Multi-Organ Failure as the Initial Presentation of Lymphocyte-Depleted Hodgkin Lymphoma in Two Patients with Human Immunodeficiency Virus.

Abstract:

:Patients with HIV-associated lymphocyte-depleted Hodgkin lymphoma (HIV-HL) often present with advanced, extranodal disease and aggressive clinical features, limiting definitive therapeutic intervention. Here we report two patients with HIV-HL who presented with multi-organ dysfunction as an initial manifestation of their malignancy. Both were initially treated with brentuximab vedotin (BV), which led only to a temporary partial response, highlighting the challenges of treatment. One patient was eventually started on nivolumab and responded very well to the immune checkpoint inhibitor. To our knowledge, this is the first case to describe successful use of nivolumab in a patient with relapsed lymphocyte-depleted HIV-HL. Prompt recognition of multi-organ dysfunction as an initial presentation of lymphocyte-depleted HIV-HL is essential to ensure rapid provision of therapy. While use of BV remains a reasonable option, earlier introduction of immunotherapy in the treatment of HL may provide an additional option in critically ill patients with lymphocyte-depleted HIV-HL.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Ding J,Kumar AJ,Wilding E,Lee ST,Law JY

doi

10.1159/000500222

subject

Has Abstract

pub_date

2020-01-01 00:00:00

pages

184-188

issue

2

eissn

0001-5792

issn

1421-9662

pii

000500222

journal_volume

143

pub_type

杂志文章
  • Initial clonal acute lymphoblastic transformation of chronic lymphocytic leukemia with (11;14) and (8;12) chromosome translocations and acquired homozygosity.

    abstract::A 69-year-old woman presented with chronic lymphocytic leukemia (CLL) diagnosed after bone marrow recovery following intensive chemotherapy for acute lymphoblastic leukemia. The retrospective diagnosis of initial blastic transformation of CLL was made. The patient eventually died, 5 months after initial blastic phase,...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205751

    authors: Archimbaud E,Charrin C,Gentilhomme O,Rimokh R,Guyotat D,Fiere D,Germain D

    更新日期:1988-01-01 00:00:00

  • In vivo models of thrombogenic potential: usefulness and limitations.

    abstract::The thrombogenicity of prothrombin complex concentrates (PCCs) has been known as a risk factor since their first clinical use about 30 years ago. The development of in vivo models to define the thrombogenic components in PCCs was instrumental in providing a logical basis for selecting in vitro assays to screen for the...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000204039

    authors: MacGregor I,McLaughlin L,Drummond O,Prowse C,Ferguson J

    更新日期:1995-01-01 00:00:00

  • Transfer of iron-dextran across the placenta.

    abstract::In pregnant mice. 55Fe-labeled iron-dextran (Imferon) is transferred across the placenta. It was detected in the bone marrow, liver, spleen and peripheral blood of the pregnant animal, as well as in the embryonic liver erythroid precursors and peripheral blood. Uptake by liver and peripheral blood cells of pregnant an...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208195

    authors: Djaldetti M,Notti I,Fishman P,Bessler H

    更新日期:1975-01-01 00:00:00

  • Thalassemia major and sickle cell disease in adolescents and young adults.

    abstract::The increased longevity of patients with thalassemia and sickle cell disease (SCD) introduces new clinical challenges due to the accumulation of disease-related morbidity, psychosocial issues and health care adjustments. Patients with thalassemia major now live into adulthood without suffering heart failure but must c...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000360235

    authors: Yacobovich J,Tamary H

    更新日期:2014-01-01 00:00:00

  • Clinical Benefit Derived from Decitabine Therapy for Advanced Phases of Myeloproliferative Neoplasms.

    abstract::Treatment options are limited for patients with advanced forms of myeloproliferative neoplasms (MPN) including blast-phase disease (MPN-BP). Decitabine has frequently been deployed but its efficacy and safety profile are not well described in this population. We retrospectively reviewed 42 patients treated with decita...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000506146

    authors: Zhou S,Tremblay D,Hoffman R,Kremyanskaya M,Najfeld V,Li L,Moshier E,Mascarenhas J

    更新日期:2021-01-01 00:00:00

  • Perls Stain Grade in Bone Marrow Aspirate Correlates with Overall Survival in Low-Risk Myelodysplastic Patients.

    abstract::Low-risk patients with myelodysplastic syndromes (MDS) are inclined to long-term accumulation of iron in the organs due mostly to red blood cell transfusion and ineffective erythropoiesis. The effect of free toxic iron species in the liver and heart sites is well known, but recent knowledge assumes that oxidant-mediat...

