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[PMID]:28821195
[Au] Autor:Bledsoe JR; Wallace ZS; Deshpande V; Richter JR; Klapman J; Cowan A; Stone JH; Ferry JA
[Ad] Endereço:Department of Pathology, UMass Memorial Medical Center,Worcester, MA.
[Ti] Título:Atypical IgG4+ Plasmacytic Proliferations and Lymphomas: Characterization of 11 Cases.
[So] Source:Am J Clin Pathol;148(3):215-235, 2017 Sep 01.
[Is] ISSN:1943-7722
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Objectives: To report the clinicopathologic features of monotypic immunoglobulin G4+ (IgG4+) lymphoid and plasmacytic proliferations. Methods: Cases were identified from the pathology files. Pathology and clinical materials were reviewed. Results: Eleven cases of monotypic IgG4+ proliferations were identified at nodal, orbital, or salivary sites. Six cases (three men, three women; age, 57-94 years) met criteria for lymphoma or plasma cell neoplasia. Most contained frequent Mott cells. Five cases (three men, two women; age, 40-80 years) had restricted proliferations of atypical/monotypic IgG4+ plasma cells in a background of reactive lymphoid hyperplasia or inflammation. Conclusions: Monotypic IgG4+ proliferations include lymphomas, plasmacytic neoplasms, and a previously uncharacterized group of proliferations not meeting criteria for conventional hematolymphoid neoplasia. Distinct features included prominent Mott cells and/or monotypic plasma cells within follicles. The proliferations were infrequently associated with IgG4-related disease (IgG4-RD). Our findings raise questions regarding the relationship between clonal IgG4+ proliferations, reactive/inflammatory processes, and IgG4-RD.
[Mh] Termos MeSH primário: Imunoglobulina G
Linfoma/patologia
Neoplasias de Plasmócitos/patologia
Plasmócitos/patologia
[Mh] Termos MeSH secundário: Idoso
Idoso de 80 Anos ou mais
Feminino
Seres Humanos
Linfoma/imunologia
Masculino
Meia-Idade
Neoplasias de Plasmócitos/imunologia
Plasmócitos/imunologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Immunoglobulin G)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170906
[Lr] Data última revisão:
170906
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170820
[St] Status:MEDLINE
[do] DOI:10.1093/AJCP/AQX067


  2 / 114 MEDLINE  
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[PMID]:28636627
[Au] Autor:Kormann R; François H; Moles T; Dantal J; Kamar N; Moreau K; Bachelet T; Heng AE; Garstka A; Colosio C; Ducloux D; Sayegh J; Savenkoff B; Viglietti D; Sberro R; Rondeau E; Peltier J
[Ad] Endereço:Service d'Urgences Néphrologiques et Transplantation Rénale, Hôpital Tenon, APHP, Université Pierre et Marie Curie, Paris, France.
[Ti] Título:Plasma cell neoplasia after kidney transplantation: French cohort series and review of the literature.
[So] Source:PLoS One;12(6):e0179406, 2017.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Although post-transplant lymphoproliferative disorder (PTLD) is the second most common type of cancer in kidney transplantation (KT), plasma cell neoplasia (PCN) occurs only rarely after KT, and little is known about its characteristics and evolution. We included twenty-two cases of post-transplant PCN occurring between 1991 and 2013. These included 12 symptomatic multiple myeloma, eight indolent myeloma and two plasmacytomas. The median age at diagnosis was 56.5 years and the median onset after transplantation was 66.7 months (2-252). Four of the eight indolent myelomas evolved into symptomatic myeloma after a median time of 33 months (6-72). PCN-related kidney graft dysfunction was observed in nine patients, including six cast nephropathies, two light chain deposition disease and one amyloidosis. Serum creatinine was higher at the time of PCN diagnosis than before, increasing from 135.7 (±71.6) to 195.9 (±123.7) µmol/l (p = 0.008). Following transplantation, the annual rate of bacterial infections was significantly higher after the diagnosis of PCN, increasing from 0.16 (±0.37) to 1.09 (±1.30) (p = 0.0005). No difference was found regarding viral infections before and after PCN. Acute rejection risk was decreased after the diagnosis of PCN (36% before versus 0% after, p = 0.004), suggesting a decreased allogeneic response. Thirteen patients (59%) died, including twelve directly related to the hematologic disease. Median graft and patient survival was 31.7 and 49.4 months, respectively. PCN after KT occurs in younger patients compared to the general population, shares the same clinical characteristics, but is associated with frequent bacterial infections and relapses of the hematologic disease that severely impact the survival of grafts and patients.
