Haematology

Author(s):  
Ian B. Wilkinson ◽  
Tim Raine ◽  
Kate Wiles ◽  
Anna Goodhart ◽  
Catriona Hall ◽  
...  

This chapter presents all aspects of haematology, including the history of haematology, iron-deficiency anaemia, anaemia of chronic disease, sideroblastic anaemia, peripheral blood film, differential white cell count, macrocytic anaemia, B12 deficiency and pernicious anaemia, haemolytic anaemia, sickle-cell anaemia, thalassaemia, bleeding disorders, coagulations pathways, blood transfusion and blood products, anticoagulants, leukaemia and the on-call junior doctor, acute lymphoblastic leukaemia, acute myeloid leukaemia, chronic myeloid leukaemia, chronic lymphocytic leukaemia, Hodgkin’s lymphoma, Non-Hodgkin’s lymphoma, pancytopenia and bone marrow failure, myeloproliferative disorders, myeloma, paraproteinaemia, amyloidosis, erythrocyte sedimentation rate (ESR), plasma viscosity (PV), hyperviscosity syndrome, spleen and splenectomy, thrombophilia, and immunosuppressive drugs.

Author(s):  
Murray Longmore ◽  
Ian B. Wilkinson ◽  
Andrew Baldwin ◽  
Elizabeth Wallin

On the taking of blood and of holidaysAnaemiaIron-deficiency anaemiaAnaemia of chronic diseaseSideroblastic anaemiaThe peripheral blood filmThe differential white cell countMacrocytic anaemiab12 deficiency and pernicious anaemiaAn approach to haemolysisCauses of haemolysisSickle-cell anaemiaThalassaemiaBleeding disorders...


2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Anamika Banerjee ◽  
Kaljit Bhuller ◽  
Rajini Sudhir ◽  
Amrita Bajaj

Abstract Background Hodgkin’s Lymphoma (HL) is a rare malignancy characterised histologically by the presence of Reed-Sternberg cells. Diagnosis of lymphomas can be difficult due to broad, non-specific presentations of disease, which can be similar to several other conditions ranging from infective, inflammatory or malignant causes, with one of the most common differentials being tuberculosis (TB). We aim to highlight the diagnostic dilemma of TB versus lymphoma with an atypical presentation of HL and explored areas for further research and improvement with a non-systematic literature review using MEDLINE database and Google Scholar. Written consent was obtained from the patient in compliance with ethical guidelines. Case presentation A 23-year-old Asian female initially presented to rheumatology with over a one-year history of neuropathic pain, alongside abnormal white cell count and inflammatory markers. This was investigated with magnetic resonance imaging resulting in an incidental finding of mediastinal mass and pulmonary infiltrates. An initial diagnosis of TB was made despite testing negative for acid-fast bacilli and anti-tubercular treatment was commenced. Four months later, following clinical deterioration and further investigations, a mediastinal biopsy assisted in diagnosing Stage IV HL. Conclusions Lymphoma is often misdiagnosed as TB, prolonging time to treatment and may adversely impact patient prognosis due to disease progression. Existing TB guidelines for smear-negative cases are not clear when to consider alternative diagnoses. In smear-negative TB, lymphoma should be considered as a differential and definitive diagnostic tests such as molecular testing and histological examination of biopsies should be considered earlier in the diagnostic work-up to prevent diagnostic delay.


Author(s):  
Toby Eyre

This chapter examines the epidemiology, genetics, clinical presentation, and classification of these diseases and presents current treatment approaches for each. First are the acute leukaemias: acute lymphoblastic leukaemia (ALL) and acute myeloid leukaemia (AML). Chronic myeloid leukaemia and chronic lymphoid leukaemias follow. Hodgkin's lymphoma is described, along with current treatment with chemotherapy and limited radiotherapy. Non-Hodgkin's lymphoma is divided into low-grade and high-grade pathology. Treatments, including chemotherapy and rituximab, are covered. Myeloma and its treatment options are reviewed, including chemotherapy, bisphosphonate therapy, and radiotherapy. Throughout this chapter is emphasized the importance of clinical trials in driving the rapid improvements in treatment of these diseases. Nursing issues related to each disease are covered within each of their specific section.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 2829-2829
Author(s):  
Peter A. Boehringer ◽  
Ming C. Kuan ◽  
Michael W. Peterson