    journal_title:Acta haematologica

    pub_type: 新闻

    doi:10.1159/000510111

    authors: Pilo F,Caocci G,Mele G,La Nasa G

    更新日期:2020-10-02 00:00:00

  • Predictive factors for cure after immunosuppressive therapy of aplastic anemia.

    abstract::In a previous study, we evaluated efficacy of repeated antilymphocyte globulin (ALG) treatment for patients with severe aplastic anemia not responding to an initial ALG treatment or relapsing after initial response to ALG. We now searched in the same cohort of patients for differences between patients who responded to...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000041005

    authors: Viollier R,Tichelli A

    更新日期:2000-01-01 00:00:00

  • Changes in peripheral blood mononuclear cell subpopulations during antithymocyte globulin therapy for severe aplastic anemia.

    abstract::The short-term effect of a domestically produced equine antithymocyte globulin (ATG) was analyzed in 6 patients with acquired severe aplastic anemia (AA). All patients received 5 doses of ATG every other day in a 60-min intravenous infusion. Five peripheral blood immunoregulatory mononuclear cell (MNC) subsets, define...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1159/000205557

    authors: López-Karpovitch X,Zarzosa ME,Cárdenas MR,Piedras J

    更新日期:1989-01-01 00:00:00

  • Phagocytic activity of leukaemic blasts.

    abstract::Phagocytic activity of leukaemic blasts in 20 adults and 16 children suffering from acute leukaemia was studied in vitro by the use of ferrioxidsaccharate. Most frequently phagocytosing blasts were encountered in myelomonocytic leukaemias. The morphological character of positive blasts resembled often that of monocyto...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208150

    authors: Neuwirtová R,Setková O,Housková J,Poch T,Dorazilová V,Donner L

    更新日期:1975-01-01 00:00:00

  • A CD5+ leukemic lymphoma with monocytoid features: an unusual B-cell lymphoma mimicking hairy-cell leukemia.

    abstract::A case of lymphoma presenting with features shared by hairy cell leukemia (HCL) and its variant, intermediate lymphocytic lymphoma (ILL) and monocytoid B-cell lymphoma (MBCL) is described. Clinical presentation and the morphological findings observed in peripheral blood and in bone marrow biopsy suggested an HCL; howe...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204496

    authors: Adami F,Chilosi M,Lestani M,Scarpa A,Zambello R,Pomponi F,Semenzato G,Menestrina F

    更新日期:1993-01-01 00:00:00

  • Angioimmunoblastic lymphadenopathy with dysproteinemia: emphasis on pathogenesis and treatment.

    abstract::Angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) is a rare lymphoproliferative disorder characterized by diffuse lymphadenopathy, fever, hepatosplenomegaly, hemolytic anemia, and polyclonal hypergammaglobulinemia. Morphologically, the involved lymph nodes demonstrate complete effacement of the normal arch...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000040811

    authors: Sallah S,Gagnon GA

    更新日期:1998-01-01 00:00:00

  • Transmission and scanning electron microscopy study on congenital dyserythropoietic anemia type I.

    abstract::An ultrastructural study of the aspirated bone marrow of a patient with congenital dyserythropoietic anemia type I is presented. Both in transmission electron microscopy (TEM) and in scanning electron microscopy (SEM) ultrastructural abnormalities of the bone marrow erythroid precursors were seen. These abnormalities ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206735

    authors: Conde E,Mazo E,Baro J,Lafarga M,Cuadrado MA,Recio M,Zubizarreta A

    更新日期:1983-01-01 00:00:00

  • Temporal response of murine pluripotent stem cells and myeloid and erythroid progenitor cells to low-dose glucan treatment.

    abstract::B6D2F1 female mice were intravenously administered 0.4 mg of glucan. 1, 5, 11, and 17 days later, the total nucleated cellularity (TNC) and the numbers of pluripotent hemopoietic stem cells (CFU-s), granulocyte-macrophage progenitor cells (GM-CFC), and erythroid colony-forming (CFU-e) and burst-forming (BFU-e) cells w...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206753

    authors: Patchen ML,MacVittie TJ

    更新日期:1983-01-01 00:00:00

  • Essential thrombocythemia terminating in acute leukemia with minimal myeloid differentiation--a brief review of recent literature.

    abstract::Essential thrombocythemia (ET), one of the chronic myeloproliferative disorders, is a clonal disorder of multipotent stem cells. Although most patients with ET have a prolonged benign course, a minority of patients may develop a blastic crisis similar to chronic myelogenous leukemia (CML). A case of ET terminating in ...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000204260

    authors: Shibata K,Shimamoto Y,Suga K,Sano M,Matsuzaki M,Yamaguchi M

    更新日期:1994-01-01 00:00:00

  • Mediastinal bulky tumour in Hodgkin's disease and prognostic value of positron emission tomography in the evaluation of post-treatment residual masses.

