Research Topics
Genomes and GenesSpecies | Roberto N MirandaSummaryAffiliation: The University of Texas Country: USA Publications
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Publications
Anaplastic large cell lymphoma involving the breast: a clinicopathologic study of 6 cases and review of the literatureRoberto N Miranda
Department of Hematopathology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA
Arch Pathol Lab Med 133:1383-90. 2009..Lymphomas involving the breast are rare, and most cases are of B-cell lineage; T-cell neoplasms represent less than 10% of all breast lymphomas...
Extranodal NK/T-cell lymphoma, nasal type, arising in association with saline breast implant: expanding the spectrum of breast implant-associated lymphomasTariq N Aladily
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Am J Surg Pathol 36:1729-34. 2012..In addition, we believe this case is important to report, because it expands the spectrum of T-cell lymphomas that can be associated with breast implants and may be a forerunner of additional cases to follow...
CD5-positive mucosa-associated lymphoid tissue (MALT) lymphoma: a clinicopathologic study of 14 casesJesse Jaso
Department of Pathology, The University of Texas Medical School at Houston, Houston, TX 77030, USA
Hum Pathol 43:1436-43. 2012..Our results show that CD5 expression is rare in MALT lymphoma, and is often associated with nongastric disease and an increased tendency to present with disseminated disease. Overall survival is excellent with appropriate therapy...
High-grade B cell lymphoma, unclassifiable, with blastoid features: an unusual morphological subgroup associated frequently with BCL2 and/or MYC gene rearrangements and a poor prognosisRashmi Kanagal-Shamanna
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Histopathology 61:945-54. 2012..At a haematopathology workshop, experts had suggested the term 'high-grade B cell lymphoma, unclassifiable, with blastoid features', and recommended further studies...
B-cell lymphomas with MYC/8q24 rearrangements and IGH@BCL2/t(14;18)(q32;q21): an aggressive disease with heterogeneous histology, germinal center B-cell immunophenotype and poor outcomeShaoying Li
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Mod Pathol 25:145-56. 2012..Tumors with extra MYC signals plus IGH@BCL2 or MYC rearrangement plus extra BCL2 signals, respectively, appear to behave as poorly as MYC/BCL2 lymphomas, possibly expanding the disease spectrum...
Myelodysplastic syndromes with deletions of chromosome 11q lack cryptic MLL rearrangement and exhibit characteristic clinicopathologic featuresSa A Wang
Department of Hematopathology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030 4009, USA
Leuk Res 35:351-7. 2011..These clinicopathological features are likely attributed to commonly deleted regions of 11q and their involved genes...
Expression of serine 194-phosphorylated Fas-associated death domain protein correlates with proliferation in B-cell non-Hodgkin lymphomasElias Drakos
Department of Hematopathology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA
Hum Pathol 42:1117-24. 2011..9, P < .0001). These data provide evidence that serine 194 phosphorylated Fas-associated death domain protein is involved in the proliferation of normal and neoplastic B cells and has features of a novel proliferation marker...
Anaplastic large cell lymphoma associated with breast implants: a report of 13 casesTariq N Aladily
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Am J Surg Pathol 36:1000-8. 2012..In contrast, patients who present with a distinct mass may have advanced stage or possibly systemic disease and have a poorer prognosis...
Splenic B-cell lymphomas with more than 55% prolymphocytes in blood: evidence for prolymphocytoid transformationDaniela Hoehn
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Hum Pathol 43:1828-38. 2012..We conclude that splenic B-cell lymphoma of various types can undergo prolymphocytoid transformation with more than 55% prolymphocytes in the blood mimicking B-cell prolymphocytic leukemia...
Pure erythroid leukemia: a reassessment of the entity using the 2008 World Health Organization classificationWei Liu
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030 4009, USA
Mod Pathol 24:375-83. 2011..These new assigned categories fail to capture the distinct features of PEL, where the phenotype of PEL correlates with a very complex karyotype and an extremely aggressive clinical course...
T-cell large granular lymphocyte leukemia associated with myelodysplastic syndrome: a clinicopathologic study of nine casesYang O Huh
Department of Hematopathology, Unit 72, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Am J Clin Pathol 131:347-56. 2009..The median hemoglobin level and absolute lymphocyte count were lower in patients with T-LGL/MDS (P < .05). The frequency of coexistent T-LGL and MDS at our institution suggests an etiologic relationship rather than simple coincidence...
Lymphomas involving the breast: a study of 106 cases comparing localized and disseminated neoplasmsSameer S Talwalkar
Department of Hematopathology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA
Am J Surg Pathol 32:1299-309. 2008..003). In the disseminated group, patients with DLBCL had a worse disease-free survival compared with patients with mucosa-associated lymphoid tissue lymphoma or follicular lymphoma (P=0.01)...
Composite mantle cell lymphoma and chronic lymphocytic leukemia/small lymphocytic lymphoma: a clinicopathologic and molecular studySylvia Hoeller
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77230 1439, USA
Hum Pathol 44:110-21. 2013..The lack of a clonal relationship between the MCL and CLL/SLL components suggests that MCL and CLL/SLL components represent distinct disease processes and do not share a common progenitor B-cell...
8p11 myeloproliferative syndrome: a reviewCourtney C Jackson
Department of Hematopathology, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA
Hum Pathol 41:461-76. 2010..The most common partner is ZNF198 on chromosome 13q12. In the current World Health Organization classification, the 8p11 myeloproliferative syndrome is designated as "myeloid and lymphoid neoplasms with FGFR1 abnormalities."..
HDM4 is overexpressed in mantle cell lymphoma and its inhibition induces p21 expression and apoptosisMei Liang
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Mod Pathol 23:381-91. 2010..Inhibition of HDM4 may serve as a potential approach in the design of therapy for patients with mantle cell lymphoma...
