Search

Summary: Management of classical Hodgkin lymphoma in older patients is challenging due to poor tolerance of the chemotherapy regimens used in younger patients. We modified the BEACOPP regimen (bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine and prednisolone), whereby bleomycin and etoposide were removed and cyclophosphamide dose was reduced, for older patients with co‐morbidities. Here we present data from the first 41 patients treated with 'ACOPP' across 3 centres, demonstrating that it can be delivered, with a favourable toxicity profile (TRM 2%) and promising efficacy (2‐year PFS and OS, 73% (95% CI: 52–94) and 93% (95% CI: 80–100) respectively). [ABSTRACT FROM AUTHOR]

The article discusses a guideline compiled by the British Society for Haematology (BSH) for the management of mantle cell lymphoma (MCL). Topics covered include first line management for early stage and advanced stage MCL as well as indications for treatment, how to determine patients fit for autologous stem cell transplant, and therapeutic algorithm for alternative immunochemotherapy, Bruton tyrosine kinase (BTK) inhibitor or other targeted therapy.

The article discusses the diagnosis and investigation of patients with mantle cell lymphoma (MCL. Topics covered include the latest information on molecular pathology, the use of positron emission tomography/computed tomography (PET/CT) scanning in staging and response assessment, and biological prognostic factors of MCL.

The article discusses the Safety and diagnostic yield of splenic core biopsy and discusses an approach using combined Haematology/Radiology assessment in a tertiary referral centre. Topics include how the core biopsy of the spleen is performed less often than in other solid organs due to a perceived increased risk of post-procedure haemorrhage.

The article offers guidelines for the management and investigation of nodular lymphocyte predominant Hodgkin lymphoma(NLPHL) disease. Topics discussed include transformation of NLPHL into diffuse large B-cell lymphoma (DLBCL), imagine and evaluation related to pretreatment of disease, and management of early stage and advance stage NLPHL with radiotherapy, rituximab monotherapy, and combined modality therapy.

The article discusses a study which identified a series of 5 consecutive patients presenting with hypomegakaryocytic thrombocytopenia (HMT) and low-to-intermediate risk myelodysplastic syndrome (MDS). Topics covered include the clinical characteristics of patients, the role of immune dysregulation in the pathophysiology of MDS, and the response of patients to ciclosporin (CsA) therapy.

Central nervous system relapse of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma There was no evidence of systemic disease on computed tomography (CT) imaging and therefore a diagnosis of primary cutaneous CD8 SP + sp aggressive epidermotropic cytotoxic T-cell lymphoma was made. Cutaneous CD8 SP + sp T-cell lymphoma is a rare and aggressive lymphoma. [Extracted from the article]

GLO:1XW/01may20:bjh16464-fig-0001.jpg PHOTO (COLOR): . gl A 32-year-old male with a history of stage 1A nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) treated four years previously with radiotherapy presented with weight loss. Contrast computed tomography (CT) of neck, thorax, abdomen and pelvis demonstrated widespread small-volume lymphadenopathy and 17-cm splenomegaly. Bone marrow trephine biopsy sections showed a hypercellular marrow with numerous large paratrabecular lymphoid aggregates. [Extracted from the article]

Contrast magnetic resonance imaging (MRI) of brain and spinal cord demonstrated abnormal thickening and leptomeningeal enhancement of all visible cranial nerves, most striking in cranial nerves III (top left) and V (top right). Whilst leptomeningeal involvement can occur synchronously with primary central nervous system lymphoma, or as a feature of relapsed systemic lymphoma, isolated primary leptomeningeal lymphoma with no parenchymal lesions is extremely rare. MRI with contrast is often the only imaging modality that demonstrates meningeal enhancement and should be used in combination with CSF analysis to confirm the diagnosis. [Extracted from the article]

A 35-year-old man was referred after thrombocytopenia was detected at occupational health screening. Full blood count showed Hb 154 g/l, WBC 6 x 10 SP 9 sp /l, platelet count 94 x 10 SP 9 sp /l, mean platelet volume 14 fl (normal range [NR] 7-11). Haemolytic anaemia may occur due to incorporation of phytosterols into red cell membranes causing stomatocytosis and reduced red cell deformability and survival. [Extracted from the article]

The article focuses on a 74-year-old man with weight loss, fatigue, and fever who was suspected with an infective or inflammatory aetiology. It says that the patient's brain imaging with magnetic resonance imaging (MRI) showed features of small vessel disease. It mentions that intravascular lymphoma is an aggressive subtype of diffuse B-cell lymphoma (IVL). Meanwhile, the clinical images of abnormal cells, reticulin stain, and abnormal lymphoid cells are presented.

The article presents a case of a 50-year-old female with a history of coeliac disease, who was presented with an acute jejunal perforation. The histology has revealed a high grade T-cell lymphoma on a background of coeliac disease, the Enteropathy associated T-cell lymphoma (EATCL). The magnetic resonance imaging (MRI) small bowel studies have been used for the treatment of the patient.

The article presents a case study of a 74-year-old man with B-cell chronic lymphocytic leukemia and anemia, who was treated with intravenous bendamustine and was admitted to hospital with fatigue. computerized tomography (CT) scan had shown no significant lymphadenopathy or renal disorders. Full blood count showed pancytopenia and Non-contrast CT imaging showed dilatation of the collecting systems of both kidneys and perinephric stranding bilaterally.

A case study of neutrophil-specific granule deficiency (NSGD) is presented. The patient was a 25-year-old male who was referred for further investigation of chronic neutropenia, monocytosis and recurrent bacterial infections from an early age. An automated full blood count showed normal hemoglobin, white blood cell and platelet count and an apparent neutropenia and monocytosis. A blood film showed neutrophils with reduced granulation and incomplete nuclear segmentation with some bilobed forms.

The article presents a case study of a 23-year-old patient with lymphadenopathy which affects his groins and axillae for 12 months. The patient underwent urea and electrolytes, lactate dehydrogenase, and blood count investigation with normal results as well as excision biopsy of a groin node. It was found out that the disease was a reaction from a tattoo pigment that undergone lymphatic migration due to the reaction generated by tattoo inks which are made from iron and mercury compounds.

The article discusses the role of positron emission tomography (PET) in the management of Hodgkin lymphoma (HL).

The article presents the case study of a 73 year old woman suffering from acute myeloid leukemia (AML) with several short histories including spontaneous bruising, petechiae and rectal bleeding. It presents the images of the blood film of the woman which shows granular myeloblasts with large nuclear indentations. It discusses that the Immunophenotyping confirmed AML but the blasts were found negative for CD34 and HLA-DR. It further discusses the AML with cup like blasts and its characteristics.