[Mh] Termos MeSH primário: Nefropatias/cirurgia
Transplante de Rim/efeitos adversos
Neoplasias de Plasmócitos/etiologia
[Mh] Termos MeSH secundário: Adulto
Idoso
Feminino
Seres Humanos
Masculino
Meia-Idade
Neoplasias de Plasmócitos/diagnóstico
Prognóstico
Estudos Retrospectivos
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171006
[Lr] Data última revisão:
171006
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170622
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0179406


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[PMID]:28395104
[Au] Autor:Chadburn A; Said J; Gratzinger D; Chan JK; de Jong D; Jaffe ES; Natkunam Y; Goodlad JR
[Ad] Endereço:From the Weill Medical College of Cornell University, New York, NY.
[Ti] Título:HHV8/KSHV-Positive Lymphoproliferative Disorders and the Spectrum of Plasmablastic and Plasma Cell Neoplasms: 2015 SH/EAHP Workshop Report-Part 3.
[So] Source:Am J Clin Pathol;147(2):171-187, 2017 Feb 01.
[Is] ISSN:1943-7722
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Objectives: The 2015 Workshop of the Society for Hematopathology/European Association for Haematopathology aimed to review immunodeficiency-related lymphoproliferative disorders with plasmablastic and plasma cell differentiation. Methods: The workshop panel reviewed human herpes virus 8 (HHV8)/Kaposi sarcoma herpesvirus (KSHV)-associated lesions and other lesions exhibiting plasma cell differentiation, including plasmablastic proliferations with features of myeloma/plasmacytoma, plasmablastic neoplasms presenting in extranodal sites and effusion-based lymphomas, and rendered a consensus diagnosis. Results: The spectrum of HHV8/KSHV-associated proliferations ranged from multicentric Castleman disease (MCD) to MCD with plasmablastic aggregates to HHV8+ diffuse large B-cell lymphoma and germinotrophic lymphoproliferative disorder. Comparisons across effusion-based lymphomas with and without HHV8/KSHV and plasmablastic lymphomas in immunodeficient and immunocompetent patients were discussed. Conclusions: The presence or absence of HHV8/KSHV is a defining feature in disorders associated with Castleman disease, although their differential diagnosis and recognition of progression may be challenging. Plasmablastic proliferations overlap with myeloma/plasmacytoma as well as extranodal and effusion-based lymphomas. The involvement of Epstein-Barr virus is typically variable.
[Mh] Termos MeSH primário: Infecções por Herpesviridae/complicações
Síndromes de Imunodeficiência/patologia
Transtornos Linfoproliferativos/patologia
Neoplasias de Plasmócitos/patologia
[Mh] Termos MeSH secundário: Adulto
Idoso
Educação
Feminino
Herpesvirus Humano 8
Seres Humanos
Síndromes de Imunodeficiência/virologia
Transtornos Linfoproliferativos/diagnóstico
Transtornos Linfoproliferativos/virologia
Masculino
Meia-Idade
Neoplasias de Plasmócitos/diagnóstico
Neoplasias de Plasmócitos/virologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170414
[Lr] Data última revisão:
170414
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170411
[St] Status:MEDLINE
[do] DOI:10.1093/ajcp/aqw218


  4 / 114 MEDLINE  
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[PMID]:27070686
[Au] Autor:Gargya V; Lucas HD; Wendel Spiczka AJ; Mahabir RC
[Ad] Endereço:From the Divisions of *General Surgery, and †Plastic and Reconstructive Surgery, Mayo Clinic Hospital, Phoenix; and ‡Department of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, AZ.