    abstract::Among the 193 patients (82 female, 111 male) treated primarily for Hodgkin's disease at our clinic between 1990 and 2001 and followed up until 2003, 42 (22%) had mediastinal bulky tumours (MBTs) by the Cotswolds criteria. The rate of MBT diagnosis was significantly greater in the early stage of the disease, these pati...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000081271

    authors: Keresztes K,Lengyel Z,Devenyi K,Vadasz G,Miltenyi Z,Illes A

    更新日期:2004-01-01 00:00:00

  • Monocytoid B cell lymphoma associated with antibodies to myelin-associated glycoprotein and sulphated glucuronyl paragloboside.

    abstract::Monocytoid B cell lymphoma (MBCL) is an immunologically and morphologically well-defined low-grade lymphoma with a predilection for lymph nodes of the parotid region. We describe an association of MBCL with anti-myelin-associated glycoprotein (MAG) polyneuropathy in a 53-year-old male. The diagnosis of stage IV MBCL w...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000046603

    authors: Donfrid M,Apostolski S,Suvajdzić N,Janković G,Cemerikić-Martinović V,Atkinson HD,Colovic M

    更新日期:2001-01-01 00:00:00

  • Relationship of lymphocyte anisocytosis in chronic lymphatic leukaemia to mouse red cell rosetting capacity and clinical stage.

    abstract::In 34 patients with chronic lymphatic leukaemia (CLL) the lymphocytes have been separated and sized using a C1000 Channelyzer. The modal volume and the volume range of the populations have been obtained and related to clinical stage and mouse red blood cell (MRBC) rosetting capacity. Over 1 year's observation with sev...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206714

    authors: Wastell HJ,Proctor SJ

    更新日期:1983-01-01 00:00:00

  • Bone marrow histological modifications induced by alpha interferon in hairy cell leukemia.

    abstract::This paper reports the bone marrow histological picture in 7 patients with hairy cell leukemia treated with recombinant interferon. Bone marrow biopsies were performed at diagnosis, after 1, 3 and 7 months from the beginning of treatment and at 12 months at treatment suspension. The main modifications observed were a ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205996

    authors: Lambertenghi-Deliliers G,Benazzi E,Cortelezzi A,Polli EE

    更新日期:1987-01-01 00:00:00

  • Benign Bence Jones gammopathy.

    abstract::A case of isolated lambda-light chain proteinemia and proteinuria is reported. During a 42-month follow-up, no sign of myelomatosis or amyloidosis developed and Bence Jones proteinuria remained nearly of the same magnitude. This case of apparently idiopathic Bence Jones gammopathy, the first lambda-type so far reporte...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207409

    authors: Paladini G,Sala PG,Santini PA

    更新日期:1980-01-01 00:00:00

  • Clinical Management of Posterior Reversible Encephalopathy Syndrome after Allogeneic Hematopoietic Stem Cell Transplantation: A Case Series and Review of the Literature.

    abstract:BACKGROUND:Posterior reversible encephalopathy syndrome (PRES) is a rare but serious complication after allogeneic hematopoietic stem cell transplantation (alloHSCT). Among others, calcineurin inhibitors (CNI) for prophylaxis of graft-versus-host disease (GvHD) may promote the development of PRES, but the pathomechanis...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000430489

    authors: Schmidt V,Prell T,Treschl A,Klink A,Hochhaus A,Sayer HG

    更新日期:2016-01-01 00:00:00

  • New cell line from hairy-cell leukaemia producing interleukin-6 after Epstein-Barr virus immortalization.

    abstract::A hairy-cell leukaemia (HCL) cell line, HCL-O, was established from the peripheral blood of a 62-year-old Japanese patient with a unique variant of HCL strongly expressing CD21, the receptor for the Epstein-Barr virus (EBV). The HCL-O cells expressed antigens similar and dissimilar to those expressed with the original...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204129

    authors: Tokioka T,Shimamoto Y,Nagumo F,Tadano J,Yamaguchi M

    更新日期:1994-01-01 00:00:00

  • Infections in hematogical cancer patients: the contribution of systematic reviews and meta-analyses.

    abstract::Systematic reviews and meta-analyses have made a major contribution to the evidence-based management of infections in cancer patients. We review the contribution of systematic reviews with regard to antibiotic, antifungal, antiviral and Pneumocystis pneumonia prophylaxis; antibiotic and antifungal treatment of febrile...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000318900

    authors: Paul M,Gafter-Gvili A,Goldberg E,Yahav D

    更新日期:2011-01-01 00:00:00

  • Characterization of a diester lipase activity in human erythrocytes.

