. Kataoka A, et al. Kurume Med J. 2011;58(4):127-30. doi: 10.2739/kurumemedj.58.127. Kurume Med J. 2011. PMID: 23047142 Free article.
Large numbers of patients with deletions of the long arm of chromosome 13 have been described. However, only a few instances have been reported of monosomy 13/r(13) mosaicism. A 31-year-old Japanese woman underwent an ultrasound tomographic screening, which detected …
Large numbers of patients with deletions of the long arm of chromosome 13 have been described. However, only a few instances have been repor …
Cytogenetic evolution patterns in non-Hodgkin's lymphoma.
Johansson B, Mertens F, Mitelman F. Johansson B, et al. Blood. 1995 Nov 15;86(10):3905-14. Blood. 1995. PMID: 7579360 Free article.

In general, the secondary aberrations were similar in lymphomas of different histologic subtypes but with the same primary abnormality, although some significant differences were discerned: +3, del(6q), +7, and +18 wee more common (P < .01) in intermediate-grade than in high-g

…
In general, the secondary aberrations were similar in lymphomas of different histologic subtypes but with the same primary abnormality, alth …
Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy.
Chen M, Yeh GP, Shih JC, Wang BT. Chen M, et al. Prenat Diagn. 2004 Feb;24(2):137-43. doi: 10.1002/pd.814. Prenat Diagn. 2004. PMID: 14974123 Review.
The process of correction appeared to exist in the placenta (indirect evidence from coexistence of trisomy 13 [46,XX,der(13;13)(q10,q10)], euploidy [46,XX], aneuploidy [46,XX,-13, +mar], and monosomy 13 [45,XX,-13] in the chorion at birth). The baby had survived bey …
The process of correction appeared to exist in the placenta (indirect evidence from coexistence of trisomy 13 [46,XX,der(13;13)(q10,q10)], e …
Close relation between 14q32/IGH translocations and chromosome 13 abnormalities in multiple myeloma: a high incidence of 11q13/CCND1 and 16q23/MAF.
Takimoto M, Ogawa K, Kato Y, Saito T, Suzuki T, Irei M, Shibuya Y, Suzuki Y, Kato M, Inoue Y, Takahashi M, Sugimori H, Miura I. Takimoto M, et al. Int J Hematol. 2008 Apr;87(3):260-5. doi: 10.1007/s12185-008-0039-x. Epub 2008 Feb 16. Int J Hematol. 2008. PMID: 18274833
Although 14q32/IGH translocations are closely related to the biological features of MM, the most consistent and powerful prognostic factor has been reported to be the loss of all (monosomy 13/-13) or part of chromosome 13 (del(13)(q14)/13q-). Our fluorescence in sit …
Although 14q32/IGH translocations are closely related to the biological features of MM, the most consistent and powerful prognostic factor h …
29 results