[Ti] Título:Is Routine Pathologic Evaluation of Sebaceous Cysts Necessary?: A 15-Year Retrospective Review of a Single Institution.
[So] Source:Ann Plast Surg;78(2):e1-e3, 2017 Feb.
[Is] ISSN:1536-3708
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:A question arose in our practice of whether all cysts considered sebaceous should be sent for pathologic evaluation. To address this controversial topic, we performed a retrospective study of our single institution's histopathology database. A natural language search of the CoPath database across the institution was undertaken using the diagnosis of sebaceous cyst, epidermal cyst, epidermoid cyst, epithelial cyst, infundibular cyst, pilar cyst, trichilemmal cyst, and steatocystoma. A surgical pathologic review of all specimens with one of these preexcision diagnoses was included in the 15-year retrospective study of 1998 to 2013. All slides were confirmed to have undergone histopathologic review, and the preexcision diagnoses were compared with the postexcision diagnoses. Chart review was undertaken in instances of a diagnosis of malignancy. A total of 13,746 samples were identified. Forty-eight specimens had histopathologic diagnosis of malignancy, for an incidence of 0.3% and with the most common malignancy being squamous cell carcinoma. Chart review showed that for all cases, the surgeons reported uncertainty with regard to the diagnosis because of history or physical characteristics, or both. In addition, a comprehensive literature review showed results consistent with our data and illustrated 19 cases during the past 10 years in which most of the findings were squamous cell carcinoma. We propose the recommendation that routine pathologic evaluation of sebaceous cysts is necessary only when clinical suspicion exists.
[Mh] Termos MeSH primário: Cisto Epidérmico/patologia
[Mh] Termos MeSH secundário: Adulto
Idoso
Idoso de 80 Anos ou mais
Carcinoma/diagnóstico
Carcinoma/patologia
Carcinoma/cirurgia
Bases de Dados Factuais
Diagnóstico Diferencial
Cisto Epidérmico/diagnóstico
Cisto Epidérmico/cirurgia
Seres Humanos
Linfoma de Células B/diagnóstico
Linfoma de Células B/patologia
Linfoma de Células B/cirurgia
Melanoma/diagnóstico
Melanoma/patologia
Melanoma/cirurgia
Meia-Idade
Neoplasias de Plasmócitos/diagnóstico
Neoplasias de Plasmócitos/patologia
Neoplasias de Plasmócitos/cirurgia
Estudos Retrospectivos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171003
[Lr] Data última revisão:
171003
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160413
[St] Status:MEDLINE
[do] DOI:10.1097/SAP.0000000000000826


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[PMID]:27604415
[Au] Autor:Caporali C; Albanese F; Binanti D; Abramo F
[Ad] Endereço:Private Practitioner, via Giovanni da Verrazzano, 19, 52100, Arezzo, Italy.
[Ti] Título:Two cases of feline paraneoplastic alopecia associated with a neuroendocrine pancreatic neoplasia and a hepatosplenic plasma cell tumour.
[So] Source:Vet Dermatol;27(6):508-e137, 2016 Dec.
[Is] ISSN:1365-3164
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Feline paraneoplastic alopecia (FPA) is a rare condition listed among the cutaneous paraneoplastic syndromes, which occurs in association with pancreatic carcinoma, cholangiocarcinoma, hepatocellular carcinoma and metastatic intestinal carcinoma. OBJECTIVES: To describe the clinicopathological findings of paraneoplastic alopecia in two cats each with an uncommon tumour not previously reported in association with FPA. ANIMALS: Paraneoplastic alopecia was associated with neuroendocrine pancreatic neoplasia in a Persian cat and with a hepatosplenic plasma cell tumour in a domestic short hair cat. RESULTS: FPA was suspected based on age, rapid onset of clinical signs, ventral distribution of alopecia, shiny appearance of the skin and telogenization/miniaturization of the follicles on histopathology. The nature of the tumours was determined through cytology, postmortem, histopathological and immunohistochemical examination, and capillary immunoelectrophoresis. A causative association between the skin lesions and the tumour was suggested by clinical and histopathological features shared with previously published cases. CONCLUSIONS AND CLINICAL IMPORTANCE: Pancreatic neuroendocrine and plasma cell tumour should be considered as differential diagnoses when evaluating FPA.