    abstract::A diester lipase activity is described in human red blood cells (RBC). Diester lipase activity acts as a membrane-bound enzyme and is assayed using intact RBC as the enzyme source. An emulsion of di-[3H]-oleoylglycerol (0.6 mM) serves as the substrate. The optimum pH for the reaction is 7.8 at 37 degrees C. Lipolytic ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206770

    authors: Somma C,Arnaud J,Boyer J

    更新日期:1983-01-01 00:00:00

  • Polymorphism of foetal haemoglobin in the Sardinian beta +-thalassaemia.

    abstract::12 thalassaemic patients from Northern Sardinia showing the beta + phenotype were examined by isoelectric focusing and high-performance liquid chromatography techniques for the determination of the variant A gamma T globin chain of the foetal haemoglobin. Two patients (16.7%) were homozygotes for the A gamma T gene va...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206057

    authors: Masala B,Formato M,Manca L,Demuro P,Gallisai D,Dore F,Longinotti M

    更新日期:1986-01-01 00:00:00

  • Chronic inflammatory bowel disease, deep-venous thrombosis and antithrombin activity.

    abstract::Of 34 patients with chronic inflammatory bowel disease (CIBD), 4 developed well-documented episodes of deep-venous thrombosis. All 4 patients had active disease at the time of thrombosis. This group was studied to determine if the tendency to deep-venous thrombosis in patients with CIBD was associated with reduced ant...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206688

    authors: Ghosh S,Mackie MJ,McVerry BA,Galloway M,Ellis A,McKay J

    更新日期:1983-01-01 00:00:00

  • Marrow suppression produced by repeated doses of cladribine.

    abstract::2-Chlorodeoxyadenosine (cladribine, Leustatin) is being used extensively in the treatment of hematologic malignancies, but relatively little is known regarding its toxicity to the normal marrow. Long-term serial hematologic observations have been made on 29 patients with multiple sclerosis undergoing experimental ther...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000204236

    authors: Beutler E,Koziol JA,McMillan R,Sipe JC,Romine JS,Carrera CJ

    更新日期:1994-01-01 00:00:00

  • The effect of dietary habits and socioeconomic status on the prevalence of iron deficiency in children of northern Greece.

    abstract:BACKGROUND:Despite encouraging reports concerning the declining prevalence of iron deficiency, this easily preventable disorder is still an existing problem in presumably developed regions. OBJECTIVE:To evaluate the prevalence of iron deficiency and relevant anemia in children residing in Northern Greece and to study ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000098273

    authors: Gompakis N,Economou M,Tsantali C,Kouloulias V,Keramida M,Athanasiou-Metaxa M

    更新日期:2007-01-01 00:00:00

  • Cytochemical method for demonstrating magnesium-activated adenosine triphosphatase in haemic cells.

    abstract::A modified cytochemical method was developed for demonstrating magnesium-activated adenosine triphosphatase in haemic cells. The enzyme was shown in a variety of normal and leukaemic, unfixed cells. The high sensitivity of this enzyme to all fixatives tried in this study hampered further exploration and characterizati...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205983

    authors: Khalaf MR,Hayhoe FG

    更新日期:1987-01-01 00:00:00

  • Serum levels of G-CSF, IL-3, IL-6 and GM-CSF after a single intraperitoneal dose of rhG-CSF in lethally irradiated B6D2F1 mice.

    abstract::The objective of this study was to assess the pharmacokinetics of rhG-CSF after a single intraperitoneal injection 2 h post-TBI in B6D2F1 lethally irradiated mice and to analyze the effect of rhG-CSF on the endogenous response of interleukin-3 (IL-3), interleukin-6 (IL-6) and granulocyte-macrophage colony-stimulating ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203604

    authors: Kádár E,Sureda A,Mangues MA,Inglés-Esteve J,Valls A,García J

    更新日期:1997-01-01 00:00:00

  • Antithrombin III during high-dose cytosine arabinoside therapy with or without asparaginase.

    abstract::Fourteen patients with hematologic neoplasia (11 acute myeloid leukemias, 2 non-Hodgkin's lymphomas and 1 blast crisis of chronic myeloid leukemia) who underwent high-dose cytosine arabinoside (HIDARAC) therapy with or without sequential asparaginase (ASNase) were investigated in order to evaluate liver toxicity and a...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000206094

    authors: Marra R,Pagano L,De Stefano V,Leone G,Bizzi B

    更新日期:1986-01-01 00:00:00