Abstract BACKGROUND More than 4 million people in the United States are chronically infected with hepatitis C virus (HCV) and approximately 800,000 will develop liver cirrhosis or present with several other extrahepatic conditions such as porphyria cutanea tarda, lichen planus, vitiligo, mixed cryoglobulinemia, membranoproliferative glomerulonephritis, and bone marrow hypoplasia. Several studies with relatively small convenience samples of HCV-infected patients seen at referral centers present controversial results regarding the association between HCV infection and B-cell lymphomas. METHODS Using the computerized database of the Department of Veterans Affairs, Fresno, California, we carried out a cross-sectional study to examine whether B-cell non-Hodgkin’s lymphoma (NHL) and other hematologic malignancies might be associated with chronic HCV infection. We examined all cases of chronic HCV infected patients (n=992) diagnosed between 1991 and 2004 and randomly matched control subjects HCV naïve (n=1,929). Demographic Distribuition Cases (n=992) Controls (n=1,929) Alive at enrollment 880 (88.7%) 1,761 (91.3%) Age (years) 53.13 53.14 gender (male) 869 (98.8%) 1,725 (98%) Period of military service (Vietnam Era) 578 (66%) 1,149 (62%) Exposure to Agent Orange 12 (2%) 35 (2%) RESULTS An increased prevalence of hematologic malignancies was found among the chronic HCV infected patients compared to the control group with an odds ratio (OR) of 3.4 (95% confidence interval [95%CI]=1.4–10, p=0.009). The prevalence of NHL (OR=4.2, 95%CI=0.7–22, p=0.1), Hodgkin’s lymphoma (p=0.1), myeloproliferative disorders (OR=4.2, 95%CI=0.7–22, p=0.1), myelodysplastic syndrome (p=0.6) and myeloma (p=0.3) was each independently statistically not significant. The chronic HCV infected group showed a prevalence of 2% for hepatocellular carcinoma (p<0.0001) and had a significantly higher rate of HIV co-infection compared to the control group (OR=6, 95%CI=3–13, p<0.0001). However, none of the chronic HCV and HIV co-infected patients presented a concomitant hematologic malignancy. The overall mortality rate in the chronic HCV infected patients was 11.3% and of the control group 8.7% (OR=1.3, 95%CI=1–1.7, p=0.028). Patients with chronic HCV infection died significantly earlier (mean age 56.7 years) compared to the subjects in the control group (mean age 63.5 years) (p<0.0001). Chronic HCV Infection and Hematologic Malignancies Cases n=880 (%, 95%CI) Controls n=1,761 (%, 95%CI) OR 95%CI p NHL 4 (0.5%, 0.2–1.2) 2 (0.1%, 0.04–0.4) 4.2 0.7–22 0.1 Hodgkin’s lymphoma 2 (0.3%, 0.07–0.8) 0 (0%, 0.001–0.2) - - 0.1 Myeloproliferative disorders 4 (0.5%, 0.2–1.2) 2 (0.1%, 0.04–0.4) 4.2 0.7–22 0.1 Myelodysplastic syndromes 0 (0%, 0.003–0.4) 2 (0.1%, 0.04–0.4) - - 0.6 Multiple Myeloma 1 (0.1%, 0.03–0.6) 0 (0%, 0.001–0.2) - - 0.3 Overall Hematologic Malignancies 11 (1.3%, 0.7–2.2) 6 (0.34%, 0.2–0.7) 3.4 1.4–10 0.009 CONCLUSIONS We report the prevalence of several hematologic malignancies in chronic HCV-infected veterans. Our study suggests that chronic HCV infection is a significant risk factor for lymphatic and stem-cell malignancies. Further larger studies are required to confirm this finding.


2008 ◽  
Author(s):  
Veronica Sanchez Varela ◽  
Sharon Bober ◽  
Andrea Ng ◽  
Peter Mauch ◽  
Christopher Recklitis

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