[Mh] Termos MeSH primário: Alopecia/veterinária
Doenças do Gato/patologia
Neoplasias de Plasmócitos/veterinária
Neoplasias Pancreáticas/veterinária
[Mh] Termos MeSH secundário: Alopecia/etiologia
Alopecia/patologia
Animais
Doenças do Gato/etiologia
Gatos
Feminino
Neoplasias de Plasmócitos/complicações
Neoplasias Pancreáticas/complicações
[Pt] Tipo de publicação:CASE REPORTS
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170502
[Lr] Data última revisão:
170502
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160909
[St] Status:MEDLINE
[do] DOI:10.1111/vde.12375


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[PMID]:27546802
[Au] Autor:Jakó J; Szerafin L
[Ad] Endereço:Hematológiai Osztály, Szabolcs-Szatmár-Bereg Megyei Jósa András Oktatókórház Nyíregyháza.
[Ti] Título:[Epidemiologic features of myeloma in Szabolcs-Szatmár-Bereg county, Hungary. Analysis of data of a 33-year period].
[Ti] Título:A myeloma epidemiológiai jellemzoi Szabolcs-Szatmár-Bereg megyében. 33 év adatainak elemzése..
[So] Source:Orv Hetil;157(34):1357-60, 2016 Aug.
[Is] ISSN:0030-6002
[Cp] País de publicação:Hungary
[La] Idioma:hun
[Ab] Resumo:INTRODUCTION: In their previous work, the authors reported findings from 30 years on the incidence of hematological malignancies in Szabolcs-Szatmár-Bereg county, Hungary. Until now there are no other studies on this topic available in Hungary. AIM: Detailed analysis of epidemiologic features of patients with myeloma. METHOD: During a 33-year period (between January 1, 1983 and December 31, 2015) 4521 adult patients with hematologic malignancies were recorded in the leukaemia/lymphoma registry of Szabolcs-Szatmár-Bereg county. Among them 440 patients with myeloma (9.73%) were registered (397 multiple myeloma, 38 solitary, bone/soft tissue plasmocytoma, 5 primary plasma cell leukaemia). RESULTS: The incidence of myeloma in Szabolcs-Szatmár-Bereg county showed an increasing tendency, with an overall incidence rate of 2.33/100 000 inhabitants/year. The male:female ratio was 45.9%:54.1%, the average age of patients was 65.1 (28-90) years, and 59.4% of the patients with multiple myeloma had IgG-type monoclonal immunoglobulin. There was no town or village in this county where the occurrence of patients with myeloma in one thousand inhabitants was significantly higher, than the average (0.78). CONCLUSIONS: The epidemiologic features of myeloma in Szabolcs-Szatmár-Bereg county - except a moderate female dominance - is essentially similar to data published in the literature. Orv. Hetil., 2016, 157(34), 1357-1360.
[Mh] Termos MeSH primário: Mieloma Múltiplo/epidemiologia
Neoplasias de Plasmócitos/epidemiologia
Plasmocitoma/epidemiologia
Sistema de Registros
[Mh] Termos MeSH secundário: Adulto
Distribuição por Idade
Idoso
Idoso de 80 Anos ou mais
Feminino
Seres Humanos
Hungria/epidemiologia
Incidência
Linfoma/epidemiologia
Masculino
Meia-Idade
Saúde Pública/tendências
Distribuição por Sexo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170706
[Lr] Data última revisão:
170706
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160823
[St] Status:MEDLINE
[do] DOI:10.1556/650.2016.30490


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[PMID]:27546545
[Au] Autor:Zajko J; Czako L; Galis B
[Ti] Título:Plasmocytoma, multiple myeloma and plasma cell neoplasms in orofacial region.
