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1.
Hematol., Transfus. Cell Ther. (Impr.) ; 44(4): 497-503, Oct.-dec. 2022. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1421520

RESUMO

ABSTRACT Introduction: People living with human immunodeficiency virus (PLWH) still face high morbidity and mortality resulting from lymphoma. Aim: To describe a population of PLWH and lymphoma in a Chilean public hospital and compare the overall survival (OS) with a previously reported cohort from the same institution. Methods: Retrospective single-center cohort study. All the patients diagnosed between 2010 and 2017 were included. Demographic and clinical variables were obtained from medical records. The overall survival (OS) was estimated in treated patients from diagnosis until death or October 2020. The OS was then compared with a cohort of patients diagnosed between 1992 and 2008. Main Results: Eighty-four patients were included. The most common histological types were Burkitt's lymphoma (BL), diffuse large B-cell lymphoma (DLBCL), Hodgkin's lymphoma (HL) and plasmablastic lymphoma (PBL) at 31%, 27%, 21% and 14%, respectively. The three-year OS for the whole cohort of BL, DLBCL, HL and PBL was 58.9%, 65.2%, 47.4%, 76.4% and 50%, respectively. Compared to the cohort of 1992 to 2008, a global increase in the OS was found after excluding HL and adjusting for age and clinical stage (HR 0.38, p = 0.002). However, when the main types were analyzed individually, the increase in the OS was statistically significant only in DLBCL (HR 0.29, p = 0.007). Most patients with DLBCL received CHOP chemotherapy, as in the previous cohort. Conclusion: The OS has improved in this population, despite no major changes in chemotherapy regimens, mainly due to the universal access to antiretroviral therapy.


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Idoso , Adulto Jovem , Linfoma Difuso de Grandes Células B , Linfoma de Burkitt , Síndrome de Imunodeficiência Adquirida , Linfoma Plasmablástico , Prognóstico , Sobrevida , Doença de Hodgkin , Estudos de Coortes
2.
Rev. colomb. gastroenterol ; 37(2): 233-236, Jan.-June 2022. graf
Artigo em Inglês | LILACS | ID: biblio-1394955

RESUMO

Abstract Introduction: Primary tumors of the anal canal other than carcinomas are rare entities; among them, anal canal lymphomas are extremely unusual and pose both a diagnostic and therapeutic challenge for the coloproctologist. Case presentation: A male patient with positive human immunodeficiency virus (HIV) with proctalgia and mass sensation at the perianal level. A concentric thickening of the walls of the lower rectum was documented by magnetic resonance imaging, with colonoscopy and biopsies with histopathology compatible with plasmablastic lymphoma. Therefore, a diverting colostomy was performed and, subsequently, the hematology service indicated chemotherapy with the EPOCH scheme. Discussion: Lymphoma of the anus represents 0.2 % of anorectal tumors, most of these are non-Hodgkin's lymphomas; Hodgkin's disease at the anorectal level is even rarer. The population with the highest risk of this entity is HIV-positive patients, such as the patient in this case, although other associated factors are described in the literature.


Resumen Introducción: los tumores primarios del canal anal diferentes a carcinomas son entidades poco frecuentes; dentro de estos, los linfomas del canal anal son extremadamente raros y generan un reto tanto diagnóstico como terapéutico para el coloproctólogo. Presentación de caso: se presenta a continuación un caso clínico de un paciente con virus de inmunodeficiencia humana (VIH) positivo con proctalgia y sensación de masa a nivel perianal, se documentó por resonancia magnética un engrosamiento concéntrico de las paredes del recto inferior, con realización de colonoscopia y biopsias con histopatología compatible con linfoma plasmablástico, por lo que se realizó una colostomía derivativa y, posteriormente, se indicó por el servicio de hematología una quimioterapia con esquema EPOCH. Discusión: el linfoma de ano representa el 0,2 % de los tumores anorrectales, la mayoría de estos corresponde a linfomas no Hodgkin, y es aún más rara la enfermedad de Hodgkin a nivel anorrectal. La población con mayor riesgo de presentar esta entidad es los pacientes con VIH positivo, como el paciente descrito en el caso, aunque existen otros factores asociados descritos en la literatura.


Assuntos
Humanos , Masculino , Adulto , Neoplasias do Ânus/patologia , Linfoma Plasmablástico/patologia , Neoplasias do Ânus/diagnóstico , Biópsia , Linfoma Plasmablástico/diagnóstico
3.
An. bras. dermatol ; 92(5,supl.1): 110-112, 2017. graf
Artigo em Inglês | LILACS | ID: biblio-887095

RESUMO

Abstract Plasmablastic lymphoma is a non-Hodgkin lymphoma characterized by its plasmacytic differentiation and predilection for the oral cavity. It is among the lymphomas most commonly associated with AIDS. This report details a case of a HIV-positive patient with a 1-month history of an exophytic mass in the gingival area of the upper left quadrant. The diagnosis of plasmablastic lymphoma was made based on its histopathological and immunophenotypical features. She was treated with chemotherapy followed by autologous hematopoietic stem cell transplantation. Despite complete resolution of the lesion, the patient died of cardiorespiratory arrest. This case illustrates plasmablastic lymphoma as the first clinical manifestation of AIDS, highlighting the importance of differentiating between a potentially malignant lesion and other pathologic processes.