[So] Source:Bratisl Lek Listy;117(7):425-7, 2016.
[Is] ISSN:0006-9248
[Cp] País de publicação:Slovakia
[La] Idioma:eng
[Ab] Resumo:A neoplastic proliferation of B cell lymphocyte is called plasma cell neoplasms, results from malignant plasma cells transformation in bone marrow. The authors present a clinical study and overview of this pathology in maxillofacial region for six years (Tab. 2, Ref. 14).
[Mh] Termos MeSH primário: Neoplasias Ósseas/patologia
Mieloma Múltiplo/patologia
Neoplasias de Plasmócitos/patologia
Plasmocitoma/patologia
[Mh] Termos MeSH secundário: Idoso
Feminino
Seres Humanos
Masculino
Neoplasias Mandibulares/diagnóstico
Neoplasias Mandibulares/cirurgia
Meia-Idade
Mieloma Múltiplo/cirurgia
Neoplasias de Plasmócitos/cirurgia
Plasma
Plasmocitoma/cirurgia
Resultado do Tratamento
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170626
[Lr] Data última revisão:
170626
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160823
[St] Status:MEDLINE


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[PMID]:27453441
[Au] Autor:Wilberger AC; Prayson RA
[Ad] Endereço:From the Department of Pathology, University of Colorado School of Medicine, Aurora.
[Ti] Título:Intracranial Involvement by Plasma Cell Neoplasms.
[So] Source:Am J Clin Pathol;146(2):156-62, 2016 Aug.
[Is] ISSN:1943-7722
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: Intracranial plasma cell neoplasms (PCNs) arising from the skull, dura, or brain parenchyma are rare tumors and there is only a limited experience in the literature with these lesions. METHODS: We performed a retrospective clinicopathologic study of fourteen cases of intracranial PCN at our institution encountered over a 26-year-period. RESULTS: The fourteen patients ranged in age from 30-74 years (median 66 years) and included seven males. For eight patients, their intracranial lesions were the initial presentation of multiple myeloma (MM). Three patients had prior history of MM; their intracranial tumors showed blastic plasma cell morphology, and all three died secondary to MM. The remaining three patients did not or have not developed MM. CONCLUSIONS: PCNs rarely arise in the intracranial compartment. Intracranial PCN may be the initial presentation of MM. Anecdotally, blastic morphology appears to manifest more aggressive behavior.
[Mh] Termos MeSH primário: Neoplasias Encefálicas/patologia
Neoplasias de Plasmócitos/patologia
[Mh] Termos MeSH secundário: Adulto
Idoso
Feminino
Seres Humanos
Masculino
Meia-Idade
Estudos Retrospectivos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1702
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:160726
[St] Status:MEDLINE
[do] DOI:10.1093/ajcp/aqw058


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[PMID]:27133529
[Au] Autor:Luo X; Kuklani R; Bains A
[Ad] Endereço:Department of Pathology and Laboratory Medicine, Temple University Hospital, Philadelphia, PA, United States. Electronic address: xunda.luo@tuhs.temple.edu.
[Ti] Título:Dual CD3 and CD4 positive plasma cell neoplasm with indistinct morphology: a diagnostic pitfall.
[So] Source:Pathology;48(4):378-80, 2016 Jun.