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Neoplasias Bucais/patologia , Neoplasias Bucais/virologia , Linfoma Relacionado a AIDS/patologia , Linfoma Plasmablástico/patologia , Linfoma Plasmablástico/virologia , Biópsia , Neoplasias Bucais/terapia , Imuno-Histoquímica , Síndrome de Imunodeficiência Adquirida/complicações , Síndrome de Imunodeficiência Adquirida/patologia , Linfoma Relacionado a AIDS/terapia , Linfoma Plasmablástico/terapia
4.
An. bras. dermatol ; 91(4): 507-509, July-Aug. 2016. graf
Artigo em Inglês | LILACS | ID: lil-792436

RESUMO

Abstract: Plasmablastic lymphoma is a rare subtype of diffuse large B-cell lymphoma more frequently diagnosed in immunosuppressed patients, mainly HIV-infected. Primary cutaneous plasmablastic lymphoma is extremely rare, and in this patient it was the first clinical manifestation of unsuspected HIV-infection.


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Neoplasias Cutâneas/patologia , Neoplasias Cutâneas/virologia , Infecções por HIV/patologia , Linfoma Relacionado a AIDS/patologia , Linfoma Plasmablástico/patologia , Linfoma Plasmablástico/virologia , Pele/patologia , Biópsia , Infecções por HIV/complicações
5.
Arch. argent. pediatr ; 114(2): e95-e99, abr. 2016. ilus
Artigo em Espanhol | LILACS, BINACIS | ID: biblio-838191

RESUMO

El linfoma plasmablástico es un subtipo raro y agresivo de linfoma no Hodgkin de células grandes B, descrito inicialmente en la cavidad oral de adultos varones con enfermedad por virus de inmunodeficiencia humana/síndrome de inmunodeficiencia adquirida. Se compone de una proliferación de células neoplásicas que se asemejan a los inmunoblastos, pero presentan inmunofenotipo característico de célula plasmática e infección latente por el virus de Epstein-Barr. En la población pediátrica, es una entidad excepcional. Presentamos el caso de una niña de 5 años de edad, con enfermedad por virus de inmunodeficiencia humana / síndrome de inmunodeficiencia adquirida de transmisión vertical con linfoma plasmablástico de cavidad oral.


Plasmablastic lymphoma is a rare and aggressive subtype of diffuse large B cell non-Hodgkin lymphoma, originally described in the oral cavity of male adults with acquired immune deficiency syndrome. It is composed of neoplastic ceils which resemble immunoblasts but present immunophenotype distinctive of plasma cell and Epstein-Barr virus latent infection. In children, it is an even rarer disease. We present a case of oral plasmablastic lymphoma in a vertically transmitted human immunodeficiency virus-positive five-year-old child.


Assuntos
Humanos , Feminino , Pré-Escolar , Soropositividade para HIV , Linfoma Plasmablástico/diagnóstico
6.
Int. arch. otorhinolaryngol. (Impr.) ; 19(4): 354-358, Oct.-Dec. 2015. ilus
Artigo em Inglês | LILACS | ID: lil-768335

RESUMO

Introduction Plasmablastic lymphoma is a rare entity that was first described in the jaws and the oral cavity of patients with human immunodeficiency virus (HIV) and acquired immunodeficiency syndrome (AIDS). Plasmablastic lymphoma is considered as a diffuse, large, B-cell lymphoma with a unique phenotype and a predilection for the oral cavity. Objectives The authors describe a case of an aggressive plasmablastic lymphoma of the oral cavity as the primary manifestation of AIDS. Resumed We report a case of plasmablastic lymphoma involving only the oral cavity as the first manifestation of AIDS. Diagnosis was confirmed by the oral lesion biopsy and the histopathologic examination that showed a dense infiltrate composed of atypical lymphocytes with numerous plasmocytes that expressed the plasma cell markers MUM-1 and CD138 and that were negative for the B-cell markers CD3, CD20, and CD45. Immunohistochemical and in situ hybridization revealed the Epstein-Barr virus genome in the atypical cells. Polymerase chain reaction was also positive for human herpesvirus-8 RNA. Conclusion The HIV serologic status should be evaluated in all patients with plasmablastic lymphoma of the oral cavity or extraoral sites.(AU)


Assuntos
Humanos , Masculino , Adulto , Síndrome de Imunodeficiência Adquirida , HIV , Linfoma Plasmablástico , Manifestações Bucais
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