[Is] ISSN:1465-3931
[Cp] País de publicação:England
[La] Idioma:eng
[Mh] Termos MeSH primário: Complexo CD3/metabolismo
Antígenos CD4/metabolismo
Neoplasias Mandibulares/diagnóstico
Neoplasias de Plasmócitos/diagnóstico
[Mh] Termos MeSH secundário: Biomarcadores Tumorais/metabolismo
Seres Humanos
Masculino
Neoplasias Mandibulares/metabolismo
Neoplasias Mandibulares/patologia
Meia-Idade
Neoplasias de Plasmócitos/metabolismo
Neoplasias de Plasmócitos/patologia
[Pt] Tipo de publicação:CASE REPORTS; LETTER
[Nm] Nome de substância:
0 (Biomarkers, Tumor); 0 (CD3 Complex); 0 (CD4 Antigens)
[Em] Mês de entrada:1704
[Cu] Atualização por classe:171116
[Lr] Data última revisão:
171116
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160503
[St] Status:MEDLINE


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[PMID]:26796980
[Au] Autor:Limvorapitak W; Srisum-Ang T; Chimres C; Warnnissorn N; Kanitsap N
[Ad] Endereço:Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Thammasat University, Pathumthani, Thailand. Electronic address: wasithep@tu.ac.th.
[Ti] Título:Accuracy of Bone Marrow Flow Cytometry Analysis in Patients With Plasma Cell Neoplasm in Thailand: A Single Institutional Study.
[So] Source:Clin Lymphoma Myeloma Leuk;16(3):e27-37, 2016 Mar.
[Is] ISSN:2152-2669
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Plasma cell neoplasm is a common hematologic malignancy. Treatment with novel agents results in favorable outcomes. Reliable investigations are required to monitor the residual disease, especially after such effective treatments. Flow cytometric analysis is a speedy and accurate method to detect abnormal cells. The aim of this study was to determine diagnostic performance of flow cytometry in the detection of abnormal plasma cells in bone marrow specimens. MATERIALS AND METHODS: We included bone marrow samples taken from patients suspected to harbor plasma cell neoplasm at the time of diagnosis or follow-up after treatment from 2013 to 2015. Flow cytometric analyses, using cluster of differentiation (CD)19/CD20/CD27/CD38/CD45/CD56/CD117/CD138 and cytoplasmic κ/λ, were done and results compared with morphologic evaluation of marrow aspirate smear, histology, and immunohistochemistry of marrow biopsy and protein electrophoretic analyses. RESULTS: A total of 154 specimens were included. Plasma cell neoplasm was detected in 56 samples (36.4%). Most abnormal plasma cells in this study were CD19-negative (CD19(-))/CD20(-)/CD27(+)/CD38(+)/CD45(-) (or weakly positive)/CD56(+)/CD117(+)/CD138(+). Light chain restriction was found only in 18 samples (32.1%). Sensitivity and specificity of flow cytometric analysis were 91.1% and 96.9%, respectively. For the follow-up cohort, sensitivity and specificity were 86.7% and 66.7%, respectively. CONCLUSION: Analysis of plasma cell neoplasm using flow cytometry has high sensitivity and specificity. As an adjunct to marrow histology and immunohistochemistry, flow cytometry can be used in diagnosis of plasma cell neoplasm and more importantly in monitoring the disease after treatment. We propose a limited panel of CD19/CD38/CD45/CD56/CD117/CD138 for detecting minimal residual disease in Thai patients.
[Mh] Termos MeSH primário: Células da Medula Óssea/metabolismo
Medula Óssea/patologia
Citometria de Fluxo
Neoplasias de Plasmócitos/diagnóstico
Neoplasias de Plasmócitos/metabolismo
[Mh] Termos MeSH secundário: Idoso
Idoso de 80 Anos ou mais
Biomarcadores
Biópsia
Células da Medula Óssea/patologia
Feminino
Citometria de Fluxo/métodos
Seres Humanos
Imunofenotipagem
Masculino
Meia-Idade
Reprodutibilidade dos Testes
Sensibilidade e Especificidade
Tailândia
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Biomarkers)
[Em] Mês de entrada:1612
[Cu] Atualização por classe:161230
[Lr] Data última revisão:
161230
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160123
[St] Status:MEDLINE



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